Synergistic effects of PD-1 antibody and chemotherapy followed by surgery-centric local treatment in patients with limited-metastatic gastric or gastroesophageal adenocarcinoma (ROSETTE trial): an open-label, single-center, randomized phase 2 trial.

IF 3.4 2区 医学 Q2 ONCOLOGY
Ying Ying Wu, Lian Chen Lee, Hong Zeng, Yuan Gu, Chen Xu, Wei Dong Chen, Zhen Bin Shen, Kun Tang Shen, Yue Hong Cui, Yi Hong Sun, Tian Shu Liu, Zhao Qing Tang, Xue Fei Wang
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引用次数: 0

Abstract

Background: Limited metastatic gastric cancer (lmGC) represents an intermediate disease stage, positioned between localized and widely disseminated gastric cancer, and has garnered increasing attention due to its distinct prognostic outcomes. Currently, there is no consensus on the optimal treatment approach for lmGC, raising the question of whether it should align more with the systemic treatment-focused approach used for metastatic gastric cancer or adopt a surgery-centric strategy similar to that used in localized disease. Previous studies have preliminarily explored combining systemic treatment and surgical resection to address both the primary tumor and metastatic lesions. However, these investigations have been constrained by limited evidence and yielded inconclusive findings.

Methods: ROSETTE trial is an open-label, randomized phase II study designed to investigate treatment strategies for patients with limited metastatic gastric or gastroesophageal adenocarcinoma. Eligible patients, confirmed through comprehensive evaluation including radiography and laparoscopy, are randomized to receive either systemic treatment followed by surgery-centric local treatment, or systemic treatment alone. Systemic treatment combines immunotherapy with chemotherapy, while the surgery-centric local treatment utilizes a surgery-centric, multi-modality approach involving resection of both primary and metastatic tumors where feasible. For unresected or unresectable metastatic lesions, alternative local therapies are provided. The primary endpoint is the 1-year event-free survival (EFS) rate. Secondary endpoints include objective response rate (ORR), disease control rate (DCR), extended EFS, overall survival (OS), pathologic complete response rate (pCR), major pathologic response rate (MPR), and R0 resection rate.

Discussion: The ROSETTE trial aims to evaluate whether systemic treatment followed by surgery-centric local treatment provides a survival advantage over the standard systemic-only approach for patients with limited metastatic gastric cancer. It seeks to build on previous research while addressing limitations such as selection bias inherent to non-randomized designs, patient recruitment challenges, and the complexities of managing surgical complications. By applying the latest evidence and a multi-modality approach, the ROSETTE trial endeavors to offer new insights into optimizing treatment strategies for patient with lmGC.

Trial registration: NCT06468280 (Registration date: 05/28/2024).

PD-1抗体和化疗后手术中心局部治疗对有限转移性胃或胃食管腺癌患者的协同作用(ROSETTE试验):一项开放标签、单中心、随机2期试验。
背景:有限转移性胃癌(lmGC)是一种介于局部胃癌和广泛弥散性胃癌之间的中间疾病阶段,由于其独特的预后结果而受到越来越多的关注。目前,对于lmGC的最佳治疗方法尚无共识,这就提出了一个问题,即它是否应该与转移性胃癌的系统性治疗方法更加一致,还是采用类似于局部疾病的手术中心策略。既往研究初步探讨了全身治疗和手术切除相结合的方法来治疗原发肿瘤和转移灶。然而,这些调查受到证据有限的限制,得出了不确定的结论。方法:ROSETTE试验是一项开放标签、随机的II期研究,旨在研究有限转移性胃或胃食管腺癌患者的治疗策略。通过包括x线摄影和腹腔镜检查在内的综合评估确认符合条件的患者,随机接受全身治疗后再进行以手术为中心的局部治疗或单独接受全身治疗。全身治疗结合免疫治疗和化疗,而以手术为中心的局部治疗采用手术为中心的多模式方法,包括在可行的情况下切除原发性和转移性肿瘤。对于未切除或不可切除的转移性病变,可提供其他局部治疗。主要终点是1年无事件生存率(EFS)。次要终点包括客观缓解率(ORR)、疾病控制率(DCR)、延长EFS、总生存期(OS)、病理完全缓解率(pCR)、主要病理缓解率(MPR)、R0切除率。讨论:ROSETTE试验旨在评估对于有限转移性胃癌患者,全身治疗后再进行以手术为中心的局部治疗是否比标准的全身治疗更有生存优势。它寻求建立在先前研究的基础上,同时解决局限性,如非随机设计固有的选择偏差,患者招募挑战,以及处理手术并发症的复杂性。通过应用最新的证据和多模式的方法,ROSETTE试验努力为优化lmGC患者的治疗策略提供新的见解。试验注册:NCT06468280(注册日期:05/28/2024)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Cancer
BMC Cancer 医学-肿瘤学
CiteScore
6.00
自引率
2.60%
发文量
1204
审稿时长
6.8 months
期刊介绍: BMC Cancer is an open access, peer-reviewed journal that considers articles on all aspects of cancer research, including the pathophysiology, prevention, diagnosis and treatment of cancers. The journal welcomes submissions concerning molecular and cellular biology, genetics, epidemiology, and clinical trials.
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