JIPANG研究的5年总生存分析:培美曲塞或长春瑞滨加顺铂治疗切除的II-IIIA期非鳞状非小细胞肺癌

IF 42.1 1区 医学 Q1 ONCOLOGY Journal of Clinical Oncology Pub Date : 2023-12-01 Epub Date: 2023-09-01 DOI:10.1200/JCO.23.00179
Hirotsugu Kenmotsu, Nobuyuki Yamamoto, Toshihiro Misumi, Kiyotaka Yoh, Haruhiro Saito, Shunichi Sugawara, Koji Yamazaki, Kazuhiko Nakagawa, Kenji Sugio, Takashi Seto, Shinichi Toyooka, Hiroshi Date, Tetsuya Mitsudomi, Isamu Okamoto, Kohei Yokoi, Hideo Saka, Hiroaki Okamoto, Yuichi Takiguchi, Toshiaki Takahashi, Masahiro Tsuboi
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引用次数: 0

摘要

临床试验通常包括在不同时间成熟的多个终点。通常基于主要终点的初始报告,可能在关键的计划共同主要或次要分析尚未可用时发布。临床试验更新提供了一个机会来传播来自发表在JCO或其他地方的研究的额外结果,这些研究的主要终点已经被报道。JIPANG研究是一项开放标签III期试验,评估培美曲塞加顺铂(PemP)与维诺瑞滨加顺铂(NP)作为辅助化疗治疗II-IIIA期非鳞状非小细胞肺癌(NSCLC)患者的疗效。在这里,我们报告了长期随访的总生存期(OS)数据。符合条件的患者被随机分配接受PemP或NP。主要终点为无复发生存期(RFS),次要终点为OS。该分析使用最后一次患者入组后5年收集的数据进行。在入组的804例患者中,783例患者符合条件(384例NP和389例PemP)。更新后的中位RFS在NP组为37.5个月,在PemP组为43.4个月,风险比为0.95 (95% CI, 0.79至1.14)。在中位随访77.3个月时,3年和5年的OS率分别为84.1%和75.6%,相对于87.0%和75.0%,风险比为1.04 (95% CI, 0.81至1.34)。这项长期随访分析显示,在该人群的RFS和OS中,PemP与NP具有相似的疗效,与历史数据相比,这是最长的OS数据之一。
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Five-Year Overall Survival Analysis of the JIPANG Study: Pemetrexed or Vinorelbine Plus Cisplatin for Resected Stage II-IIIA Nonsquamous Non-Small-Cell Lung Cancer.

Clinical trials frequently include multiple end points that mature at different times. The initial report, typically based on the primary end point, may be published when key planned co-primary or secondary analyses are not yet available. Clinical Trial Updates provide an opportunity to disseminate additional results from studies, published in JCO or elsewhere, for which the primary end point has already been reported.The JIPANG study is an open-label phase III trial evaluating the efficacy of pemetrexed plus cisplatin (PemP) versus vinorelbine plus cisplatin (NP) as adjuvant chemotherapy in patients with stage II-IIIA nonsquamous non-small-cell lung cancer (NSCLC). Here, we report the long follow-up overall survival (OS) data. Eligible patients were randomly assigned to receive either PemP or NP. The primary end point was recurrence-free survival (RFS), and the secondary end point included OS. This analysis was performed using data collected 5 years after the last patient enrollment. Among 804 patients enrolled, 783 patients were eligible (384 for NP and 389 for PemP). The updated median RFS was 37.5 months in the NP arm and 43.4 months in the PemP arm with a hazard ratio of 0.95 (95% CI, 0.79 to 1.14). At a median follow-up of 77.3 months, the OS rates at 3 and 5 years were 84.1% and 75.6% versus 87.0% and 75.0% with a hazard ratio of 1.04 (95% CI, 0.81 to 1.34). This long-term follow-up analysis showed that PemP had similar efficacy to NP in both RFS and OS for this population, with one of the longest OS data compared with the historical data.

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来源期刊
Journal of Clinical Oncology
Journal of Clinical Oncology 医学-肿瘤学
CiteScore
41.20
自引率
2.20%
发文量
8215
审稿时长
2 months
期刊介绍: The Journal of Clinical Oncology serves its readers as the single most credible, authoritative resource for disseminating significant clinical oncology research. In print and in electronic format, JCO strives to publish the highest quality articles dedicated to clinical research. Original Reports remain the focus of JCO, but this scientific communication is enhanced by appropriately selected Editorials, Commentaries, Reviews, and other work that relate to the care of patients with cancer.
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