| Autor: |
Chua, Wei Ming, Lam, Winnie Wing‐Chuen, Tong, Aaron Kian‐Ti, Sultana, Rehena, Kua, Sandra Mei Yu, Kanesvaran, Ravindran, Wong, Alvin Seng Cheong, Tay, Kae Jack, Cheng, Tai Jit Lenith, Ng, David Chee Eng, Thang, Sue Ping |
| Předmět: |
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| Zdroj: |
Asia Pacific Journal of Clinical Oncology; Oct2024, Vol. 20 Issue 5, p572-581, 10p |
| Abstrakt: |
Aim: Lutetium‐177 (Lu‐177) prostate‐specific membrane antigen radioligand therapy (PSMA‐RLT) is a promising therapy for metastatic castration‐resistant prostate cancer (mCRPC), but there is limited data of its efficacy and safety in Asian population. We aim to explore the clinical outcomes of Lu‐177 PSMA‐RLT in this population. Methods: We evaluated 84 patients with progressive mCRPC receiving Lu‐177 PSMA‐RLT between 9 May 2018 and 21 February 2022. Lu‐177‐PSMA‐I&T was administered at 6–8‐week intervals. Primary end point was overall survival (OS), and secondary end points included prostate‐specific antigen (PSA) progression‐free survival (PFS), PSA response rate, clinical response, toxicity assessment, and prognostic indicators. Results: The median OS and PSA PFS were 12.2 and 5.2 months, respectively. PSA decline of ≥50% was observed in 51.8% of patients. Patients achieving PSA response had longer median OS (15.0 vs. 9.5 months, p =.03) and PSA PFS (6.5 vs. 2.9 months, p <.001). Pain score improvement was seen in 19 out of 34 patients. A hematotoxicity of ≥grade 3 was observed in 13 out of 78 patients. Multivariable analyses showed that PSA velocity, alkaline phosphatase, hemoglobin (Hb), and the number of treatment cycles were independent prognostic indicators for OS. The retrospective design was the main limitation of the study. Conclusions: Our study demonstrated a similar safety and efficacy of Lu‐177 PSMA‐RLT in Asian mCRPC patients compared to the existing literature. A PSA decline ≥50% was associated with longer OS and PSA PFS. Several prognostic indicators for patient outcomes were also identified. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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