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帕博利珠单抗治疗晚期尿路上皮癌停药后未发生疾病进展:全国队列研究。

Discontinuation of pembrolizumab for advanced urothelial carcinoma without disease progression: Nationwide cohort study.

机构信息

Department of Urology, Kyoto University Graduate School of Medicine, Kyoto, Japan.

Department of Urology, Harasanshin Hospital, Fukuoka, Japan.

出版信息

Cancer Med. 2023 Feb;12(3):2325-2332. doi: 10.1002/cam4.5057. Epub 2022 Jul 21.

DOI:10.1002/cam4.5057
PMID:35864744
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9939199/
Abstract

Pembrolizumab, an anti-programmed death 1 monoclonal antibody, has revolutionized the treatment of metastatic urothelial carcinoma. However, the optimal treatment duration for treatment responders has not been established. To address this, we retrospectively assess the treatment outcomes and duration of pembrolizumab for patients whose best response was complete response (CR) or partial response (PR) in a Japanese nationwide cohort of platinum-refractory metastatic urothelial carcinoma. Of 203 patients whose best response was CR or PR, 83 patients discontinued pembrolizumab before progression. The median pembrolizumab treatment duration was 6.9 months. The 2-year relapse-free survival (RFS), treatment-free survival, and OS rates after discontinuation were 49.0%, 57.4%, and 74.5%, respectively. CR, higher hemoglobin levels, and a better Eastern Cooperative Oncology Group performance status at the time of discontinuation were associated with significantly better RFS. Pembrolizumab was re-administered to 12 patients. Pembrolizumab re-challenge resulted in CR, PR, stable disease, and progressive disease in six, three, two, and one patient, respectively. Propensity score-matched landmark analysis revealed no significant OS difference between patients who continued or discontinued pembrolizumab at 6, 12, and 18 months (p = 0.91, 0.99, and 0.25, respectively). Our findings demonstrated that patients with objective responses had favorable survival outcomes and suggested that pembrolizumab could be discontinued safely in this population. This study should drive further efforts to optimize the treatment duration for pembrolizumab responders.

摘要

派姆单抗是一种抗程序性死亡 1 单克隆抗体,彻底改变了转移性尿路上皮癌的治疗方法。然而,对于治疗应答者的最佳治疗持续时间尚未确定。为了解决这个问题,我们回顾性评估了在日本全国铂类难治性转移性尿路上皮癌队列中,对最佳反应为完全缓解(CR)或部分缓解(PR)的患者使用派姆单抗的治疗结果和持续时间。在 203 名最佳反应为 CR 或 PR 的患者中,有 83 名患者在进展前停止了派姆单抗治疗。派姆单抗治疗的中位持续时间为 6.9 个月。停药后 2 年无复发生存(RFS)、无治疗生存和总生存(OS)率分别为 49.0%、57.4%和 74.5%。CR、较高的血红蛋白水平以及停药时较好的东部合作肿瘤学组表现状态与 RFS 显著改善相关。12 名患者重新接受了派姆单抗治疗。重新使用派姆单抗治疗后,6 名、3 名、2 名和 1 名患者的反应分别为 CR、PR、疾病稳定和疾病进展。倾向评分匹配的里程碑分析显示,在 6、12 和 18 个月时继续或停止派姆单抗治疗的患者之间,OS 无显著差异(p=0.91、0.99 和 0.25)。我们的研究结果表明,有客观反应的患者有较好的生存结果,并表明在这一人群中可以安全地停止使用派姆单抗。这项研究应该进一步努力优化派姆单抗应答者的治疗持续时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c920/9939199/1ba1de57ddbe/CAM4-12-2325-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c920/9939199/e0ad1fefb325/CAM4-12-2325-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c920/9939199/e09d6579e317/CAM4-12-2325-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c920/9939199/b1fc5ee676e2/CAM4-12-2325-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c920/9939199/1ba1de57ddbe/CAM4-12-2325-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c920/9939199/e0ad1fefb325/CAM4-12-2325-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c920/9939199/e09d6579e317/CAM4-12-2325-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c920/9939199/b1fc5ee676e2/CAM4-12-2325-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c920/9939199/1ba1de57ddbe/CAM4-12-2325-g004.jpg

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