从酪氨酸激酶抑制剂时代到免疫肿瘤学时代,晚期非透明细胞肾细胞癌患者的预后变化。

IF 2.4 3区 医学 Q3 ONCOLOGY
Hiroki Ishihara, Yuki Nemoto, Shinsuke Mizoguchi, Koichi Nishimura, Takashi Ikeda, Hironori Fukuda, Kazuhiko Yoshida, Hiroaki Shimmura, Yasunobu Hashimoto, Junpei Iizuka, Tsunenori Kondo, Toshio Takagi
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引用次数: 0

摘要

背景:免疫肿瘤学(IO)疗法对晚期非透明细胞肾细胞癌(nccRCC)患者的治疗效果尚不明确:免疫肿瘤学(IO)疗法对晚期非透明细胞肾细胞癌(nccRCC)患者的治疗效果尚不明确:我们回顾了93名晚期nccRCC患者的临床数据,这些患者在我们的附属机构接受了一线系统治疗,包括IO联合治疗和酪氨酸激酶抑制剂(TKI)单药治疗。根据作为标准疗法实施的时期,将患者分为 IO 和 TKI 两个时期。比较了IO和TKI时期的生存率和肿瘤反应结果:93名患者中,50人(54%)和43人(46%)分别被归入IO时代和TKI时代组。无进展生存期(PFS)和总生存期(OS)在 IO 时代明显长于 TKI 时代(中位 PFS:8.97 个月 vs. 4.96 个月,p = 0.0152;中位 OS:38.4 个月 vs. 13.5 个月):38.4个月对13.5个月,p = 0.0001)。在使用其他协变量进行调整后,治疗年代是影响 PFS(危险比:0.59,p = 0.0235)和 OS(危险比:0.27,p 结论:治疗年代与 PFS 和 OS 的影响显著相关:在 nccRCC 患者中,IO 治疗的实施与更长的生存期显著相关。还需要进一步研究,以便在这一人群中使用多种 IO 联合疗法方案,建立更有效的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Changes in outcome of patients with advanced non-clear cell renal cell carcinoma from the tyrosine kinase inhibitor era to the immuno-oncology era.

Changes in outcome of patients with advanced non-clear cell renal cell carcinoma from the tyrosine kinase inhibitor era to the immuno-oncology era.

Background: The therapeutic benefit of immuno-oncology (IO) therapy for patients with advanced non-clear-cell renal cell carcinoma (nccRCC) remains unclear.

Patients and methods: We reviewed clinical data from 93 patients with advanced nccRCC who received first-line systemic therapy including IO combination therapy and tyrosine kinase inhibitor (TKI) monotherapy at our affiliated institutions. Patients were divided based on the period when the treatment was implemented as the standard of care into the IO and TKI eras. Survival and tumor response outcomes were compared between the IO and TKI eras.

Results: Of the 93 patients, 50 (54%) and 43 (46%) were categorized as IO era and TKI era groups, respectively. Progression-free survival (PFS) and overall survival (OS) were significantly longer in the IO era than in the TKI era (median PFS: 8.97 vs. 4.96 months, p = 0.0152; median OS: 38.4 vs. 13.5 months, p = 0.0001). After the adjustment using other covariates, the treatment era was an independent factor for PFS (hazard ratio: 0.59, p = 0.0235) and OS (hazard ratio: 0.27, p < 0.0001). Objective response and disease control rates was not significantly different between the treatment eras (26% vs. 16.3%, p = 0.268; 62% vs. 62.8%, p = 0.594).

Conclusion: The implementation of IO therapy was significantly associated with longer survival in the nccRCC population. Further studies are needed to establish a more effective treatment strategy in this population using multiple regimens of IO combination therapy.

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来源期刊
CiteScore
6.80
自引率
3.00%
发文量
175
审稿时长
2 months
期刊介绍: The International Journal of Clinical Oncology (IJCO) welcomes original research papers on all aspects of clinical oncology that report the results of novel and timely investigations. Reports on clinical trials are encouraged. Experimental studies will also be accepted if they have obvious relevance to clinical oncology. Membership in the Japan Society of Clinical Oncology is not a prerequisite for submission to the journal. Papers are received on the understanding that: their contents have not been published in whole or in part elsewhere; that they are subject to peer review by at least two referees and the Editors, and to editorial revision of the language and contents; and that the Editors are responsible for their acceptance, rejection, and order of publication.
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