Outcome of immunotherapy in adrenocortical carcinoma: a retrospective cohort study

医学 肾上腺皮质癌 无容量 内科学 相伴的 回顾性队列研究 彭布罗利珠单抗 米托坦 无进展生存期 队列 胃肠病学 肾细胞癌 不利影响 免疫疗法 泌尿科 肿瘤科 总体生存率 外科 癌症
作者
Hanna Remde,Laura Schmidt-Pennington,Miriam Reuter,Laura‐Sophie Landwehr,Marie M. Jensen,Harald Lahner,Otilia Kimpel,Barbara Altieri,Katharina Laubner,J. Schreiner,Joerg Bojunga,Stefan Kircher,Catarina Alisa Kunze,Anne Pohrt,Maria‐Veronica Teleanu,Daniel Hübschmann,Albrecht Stenzinger,Hanno Glimm,Stefan Fröhling,Martin Faßnacht,Knut Mai,Matthias Kroiß
出处
期刊:European journal of endocrinology [Bioscientifica]
卷期号:188 (6): 485-493 被引量:6
标识
DOI:10.1093/ejendo/lvad054
摘要

Abstract Objective Clinical trials with immune checkpoint inhibitors (ICI) in adrenocortical carcinoma (ACC) have yielded contradictory results. We aimed to evaluate treatment response and safety of ICI in ACC in a real-life setting. Design Retrospective cohort study of 54 patients with advanced ACC receiving ICI as compassionate use at 6 German reference centres between 2016 and 2022. Methods Objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), overall survival (OS), and treatment-related adverse events (TRAE) were assessed. Results In 52 patients surviving at least 4 weeks after initiation of ICI, ORR was 13.5% (6-26) and DCR was 24% (16-41). PFS was 3.0 months (95% CI, 2.3-3.7). In all patients, median OS was 10.4 months (3.8-17). 17 TRAE occurred in 15 patients, which was associated with a longer PFS of 5.5 (1.9-9.2) vs 2.5 (2.0-3.0) months (HR 0.29, 95% CI, 0.13-0.66, P = 0.001) and OS of 28.2 (9.5-46.8) vs 7.0 (4.1-10.2) months (HR 0.34, 95% CI, 0.12-0.93). Positive tissue staining for programmed cell death ligand 1 (PD-L1) was associated with a longer PFS of 3.2 (2.6-3.8) vs 2.3 (1.6-3.0, P < 0.05) months. Adjusted for concomitant mitotane use, treatment with nivolumab was associated with lower risk of progression (HR 0.36, 0.15-0.90) and death (HR 0.20, 0.06-0.72) compared to pembrolizumab. Conclusions In the real-life setting, we observe a response comparable to other second-line therapies and an acceptable safety profile in ACC patients receiving different ICI. The relevance of PD-L1 as a marker of response and the potentially more favourable outcome in nivolumab-treated patients require confirmation.

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