Safety, pharmacokinetics, and dosimetry of 177Lu-AB-3PRGD2 in patients with advanced integrin αvβ3-positive tumors: A first-in-human study

Safety, pharmacokinetics, and dosimetry of ¹⁷⁷Lu-AB-3PRGD2 in patients with advanced integrin α_vβ₃-positive tumors: A first-in-human study

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Huimin Sui^a^,^*, Feng Guo^b, Hongfei Liu^c, Rongxi Wang^a, Linlin Li^a, Jiarou Wang^a, Chenhao Jia^a, Jialin Xiang^a, Yingkui Liang^b^,^*, Xiaohong Chen^c^,^*, Zhaohui Zhu^a^,^*, Fan Wang^d^,^*

Acta Pharmaceutica Sinica B | 2025, 15(2) : 669 - 680

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Acta Pharmaceutica Sinica B | 2025, 15(2): 669-680

• ORIGINAL ARTICLE •

Safety, pharmacokinetics, and dosimetry of ¹⁷⁷Lu-AB-3PRGD2 in patients with advanced integrin α_vβ₃-positive tumors: A first-in-human study

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Huimin Sui^a^,^*, Feng Guo^b, Hongfei Liu^c, Rongxi Wang^a, Linlin Li^a, Jiarou Wang^a, Chenhao Jia^a, Jialin Xiang^a, Yingkui Liang^b^,^*, Xiaohong Chen^c^,^*, Zhaohui Zhu^a^,^*, Fan Wang^d^,^*

Affiliations

^aDepartment of Nuclear Medicine, State Key Laboratory of Complex Severe and Rare Diseases, Beijing Key Laboratory of Molecular Targeted Diagnosis and Therapy in Nuclear Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing 100730, China

^bDepartment of Nuclear Medicine, Sixth Medical Center of PLA General Hospital, Beijing 100048, China

^cDepartment of Otolaryngology-Head and Neck Surgery, Beijing Tongren Hospital, Capital Medical University, Beijing 100730, China

^dMedical Isotopes Research Center and Department of Radiation Medicine, State Key Laboratory of Natural and Biomimetic Drugs, School of Basic Medical Sciences, International Cancer Institute, Peking University, Beijing 100191, China

About Author:

E-mail addresses:suihm513@163.com (Huimin Sui)

liangyingkui2012@sina.com (Yingkui Liang)

trchxh@163.com (Xiaohong Chen)

13611093752@163.com (Zhaohui Zhu)

wangfan@bjmu.edu.com (Fan Wang).

Author contributions

Huimin Sui: Writing – review & editing, Writing – original draft, Visualization, Software, Resources, Project administration, Methodology, Investigation, Formal analysis, Data curation, Conceptualization. Feng Guo: Resources, Investigation. Hongfei Liu: Resources, Investigation. Rongxi Wang: Visualization, Data curation. Linlin Li: Visualization, Data curation. Jiarou Wang: Visualization, Data curation. Chenhao Jia: Visualization. Jialin Xiang: Visualization. Yingkui Liang: Writing – review & editing, Supervision, Resources, Methodology, Conceptualization. Xiaohong Chen: Writing – review & editing, Supervision, Resources, Methodology, Conceptualization. Zhaohui Zhu: Writing – review & editing, Supervision, Resources, Project administration, Methodology, Funding acquisition, Conceptualization. Fan Wang: Writing – review & editing, Supervision, Resources, Methodology, Funding acquisition, Conceptualization.

doi: 10.1016/j.apsb.2024.10.012

Outline

Abstract

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Integrin α_vβ₃ is overexpressed in various tumor cells and angiogenesis. To date, no drug has been proven to target it for therapy. A first-in-human study was designed to investigate the safety, pharmacokinetics, and dosimetry of ¹⁷⁷Lu-AB-3PRGD2, a novel integrin α_vβ₃-targeting radionuclide drug with an albumin-binding motif to optimize the pharmacokinetics. Ten patients (3 men, 7 women; aged 45 ± 16 years) with integrin α_vβ₃-avid tumors were recruited to accept ¹⁷⁷Lu-AB-3PRGD2 injection in a dosage of 1.57 ± 0.08 GBq (42.32 ± 2.11 mCi), followed by serial scans to obtain its dynamic distribution in the body. Safety tests were performed before and every 2 weeks after the treatment for 6–8 weeks. No adverse event over grade 3 was observed. ¹⁷⁷Lu-AB-3PRGD2 was excreted mainly through the urinary system, with intense radioactivity in the kidneys and bladder. Moderate distribution was found in the liver, spleen, and intestines. The estimated blood half-life was 2.85 ± 2.17 h. The whole-body effective dose was 0.251 ± 0.047 mSv/MBq. The absorbed doses were 0.157 ± 0.032 mGy/MBq in red bone marrow and 0.684 ± 0.132 mGy/MBq in kidneys. This first-in-human study of ¹⁷⁷Lu-AB-3PRGD2 treatment indicates its promising potential for targeted radionuclide therapy of integrin α_vβ₃-avid tumors. It merits further studies in more patients with escalating doses and multiple treatment courses.

Key words

¹⁷⁷Lu-AB-3PRGD2 / Integrin α_vβ₃ / Targeted radionuclide therapy / First-in-human study / Pharmacokinetics / Dosimetry / Safety / Advanced tumors

Cite this Article

Huimin Sui, Feng Guo, Hongfei Liu, Rongxi Wang, Linlin Li, Jiarou Wang, Chenhao Jia, Jialin Xiang, Yingkui Liang, Xiaohong Chen, Zhaohui Zhu, Fan Wang. Safety, pharmacokinetics, and dosimetry of ¹⁷⁷Lu-AB-3PRGD2 in patients with advanced integrin α_vβ₃-positive tumors: A first-in-human study[J]. Acta Pharmaceutica Sinica B, 2025 , 15 (2) : 669 -680 . DOI: 10.1016/j.apsb.2024.10.012

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1.　Introduction

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Integrin α_vβ₃ is significantly overexpressed on various tumor cells and the neovascular endothelial cells^1,2. It plays a crucial role in the growth, invasion, and metastasis of malignant tumors, but expresses at deficient levels in mature vascular endothelial cells and most normal organs, making it a hot target for diagnosis and therapy of broad-spectrum tumors^3—5. The Lasker Prize for Basic Medical Research in 2022 was bestowed upon three scientists for their discovery of integrins¹. However, up to now, no drug has been approved for the integrin α_vβ₃-targeted diagnosis or therapy.

A variety of arginine-glycine-aspartate (RGD) peptides have been recognized to specifically bind to integrin α_vβ₃^6,7. In the last few decades, RGD peptide-based radiopharmaceuticals have been widely studied for molecular imaging of integrin α_vβ₃-positive tumors with high integrin α_vβ₃ expression, including lung cancer, breast cancer, and other malignancies^8—10. Several diagnostic drugs targeting integrin α_vβ₃, including ^99mTc-3PRGD2 and ⁶⁸Ga-PRGD2, have been preliminarily validated by our group for imaging of lung cancer and other tumors via single photon emission computed tomography/computed tomography (SPECT/CT) or positron emission tomography/computed tomography (PET/CT)^11—14, with a promising prospect for its clinical application. However, the integrin α_vβ₃-targeted therapy studies are relatively few and mainly limited to preclinical research.

Targeted radionuclide therapy (TRT) is a promising method that uses radiolabeled targeting vectors to emit charged particles to treat advanced tumors¹⁵. These vectors can specifically seek the molecular or functional targets overexpressed in tumors and systemically treat the local and metastatic tumors through intravenous administration¹⁶. ¹⁷⁷Lu-DOTATATE and ¹⁷⁷Lu-PSMA-617 have achieved tremendous success in the treatment of advanced neuroendocrine tumors and castration-resistant prostate cancer, respectively^17,18. Radionuclide therapy using labeled RGD peptide analogs to target the integrin α_vβ₃-avid tumors holds promise and may have broader clinical applications in the treatment of a variety of malignancies⁶.

A few RGD-based TRT studies have been reported in animal models^19—24. Both ¹⁷⁷Lu and ⁹⁰Y were used for labeling RGD peptides to treat integrin α_vβ₃-avid tumors, however, ¹⁷⁷Lu was preferred for its relatively lower toxicity^19,20. Multivalent, PEGylated, cyclic RGD peptides were proved to have high tumor-targeting capability and therapeutic effects^20,21. Although our prior study indicated that ¹⁷⁷Lu-3PRGD2 treatment probes could significantly inhibit the growth of U87-MG tumors, there was still significant room for optimization regarding the limitation of rapid drug clearance and low tumor uptake²⁰. Serum albumin, a protein that is abundant in serum, can be reversibly bound by negatively charged or hydrophobic small molecules, making it possible to produce long-acting therapeutic drugs to reduce the frequency and dosage of radiopharmaceuticals²². Albumin binders, such as Evans blue (EB) and palmitic acid, were introduced to synthesize ¹⁷⁷Lu-EB-RGD and ¹⁷⁷Lu-Palm-3PRGD2, which showed a significant increase of tumor uptake and retention, leading to enhanced efficacy of targeted therapy compared to ¹⁷⁷Lu-RGD and ¹⁷⁷Lu-3PRGD2, respectively^23,24.

Here, we present a novel radionuclide therapeutic drug candidate, ¹⁷⁷Lu-AB-3PRGD2, with a PEGylated cyclic RGD dimer to target integrin α_vβ₃ and an albumin-binding motif to optimize the pharmacokinetics. This first-in-human study was designed to investigate the safety, pharmacokinetics, and dosimetry of ¹⁷⁷Lu-AB-3PRGD2 in patients with integrin α_vβ₃-avid tumors demonstrated by ⁶⁸Ga-DOTA-3PRGD2 PET/CT.

2.　Materials and methods

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2.1.　 Patient recruitment

This prospective study was approved by the Institutional Review Board of the Peking Union Medical College Hospital (ZS-2868), and written informed consent was obtained from each participant. The study was registered at ClinicalTrials.gov (NCT05013086). From February of 2023 to October of 2023, 10 patients (3 men, 7 women) aged 23–70 (45 ± 16) years with body mass index (BMI) of 13.40–29.30 (20.79 ± 5.13) kg/m² were recruited, including 8 patients with adenoid cystic carcinoma (ACC), 1 patient with intrahepatic cholangiocarcinoma (ICC), and 1 patient with uterine leiomyosarcoma (uLMS). The main characteristics of participants are listed in Table 1.

The inclusion criteria were: (1) age >18 years old; (2) with precise pathological diagnosis and have failed or progressed after conventional clinical treatments, including surgery, chemotherapy, or radiotherapy; (3) baseline ⁶⁸Ga-DOTA-3PRGD2 PET/CT revealed at least one avid lesion with uptake higher than normal liver; (4) expected survival time >6 months; (5) liver and kidney functions and blood routine tests were generally normal, or with white blood cells (WBC) ≥2.5 × 10⁹/L, platelets (PLT) ≥100 × 10⁹/L, hemoglobin (HB) ≥90 g/L; total bilirubin ≤1.5 × the institutional upper limit of normal (ULN), alanine aminotransferase (ALT) or aspartate aminotransferase (AST) ≤3.0 × ULN or ≤5.0 × ULN (liver metastasis), serum creatinine (Cr) ≤1.5 × ULN. The exclusion criteria were: (1) received Strontium-89, Samarium-153, Radium-223, or any other radionuclide treatment within 6 months; (2) received chemotherapy, radiotherapy, immunotherapy, or clinical trial drugs within 28 days; (3) with claustrophobia or radiation phobia; (4) in serious illness with difficulty for further diagnosis and treatment. The trail profile is displayed in Fig. 1.

2.2.　 PET/CT examinations

All patients underwent both ⁶⁸Ga-DOTA-3PRGD2 PET/CT and ¹⁸F-FDG PET/CT examinations within two weeks before ¹⁷⁷Lu-AB-3PRGD2 treatment, and the time interval between ⁶⁸Ga-DOTA-3PRGD2 and ¹⁸F-FDG PET/CT was within 48 h. After intravenous injection of ⁶⁸Ga-DOTA-3PRGD2 in a dosage of 1.48–1.85 MBq (0.04–0.05 mCi) per kg body weight or ¹⁸F-FDG in a dosage of 5.55–7.40 (0.15–0.20) mCi/kg, the patients rested quietly for approximately 45 or 60 min, respectively. Whole-body PET/CT was performed using a PoleStar m660 PET/CT scanner (SinoUnion Healthcare Inc., Beijing, China). Whole-body imaging was performed from mid-thigh to the top of the head. A low-dose CT scan was first performed for positioning, followed by a PET scan with 5–6 bed positions depending on the height of the patient, with each bed position scanning for 2 min. The ordered-subset expectation maximization (OSEM) method was used to reconstruct the PET image data (SinoUnion PoleStar: 2 iterations, 10 subsets, Gaussian filter, half-maximum width 4.5 mm, matrix 192 × 192), and attenuation correction was performed with the low-dose CT.

⁶⁸Ga-DOTA-3PRGD2 and ¹⁸F-FDG PET/CT scans were repeated 6–8 weeks after the treatment for response evaluation.

2.3.　 Synthesis and quality control of ¹⁷⁷Lu-AB-3PRGD2

No carrier-added ¹⁷⁷LuCl₃ for clinical use was purchased from ITM (Germany), with a specific activity of ≥3000 GBq/mg and a concentration of 36–44 GBq/mL. Typically, 3.7 GBq (100 mCi) ¹⁷⁷LuCl₃ was added to 200 μL of 0.5 mol/L NaOAc (pH 5.6), and the ¹⁷⁷Lu dilution was injected into the vial with 100 μg of DOTA-AB-3PRGD2 (Fig. 2A) provided by the Medical Isotopes Research Center, School of Basic Medical Sciences, Peking University. The mixture was heated in an upright position at 100 ℃ for 30 min, then purified through a C18 cartridge and sterilized through a 0.22-μm aseptic filtration membrane. Radiochemical purity was tested using analytical thin-layer chromatography (Bioscan, USA). CH3OH: NH₄OAc (1:1, v/v) was used as the developing solution. The radioactive labeling yield was greater than 90%, and after purification, the radiochemical purity of ¹⁷⁷Lu-AB-3PRGD2 should exceed 95% before clinical use (Fig. 2B). The sterility test and bacterial endotoxin test performed according to the Chinese Pharmacopoeia 2020 were negative for 3 consecutive batches to qualify the clinical use of subsequent batches.

2.4.　 ¹⁷⁷Lu-AB-3PRGD2 treatment

¹⁷⁷Lu-AB-3PRGD2 was diluted in 30 mL physiological saline to obtain ¹⁷⁷Lu-AB-3PRGD2 injection. The ¹⁷⁷Lu-AB-3PRGD2 treatment was performed in the ward for radionuclide therapy. The administered radioactivity was 1.56 ± 0.08 GBq (42.32 ± 2.11 mCi) for the patients and the dose for each patient is listed in Table 1.

2.5.　 Whole body planar and SPECT/CT

Whole-body planar scans of the patients after ¹⁷⁷Lu-AB-3PRGD2 injection and a SPECT/CT scan of the abdomen were performed using a Philips Precedence scanner (Philips Healthcare, Andover, Massachusetts, USA) with medium-energy general-purpose collimators, peaking at 208 KeV with a 20% energy window. The whole-body planar images were acquired at 3 ± 0.5, 24 ± 1, 48 ± 1, 72 ± 1, 96 ± 1, 120 ± 1, and 168 ± 1 h after the ¹⁷⁷Lu-AB-3PRGD2 injection, using an acquisition matrix of 256 × 1024 and a scan speed of 15 cm/min. The dual-head SPECT/CT scans were acquired at 72 or 96 h post-injection, with each head acquiring 32 frames in a 40 s exposure time per frame. Low-dose CT was obtained for positioning and attenuation correction.

2.6.　 Blood sample collection and count measurement

After the injection of ¹⁷⁷Lu-AB-3PRGD2, 1–2 mL of venous blood was drawn at 5 ± 1 min, 3 ± 0.5 h, 24 ± 1 h, 72 ± 1 h, and 168 ± 1 h to measure the radioactivity using a Cobra II auto-gamma counter (Perkin-Elmer).

2.7.　 Adverse events collection and safety tests

Adverse events and subjective health complaints were collected after treatment. Laboratory tests, including blood routine tests and hepatic and renal function tests, were performed before and every two weeks until 6–8 weeks later. The adverse events and laboratory tests were categorized according to the Common Toxicity Criteria for Adverse Events 5.0 (CTCAE V5.0).

2.8.　 Dosimetry analysis

Hermes Hybrid Viewer Dosimetry module (HERMES Medical Solutions Inc., Greenville, MA, USA) was used to derive the absorbed doses of the organs and whole-body effective doses. The volumes of individual organs, including the brain, heart, kidneys, liver, lungs, pancreas, red bone marrow, spleen, and urinary bladder, were delineated on serial SPECT/CT slice-by-slice and projected onto the whole-body images to obtain their residence time and other values. The residence times of different patients were determined by fitting the time–activity curves obtained from multiple time-point imaging data and calculating the integral under the curves.

The dosimetry module in conjunction with Olinda/EXM uses the well-established MIRD technique to determine organ and whole-body doses from the radionuclide within the body. The equations for absorbed dose in an organ are shown in Eqs. (1), (2):

D r κ = ∑ h A ˜ h S (r κ ← r h)

(1)

where r_k represents a target region, r_h represents a source region, Ã_h is the cumulated activity (integrated area under time activity curve), and S is a factor to convert the integrated activity into absorbed dose.

S (r κ ← r h) = κ ∑ i n i E i Φ i (r κ ← r h) m r κ

(2)

where n_i is the number of radiations with energy E emitted per nuclear transition, E_i is the energy per radiation (MeV), ϕ_i is the fraction of energy emitted that is absorbed in the target, m is the mass of the target region and k is the proportionality constant.

2.9.　 Statistical analysis

Calculations were performed using the SPSS software (IBM SPSS Statistics for Windows, version 25.0; Armonk, NY, USA). Continuous variables are summarized as mean ± standard deviations (SD). Categorical variables were described as numbers and percentages. Detailed correlations between the pre-therapy standardized uptake value (SUV) of ⁶⁸Ga-DOTA-3PRGD2 and the effective absorbed dose of the main normal organs were assessed using Spearman's rank correlation coefficient. The mean counts obtained by SPECT/CT were defined as counts_mean. All tests were two-sided, and P < 0.05 was considered statistically significant.

3.　Results

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3.1.　 Safety and toxicity

No remarkable acute adverse event was reported during the ¹⁷⁷Lu-AB-3PRGD2 injection. During the follow-ups, there was no instance of life-threatening grade 4 or 5 toxicity observed in any of the patients. No significant change was found in blood white blood cell counts (P = 0.495), hemoglobin level (P = 0.837), platelet counts (P = 0.459), and serum alanine aminotransferase (ALT) level (P = 0.630), aspartate aminotransferase (AST) level (P = 0.925), creatinine level (P = 0.645) before and after treatment (Fig. 3A‒F).

Adverse events were found in 3 patients (3/10, 30%) (Fig. 3, Table 2). A maximum of grade 3 elevations of ALT and AST was observed in patient No. 8 in the 6th week after treatment, which decreased significantly 2 weeks later without special treatment. Patient No. 3 also showed a maximum of grade 2 ALT elevation and grade 1 AST elevation that recovered two weeks later. Both patients had confounding factors, including multiple intrahepatic cholangiocarcinoma in patient No. 8 and liver metastasis of ACC in Patient No. 3. In addition, Patient No. 7 with borderline hemoglobin reported a grade 2 reduction 2 weeks after therapy, which was partly recovered 4 weeks after the therapy.

3.2.　 Pharmacokinetics

¹⁷⁷Lu-AB-3PRGD2 was excreted mainly through the urinary system, with intense radioactivity in the bladder and kidneys. Radioactivity could also be observed in the intestine, which was changed over time. Moderate physiological uptake was found in the liver and spleen. There was very low uptake in the brain. Representative images of the patients are shown in Fig. 4A‒D.

The uptakes in the percentage of injection activity for normal organs and tumor lesions are shown in Fig. 5A and B. The urinary bladder had the highest residence time (8.45 h), followed by the liver (3.96 h), heart (2.06 h), and red bone marrow (2.03 h) (Fig. 5C, Table 3). The decay curve of counts per minute (CPM) for ¹⁷⁷Lu-AB-3PRGD2 over time was plotted based on blood samples extracted at 5 min and 3, 24, 72, and 168 h (Fig. 5D) and the fitted exponential decay curve. Based on the fitted model, the estimated half-life of ¹⁷⁷Lu-AB-3PRGD2 in blood was approximately 2.85 ± 2.17 h.

3.3.　 Dosimetry of normal organs

The whole-body effective dose of ¹⁷⁷Lu-AB-3PRGD2 was 0.251 ± 0.047 mSv/MBq. The absorbed doses of normal organs are shown in Table 3. The average red bone marrow dose was 0.157 ± 0.032 mGy/MBq. The absorbed dose of the kidneys was 0.684 ± 0.132 mGy/MBq, and the absorbed dose of the bladder was 1.852 ± 1.047 mGy/MBq. Furthermore, a systemic dose of 0.128 ± 0.013 mGy/MBq demonstrated the non-targeted systemic distribution of the radiopharmaceutical.

3.4.　 Correlation of SUV and absorbed doses in normal organs

Linear regression analysis showed a high positive correlation of ⁶⁸Ga-DOTA-3PRGD2 SUV_mean and ¹⁷⁷Lu-AB-3PRGD2 counts_mean in normal organs at different time points, with the highest R-value at 24 h (R = 0.830 at 3 h, P < 0.001; R = 0.840 at 24 h, P < 0.001; R = 0.790 at 48 h, P < 0.001; R = 0.760 at 72 h, P < 0.001; R = 0.760 at 96 h, P < 0.001; R = 0.730 at 120 h, P < 0.001; R = 0.700 at 168 h, P < 0.001) (Fig. 6).

The SUV_max and SUV_mean of ⁶⁸Ga-DOTA-3PRGD2 correlated with the absorbed doses of ¹⁷⁷Lu-AB-3PRGD2 in normal organs (R = 0.360 for SUV_max, P < 0.001; R = 0.340 for SUV_mean, P < 0.001) (Fig. 7A).

3.5.　 Correlation of SUV and absorbed doses in tumor lesions

From the 10 patients, a total of 40 tumors were measured, including 5 head and neck soft tissue lesions, 14 lung metastases, 11 bone metastases, 5 liver metastases, 3 pleural metastases, and 2 lymph node metastases, with no more than 2 lesions from each organ of each patient. The SUV_max and SUV_mean of ⁶⁸Ga-DOTA-3PRGD2 in the tumor lesions correlated significantly with the corresponding absorbed doses of ¹⁷⁷Lu-AB-3PRGD2 (R = 0.780 for SUV_max, P < 0.001; R = 0.790 for SUV_mean, P < 0.001) (Fig. 7B).

3.6.　 Response assessment

In the symptom assessment (Table 4), three patients with ACC experienced worsened symptoms, including one patient with worsening visual acuity, one with more oral bleeding, and one with decreased physical strength and worsening fatigue. Three patients felt lessened symptoms, including one ICC patient with better appetite and 3-kg body weight gain within 8 weeks, one ACC patient with reduced pain caused by bone metastases, and one ACC patient with less coughing caused by lung metastases. According to PERCIST 1.0²⁵, the partial response rate was 10% (1/10), the stable disease rate was 80% (8/10), and the progressive disease rate was 10% (1/10). According to RECIST 1.1²⁶, nine patients exhibited stable disease, and one patient showed disease progression. The images of the patient with partial response, according to PERCIST 1.0, are shown in Fig. 8A and B.

4.　Discussion

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In this prospective pilot study, a novel radionuclide drug candidate targeting integrin α_vβ₃ with PEGylated cyclic RGD dimmers and an albumin-binding motif, ¹⁷⁷Lu-AB-3PRGD2, was translated into a first-in-human clinical trial in patients with integrin α_vβ₃-avid tumors, mostly adenoid cystic carcinoma. The primary outcome was to obtain the pharmacokinetics and dosimetry of ¹⁷⁷Lu-AB-3PRGD2 in human beings and the second outcome was the evaluation of the preliminary safety data and possible responses to the single-dose treatment.

According to this study, ¹⁷⁷Lu-AB-3PRGD2 was predominantly excreted through the renal-urinary pathway, with the most intense radioactivity observed and the highest absorbed doses in the bladder and followed by the kidneys, similar to the other RGD-based peptides in human being^27—29. The established tolerance absorbed-dose limit for the kidneys was 23 Gy³⁰. According to our dosimetry data 0.684 ± 0.132 mGy/MBq for kidneys, the maximum dosing activities in the kidneys would be 33.625 ± 6.489 GBq, which was 22.7 times the current administered dose. Moreover, the kidneys, once regarded as the critical organ for radiation toxicity, showed excellent tolerance to radiation doses as high as 50–60 Gy in selected cases³¹. ¹⁷⁷Lu-labeled peptides appeared to be well tolerated even in patients with preexisting chronic kidney disease stage 3, with a low incidence of permanent major nephrotoxicity³². No evidence of nephrotoxicity and no adverse event related to the urinary system was observed in this study. However, further researchers still need to pay attention to the nephrotoxicity of higher doses of ¹⁷⁷Lu-AB-3PRGD2 treatment with multiple courses.

Moderate physiological uptake was found in the liver, with a residence time of 3.96 ± 0.55 h and an absorbed dose of 0.204 ± 0.028 mGy/MBq. Among the 10 participants, two (20%) suffered from adverse events of liver function tests. One patient with grade 3 elevated ALT and AST levels had intrahepatic cholangiocarcinoma accompanied by liver metastases, who had been found with grade 1 elevation of ALT and AST levels before treatment. Another patient with grade 2 elevation of ALT and grade 1 elevation of AST levels had liver metastases of adenoid cystic carcinoma. His ALT and AST levels were transient and returned to normal in the 4th week after treatment and subsequent follow-ups. Although no confirmed hepatotoxicity has been established with the ¹⁷⁷Lu-AB-3PRGD2 treatment, it might be necessary to closely monitor liver function in further studies.

Radioactivity could also be observed in the intestine, which was changed over time, indicating partial hepato-intestinal excretion of ¹⁷⁷Lu-AB-3PRGD2. No adverse event related to the gastrointestinal system was observed in this study. The accurate percentage of excretion from the renal-urinary system and the hepato-intestinal route needed further studies to collect and measure radioactivity in urine and feces, respectively. The excretion of ^99mTc-Maraciclatide in healthy volunteers was reported as 55% and 16% through the urinary pathway and intestinal tract, respectively²⁸.

With an albumin-binding motif reversibly binding to serum albumin to optimize the pharmacokinetics, the estimated half-life of ¹⁷⁷Lu-AB-3PRGD2 in the blood was 2.85 ± 2.17 h, which was much longer than the 8.6 min plasma half-life of a reported RGD dimmer [⁶⁸Ga]Ga-NODAGA-E[c(RGDyK)]₂ for PET imaging²⁹. An albumin-binding motif could provide more chances for the target binding and remarkably increase the radioactivity accumulation in the tumor, as reported in our prior studies using Evan's blue and similar albumin binding moiety^31—33. However, this may also increase the possibility of toxicity to normal organs, especially to red bone marrow causing hematological toxicity. In this study, only a patient with uterine leiomyosarcoma developed a grade 2 anemia two weeks after the treatment. She had borderline anemia before treatment and the changes were partly recovered 4 weeks after the therapy.

Many radionuclide-labeled RGD derivatives have been developed to specifically target integrin α_vβ₃, and several approaches have been investigated to improve the pharmacokinetics and tumor accumulation of these derivatives, including their combination with glycosyl, hydrophilic amino acids, PEGs, dimeric or polymeric derivative^5—9. Reversibly binding to serum albumin is also one of the strategies to make it possible to produce long-acting therapeutic drugs to reduce the frequency and dosage of radiopharmaceuticals, which showed a significant increase of tumor uptake and retention, leading to enhanced efficacy of targeted therapy^22—24. However, along with the increase of tumor uptake, the absorption of non-targeted organs such as the kidneys, liver, and red bone marrow may also increase^33—35. Therefore, potential nephrotoxicity, hepatotoxicity, and hematological toxicity concerns still require careful attention in therapeutic research. In this study, intense to moderate physiological uptake of ¹⁷⁷Lu-AB-3PRGD2 was observed in the bladder, kidneys, liver, spleen, and intestines, the safety profile suggested that ¹⁷⁷Lu-AB-3PRGD2 was generally well tolerated by patients, with no significant acute adverse events or life-threatening toxicities. None of the patients experienced grade 4 or 5 toxicity, indicating that a dosage of 1.57 ± 0.08 MBq (42.32 ± 2.11 mCi) was relatively safe and in line with the therapeutic aim of providing an effective dose to the target tissue while preserving the normal organ system. However, the occurrence of possible drug-related adverse events in some patients, although not life-threatening, emphasizes the necessity of careful monitoring of these toxicities associated with the therapy in further studies with escalating doses and multiple treatment courses.

There were highly significant correlations between the ⁶⁸Ga-DOTA-3PRGD2 distribution on PET/CT and the ¹⁷⁷Lu-AB-3PRGD2 distribution on SPECT/CT. Furthermore, there were also positive correlations between the SUV_max or SUV_mean on ⁶⁸Ga-DOTA-3PRGD2 PET/CT and the absorbed doses of ¹⁷⁷Lu-AB-3PRGD2 in normal organs and tumors. These suggested that ⁶⁸Ga-DOTA-3PRGD2 PET/CT could be a robust and reliable method to select patients who might benefit from the ¹⁷⁷Lu-AB-3PRGD2 treatment.

Most patients in this study had stable conditions after treatment. However, three patients reported symptom improvement and one patient showed an ¹⁸F-FDG uptake decrease, indicating positive responses to the current single low-dose treatment and providing a foundation for subsequent escalating and multi-dose treatments with ¹⁷⁷Lu-AB-3PRGD2.

This study had several limitations: First, the treatment dosage of ¹⁷⁷Lu-AB-3PRGD2 was relatively low as a pilot study mainly focusing on pharmacokinetics and dosimetry, making the safety evaluations insufficient for routine clinical radionuclide therapy with full dose. Second, only a single dose was administered to each patient, whereas 4–6 courses were usually adopted in a routine clinical setting. In addition, the number of patients was small and the disease types were limited in this study. Moreover, the follow-up period was only 6–8 weeks, an interval duration of two consecutive treatment courses. However, in light of the promising findings in this preliminary pilot study, further studies were warranted with escalated doses and multiple courses in a more diverse patient population to verify the safety and efficacy of ¹⁷⁷Lu-AB-3PRGD2. Furthermore, an extended follow-up period would be beneficial for assessing the long-term safety and overall survival of the new treatment strategy.

5.　Conclusions

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This prospective first-in-human pilot study of ¹⁷⁷Lu-AB-3PRGD2, a novel integrin α_vβ₃-targeting drug with an albumin-binding motif, preliminarily indicates its safety in human beings and demonstrates an optimal pharmacokinetics and dosimetry as a potential candidate drug for radionuclide therapy. ⁶⁸Ga-DOTA-3PRGD2 PET/CT can help to select patients who may benefit from the ¹⁷⁷Lu-AB-3PRGD2 therapy and evaluate the integrin α_vβ₃-avid tumors. The promising results of this study merit further investigations of ¹⁷⁷Lu-AB-3PRGD2 treatment in more patients with escalating doses and multiple courses, and subsequently, conduct long-term evaluations to determine its safety and efficacy.

References

Less

Fagerholm

. Integrins in health and disease. N Engl J Med 2022;387:1519—21.

Barczyk

, Carracedo

, Gullberg

. Integrins. Cell Tissue Res 2010;339:269—80.

Liu

, Wu

, Dong

, Liu

. Integrins in cancer: emerging mechanisms and therapeutic opportunities. Pharmacol Ther 2023;247:108458.

Slack

, Macdonald

SJF

, Roper

, Jenkins

, Hatley

RJD

. Emerging therapeutic opportunities for integrin inhibitors. Nat Rev Drug Discov 2022;21:60—78.

Ludwig

, Kessler

, Kossatz

, Reuning

. RGD-binding integrins revisited: how recently discovered functions and novel synthetic ligands (re-)shape an ever-evolving field. Cancers (Basel) 2021;13:1711.

Badipa

, Alirezapour

, Yousefnia

. An overview of radiolabeled RGD peptides for theranostic applications. Curr Radiopharm 2023;16:107—22.

Sani

, Messe

, Fuchs

, Pierrevelcin

, Laquerriere

, Entz-Werle

, et al. Biological relevance of RGD-integrin subtype-specific ligands in cancer. Chembiochem 2021;22:1151—60.

, Chen

, Yu

, Yuan

. Preliminary clinical application of RGD-containing peptides as PET radiotracers for imaging tumors. Front Oncol 2022;12:837952.

Chen

, Niu

, Wu

, Chen

. Clinical application of radiolabeled RGD peptides for PET imaging of integrin αvβ3. Theranostics 2016;6:78—92.

10.

Xiao

, Xin

. Advances in clinical oncology research on ^99mTc-3PRGD2 SPECT Imaging. Front Oncol 2022;12:898764.

11.

Jin

, Liang

, Wang

, Meng

, Jia

, Shi

, et al. Integrin imaging with ^99mTc-3PRGD2 SPECT/CT shows high specificity in the diagnosis of lymph node metastasis from non-small cell lung cancer. Radiology 2016;281:958—66.

12.

Zhu

, Miao

, Li

, Dai

, Ma

, Wang

, et al. ^99mTc-3PRGD2 for integrin receptor imaging of lung cancer: a multicenter study. J Nucl Med 2012;53:716—22.

13.

Zheng

, Liang

, Zhang

, Lang

, Zhang

, Li

, et al. ⁶⁸Ga-NOTA-PRGD2 PET/CT for integrin imaging in patients with lung cancer. J Nucl Med 2015;56:1823—7.

14.

, Zhang

, Ji

, Zhao

, Zheng

, Qiao

, et al. Combined ⁶⁸Ga-NOTA-PRGD2 and ¹⁸F-FDG PET/CT can discriminate uncommon meningioma mimicking high-grade glioma. Clin Nucl Med 2018;43:648—54.

15.

Goldsmith

. Targeted radionuclide therapy: a historical and personal review. Semin Nucl Med 2020;50:87—97.

16.

Gill

, Falzone

, Du

, Vallis

. Targeted radionuclide therapy in combined-modality regimens. Lancet Oncol 2017;18:e414—23.

17.

Strosberg

, El-Haddad

, Wolin

, Hendifar

, Yao

, Chasen

, et al. Phase 3 trial of ¹⁷⁷Lu-Dotatate for midgut neuroendocrine tumors. N Engl J Med 2017;376:125—35.

18.

Sartor

, de Bono

, Chi

, Fizazi

, Herrmann

, Rahbar

, et al. Lutetium-177-PSMA-617 for metastatic castration-resistant prostate cancer. N Engl J Med 2021;385:1091—103.

19.

Bozon-Petitprin

, Bacot

, Gauchez

, Ahmadi

, Bourre

, Marti-Batlle

, et al. Targeted radionuclide therapy with RAFT-RGD radiolabelled with ⁹⁰Y or ¹⁷⁷Lu in a mouse model of αvβ3-expressing tumors. Eur J Nucl Med Mol Imaging 2015;42:252—63.

20.

Shi

, Fan

, Dong

, Liu

, Jia

, Zhao

, et al. Anti-tumor effect of integrin targeted ¹⁷⁷Lu-3PRGD2 and combined therapy with Endostar. Theranostics 2014;4:256—66.

21.

Pirooznia

, Abdi

, Beiki

, Emami

, Arab

, Sabzevari

, et al. ¹⁷⁷Lu-labeled cyclic RGD peptide as an imaging and targeted radionuclide therapeutic agent in non-small cell lung cancer: biological evaluation and preclinical study. Bioorg Chem 2020;102:104100.

22.

Lau

, Jacobson

, Niu

, Lin

, Bénard

, Chen

. Bench to bedside: albumin binders for improved cancer radioligand therapies. Bioconjug Chem 2019;30:487—502.

23.

Zhao

, Chen

, Guo

, Fu

, Yao

, Fu

, et al. Targeted radionuclide therapy in patient-derived xenografts using ¹⁷⁷Lu-EB-RGD. Mol Cancer Ther 2020;19:2034—43.

24.

Yang

, Gao

, Luo

, Zhao

, Luo

, Shi

, et al. Palmitic acid-conjugated radiopharmaceutical for integrin α_vβ₃-targeted radionuclide therapy. Pharmaceutics 2022;14:1327.

25.

Wahl

, Jacene

, Kasamon

, Lodge

. From RECIST to PERCIST: evolving considerations for PET response criteria in solid tumors. J Nucl Med 2009;50:122S—50S.

26.

Eisenhauer

, Therasse

, Bogaerts

, Schwartz

, Sargent

, Ford

, et al. New response evaluation criteria in solid tumors: revised RECIST guideline (version 1.1). Eur J Cancer 2009;45:228—47.

27.

Doss

, Kolb

, Zhang

, Bélanger

, Stubbs

, Stabin

, et al. Biodistribution and radiation dosimetry of the integrin marker ¹⁸F-RGD-K5 determined from whole-body PET/CT in monkeys and humans. J Nucl Med 2012;53:787—95.

28.

Gibbons

, Perkins

, Barnett

. Safety, biodistribution and radiation dosimetry of the Arg-Gly-Asp peptide ^99mTc-maraciclatide in healthy volunteers. Nucl Med Commun 2024;45:295—303.

29.

Clausen

, Carlsen

, Christensen

, Madsen

, Brandt-Larsen

, Klausen

, et al. First-in-human study of [⁶⁸Ga]Ga-NODAGA-E[c(RGDyK)](2) PET for integrin α_vβ₃ imaging in patients with breast cancer and neuroendocrine neoplasms: safety, dosimetry, and tumor imaging ability. Diagnostics 2022;12:851.

30.

Del Prete

, Buteau

, Arsenault

, Saighi

, Bouchard

, Beaulieu

, et al. Personalized ¹⁷⁷Lu-octreotate peptide receptor radionuclide therapy of neuroendocrine tumors: initial results from the P-PRRT trial. Eur J Nucl Med Mol Imaging 2019;46:728—42.

31.

Parihar

, Chopra

, Prasad

. Nephrotoxicity after radionuclide therapies. Transl Oncol 2022;15:101295.

32.

Alsadik

, Gnanasegaran

, Chen

, Mandair

, Toumpanakis

, Caplin

, et al. Safety of peptide receptor radionuclide therapy with ¹⁷⁷Lu-DOTATATE in neuroendocrine tumor patients with chronic kidney disease. J Nucl Med 2022;63:1503—8.

33.

Zang

, Fan

, Wang

, Liu

, Wang

, Li

, et al. First-in-human study of ¹⁷⁷Lu-EB-PSMA-617 in patients with metastatic castration-resistant prostate cancer. Eur J Nucl Med Mol Imaging 2019;46:148—58.

34.

Zhang

, Wang

, Jacobson

, Cheng

, Niu

, Li

, et al. Safety, Pharmacokinetics, and dosimetry of a long-acting radiolabeled somatostatin analog ¹⁷⁷Lu-DOTA-EB-TATE in patients with advanced metastatic neuroendocrine tumors. J Nucl Med 2018;59:1699—705.

35.

, Wang

, Jin

, Zang

, et al. Comparison of novel PSMA-targeting [¹⁷⁷Lu]Lu-P17-087 with its albumin binding derivative [¹⁷⁷Lu]Lu-P17-088 in metastatic castration-resistant prostate cancer patients: a first-in-human study. Eur J Nucl Med Mol Imaging 2024;51:2794—805.

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Year 2025 volume 15 Issue 2

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doi: 10.1016/j.apsb.2024.10.012

Receive Date：2024-06-16
Online Date：2026-09-17

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Received：2024-06-16
Revised：2024-09-18
Accepted：2024-09-25

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^bDepartment of Nuclear Medicine, Sixth Medical Center of PLA General Hospital, Beijing 100048, China

^cDepartment of Otolaryngology-Head and Neck Surgery, Beijing Tongren Hospital, Capital Medical University, Beijing 100730, China

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^* Corresponding authors.

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表12种不同金属材料的力学参数

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

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Table 1 Main characteristics of the participants.

Patient number	Gender	Age	BMI (kg/m²)	Pathology	Lesion location	Prior treatment	Dose: GBq (mCi)
1	F	36	19.1	ACC	Head and neck, lung, bone	Surgery, radiotherapy	1.38 (37.40)
2	M	57	26.3	ACC	Head and neck, lung, pleura, intercostal space	Surgery, chemotherapy, radiotherapy	1.48 (40.10)
3	M	50	29.3	ACC	Lung, pleura, bone, liver	Surgery, radiotherapy	1.56 (42.10)
4	M	48	22.6	ACC	Lung	Surgery, targeted therapy	1.63 (44.00)
5	F	27	13.4	ACC	Head and neck, bone	Surgery, radiotherapy, targeted therapy	1.56 (42.20)
6	F	27	21.3	ACC	Head and neck, liver, bone	Surgery, radiotherapy	1.62 (43.90)
7	F	70	24.2	uLMS	Lymph node, lung	Surgery, radiotherapy, immunotherapy	1.62 (43.70)
8	F	52	20.8	ICC	Lymph node, liver	Surgery, TACE, targeted therapy, immunotherapy	1.58 (42.80)
9	F	23	16.9	ACC	Bone	Surgery, chemotherapy, radiotherapy, targeted therapy	1.59 (42.90)
10	F	57	14.0	ACC	Head and neck, lung, bone	Surgery, chemotherapy, radiotherapy, targeted therapy	1.63 (44.10)

ACC: adenoid cystic carcinoma; ICC: intrahepatic cholangiocarcinoma; uLMS: uterine leiomyosarcoma; TACE: transcatheter arterial chemoembolization.

Table 2 Adverse events reported in each patient during the follow-ups assessed according to CTCAE 5.0.

Patient number	Baseline status	Grade of adverse event/week
Patient number	Baseline status	2	4	6	8
1	Normal	0	0	0	–
2	Normal	0	0	0	–
3	ALT: 35.1 U/LAST: 19.9 U/L	21	00	00	––
4	Normal	0	0	0	–
5	Normal	0	0	0	–
6	ALT: 141.5 U/LAST: 115.0 U/L	0	0	0	–
7	HB: 108 g/L	2	1	1	–
8	ALT: 32.5 U/LAST: 45.0 U/L	00	10	33	31
9	WBC: 2.62 × 10⁹/L	0	0	0	–
10	Normal	0	0	0	–

ALT: alanine aminotransferase; AST: aspartate aminotransferase; HB: Hemoglobin; WBC: white blood cells.

Table 3 Residence time and absorbed doses in main organs and the effective dose.

Target organ	Residence time (h)	Absorbed dose (mGy/MBq) or effective dose (mSv/MBq)
Brain	0.14 ± 0.05	0.012 ± 0.003
Heart	2.06 ± 0.84	0.273 ± 0.074
Kidneys	1.30 ± 0.37 (left)1.12 ± 0.18 (right)	0.684 ± 0.132
Liver	3.96 ± 0.55	0.204 ± 0.028
Lungs	1.13 ± 0.62 (left)1.98 ± 2.70 (right)	0.232 ± 0.198
Pancreas	0.17 ± 0.09	0.120 ± 0.058
Red marrow	2.03 ± 0.80	0.157 ± 0.032
Spleen	0.95 ± 1.14	0.359 ± 0.162
Intestine	1.28 ± 0.32	0.092 ± 0.024
Urinary bladder	8.45 ± 5.01	1.852 ± 1.047
Total body	–	0.128 ± 0.013
Effective dose	–	0.251 ± 0.047

Table 4 Response assessment of the participant patients.

Response	Symptomatic evaluation n (%)	PERCIST 1.0 n (%)	RECIST 1.1 n (%)
Complete response	0 (0%)	0 (0%)	0 (0%)
Partial response	3 (30%)	1 (10%)	0 (0%)
Stable disease	4 (40%)	8 (80%)	9 (90%)
Progressive disease	3 (30%)	1 (10%)	1 (10%)

Figure 1 Trail profile.

Figure 2 The precursor structure and radiochemical purity of ¹⁷⁷Lu-AB-3PRGD2. (A) Structural formula of DOTA-AB-3PRGD2. The molecular formula is C₁₃₇H₂₁₅IN₃₀O₄₅S, and molecular weight is 3161.36. (B) Radiochemical purity of ¹⁷⁷Lu-AB-3PRGD2.

Figure 3 Serial changes of main indicators for hematological toxicity (A–C), hepatotoxicity (D–E), and nephrotoxicity (F) at baseline and 2, 4, 6, and 8 weeks after the ¹⁷⁷Lu-AB-3PRGD2 treatment. WBC: blood white blood cell counts; HB: blood hemoglobin level; PLT: blood platelet counts; ALT: serum alanine aminotransferase level; AST: serum aspartate aminotransferase level; and Cr: serum creatinine level.

Figure 4 Representative ⁶⁸Ga-DOTA-3PRGD2 PET/CT and ¹⁷⁷Lu-AB-3PRGD2 whole body planar scan and SPECT/CT images in a 52-year-old women. ¹⁷⁷Lu-AB-3PRGD2 accumulated in the intrahepatic cholangiocarcinoma and liver metastases. (A) ⁶⁸Ga-DOTA-3PRGD2 PET/CT, (B) ¹⁸F-FDG PET/CT, (C) ¹⁷⁷Lu-AB-3PRGD2 whole-body anterior planar images at different time points, (D) ¹⁷⁷Lu-AB-3PRGD2 SPECT/CT at 72 h.

Figure 5 Pharmacokinetics of ¹⁷⁷Lu-AB-3PRGD2 in the patients. (A) Changes of normal organ uptake in percentage of injection activity over time; (B) Changes of lesion uptake in percentage of injection activity over time; (C) Residence times of ¹⁷⁷Lu-AB-3PRGD2 in normal organs; (D) Radioactive curve of ¹⁷⁷Lu-AB-3PRGD2 in the blood of the participants (n = 10). CPM: decay-corrected counts per minute.

Figure 6 Correlation between the SUVmean of normal organs on ⁶⁸Ga-DOTA-3PRGD2 PET/CT and the corresponding counts_mean on ¹⁷⁷Lu-AB-3PRGD2 planar scans at different time points.

Figure 7 Correlation between the SUVmax (left) and SUVmean (right) of ⁶⁸Ga-DOTA-3PRGD2 and ¹⁷⁷Lu-AB-3PRGD2 absorbed dose of normal organs (A) and tumors (B).

Figure 8 Comparison of ¹⁸F-FDG PET/CT images with a single dose of 1.62 GBq (43.70 mCi) ¹⁷⁷Lu-AB-3PRGD2 treatment in a 70-year-old patient with uterine leiomyosarcoma. (A) The baseline images of maximum intensity projection (left) and pelvic transaxial view of PET, CT and PET/CT (right, from top to bottom); (B) The follow-up images 6 weeks after the treatment, with a remarkably decrease of the SUV_max from 12.0 to 4.6 in a pelvic lymph node metastasis (red arrow), but a mild change of the SUV_max from 22.7 to 22.4 in a larger lung metastasis (black arrow).

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