Prognostic Significance of Baseline Clinical and [68Ga]Ga-PSMA PET Derived Parameters on Biochemical Response, Overall Survival, and PSA Progression-Free Survival in Metastatic Castration-Resistant Prostate Cancer (mCRPC) Patients Undergoing [177Lu]Lu-PSMA Therapy.

Esmail Jafari, Reyhaneh Manafi-Farid, Hojjat Ahmadzadehfar, Fatemeh Salek, Narges Jokar, Ahmad Keshavarz, GhasemAli Divband, Habibollah Dadgar, Farshad Zohrabi, Majid Assadi
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Abstract

Background: In this study, we sought to identify the clinical baseline characteristics and pre-therapy 68Ga-PSMA PET derived parameters that can have impact on PSA (biochemical) response, OS and PSA PFS in patients with metastatic castration-resistant prostate cancer (mCRPC) who undergo RLT with [177Lu]Lu-PSMA-617.

Methods: Various pre-treatment clinical and PSMA PET derived parameters were gathered and computed. We used PSA response as the criteria for more than a 50% decrease in PSA level, and OS and PSA PFS as endpoints. We assessed the collected parameters in relation to PSA response. Additionally, we employed univariable Cox regression and Kaplan-Meier analysis with log rank to evaluate the influence of the parameters on OS and PFS.

Results: A total of 125 mCRPC patients were included in this study. The median age was 68 years (range: 49-89). Among the cases, 77 patients (62%) showed PSARS, while 48 patients (38%) did not show PSA response. The median OS was 14 months (range: 1-60), and the median PSA-PFS was 10 months (range: 1-56). Age, prior history of chemotherapy, and SUVmax had a significant impact on PSA response (p<0.05). PSA response, RBC count, hemoglobin, hematocrit, neutrophil to lymphocyte ratio (NLR), alkaline phosphatase (ALP), number of metastases, wbPSMA-TV, and wbTL-PSMA significantly affected OS. GS, platelet count, NLR, and number of metastases were found to have a significant impact on PSA PFS.

Conclusion: We have identified several baseline clinical and PSMA PET derived parameters that can serve as prognostic factors for predicting PSA response, OS, and PSA PFS after RLT. Based on the findings, we believe that these clinical baseline characteristics can assist nuclear medicine specialists in identifying RLT responders who have long-term survival and PFS.

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接受[177Lu]Lu-PSMA治疗的转移性钙化抗性前列腺癌(mCRPC)患者的基线临床参数和[68Ga]Ga-PSMA PET衍生参数对生化反应、总生存期和PSA无进展生存期的预后意义。
研究背景在这项研究中,我们试图确定接受[177Lu]Lu-PSMA-617 RLT治疗的转移性去势抵抗性前列腺癌(mCRPC)患者的临床基线特征和治疗前68Ga-PSMA PET衍生参数,这些参数可能会对PSA(生化)反应、OS和PSA PFS产生影响:收集并计算治疗前的各种临床参数和 PSMA PET 派生参数。我们以 PSA 水平下降 50% 以上为 PSA 反应标准,以 OS 和 PSA PFS 为终点。我们评估了所收集参数与 PSA 反应的关系。此外,我们还采用了单变量 Cox 回归和 Kaplan-Meier 对数秩分析来评估参数对 OS 和 PFS 的影响:本研究共纳入了 125 例 mCRPC 患者。中位年龄为68岁(范围:49-89岁)。其中,77 例患者(62%)出现 PSARS,48 例患者(38%)未出现 PSA 反应。中位 OS 为 14 个月(范围:1-60),中位 PSA-PFS 为 10 个月(范围:1-56)。年龄、既往化疗史和 SUVmax 对 PSA 反应有显著影响(p 结论:我们发现了一些基线临床参数和 PSMA PET 导出参数,这些参数可作为预测 RLT 后 PSA 反应、OS 和 PSA PFS 的预后因素。基于这些研究结果,我们认为这些临床基线特征可以帮助核医学专家识别RLT反应者的长期生存和PFS。
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