转移性肾上腺皮质癌全身治疗的疗效:前瞻性临床试验的荟萃分析。

Endocrine oncology (Bristol, England) Pub Date : 2025-09-05 eCollection Date: 2025-01-01 DOI:10.1530/EO-25-0027
S Shekar, A Hall, J Pham, M Crumbaker, J Liu, B Talmor, H W Sim, A M Joshua
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引用次数: 0

摘要

目的:评估转移性肾上腺皮质癌(mACC)全身治疗疗效的合并前瞻性试验数据,结合治疗方式和治疗线的亚组分析,建立生存和反应基准。方法:纳入2010年至2023年7月发表的mACC全身治疗方案的前瞻性试验。主要终点是总生存期(OS)、无进展生存期(PFS)和客观缓解率(orr)。采用随机效应模型和方差逆方法对ORR进行对数变换和汇总。对PFS和OS的Kaplan-Meier曲线进行数字化处理,并采用dersimonan - laird方法的多元扩展构建汇总曲线。结果:在24项研究中,纳入880例患者:386例接受化疗,169例接受免疫治疗,288例接受靶向治疗,37例接受其他治疗。治疗设置为一线(383例,44%),二线或以上(471,54%),未报告(26,3%)。合并ORR为9.0% (95% CI 6.0-13.2),异质性中等(I 2 = 54.2%, P < 0.01)。亚组分析显示,靶向治疗的orr为2.9%,化疗为12.3%,免疫治疗为15.3%。合并中位OS为9.9个月(95% CI 7.7-11.9),合并中位PFS为2.6个月(95% CI 1.9-3.6)。12个月OS率为41.6% (95% CI 33.1-51.2), 6个月PFS率为24.0% (95% CI 15.2-37.8)。结论:该分析为mACC的全身治疗建立了当代基准。虽然化疗和免疫治疗提供适度的生存益处,但靶向治疗的有限有效性突出了可操作的分子生物标志物的缺乏。未来的试验应旨在超越本分析中确定的生存结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Efficacy of systemic therapy in metastatic adrenocortical carcinoma: a meta-analysis of prospective clinical trials.

Efficacy of systemic therapy in metastatic adrenocortical carcinoma: a meta-analysis of prospective clinical trials.

Efficacy of systemic therapy in metastatic adrenocortical carcinoma: a meta-analysis of prospective clinical trials.

Efficacy of systemic therapy in metastatic adrenocortical carcinoma: a meta-analysis of prospective clinical trials.

Objective: To evaluate pooled prospective trial data investigating efficacy of systemic therapies in metastatic adrenocortical carcinoma (mACC), incorporating subgroup analyses by treatment modality and line, establishing survival and response benchmarks.

Methods: Prospective trials of systemic therapy regimens in mACC published from 2010 to July 2023 were included. Primary endpoints were overall survival (OS), progression-free survival (PFS), and objective response rates (ORRs). ORR was logit-transformed and pooled using a random effects model and inverse variance method. Kaplan-Meier curves for PFS and OS were digitised, and summary curves were constructed using a multivariate extension of the DerSimonian-Laird method.

Results: Across twenty-four studies, 880 patients were included: 386 received chemotherapy, 169 immunotherapies, 288 targeted therapies, and 37 other therapies. Treatment settings were first-line (383 patients, 44%), second-line or beyond (471, 54%), and not reported (26, 3%). Pooled ORR was 9.0% (95% CI 6.0-13.2) with moderate heterogeneity (I 2 = 54.2%, P < 0.01). Subgroup analysis showed ORRs of 2.9% for targeted therapy, 12.3% for chemotherapy, and 15.3% for immunotherapy. Pooled median OS was 9.9 months (95% CI 7.7-11.9) and pooled median PFS 2.6 months (95% CI 1.9-3.6). The 12-month OS rate was 41.6% (95% CI 33.1-51.2) and the 6-month PFS rate was 24.0% (95% CI 15.2-37.8).

Conclusion: This analysis establishes contemporary benchmarks for systemic treatments in mACC. While chemotherapy and immunotherapy offer modest survival benefits, the limited effectiveness of targeted therapy highlights the paucity of actionable molecular biomarkers. Future trials should aim to surpass the survival outcomes identified in this analysis.

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