胃肿瘤辅助放化疗的安全性中期分析结果2试验:一项多中心、随机的III期临床试验

IF 1.9 Q2 MEDICINE, GENERAL & INTERNAL
S. Park, Jeeyun Lee, T. Sohn, D. Lim, Kyoung-Mee Kim, J. An, M. Choi, Jun Ho Lee, J. Bae, Sung Kim, Su Jin Lee, Seung-Tae Kim, Joon-Oh Park, Y. Park, Ho Yeong Lim, W. Kang
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引用次数: 2

摘要

目的:进行胃肿瘤辅助放化疗2 (ARTIST 2)试验,比较辅助化疗方案与放化疗方案在d2切除、淋巴结阳性、2期或3期胃癌中的疗效。方法:在这项前瞻性、多中心、III期试验中,我们将患者随机分配到三个治疗组:接受辅助S-1治疗1年,S-1 +奥沙利铂(SOX)治疗6个月,或SOX +放化疗(SOXRT)。在此,我们报告了接受辅助化疗或放化疗的患者的安全性结果。结果:在2013年2月至2017年12月期间登记的514名患者中,499名完成或停止指定研究治疗的患者被纳入本分析。三个治疗组总体耐受良好,总体治疗完成率为94% (S-1组为96%,SOX组为93%,SOXRT组为92%)。SOXRT组放射治疗的中位剂量为4500 cGy(范围0 - 4500 cGy)。最常见的不良事件是S-1组的疲劳(29%)和SOX和SOXRT组的周围神经病变(分别为59%和50%)。结论:我们的初步数据证实,ARTIST 2试验没有明显的安全性问题(ClinicalTrials.gov, NCT0176146)。根据独立数据监测委员会的数据,患者收益正在进行中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Results from the safety interim analysis of the adjuvant chemoradiotherapy in stomach tumors 2 trial: a multicenter, randomized phase III clinical trial
Purpose: The Adjuvant chemoRadioTherapy In Stomach Tumors 2 (ARTIST 2) trial was conducted to compare the efficacy between adjuvant chemotherapy regimens and chemoradiotherapy in D2-resected, node-positive, stage 2 or 3 gastric cancer. Methods: In this prospective, multicenter, phase III trial, we randomly assigned patients to three treatment arms: patients who receive adjuvant S-1 for 1 year, S-1 plus oxaliplatin (SOX) for 6 months, or SOX plus chemoradiotherapy (SOXRT). Herein, we report the safety outcomes of patients who received adjuvant chemotherapy or chemoradiotherapy. Results: Among a total of 514 patients registered between February 2013 and December 2017, 499 patients who either completed or discontinued the assigned study treatments were included in the present analysis. All the three treatment arms were generally well-tolerated, with the overall treatment completion rate of 94% (96% in S-1, 93% in SOX, and 92% in SOXRT). The median delivered dose of radiotherapy in the SOXRT arm was 4,500 cGy (range, 0 to 4,500 cGy). The most frequently observed adverse events were fatigue (29%) in S-1 arm and peripheral neuropathy in the SOX and SOXRT arms (59% and 50%, respectively). Conclusion: Our preliminary data confirm that there are no significant safety concerns in ARTIST 2 trial (ClinicalTrials.gov, NCT0176146). According to the Independent Data Monitoring Committee, patient accrual is underway.
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Precision and Future Medicine
Precision and Future Medicine MEDICINE, GENERAL & INTERNAL-
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