Article(id=1239268422064853880, tenantId=1146029695717560320, journalId=1205117082300743687, issueId=1239268417962832543, articleNumber=null, orderNo=null, doi=10.14109/j.cnki.xyylc.2024.07.05, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1666800000000, receivedDateStr=2022-10-27, revisedDate=null, revisedDateStr=null, acceptedDate=1711296000000, acceptedDateStr=2024-03-25, onlineDate=1773394216313, onlineDateStr=2026-03-13, pubDate=1721836800000, pubDateStr=2024-07-25, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1773394216313, onlineIssueDateStr=2026-03-13, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1773394216313, creator=13701087609, updateTime=1773394216313, updator=13701087609, issue=Issue{id=1239268417962832543, tenantId=1146029695717560320, journalId=1205117082300743687, year='2024', volume='43', issue='7', pageStart='481', pageEnd='560', issueExtLink='null', onlineDate='null', pubDate='null', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1773394215336, creator=13701087609, updateTime=1773394445099, updator=13701087609, preIssue=null, nextIssue=null, ext={EN=IssueExt(id=1239269381725810851, tenantId=1146029695717560320, journalId=1205117082300743687, issueId=1239268417962832543, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1239269381725810852, tenantId=1146029695717560320, journalId=1205117082300743687, issueId=1239268417962832543, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null}, startPage=510, endPage=513, ext={EN=ArticleExt(id=1239268422945657748, articleId=1239268422064853880, tenantId=1146029695717560320, journalId=1205117082300743687, language=EN, title=A new drug in treating intrahepatic cholangiocarcinoma : FGFR1-4 inhibitor futibatinib, columnId=1239174991388930543, journalTitle=Chinese Journal of New Drugs and Clinical Remedies, columnName=New Drug Introduction, runingTitle=null, highlight=null, articleAbstract=

Intrahepatic cholangiocarcinoma (ICC) is a malignant tumor that occurs in the biliary system, with a hidden onset, poor overall prognosis and high mortality. Futibatinib is a fibroblast growth factor receptor (FGFR) 1-4 inhibitor, which was approved by the U.S. Food and Drug Administration in 2022 for the treatment of adult patients with previously treated, unresectable, locally advanced or metastatic ICC with FGFR2 gene fusions or other rearrangements. Phase Ⅰ and Ⅱ clinical trials have shown that futibatinib has good clinical effect on ICC, which can significantly improve the objective response rate and prolong the survival time of ICC patients. The common adverse events include hyperphosphatemia, diarrhea, constipation, and dry mouth, with a high incidence of adverse events.

, correspAuthors=null, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, authorCompany=null, fund=null, authors=null, authorsList=Pan-pan DI, Xiao-qin XING, Hai LIANG, Shu-yun JIA), CN=ArticleExt(id=1239268423545443257, articleId=1239268422064853880, tenantId=1146029695717560320, journalId=1205117082300743687, language=CN, title=治疗肝内胆管癌新药:泛FGFR抑制剂福巴替尼, columnId=1239174991577674232, journalTitle=中国新药与临床杂志, columnName=新药介绍, runingTitle=null, highlight=null, articleAbstract=

肝内胆管癌(ICC)是一种发生于胆管系统的恶性肿瘤,起病隐匿,患者总体预后较差,死亡率较高。福巴替尼是一种泛成纤维细胞生长因子受体(FGFR)抑制剂,于2022年被美国食品和药物管理局批准上市,用于既往治疗过的、不可切除的局部晚期或转移性且伴有FGFR2基因融合或其他重排的ICC成年患者。Ⅰ期和Ⅱ期临床试验表明,福巴替尼对ICC具有良好的治疗效果,可显著提高ICC患者的客观缓解率并延长患者的生存时间;其常见不良事件包括高磷血症、腹泻、便秘及口干等,不良事件发生率较高。

, correspAuthors=null, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=《中国新药与临床杂志》编辑部, extLink=null, articleAbsUrl=null, sourceXml=CzV0EBJbR8dL2Innvr9/ww==, magXml=G/CxT8PTjYMWomejDBVisA==, pdfUrl=null, pdf=k59Z3aEwSu9ZcfN341yJGw==, pdfFileSize=1791469, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=SxVo2w6/n0SHi+XzgTrjEQ==, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=B5Ky1LhUuje2a5TpQu4vQw==, mapNumber=null, authorCompany=null, fund=null, authors=

狄潘潘,男,主管药师,硕士,主要从事医院药学、数据挖掘与处理的研究,E-mail:

, authorsList=狄潘潘, 邢晓勤, 梁海, 贾淑云)}, authors=[Author(id=1239268423880987601, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, orderNo=0, firstName=null, middleName=null, lastName=null, nameCn=null, orcid=null, stid=null, country=null, authorPic=null, dead=0, email=13285687999@sina.cn, emailSecond=null, emailThird=null, correspondingAuthor=0, authorType=1, ext={EN=AuthorExt(id=1239268423969067993, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, authorId=1239268423880987601, language=EN, stringName=Pan-pan DI, firstName=Pan-pan, middleName=null, lastName=DI, prefix=null, suffix=null, authorComment=null, nameInitials=null, affiliation=null, department=null, xref=null, address=Department of Pharmacy, the Affiliated Bozhou Hospital of Anhui Medical University, Bozhou ANHUI 236800, China, bio=null, bioImg=null, bioContent=null, aboutCorrespAuthor=null), CN=AuthorExt(id=1239268424040371165, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, authorId=1239268423880987601, language=CN, stringName=狄潘潘, firstName=null, middleName=null, lastName=null, prefix=null, suffix=null, authorComment=null, nameInitials=null, affiliation=null, department=null, xref=null, address=安徽医科大学附属亳州医院 药学部,安徽 亳州 236800, bio={"content":"

狄潘潘,男,主管药师,硕士,主要从事医院药学、数据挖掘与处理的研究,E-mail:

"}, bioImg=null, bioContent=

狄潘潘,男,主管药师,硕士,主要从事医院药学、数据挖掘与处理的研究,E-mail:

, aboutCorrespAuthor=null)}, companyList=[AuthorCompany(id=1239268423792907208, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, xref=null, ext=[AuthorCompanyExt(id=1239268423801295817, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, companyId=1239268423792907208, language=EN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=Department of Pharmacy, the Affiliated Bozhou Hospital of Anhui Medical University, Bozhou ANHUI 236800, China), AuthorCompanyExt(id=1239268423813878730, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, companyId=1239268423792907208, language=CN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=安徽医科大学附属亳州医院 药学部,安徽 亳州 236800)])]), Author(id=1239268424141034468, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, orderNo=1, firstName=null, middleName=null, lastName=null, nameCn=null, orcid=null, stid=null, country=null, authorPic=null, dead=0, email=null, emailSecond=null, emailThird=null, correspondingAuthor=0, authorType=1, ext={EN=AuthorExt(id=1239268424266863595, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, authorId=1239268424141034468, language=EN, stringName=Xiao-qin XING, firstName=Xiao-qin, middleName=null, lastName=XING, prefix=null, suffix=null, authorComment=null, nameInitials=null, affiliation=null, department=null, xref=null, address=Department of Pharmacy, the Affiliated Bozhou Hospital of Anhui Medical University, Bozhou ANHUI 236800, China, bio=null, bioImg=null, bioContent=null, aboutCorrespAuthor=null), CN=AuthorExt(id=1239268424346555376, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, authorId=1239268424141034468, language=CN, stringName=邢晓勤, firstName=null, middleName=null, lastName=null, prefix=null, suffix=null, authorComment=null, nameInitials=null, affiliation=null, department=null, xref=null, address=安徽医科大学附属亳州医院 药学部,安徽 亳州 236800, bio=null, bioImg=null, bioContent=null, aboutCorrespAuthor=null)}, companyList=[AuthorCompany(id=1239268423792907208, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, xref=null, ext=[AuthorCompanyExt(id=1239268423801295817, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, companyId=1239268423792907208, language=EN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=Department of Pharmacy, the Affiliated Bozhou Hospital of Anhui Medical University, Bozhou ANHUI 236800, China), AuthorCompanyExt(id=1239268423813878730, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, companyId=1239268423792907208, language=CN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=安徽医科大学附属亳州医院 药学部,安徽 亳州 236800)])]), Author(id=1239268424443024376, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, orderNo=2, firstName=null, middleName=null, lastName=null, nameCn=null, orcid=null, stid=null, country=null, authorPic=null, dead=0, email=null, emailSecond=null, emailThird=null, correspondingAuthor=0, authorType=1, ext={EN=AuthorExt(id=1239268424539493376, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, authorId=1239268424443024376, language=EN, stringName=Hai LIANG, firstName=Hai, middleName=null, lastName=LIANG, prefix=null, suffix=null, authorComment=null, nameInitials=null, affiliation=null, department=null, xref=null, address=Department of Pharmacy, the Affiliated Bozhou Hospital of Anhui Medical University, Bozhou ANHUI 236800, China, bio=null, bioImg=null, bioContent=null, aboutCorrespAuthor=null), CN=AuthorExt(id=1239268424606601223, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, authorId=1239268424443024376, language=CN, stringName=梁海, firstName=null, middleName=null, lastName=null, prefix=null, suffix=null, authorComment=null, nameInitials=null, affiliation=null, department=null, xref=null, address=安徽医科大学附属亳州医院 药学部,安徽 亳州 236800, bio=null, bioImg=null, bioContent=null, aboutCorrespAuthor=null)}, companyList=[AuthorCompany(id=1239268423792907208, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, xref=null, ext=[AuthorCompanyExt(id=1239268423801295817, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, companyId=1239268423792907208, language=EN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=Department of Pharmacy, the Affiliated Bozhou Hospital of Anhui Medical University, Bozhou ANHUI 236800, China), AuthorCompanyExt(id=1239268423813878730, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, companyId=1239268423792907208, language=CN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=安徽医科大学附属亳州医院 药学部,安徽 亳州 236800)])]), Author(id=1239268424673710094, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, orderNo=3, firstName=null, middleName=null, lastName=null, nameCn=null, orcid=null, stid=null, country=null, authorPic=null, dead=0, email=null, emailSecond=null, emailThird=null, correspondingAuthor=0, authorType=1, ext={EN=AuthorExt(id=1239268424786956307, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, authorId=1239268424673710094, language=EN, stringName=Shu-yun JIA, firstName=Shu-yun, middleName=null, lastName=JIA, prefix=null, suffix=null, authorComment=null, nameInitials=null, affiliation=null, department=null, xref=null, address=Department of Pharmacy, the Affiliated Bozhou Hospital of Anhui Medical University, Bozhou ANHUI 236800, China, bio=null, bioImg=null, bioContent=null, aboutCorrespAuthor=null), CN=AuthorExt(id=1239268424858259480, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, authorId=1239268424673710094, language=CN, stringName=贾淑云, firstName=null, middleName=null, lastName=null, prefix=null, suffix=null, authorComment=null, nameInitials=null, affiliation=null, department=null, xref=null, address=安徽医科大学附属亳州医院 药学部,安徽 亳州 236800, bio=null, bioImg=null, bioContent=null, aboutCorrespAuthor=null)}, companyList=[AuthorCompany(id=1239268423792907208, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, xref=null, ext=[AuthorCompanyExt(id=1239268423801295817, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, companyId=1239268423792907208, language=EN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=Department of Pharmacy, the Affiliated Bozhou Hospital of Anhui Medical University, Bozhou ANHUI 236800, China), AuthorCompanyExt(id=1239268423813878730, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, companyId=1239268423792907208, language=CN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=安徽医科大学附属亳州医院 药学部,安徽 亳州 236800)])])], keywords=[Keyword(id=1239268424971505699, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, language=EN, orderNo=1, keyword=intrahepatic cholangiocarcinoma), Keyword(id=1239268425063780392, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, language=EN, orderNo=2, keyword=futibatinib), Keyword(id=1239268425181220910, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, language=EN, orderNo=3, keyword=fibroblast growth factors), Keyword(id=1239268425273495604, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, language=EN, orderNo=4, keyword=antineoplastic agents), Keyword(id=1239268425348993082, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, language=CN, orderNo=1, keyword=肝内胆管癌), Keyword(id=1239268425453850686, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, language=CN, orderNo=2, keyword=福巴替尼), Keyword(id=1239268426502426692, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, language=CN, orderNo=3, keyword=成纤维细胞生长因子), Keyword(id=1239268426586312781, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, language=CN, orderNo=4, keyword=抗肿瘤药)], refs=[Reference(id=1239268427274178675, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, doi=null, pmid=null, pmcid=null, year=2019, volume=39, issue=Suppl 1, pageStart=7, pageEnd=18, url=null, language=null, rfNumber=[1], rfOrder=0, authorNames=KENDALL T, VERHEIJ J, GAUDIO E, journalName=Liver Int, refType=null, unstructuredReference=KENDALL T, VERHEIJ J, GAUDIO E, et al. Anatomical, histomorphological and molecular classification of cholangiocarcinoma[J]. Liver Int, 2019, 39(Suppl 1): 7-18., articleTitle=Anatomical, histomorphological and molecular classification of cholangiocarcinoma, refAbstract=null), Reference(id=1239268427349676152, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, doi=null, pmid=null, pmcid=null, year=2019, volume=39, issue=Suppl 1, pageStart=19, pageEnd=31, url=null, language=null, rfNumber=[2], rfOrder=1, authorNames=KHAN SA, TAVOLARI S, BRANDI G, journalName=Liver Int, refType=null, unstructuredReference=KHAN SA, TAVOLARI S, BRANDI G. Cholangiocarcinoma: epidemiology and risk factors[J]. Liver Int, 2019, 39(Suppl 1):19-31., articleTitle=Cholangiocarcinoma: epidemiology and risk factors, refAbstract=null), Reference(id=1239268427454533755, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, doi=null, pmid=null, pmcid=null, year=2020, volume=17, issue=9, pageStart=557, pageEnd=588, url=null, language=null, rfNumber=[3], rfOrder=2, authorNames=BANALES JM, MARIN JJG, LAMARCA A, journalName=Nat Rev Gastroenterol Hepatol, refType=null, unstructuredReference=BANALES JM, MARIN JJG, LAMARCA A, et al. Cholangiocarcinoma 2020: the next horizon in mechanisms and management[J]. Nat Rev Gastroenterol Hepatol, 2020, 17(9):557-588., articleTitle=Cholangiocarcinoma 2020: the next horizon in mechanisms and management, refAbstract=null), Reference(id=1239268427580362881, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, doi=null, pmid=null, pmcid=null, year=2021, volume=21, issue=1, pageStart=497, pageEnd=null, url=null, language=null, rfNumber=[4], rfOrder=3, authorNames=TAWARUNGRUANG C, KHUNTIKEO N, CHAMADOL N, journalName=BMC Cancer, refType=null, unstructuredReference=TAWARUNGRUANG C, KHUNTIKEO N, CHAMADOL N, et al. Survival after surgery among patients with cholangiocarcinoma in Northeast Thailand according to anatomical and morphological classification[J]. BMC Cancer, 2021, 21(1): 497., articleTitle=Survival after surgery among patients with cholangiocarcinoma in Northeast Thailand according to anatomical and morphological classification, refAbstract=null), Reference(id=1239268427693609093, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, doi=null, pmid=null, pmcid=null, year=2021, volume=10, issue=11, pageStart=2873, pageEnd=null, url=null, language=null, rfNumber=[5], rfOrder=4, authorNames=LAWAL B, KUO YC, TANG SL, journalName=Cells, refType=null, unstructuredReference=LAWAL B, KUO YC, TANG SL, et al. Transcriptomic-based identification of the immuno-oncogenic signature of cholangiocarcinoma for HLC-018 multi-target therapy exploration[J]. Cells, 2021, 10(11): 2873., articleTitle=Transcriptomic-based identification of the immuno-oncogenic signature of cholangiocarcinoma for HLC-018 multi-target therapy exploration, refAbstract=null), Reference(id=1239268427769106566, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, doi=null, pmid=null, pmcid=null, year=null, volume=null, issue=null, pageStart=null, pageEnd=null, url=null, language=null, rfNumber=[6], rfOrder=5, authorNames=FDA, journalName=null, refType=null, unstructuredReference=FDA. Futibatinib tablets, for oral use[EB/OL]. (2022-09-30)[2022-10-22]. https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/214801Orig1s000lbledt.pdf., articleTitle=Futibatinib tablets, for oral use, refAbstract=null), Reference(id=1239268427873964169, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, doi=null, pmid=null, pmcid=null, year=2023, volume=31, issue=2, pageStart=86, pageEnd=null, url=null, language=null, rfNumber=[7], rfOrder=6, authorNames=MERICBERNSTAM F, HOLLEBECQUE A, 赵义军, journalName=肝胆外科杂志, refType=null, unstructuredReference=MERICBERNSTAM F, HOLLEBECQUE A, 赵义军, 等. Futibatinib治疗FGFR2重排肝内胆管癌[J]. 肝胆外科杂志,2023, 31(2): 86., articleTitle=Futibatinib治疗FGFR2重排肝内胆管癌, refAbstract=null), Reference(id=1239268427991404688, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, doi=null, pmid=null, pmcid=null, year=2023, volume=31, issue=2, pageStart=86, pageEnd=null, url=null, language=null, rfNumber=[7], rfOrder=7, authorNames=MERICBERNSTAM F, HOLLEBECQUE A, ZHAO YJ, journalName=J Hepatobiliary Surg, refType=null, unstructuredReference=MERICBERNSTAM F, HOLLEBECQUE A, ZHAO YJ, et al. Futibatinib for FGFR2-rearranged intrahepatic cholangiocarcinoma lipika goyal[J]. J Hepatobiliary Surg, 2023,31(2): 86., articleTitle=Futibatinib for FGFR2-rearranged intrahepatic cholangiocarcinoma lipika goyal, refAbstract=null), Reference(id=1239268428087873683, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, doi=null, pmid=null, pmcid=null, year=2016, volume=22, issue=1, pageStart=259, pageEnd=267, url=null, language=null, rfNumber=[8], rfOrder=8, authorNames=HELSTEN T, ELKIN S, ARTHUR E, journalName=Clin Cancer Res, refType=null, unstructuredReference=HELSTEN T, ELKIN S, ARTHUR E, et al. The FGFR landscape in cancer: analysis of 4 853 tumors by next-generation sequencing FGFR aberrations in cancer[J]. Clin Cancer Res, 2016, 22(1):259-267., articleTitle=The FGFR landscape in cancer: analysis of 4 853 tumors by next-generation sequencing FGFR aberrations in cancer, refAbstract=null), Reference(id=1239268428175954071, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, doi=null, pmid=null, pmcid=null, year=2021, volume=75, issue=1, pageStart=711, pageEnd=719, url=null, language=null, rfNumber=[9], rfOrder=9, authorNames=SZYBOWSKA P, HAUGSTEN EM, WIEDLOCHA A, journalName=Adv Hyg Expe Med, refType=null, unstructuredReference=SZYBOWSKA P, HAUGSTEN EM, WIEDLOCHA A. The canonical FGF-FGFR signaling system at the molecular level[J]. Adv Hyg Expe Med, 2021, 75(1): 711-719., articleTitle=The canonical FGF-FGFR signaling system at the molecular level, refAbstract=null), Reference(id=1239268428259840154, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, doi=null, pmid=null, pmcid=null, year=2017, volume=8, issue=9, pageStart=null, pageEnd=null, url=null, language=null, rfNumber=[10], rfOrder=10, authorNames=CHAE YK, RANGANATH K, HAMMERMAN PS, journalName=Oncotarget, refType=null, unstructuredReference=CHAE YK, RANGANATH K, HAMMERMAN PS, et al. Inhibition of the fibroblast growth factor receptor (FGFR) pathway: the current landscape and barriers to clinical application[J]. Oncotarget, 2017, 8(9): 16052., articleTitle=Inhibition of the fibroblast growth factor receptor (FGFR) pathway: the current landscape and barriers to clinical application, refAbstract=null), Reference(id=1239268428385669279, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, doi=null, pmid=null, pmcid=null, year=2016, volume=53, issue=null, pageStart=126, pageEnd=135, url=null, language=null, rfNumber=[11], rfOrder=11, authorNames=TANNER Y, GROSE RP, journalName=Semin Cell Dev Biol, refType=null, unstructuredReference=TANNER Y, GROSE RP. Dysregulated FGF signalling in neoplastic disorders[J]. Semin Cell Dev Biol, 2016, 53 : 126-135., articleTitle=Dysregulated FGF signalling in neoplastic disorders, refAbstract=null), Reference(id=1239268428477943971, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, doi=null, pmid=null, pmcid=null, year=2020, volume=12, issue=8, pageStart=2308, pageEnd=null, url=null, language=null, rfNumber=[12], rfOrder=12, authorNames=MASSA A, VARAMO C, VITA F, journalName=Cancers, refType=null, unstructuredReference=MASSA A, VARAMO C, VITA F, et al. Evolution of the experimental models of cholangiocarcinoma[J]. Cancers, 2020, 12(8): 2308., articleTitle=Evolution of the experimental models of cholangiocarcinoma, refAbstract=null), Reference(id=1239268428540858535, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, doi=null, pmid=null, pmcid=null, year=2021, volume=40, issue=7, pageStart=503, pageEnd=506, url=null, language=null, rfNumber=[13], rfOrder=13, authorNames=黄 璐, 童 颖, 熊传爽, journalName=中国新药与临床杂志, refType=null, unstructuredReference=黄 璐,童 颖,熊传爽,等.治疗胆管癌新药:成纤维细胞生长因子受体1/2/3抑制剂pemigatinib[J].中国新药与临床杂志, 2021, 40(7): 503-506., articleTitle=治疗胆管癌新药:成纤维细胞生长因子受体1/2/3抑制剂pemigatinib, refAbstract=null), Reference(id=1239268428620550314, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, doi=null, pmid=null, pmcid=null, year=2021, volume=40, issue=7, pageStart=503, pageEnd=506, url=null, language=null, rfNumber=[13], rfOrder=14, authorNames=HUANG L, TONG Y, XIONG CS, journalName=Chin J New Drugs Clin Rem, refType=null, unstructuredReference=HUANG L, TONG Y, XIONG CS, et al. A new drug in treating cholangiocarcinoma: FGFR1/2/3 inhibitor pemigatinib [J]. Chin J New Drugs Clin Rem, 2021, 40(7): 503-506., articleTitle=A new drug in treating cholangiocarcinoma: FGFR1/2/3 inhibitor pemigatinib, refAbstract=null), Reference(id=1239268428721213614, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, doi=null, pmid=null, pmcid=null, year=2020, volume=31, issue=10, pageStart=1405, pageEnd=1412, url=null, language=null, rfNumber=[14], rfOrder=15, authorNames=BAHLEDA R, MERIC-BERNSTAM F, GOYAL L, journalName=Ann Oncol, refType=null, unstructuredReference=BAHLEDA R, MERIC-BERNSTAM F, GOYAL L, et al. Phase Ⅰ, first-in-human study of futibatinib, a highly selective, irreversible FGFR1–4 inhibitor in patients with advanced solid tumors[J]. Ann Oncol, 2020, 31(10): 1405-1412., articleTitle=Phase Ⅰ, first-in-human study of futibatinib, a highly selective, irreversible FGFR1–4 inhibitor in patients with advanced solid tumors, refAbstract=null), Reference(id=1239268428805099698, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, doi=null, pmid=null, pmcid=null, year=2020, volume=80, issue=22, pageStart=4986, pageEnd=4997, url=null, language=null, rfNumber=[15], rfOrder=16, authorNames=SOOTOME H, FUJITA H, ITO K, journalName=Cancer Res, refType=null, unstructuredReference=SOOTOME H, FUJITA H, ITO K, et al. Futibatinib is a novel irreversible FGFR1-4 inhibitor that shows selective antitumor activity against FGFR-deregulated tumors[J]. Cancer Res, 2020, 80(22): 4986-4997., articleTitle=Futibatinib is a novel irreversible FGFR1-4 inhibitor that shows selective antitumor activity against FGFR-deregulated tumors, refAbstract=null), Reference(id=1239268428893180086, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, doi=null, pmid=null, pmcid=null, year=2022, volume=12, issue=2, pageStart=402, pageEnd=415, url=null, language=null, rfNumber=[16], rfOrder=17, authorNames=MERIC-BERNSTAM F, BAHLEDA R, HIERRO C, journalName=Cancer Discov, refType=null, unstructuredReference=MERIC-BERNSTAM F, BAHLEDA R, HIERRO C, et al. Futibatinib, an irreversible FGFR1-4 inhibitor, in patients with advanced solid tumors harboring FGF/FGFR aberrations: a phase Ⅰ dose-expansion study[J]. Cancer Discov, 2022, 12(2): 402-415., articleTitle=Futibatinib, an irreversible FGFR1-4 inhibitor, in patients with advanced solid tumors harboring FGF/FGFR aberrations: a phase Ⅰ dose-expansion study, refAbstract=null), Reference(id=1239268428964483257, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, doi=null, pmid=null, pmcid=null, year=2020, volume=38, issue=Suppl 15, pageStart=108, pageEnd=null, url=null, language=null, rfNumber=[17], rfOrder=18, authorNames=GOYAL L, MERIC-BERNSTAM F, HOLLEBECQUE A, journalName=J Clin Oncol, refType=null, unstructuredReference=GOYAL L, MERIC-BERNSTAM F, HOLLEBECQUE A, et al. FOENIX-CCA2: a phase Ⅱ, open-label, multicenter study of futibatinib in patients(pts) with intrahepatic cholangiocarcinoma(iCCA) harboring FGFR2 gene fusions or other rearrangements[J]. J Clin Oncol, 2020, 38(Suppl 15): 108., articleTitle=FOENIX-CCA2: a phase Ⅱ, open-label, multicenter study of futibatinib in patients(pts) with intrahepatic cholangiocarcinoma(iCCA) harboring FGFR2 gene fusions or other rearrangements, refAbstract=null), Reference(id=1239268429056757948, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, doi=null, pmid=null, pmcid=null, year=2023, volume=388, issue=3, pageStart=228, pageEnd=239, url=null, language=null, rfNumber=[18], rfOrder=19, authorNames=GOYAL L, MERIC-BERNSTAM F, HOLLEBECQUE A, journalName=N Engl J Med, refType=null, unstructuredReference=GOYAL L, MERIC-BERNSTAM F, HOLLEBECQUE A, et al. Futibatinib for FGFR2-rearranged intrahepatic cholangiocarcinoma[J]. N Engl J Med, 2023, 388(3): 228-239., articleTitle=Futibatinib for FGFR2-rearranged intrahepatic cholangiocarcinoma, refAbstract=null), Reference(id=1239268429119672512, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, doi=null, pmid=null, pmcid=null, year=2020, volume=38, issue=Suppl 4, pageStart=null, pageEnd=null, url=null, language=null, rfNumber=[19], rfOrder=20, authorNames=BORAD MJ, BRIDGEWATER JA, MORIZANE C, journalName=J Clin Oncol, refType=null, unstructuredReference=BORAD MJ, BRIDGEWATER JA, MORIZANE C, et al. A phase Ⅲ study of futibatinib(TAS-120) versus gemcitabine-cisplatin(gem-cis) chemotherapy as first-line(1L) treatment for patients(pts) with advanced(adv) cholangiocarcinoma(CCA) harboring fibroblast growth factor receptor 2(FGFR2) gene rearrangements(FOENIX-CCA3)[J]. J Clin Oncol, 2020, 38(Suppl 4):TPS600., articleTitle=A phase Ⅲ study of futibatinib(TAS-120) versus gemcitabine-cisplatin(gem-cis) chemotherapy as first-line(1L) treatment for patients(pts) with advanced(adv) cholangiocarcinoma(CCA) harboring fibroblast growth factor receptor 2(FGFR2) gene rearrangements(FOENIX-CCA3), refAbstract=null), Reference(id=1239268429190975685, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, doi=null, pmid=null, pmcid=null, year=2021, volume=138, issue=Suppl 1, pageStart=3656, pageEnd=null, url=null, language=null, rfNumber=[20], rfOrder=21, authorNames=KILADJIAN JJ, SHITARA K, ROSEN LS, journalName=Blood, refType=null, unstructuredReference=KILADJIAN JJ, SHITARA K, ROSEN LS, et al. A phase 2 study of futibatinib (TAS-120) in patients with myeloid or lymphoid neoplasms harboring fibroblast growth factor receptor (FGFR) 1 rearrangements[J]. Blood, 2021, 138(Suppl 1): 3656., articleTitle=A phase 2 study of futibatinib (TAS-120) in patients with myeloid or lymphoid neoplasms harboring fibroblast growth factor receptor (FGFR) 1 rearrangements, refAbstract=null), Reference(id=1239268429371330761, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, doi=null, pmid=null, pmcid=null, year=2022, volume=82, issue=Suppl 4, pageStart=P1, pageEnd=P18, url=null, language=null, rfNumber=[21], rfOrder=22, authorNames=DAMODARAN S, UNNI N, GIRIDHAR KV, journalName=Cancer Res, refType=null, unstructuredReference=DAMODARAN S, UNNI N, GIRIDHAR KV, et al. Futibatinib in combination with fulvestrant in patients with metastatic breast cancer (MBC) harboring high-level FGFR1 amplification:preliminary data from a phase 2 study[J]. Cancer Res, 2022, 82(Suppl 4): P1-P18., articleTitle=Futibatinib in combination with fulvestrant in patients with metastatic breast cancer (MBC) harboring high-level FGFR1 amplification:preliminary data from a phase 2 study, refAbstract=null), Reference(id=1239268429455216845, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, doi=null, pmid=null, pmcid=null, year=2022, volume=40, issue=Suppl 6, pageStart=501, pageEnd=null, url=null, language=null, rfNumber=[22], rfOrder=23, authorNames=KOSHKIN VS, SONPAVDE GP, HWANG C, journalName=J Clin Oncol, refType=null, unstructuredReference=KOSHKIN VS, SONPAVDE GP, HWANG C, et al. Futibatinib plus pembrolizumab in patients (pts) with advanced or metastatic urothelial carcinoma (mUC): Preliminary safety results from a phase 2 study[J]. J Clin Oncol, 2022, 40(Suppl 6): 501., articleTitle=Futibatinib plus pembrolizumab in patients (pts) with advanced or metastatic urothelial carcinoma (mUC): Preliminary safety results from a phase 2 study, refAbstract=null), Reference(id=1239268429547491534, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, doi=null, pmid=null, pmcid=null, year=2022, volume=33, issue=null, pageStart=null, pageEnd=null, url=null, language=null, rfNumber=[23], rfOrder=24, authorNames=RODON J, O’NEIL B, WACHECK V, journalName=Ann Oncol, refType=null, unstructuredReference=RODON J, O’NEIL B, WACHECK V, et al. 1198TiP a phase Ⅰb/Ⅱ open-label, nonrandomized study of FGFR inhibitor futibatinib in combination with MEK inhibitor binimetinib in patients with advanced KRAS-mutant cancer[J]. Ann Oncol, 2022, 33:S1096., articleTitle=1198TiP a phase Ⅰb/Ⅱ open-label, nonrandomized study of FGFR inhibitor futibatinib in combination with MEK inhibitor binimetinib in patients with advanced KRAS-mutant cancer, refAbstract=null)], funds=[Fund(id=1239268427026714726, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, awardId=by2023006, language=CN, fundingSource=亳州市人民医院院级科研项目(by2023006), fundOrder=null, country=null), Fund(id=1239268427118989420, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, awardId=2023xkj091, language=CN, fundingSource=安徽医科大学校基金资助项目(2023xkj091), fundOrder=null, country=null)], companyList=[AuthorCompany(id=1239268423792907208, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, xref=null, ext=[AuthorCompanyExt(id=1239268423801295817, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, companyId=1239268423792907208, language=EN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=Department of Pharmacy, the Affiliated Bozhou Hospital of Anhui Medical University, Bozhou ANHUI 236800, China), AuthorCompanyExt(id=1239268423813878730, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, companyId=1239268423792907208, language=CN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=安徽医科大学附属亳州医院 药学部,安徽 亳州 236800)])], figs=[ArticleFig(id=1239268426733113427, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, language=EN, label=null, caption=null, figureFileSmall=+1PSHCogcEsOyqbCsXey9w==, figureFileBig=SxVo2w6/n0SHi+XzgTrjEQ==, tableContent=null), ArticleFig(id=1239268426837971034, tenantId=1146029695717560320, journalId=1205117082300743687, articleId=1239268422064853880, language=CN, label=图1, caption=福巴替尼的化学结构式, figureFileSmall=+1PSHCogcEsOyqbCsXey9w==, figureFileBig=SxVo2w6/n0SHi+XzgTrjEQ==, tableContent=null)], attaches=null, journal=Journal(id=1205114437246812164, delFlag=0, nameCn=中国新药与临床杂志, nameEn=Chinese Journal of New Drugs and Clinical Remedies, nameHistory1=null, nameHistory2=null, issn=1007-7669, eissn=, cn=31-1746/R, coden=null, periodic=月刊, language=CN, oaType=1, ccby=null, superviseOffice=null, ownerOffice=null, pubOffice=null, editorOffice=null, officeType=null, aims=null, clcCode=null, officeProv=null, officeCity=null, officeAddr=null, officeZip=null, officeEmail=, officePhone=, editDirector=null, officeDirector=null, officeDirectorPhone=null, officeStaffNum=null, officeEmpNum=null, coverPicUrl=4CRZH/cEJmlFWJuWhAUDig==, journalPrice=null, startedYear=null, abbrevIsoEn=Chinese Journal of New Drugs and Clinical Remedies, journalRemark=null, publicationField=null, createdTime=1765251271787, updatedTime=1765252216403, createdBy=18614031015, updatedBy=13701087609, firstLetterCn=C, firstLetterEn=C, subjectCode=Life Sciences, subjectName=生命医学, subjectCodeEn=Life Sciences, subjectNameEn=null, picCn=4CRZH/cEJmlFWJuWhAUDig==, picEn=N3vp8/tZorUwVBJknBXdng==, jcr=null, cjcr=null, exts=[JournalExt(id=1205118399413203150, language=CN, name=中国新药与临床杂志, nameHistory1=null, nameHistory2=null, managedBy=, sponsoredBy=, publishedBy=, editorOffice=, officeProv=null, officeCity=null, officeAddr=, officeZip=, editDirector=, officeDirector=null, officePhone=null, coverPicUrl=null, journalRemark=, submitArticleUrl=null, websiteUrl=, createdTime=1765252216437, updatedTime=1765252216437, createdBy=13701087609, updatedBy=13701087609, submissionGuidelinesUrl=, submissionAuthorUrl=http://xyyl.cbpt.cnki.net/index.aspx?t=1, submissionEditorUrl=http://xyyl.cbpt.cnki.net/index.aspx?t=3, submissionReviewUrl=http://xyyl.cbpt.cnki.net/index.aspx?t=2, submissionCeEditorUrl=, submissionAeEditorUrl=, option={"copyright":""}), JournalExt(id=1205118399467729103, language=EN, name=Chinese Journal of New Drugs and Clinical Remedies, nameHistory1=null, nameHistory2=null, managedBy=, sponsoredBy=, publishedBy=, editorOffice=, officeProv=null, officeCity=null, officeAddr=, officeZip=, editDirector=, officeDirector=null, officePhone=null, coverPicUrl=null, journalRemark=, submitArticleUrl=null, websiteUrl=, createdTime=1765252216450, updatedTime=1765252216450, createdBy=13701087609, updatedBy=13701087609, submissionGuidelinesUrl=, submissionAuthorUrl=http://xyyl.cbpt.cnki.net/index.aspx?t=1, submissionEditorUrl=http://xyyl.cbpt.cnki.net/index.aspx?t=3, submissionReviewUrl=http://xyyl.cbpt.cnki.net/index.aspx?t=2, submissionCeEditorUrl=, submissionAeEditorUrl=, option={"copyright":""})], databaseList=null, tenantJournalId=1205117082300743687, websiteList=[Website(id=1205118568049389783, webName=null, webTitle=null, webDomain=null, webCopyrigh=null, webIpcNo=null, seoTitle=null, seoKeywords=null, seoDescription=null, tenantJournalId=null, journalId=1205117082300743687, journalNameCn=null, journalNameEn=null, grayFlag=null, tenantId=1146029695717560320, platformId=null, journalGroupId=null, journalGroupNameCn=null, journalGroupNameEn=null, type=1, domain=https://castjournals.cast.org.cn/joweb/zgxyylczz/CN, language=CN, createTime=1765252256643, createBy=18614031015, updateTime=1765252598399, updateBy=18614031015, name=中国新药与临床杂志-中文, tplId=1146099689490845704, title=中国新药与临床杂志, delFlag=0, indexPage=/home, props=[WebsiteProps(id=1205154564317098673, tenantId=1146029695717560320, journalId=null, journalGroupId=null, siteId=1205118568049389783, code=articleTextType, value=kx, createTime=1765260838822, updateTime=1765260838822, creator=18614031015, updator=18614031015), WebsiteProps(id=1205154564300321454, tenantId=1146029695717560320, journalId=null, journalGroupId=null, siteId=1205118568049389783, code=banner, value=null, createTime=1765260838818, updateTime=1765260838818, creator=18614031015, updator=18614031015), WebsiteProps(id=1205154564333875892, tenantId=1146029695717560320, journalId=null, journalGroupId=null, siteId=1205118568049389783, code=grayFlag, value=0, createTime=1765260838826, updateTime=1765260838826, creator=18614031015, updator=18614031015), WebsiteProps(id=1205154564296127149, tenantId=1146029695717560320, journalId=null, journalGroupId=null, siteId=1205118568049389783, code=logo, value=https://castjournals.cast.org.cn/joweb/zgxyylczz/CN/file/pic?fileId=EPNvNLzzPrR2hCakA9eyOQ==, createTime=1765260838817, updateTime=1765260838817, creator=18614031015, updator=18614031015), WebsiteProps(id=1205154564354847414, tenantId=1146029695717560320, journalId=null, journalGroupId=null, siteId=1205118568049389783, code=minRunFlag, value=0, createTime=1765260838831, updateTime=1765260838831, creator=18614031015, updator=18614031015), WebsiteProps(id=1205154564312904368, tenantId=1146029695717560320, journalId=null, journalGroupId=null, siteId=1205118568049389783, code=picServerUrl, value=https://castjournals.cast.org.cn/joweb/zgxyylczz/CN/file/pic, createTime=1765260838821, updateTime=1765260838821, creator=18614031015, updator=18614031015), WebsiteProps(id=1205154564342264501, tenantId=1146029695717560320, journalId=null, journalGroupId=null, siteId=1205118568049389783, code=silenceFlag, value=0, createTime=1765260838828, updateTime=1765260838828, creator=18614031015, updator=18614031015), WebsiteProps(id=1205154564308710063, tenantId=1146029695717560320, journalId=null, journalGroupId=null, siteId=1205118568049389783, code=staticResourcePath, value=https://castjournals.cast.org.cn/joweb/cast_kjdb_cn_619/, createTime=1765260838820, updateTime=1765260838820, creator=18614031015, updator=18614031015), WebsiteProps(id=1205154564325487282, tenantId=1146029695717560320, journalId=null, journalGroupId=null, siteId=1205118568049389783, code=themeColor, value=null, createTime=1765260838824, updateTime=1765260838824, creator=18614031015, updator=18614031015), WebsiteProps(id=1205154564329681587, tenantId=1146029695717560320, journalId=null, journalGroupId=null, siteId=1205118568049389783, code=themeStyle, value=null, createTime=1765260838825, updateTime=1765260838825, creator=18614031015, updator=18614031015)]), Website(id=1205118568124887278, webName=null, webTitle=null, webDomain=null, webCopyrigh=null, webIpcNo=null, seoTitle=null, seoKeywords=null, seoDescription=null, tenantJournalId=null, journalId=1205117082300743687, journalNameCn=null, journalNameEn=null, grayFlag=null, tenantId=1146029695717560320, platformId=null, journalGroupId=null, journalGroupNameCn=null, journalGroupNameEn=null, type=1, domain=https://castjournals.cast.org.cn/joweb/zgxyylczz/EN, language=EN, createTime=1765252256661, createBy=18614031015, updateTime=1765252618802, updateBy=18614031015, name=中国新药与临床杂志-英文, tplId=1146101810881728533, title=Chinese Journal of New Drugs and Clinical Remedies, delFlag=0, indexPage=/home, props=[WebsiteProps(id=1205154594314756492, tenantId=1146029695717560320, journalId=null, journalGroupId=null, siteId=1205118568124887278, code=articleTextType, value=kx, createTime=1765260845974, updateTime=1765260845974, creator=18614031015, updator=18614031015), WebsiteProps(id=1205154594297979273, tenantId=1146029695717560320, journalId=null, journalGroupId=null, siteId=1205118568124887278, code=banner, value=null, createTime=1765260845970, updateTime=1765260845970, creator=18614031015, updator=18614031015), WebsiteProps(id=1205154594331533711, tenantId=1146029695717560320, journalId=null, journalGroupId=null, siteId=1205118568124887278, code=grayFlag, value=0, createTime=1765260845978, updateTime=1765260845978, creator=18614031015, updator=18614031015), WebsiteProps(id=1205154594289590664, tenantId=1146029695717560320, journalId=null, journalGroupId=null, siteId=1205118568124887278, code=logo, value=https://castjournals.cast.org.cn/joweb/zgxyylczz/EN/file/pic?fileId=EPNvNLzzPrR2hCakA9eyOQ==, createTime=1765260845968, updateTime=1765260845968, creator=18614031015, updator=18614031015), WebsiteProps(id=1205154594344116625, tenantId=1146029695717560320, journalId=null, journalGroupId=null, siteId=1205118568124887278, code=minRunFlag, value=0, createTime=1765260845981, updateTime=1765260845981, creator=18614031015, updator=18614031015), WebsiteProps(id=1205154594310562187, tenantId=1146029695717560320, journalId=null, journalGroupId=null, siteId=1205118568124887278, code=picServerUrl, value=https://castjournals.cast.org.cn/joweb/zgxyylczz/EN/file/pic, createTime=1765260845973, updateTime=1765260845973, creator=18614031015, updator=18614031015), WebsiteProps(id=1205154594335728016, tenantId=1146029695717560320, journalId=null, journalGroupId=null, siteId=1205118568124887278, code=silenceFlag, value=0, createTime=1765260845979, updateTime=1765260845979, creator=18614031015, updator=18614031015), WebsiteProps(id=1205154594302173578, tenantId=1146029695717560320, journalId=null, journalGroupId=null, siteId=1205118568124887278, code=staticResourcePath, value=https://castjournals.cast.org.cn/joweb/cast_kjdb_en_623/, createTime=1765260845971, updateTime=1765260845971, creator=18614031015, updator=18614031015), WebsiteProps(id=1205154594323145101, tenantId=1146029695717560320, journalId=null, journalGroupId=null, siteId=1205118568124887278, code=themeColor, value=null, createTime=1765260845976, updateTime=1765260845976, creator=18614031015, updator=18614031015), WebsiteProps(id=1205154594327339406, tenantId=1146029695717560320, journalId=null, journalGroupId=null, siteId=1205118568124887278, code=themeStyle, value=null, createTime=1765260845977, updateTime=1765260845977, creator=18614031015, updator=18614031015)])], journalTitle=中国新药与临床杂志, weixinUrl=null, journalUrl=null, iacademicId=null, status=1, seqNo=null, journalTitleEn=Chinese Journal of New Drugs and Clinical Remedies, journalPhotoCn=4CRZH/cEJmlFWJuWhAUDig==, journalPhotoEn=N3vp8/tZorUwVBJknBXdng==, journalFirstLetter=C, journalRecommend=null, journalNew=null, journalCollection=null, jcrJf=null, cjcrJf=null, jcrJfStr=null, cjcrJfStr=null, submissionFirstDecision=null, sciSubjectClassification=null, casSubjectClassification=null, citeScore=null, totalCitationFrequency=null, icpCode=null, psCode=null, advertisingLicenseCode=null, copyrightInformation=null, country=null, option=, provinceCode=null, provinceName=null, collectFlag=false), detailUrlCn=https://castjournals.cast.org.cn/joweb/zgxyylczz/CN/10.14109/j.cnki.xyylc.2024.07.05, detailUrlEn=https://castjournals.cast.org.cn/joweb/zgxyylczz/EN/10.14109/j.cnki.xyylc.2024.07.05, pdfUrlCn=https://castjournals.cast.org.cn/joweb/zgxyylczz/CN/PDF/10.14109/j.cnki.xyylc.2024.07.05, pdfUrlEn=https://castjournals.cast.org.cn/joweb/zgxyylczz/EN/PDF/10.14109/j.cnki.xyylc.2024.07.05, aliStartDate=null, aliEndDate=null, collectionFlag=false, citedCount=null, citedUrl=null, reference=null)
收藏切换
治疗肝内胆管癌新药:泛FGFR抑制剂福巴替尼
收藏切换
PDF下载
狄潘潘 , 邢晓勤 , 梁海 , 贾淑云
中国新药与临床杂志 | 新药介绍 2024,43(7): 510-513
收起
收藏切换
中国新药与临床杂志 | 新药介绍 2024, 43(7): 510-513
治疗肝内胆管癌新药:泛FGFR抑制剂福巴替尼
全屏
狄潘潘 , 邢晓勤, 梁海, 贾淑云
作者信息
  • 安徽医科大学附属亳州医院 药学部,安徽 亳州 236800
  • 狄潘潘,男,主管药师,硕士,主要从事医院药学、数据挖掘与处理的研究,E-mail:

A new drug in treating intrahepatic cholangiocarcinoma : FGFR1-4 inhibitor futibatinib
Pan-pan DI , Xiao-qin XING, Hai LIANG, Shu-yun JIA
Affiliations
  • Department of Pharmacy, the Affiliated Bozhou Hospital of Anhui Medical University, Bozhou ANHUI 236800, China
出版时间: 2024-07-25 doi: 10.14109/j.cnki.xyylc.2024.07.05
文章导航
收藏切换

肝内胆管癌(ICC)是一种发生于胆管系统的恶性肿瘤,起病隐匿,患者总体预后较差,死亡率较高。福巴替尼是一种泛成纤维细胞生长因子受体(FGFR)抑制剂,于2022年被美国食品和药物管理局批准上市,用于既往治疗过的、不可切除的局部晚期或转移性且伴有FGFR2基因融合或其他重排的ICC成年患者。Ⅰ期和Ⅱ期临床试验表明,福巴替尼对ICC具有良好的治疗效果,可显著提高ICC患者的客观缓解率并延长患者的生存时间;其常见不良事件包括高磷血症、腹泻、便秘及口干等,不良事件发生率较高。

肝内胆管癌  /  福巴替尼  /  成纤维细胞生长因子  /  抗肿瘤药

Intrahepatic cholangiocarcinoma (ICC) is a malignant tumor that occurs in the biliary system, with a hidden onset, poor overall prognosis and high mortality. Futibatinib is a fibroblast growth factor receptor (FGFR) 1-4 inhibitor, which was approved by the U.S. Food and Drug Administration in 2022 for the treatment of adult patients with previously treated, unresectable, locally advanced or metastatic ICC with FGFR2 gene fusions or other rearrangements. Phase Ⅰ and Ⅱ clinical trials have shown that futibatinib has good clinical effect on ICC, which can significantly improve the objective response rate and prolong the survival time of ICC patients. The common adverse events include hyperphosphatemia, diarrhea, constipation, and dry mouth, with a high incidence of adverse events.

intrahepatic cholangiocarcinoma  /  futibatinib  /  fibroblast growth factors  /  antineoplastic agents
狄潘潘, 邢晓勤, 梁海, 贾淑云. 治疗肝内胆管癌新药:泛FGFR抑制剂福巴替尼. 中国新药与临床杂志, 2024 , 43 (7) : 510 -513 . DOI: 10.14109/j.cnki.xyylc.2024.07.05
Pan-pan DI, Xiao-qin XING, Hai LIANG, Shu-yun JIA. A new drug in treating intrahepatic cholangiocarcinoma : FGFR1-4 inhibitor futibatinib[J]. Chinese Journal of New Drugs and Clinical Remedies, 2024 , 43 (7) : 510 -513 . DOI: 10.14109/j.cnki.xyylc.2024.07.05
胆管癌(cholangiocarcinoma,CC)是一种具有致命性的上皮细胞恶性肿瘤。基于其解剖位置的不同,胆管癌又可细分为肝内胆管癌(intrahepatic cholangiocarcinoma,ICC)、肝门周围胆管癌和远端胆管癌[1]。世界上大多数地区人群的ICC发病率高峰年龄为70岁[2]。虽然CC的发病率在不同地区有明显差异,但总体发病率和死亡率呈逐年上升趋势,且男性发病率和死亡率稍高于女性[3]。目前,手术切除仍然是ICC的主要治疗方式,术后5年生存率约为25%[4]。多数ICC患者在ICC初期因没有明显的临床症状,导致在诊断时已处于晚期,无法进行手术,只能选择化疗。由于ICC的高度促结缔组织增生特性、丰富的肿瘤微环境以及遗传异质性,使其对化疗药物具有较高的耐药性[5],因此化疗效果很不理想。
福巴替尼(futibatinib)是一种成纤维细胞生长因子受体(fibroblast growth factor receptor,FGFR)抑制剂,分子结构见图1,该药于2022年9月30日获美国食品和药物管理局(FDA)批准上市,用于既往治疗过的、不可切除的局部晚期或转移性且伴有FGFR2基因融合或其他重排的ICC成年患者[6]。FDA曾授予福巴替尼孤儿药资格、突破性疗法认定及优先审评资格等。国内较早的关于福巴替尼的报道为短篇国外医学文摘[7],仅简单描述了关于福巴替尼的Ⅱ期临床试验数据,并未对福巴替尼的作用机制、药动学、临床前研究等进行阐述,也未对其临床疗效及安全性等进行详细描述。为使国内学者对福巴替尼有更为深入的了解,也为给国内相关学者研发FGFR抑制剂提供一定的参考,本文就福巴替尼的作用机制、药动学、临床前研究、临床研究及安全性等信息进行介绍。
FGFR由细胞外配体结构域、跨膜结构域和胞内酪氨酸激酶结构域组成,包括FGFR1、FGFR2、FGFR3、FGFR4四种亚型,可与其配体成纤维细胞生长因子(FGF)构成FGF/FGFR信号通路[8,9]。当FGF被释放后,其可与FGFR结合而发生二聚化和酪氨酸激酶结构域的自磷酸化[10],然后再激活一系列的下游信号通路[11]。激活后的FGF/FGFR信号通路在细胞分化、迁移、有丝分裂和细胞死亡中发挥了重要作用。研究表明,当FGFR基因发生突变、融合/重排、扩增及易位时,会导致FGF/FGFR通路的异常激活,致使该通路所调控的正常生理功能发生紊乱,从而导致多种癌症的发生发展,如ICC、尿路上皮癌和其他实体瘤等[12]。福巴替尼是一种不可逆的泛FGFR小分子抑制剂,可与FGFR1~4共价结合而抑制FGFR的磷酸化和下游信号的传导,从而对过度表达FGFR的肿瘤细胞产生增殖抑制作用。而FGFR2基因的融合/重排主要发生于ICC中[13],因此福巴替尼适用于伴FGFR2融合/重排的ICC患者。
口服给药后,福巴替尼的药时曲线下面积(AUC)和最大血浆浓度(cmax)在8~80 mg剂量范围内随剂量增加而增大,继续增大剂量其AUC和cmax几乎不再变化。在8~200 mg剂量范围内,cmax的增加幅度与给药剂量不成正比。对患者重复给药未观察到明显的药物积累,且8~200 mg的剂量都可在给药周期(21 d)结束时达到稳态浓度[14]。给药后,福巴替尼达cmax的中位时间约为2 h(1.2~22.8 h)。高热量和高脂饮食可使福巴替尼的AUC降低11%,cmax降低42%。福巴替尼的表观分布容积为66 L,体外血浆蛋白结合率为95%。福巴替尼的平均消除半衰期约为3 h,血浆清除率为20 L·h-1。福巴替尼主要由细胞色素P450(cytochrome P450,CYP)3A代谢,放射性试验显示,口服福巴替尼20 mg后,血浆中约有59%的药物原型,约91%的药物经粪便排出,9%经尿液排出[6]
福巴替尼对FGFR1~4激酶活性的抑制呈剂量依赖性,其对FGFR1、FGFR2、FGFR3、FGFR4的半数抑制浓度(IC50)分别为(1.8±0.4)、(1.4±0.3)、(1.6±0.1)、(3.7±0.4)nmol·L-1。SOOTOME等[15]使用100 nmol·L-1的福巴替尼对296种人类激酶进行了评估,并采用迁移率检测法对激酶的磷酸化肽段进行定量分析,结果显示,仅有3种非FGFR激酶表现出50%以上的抑制作用,说明福巴替尼对FGFR1~4具有较强的选择性。基于福巴替尼可在体外与FGFR2激酶结构域结合的特性,该研究检测了福巴替尼在FGFR失调控的细胞系中对FGFR磷酸化和信号转导的影响。结果表明,使用福巴替尼处理FGFR2扩增的胃癌细胞30 min后,福巴替尼对FGFR的磷酸化表现出浓度依赖性抑制,酶联免疫吸附法测得的IC50值为(4.9±0.1)nmol·L-1[15]。细胞实验表明,对于大多数具有FGFR基因畸变的癌细胞,福巴替尼的IC50介于1~50 nmol·L-1,但膀胱癌细胞和多发性骨髓瘤细胞对福巴替尼不敏感[15]
一项针对晚期实体瘤患者的Ⅰ期临床试验纳入了86例患者,其中42例患者给予福巴替尼8~200 mg,每周3次,44例患者给予福巴替尼4~24 mg,每日1次,两组患者的治疗周期均为21 d。结果,每周3次队列中有1例使用福巴替尼8 mg的患者报告了剂量限制毒性,然而该队列中使用其他剂量(包括最高剂量200 mg)的患者未观察到剂量限制毒性;在每日1次队列中,接受4、8、16、20 mg福巴替尼的患者也未观察到剂量限制毒性,但在9例使用了24 mg剂量的可评估剂量限制毒性的患者中,有3例报告了剂量限制毒性,因此20 mg每日1次被定为福巴替尼的最大耐受剂量,也是Ⅱ期临床试验的推荐剂量[14]
MERIC-BERNSTAM等[16]开展了一项Ⅰ期临床试验,以研究福巴替尼在FGFR异常肿瘤中的临床活性。该研究最终纳入了83例局部晚期CC患者(其中61例为ICC患者),其中59例(71.1%)患者存在FGFR2融合/重排,15例(18.1%)存在FGFR2突变,3例(3.6%)同时存在FGFR2融合和突变。治疗方案分为两种,方案1为福巴替尼20 mg,每日1次(n=64);方案2为福巴替尼16 mg,每日1次(n=19),两种方案均以21 d为1个治疗周期。结果显示,方案1的客观缓解率(ORR)为15.6%[95%置信区间(CI)为7.8%~26.9%],疾病控制率(DCR)为71.9%,中位反应持续时间(DOR)为5.3个月(95%CI为1.9~9.9个月),中位无进展生存期(PFS)为5.1个月(95%CI为3.7~9.0个月),6个月的PFS率为46.0%(95%CI为31.6%~59.3%)。进一步研究显示,42例接受方案1治疗并伴有FGFR2融合/重排的ICC患者的ORR为16.7%(95%CI为7.0%~34.1%),DCR为78.6%(95%CI为63.2%~89.7%),中位DOR为6.9个月,中位PFS为6.0个月(95%CI为3.7~9.0个月)。接受方案2治疗的患者都获得了持久的缓解(3.5~20.4个月),其中8例ICC患者经历了部分缓解(PR)。而对于先前接受过其他FGFR抑制剂治疗并产生耐药的患者,有17.9%的患者亦对福巴替尼治疗有反应。该研究表明,福巴替尼对CC,尤其是伴有FGFR2融合/重排的ICC患者具有良好的抗肿瘤活性。
FOENIX-CCA2试验(NCT02052778)是一项单臂、多中心Ⅱ期研究,旨在评估至少1次治疗失败的局部晚期或转移性不可切除并伴有FGFR2基因融合/重排的ICC患者使用福巴替尼的有效性[17]。该研究共纳入了103例之前未接受过FGFR抑制剂治疗的ICC患者,患者体能状态美国东部肿瘤协作组(ECOG)评分为0~1分,之前接受过至少1、2、3种及以上治疗方案的患者分别为44.8%、28.4%和26.9%。103例ICC患者均接受口服福巴替尼20 mg每日1次,21 d为一周期的治疗,直至疾病进展或出现不可耐受的毒性。主要研究终点为ORR,次要终点包括DCR和DOR。2020年5月,该研究报告了随访时间≥6个月的67例患者的数据,总ORR为34.3%(全部为PR,n=23),DCR为76.1%,中位DOR为6.2个月(2.1~14.2个月)。同年10月,GOYAL等[18]更新了FOENIX-CCA2试验的临床数据,确定总ORR为41.7%(43/103),平均DOR为9.7个月,72%的患者DOR≥6个月,DCR为82.5%,中位PFS为9.0个月,中位总生存期(OS)为21.7个月,12个月OS率为72.0%。
目前正在进行的Ⅲ期研究FOENIX-CCA3试验,其目的是对比福巴替尼和吉西他滨+顺铂一线治疗局部晚期或转移性ICC并伴有FGFR2基因重排患者的疗效,研究的主要终点是PFS,次要终点包括ORR、DCR、OS和安全性。但该研究目前尚未公布任何试验数据[19]。除ICC外,福巴替尼还有多个适应证处于临床研究阶段,如髓样和淋巴样肿瘤[20]、转移性乳腺癌[21]、尿路上皮癌[22]及非小细胞肺癌[23]等。
Ⅰ期临床试验显示,170例接受福巴替尼20 mg,每日1次的患者中,有168例(98.8%)患者发生了治疗相关不良事件。最常见的不良事件是高磷血症(81.2%)、腹泻(32.9%)、便秘(31.8%)、恶心(28.2%)、疲劳(25.3%)和呕吐(25.3%)。其中,有97例患者(57.1%)报告了3级不良事件,发生率>5%的3级不良事件为高磷血症(22.4%)、丙氨酸转氨酶升高(9.4%)、天冬氨酸转氨酶升高(5.3%)、贫血(5.3%)和疲劳(5.3%);9例患者(5.3%)报告了4级治疗相关不良事件,但只有1例γ-谷氨酰转移酶升高被认为与治疗相关[16]。在Ⅱ期临床试验中,最常见的治疗相关不良事件为高磷血症(79.1%)、腹泻(37.3%)和口干(32.8%);分别有65.7%和53.7%的患者因不良事件而需要延迟给药或减少剂量,6.0%的患者因不良事件停止了治疗[17]。福巴替尼还可能会引起视网膜色素上皮层脱离、干眼症和角膜炎,对于在福巴替尼治疗期间出现眼部不适的患者应及时进行眼科检查,及时调整用药剂量。福巴替尼还会引起胎儿畸形、生长迟缓和胎儿死亡,因此FDA建议有生殖需求的患者在福巴替尼治疗期间和最后1次治疗后1周内应采取有效的避孕措施[6]
作为第三代FGFR抑制剂,福巴替尼对不可切除的局部晚期或转移性并伴有FGFR2基因融合/重排的ICC患者具有良好的治疗效果。虽然福巴替尼的不良事件发生率较高,但其Ⅰ期和Ⅱ期临床试验结果已显示出令人鼓舞的抗肿瘤活性,能为ICC患者带来较好的ORR、DCR及PFS。由于福巴替尼刚上市,其在ICC中的临床数据还不够充分,期待有更多的福巴替尼上市后真实世界证据以进一步指导患者用药。
  • 亳州市人民医院院级科研项目(by2023006)
  • 安徽医科大学校基金资助项目(2023xkj091)
参考文献 引证文献
排序方式:
[1]
KENDALL T, VERHEIJ J, GAUDIO E, et al. Anatomical, histomorphological and molecular classification of cholangiocarcinoma[J]. Liver Int, 2019, 39(Suppl 1): 7-18.
[2]
KHAN SA, TAVOLARI S, BRANDI G. Cholangiocarcinoma: epidemiology and risk factors[J]. Liver Int, 2019, 39(Suppl 1):19-31.
[3]
BANALES JM, MARIN JJG, LAMARCA A, et al. Cholangiocarcinoma 2020: the next horizon in mechanisms and management[J]. Nat Rev Gastroenterol Hepatol, 2020, 17(9):557-588.
[4]
TAWARUNGRUANG C, KHUNTIKEO N, CHAMADOL N, et al. Survival after surgery among patients with cholangiocarcinoma in Northeast Thailand according to anatomical and morphological classification[J]. BMC Cancer, 2021, 21(1): 497.
[5]
LAWAL B, KUO YC, TANG SL, et al. Transcriptomic-based identification of the immuno-oncogenic signature of cholangiocarcinoma for HLC-018 multi-target therapy exploration[J]. Cells, 2021, 10(11): 2873.
[6]
FDA. Futibatinib tablets, for oral use[EB/OL]. (2022-09-30)[2022-10-22]. https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/214801Orig1s000lbledt.pdf.
[7]
MERICBERNSTAM F, HOLLEBECQUE A, 赵义军, 等. Futibatinib治疗FGFR2重排肝内胆管癌[J]. 肝胆外科杂志,2023, 31(2): 86.
MERICBERNSTAM F, HOLLEBECQUE A, ZHAO YJ, et al. Futibatinib for FGFR2-rearranged intrahepatic cholangiocarcinoma lipika goyal[J]. J Hepatobiliary Surg, 2023,31(2): 86.
[8]
HELSTEN T, ELKIN S, ARTHUR E, et al. The FGFR landscape in cancer: analysis of 4 853 tumors by next-generation sequencing FGFR aberrations in cancer[J]. Clin Cancer Res, 2016, 22(1):259-267.
[9]
SZYBOWSKA P, HAUGSTEN EM, WIEDLOCHA A. The canonical FGF-FGFR signaling system at the molecular level[J]. Adv Hyg Expe Med, 2021, 75(1): 711-719.
[10]
CHAE YK, RANGANATH K, HAMMERMAN PS, et al. Inhibition of the fibroblast growth factor receptor (FGFR) pathway: the current landscape and barriers to clinical application[J]. Oncotarget, 2017, 8(9): 16052.
[11]
TANNER Y, GROSE RP. Dysregulated FGF signalling in neoplastic disorders[J]. Semin Cell Dev Biol, 2016, 53 : 126-135.
[12]
MASSA A, VARAMO C, VITA F, et al. Evolution of the experimental models of cholangiocarcinoma[J]. Cancers, 2020, 12(8): 2308.
[13]
黄 璐,童 颖,熊传爽,等.治疗胆管癌新药:成纤维细胞生长因子受体1/2/3抑制剂pemigatinib[J].中国新药与临床杂志, 2021, 40(7): 503-506.
HUANG L, TONG Y, XIONG CS, et al. A new drug in treating cholangiocarcinoma: FGFR1/2/3 inhibitor pemigatinib [J]. Chin J New Drugs Clin Rem, 2021, 40(7): 503-506.
[14]
BAHLEDA R, MERIC-BERNSTAM F, GOYAL L, et al. Phase Ⅰ, first-in-human study of futibatinib, a highly selective, irreversible FGFR1–4 inhibitor in patients with advanced solid tumors[J]. Ann Oncol, 2020, 31(10): 1405-1412.
[15]
SOOTOME H, FUJITA H, ITO K, et al. Futibatinib is a novel irreversible FGFR1-4 inhibitor that shows selective antitumor activity against FGFR-deregulated tumors[J]. Cancer Res, 2020, 80(22): 4986-4997.
[16]
MERIC-BERNSTAM F, BAHLEDA R, HIERRO C, et al. Futibatinib, an irreversible FGFR1-4 inhibitor, in patients with advanced solid tumors harboring FGF/FGFR aberrations: a phase Ⅰ dose-expansion study[J]. Cancer Discov, 2022, 12(2): 402-415.
[17]
GOYAL L, MERIC-BERNSTAM F, HOLLEBECQUE A, et al. FOENIX-CCA2: a phase Ⅱ, open-label, multicenter study of futibatinib in patients(pts) with intrahepatic cholangiocarcinoma(iCCA) harboring FGFR2 gene fusions or other rearrangements[J]. J Clin Oncol, 2020, 38(Suppl 15): 108.
[18]
GOYAL L, MERIC-BERNSTAM F, HOLLEBECQUE A, et al. Futibatinib for FGFR2-rearranged intrahepatic cholangiocarcinoma[J]. N Engl J Med, 2023, 388(3): 228-239.
[19]
BORAD MJ, BRIDGEWATER JA, MORIZANE C, et al. A phase Ⅲ study of futibatinib(TAS-120) versus gemcitabine-cisplatin(gem-cis) chemotherapy as first-line(1L) treatment for patients(pts) with advanced(adv) cholangiocarcinoma(CCA) harboring fibroblast growth factor receptor 2(FGFR2) gene rearrangements(FOENIX-CCA3)[J]. J Clin Oncol, 2020, 38(Suppl 4):TPS600.
[20]
KILADJIAN JJ, SHITARA K, ROSEN LS, et al. A phase 2 study of futibatinib (TAS-120) in patients with myeloid or lymphoid neoplasms harboring fibroblast growth factor receptor (FGFR) 1 rearrangements[J]. Blood, 2021, 138(Suppl 1): 3656.
[21]
DAMODARAN S, UNNI N, GIRIDHAR KV, et al. Futibatinib in combination with fulvestrant in patients with metastatic breast cancer (MBC) harboring high-level FGFR1 amplification:preliminary data from a phase 2 study[J]. Cancer Res, 2022, 82(Suppl 4): P1-P18.
[22]
KOSHKIN VS, SONPAVDE GP, HWANG C, et al. Futibatinib plus pembrolizumab in patients (pts) with advanced or metastatic urothelial carcinoma (mUC): Preliminary safety results from a phase 2 study[J]. J Clin Oncol, 2022, 40(Suppl 6): 501.
[23]
RODON J, O’NEIL B, WACHECK V, et al. 1198TiP a phase Ⅰb/Ⅱ open-label, nonrandomized study of FGFR inhibitor futibatinib in combination with MEK inhibitor binimetinib in patients with advanced KRAS-mutant cancer[J]. Ann Oncol, 2022, 33:S1096.
2024年第43卷第7期
PDF下载
80
33
引用本文
BibTeX
文章信息
doi: 10.14109/j.cnki.xyylc.2024.07.05
  • 接收时间:2022-10-27
  • 首发时间:2026-03-13
  • 出版时间:2024-07-25
补充材料
相关文章
文章信息
作者
出版历史
  • 收稿日期:2022-10-27
  • 录用日期:2024-03-25
基金
亳州市人民医院院级科研项目(by2023006)
安徽医科大学校基金资助项目(2023xkj091)
作者信息
    安徽医科大学附属亳州医院 药学部,安徽 亳州 236800
参考文献
分享链接
https://castjournals.cast.org.cn/joweb/zgxyylczz/CN/10.14109/j.cnki.xyylc.2024.07.05
分享至
全文二维码

扫描看全文

引用本文
BibTeX
本文的引用情况
2种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
关闭全屏