Safety and efficacy of 177Lu-FAPI-XT radioligand therapy in patients with advanced sarcoma and other cancer entities: first-in-human, dose-escalation study

‌PURPOSE‌: This phase I, first-in-human study evaluated the safety, dosimetry, and preliminary efficacy of <sup>177</sup>Lu-FAPI-XT, a novel fibroblast activation protein (FAP)-targeted radioligand, in patients with advanced solid tumors refractory to standard therapies. ‌METHODS‌: This open-label, non-randomized, dose-escalation, investigator-initiated trial had a "accelerated titration" and "3 + 3" design involved a 6-week <sup>177</sup>Lu-FAPI-XT treatment cycle in patients with advanced-stage solid tumors at 3.7GBq initially, with subsequent cohorts receiving an incremental 1.85GBq dose increase until dose limiting toxicity (DLT) was observed. ‌RESULTS‌: <sup>177</sup>Lu-FAPI-XT was well tolerated and no DLT or grade ≥ 3 treatment-related adverse events (TRAE) were observed. The whole-body effective dose was 0.039 ± 0.013 Sv/GBq. The mean effective half-lives for the whole-body and tumor lesions were 52.13 ± 12.33 h and 31.78 ± 15.03 h, respectively. According to RECIST stable disease (SD) were observed in 5 (5/14, 35.7%) patients, with the highest benefit observed in fibroblastic sarcoma subtypes with SD presented in 4 (4/8, 50%) patients. The median progression-free survival (PFS) was 4.63 m (95%CI: 1.25, NE). Metabolic reductions on PET/CT were observed in 2 sarcoma cases. (URL: hclinicaltrials.gov . Trial registration: NCT06211647, NCT06197139. Registered 4 January 2024.) ‌CONCLUSION‌: <sup>177</sup>Lu-FAPI-XT demonstrated a favorable safety profile, with preliminary signs of tumor response observed. Complete/partial response deficiency in <sup>177</sup>Lu-FAPI-XT therapy necessitate optimized strategies for efficacy improvement.

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Journal
European Journal of Nuclear Medicine and Molecular Imaging
Published
2025-10-15
DOI
https://doi.org/10.1007/s00259-025-07617-0
Primary Topic
Peptidase Inhibition and Analysis
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article
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article

Safety and efficacy of 177Lu-FAPI-XT radioligand therapy in patients with advanced sarcoma and other cancer entities: first-in-human, dose-escalation study

Shasha Sun, Ruimin Wang, Rui Guo, Ji Hu et al.
European Journal of Nuclear Medicine and Molecular Imaging
Peptidase Inhibition and Analysis
article

Safety and efficacy of 177Lu-FAPI-XT radioligand therapy in patients with advanced sarcoma and other cancer entities: first-in-human, dose-escalation study

Shasha Sun, Ruimin Wang, Rui Guo, Ji Hu, Zhi Yang, Shuwei Sun, Jiayong Liu, Xiaojun Zhang, Honghong Liu
article en

Abstract

‌PURPOSE‌: This phase I, first-in-human study evaluated the safety, dosimetry, and preliminary efficacy of <sup>177</sup>Lu-FAPI-XT, a novel fibroblast activation protein (FAP)-targeted radioligand, in patients with advanced solid tumors refractory to standard therapies. ‌METHODS‌: This open-label, non-randomized, dose-escalation, investigator-initiated trial had a "accelerated titration" and "3 + 3" design involved a 6-week <sup>177</sup>Lu-FAPI-XT treatment cycle in patients with advanced-stage solid tumors at 3.7GBq initially, with subsequent cohorts receiving an incremental 1.85GBq dose increase until dose limiting toxicity (DLT) was observed. ‌RESULTS‌: <sup>177</sup>Lu-FAPI-XT was well tolerated and no DLT or grade ≥ 3 treatment-related adverse events (TRAE) were observed. The whole-body effective dose was 0.039 ± 0.013 Sv/GBq. The mean effective half-lives for the whole-body and tumor lesions were 52.13 ± 12.33 h and 31.78 ± 15.03 h, respectively. According to RECIST stable disease (SD) were observed in 5 (5/14, 35.7%) patients, with the highest benefit observed in fibroblastic sarcoma subtypes with SD presented in 4 (4/8, 50%) patients. The median progression-free survival (PFS) was 4.63 m (95%CI: 1.25, NE). Metabolic reductions on PET/CT were observed in 2 sarcoma cases. (URL: hclinicaltrials.gov . Trial registration: NCT06211647, NCT06197139. Registered 4 January 2024.) ‌CONCLUSION‌: <sup>177</sup>Lu-FAPI-XT demonstrated a favorable safety profile, with preliminary signs of tumor response observed. Complete/partial response deficiency in <sup>177</sup>Lu-FAPI-XT therapy necessitate optimized strategies for efficacy improvement.

European Journal of Nuclear Medicine and Molecular ImagingVol. 53(3)
Peking University (CN), Chinese PLA General Hospital (CN), China National Pharmaceutical Group Corporation (China) (CN), Peking University Cancer Hospital (CN), Ministry of Education (ET)
Openalex Percentile: Top 60%
Peptidase Inhibition and Analysis
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