Pembrolizumab、放疗和手术与放疗和手术治疗III期四肢软组织肉瘤的安全性和有效性(SU2C-SARC032):开放标签随机临床试验

Yvonne M Mowery, Karla V Ballman, Angela M Hong, Scott M Schuetze, Andrew J Wagner, Varun Monga, Rachel S Heise, Steven Attia, Edwin Choy, Melissa A Burgess, Susie Bae, David I Pryor, Brian A Van Tine, Gabriel Tinoco, Bartosz Chmielowski, Carolyn Freeman, Alessandro Gronchi, Christian F Meyer, Mark A Dickson, Lee Hartner, David G Kirsch
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引用次数: 0

摘要

背景约有一半的局部高危四肢软组织肉瘤患者会发生转移。我们的目的是评估在术前放疗和手术的基础上加用 pembrolizumab 是否能提高无病生存率。方法我们完成了一项开放标签、随机临床试验,对象是 2 级或 3 级、III 期未分化多形性肉瘤或四肢和肢腰部的已分化或多形性脂肪肉瘤患者。澳大利亚、加拿大、意大利和美国的 20 家学术机构招募了患者。患者被随机分配到术前放疗然后手术(对照组)或术前使用 Pembrolizumab 并进行放疗(在首次使用 Pembrolizumab 1-14 天后开始)然后手术并术后使用 Pembrolizumab(实验组)。Pembrolizumab(200 毫克,静脉注射,每 3 周一次)以 3 个新辅助周期(放疗前、放疗中和放疗后)和 14 个或更少的辅助周期进行治疗。主要终点为无病生存期。本研究已在ClincialTrials.gov(NCT03092323)注册。研究结果2017年11月18日至2023年11月14日期间,143名参与者被随机分配接受治疗。对中位随访时间为43个月的127名患者进行的修正意向治疗分析表明,实验组(n=64)的无病生存期明显长于对照组(n=63;对数秩单侧p=0-035;危险比[HR]0-61;90% CI 0-39-0-96)。加入 pembrolizumab 后,2 年无病生存率提高了 15%:对照组和实验组的2年无病生存率分别为52%(90% CI 42-64)和67%(90% CI 58-78)。在意向治疗患者群体中,使用pembrolizumab后,无病生存期同样得到了改善(HR 0-61 [90% CI 0-39-0-95])。实验组(56%)的3级或以上不良事件发生率高于对照组(31%)。释义在术前放疗和手术中加入pembrolizumab可提高III期未分化多形性肉瘤和四肢多形性或已分化脂肪肉瘤患者的无病生存率,为这些患者提供了一种很有前景的新治疗方案。
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Safety and efficacy of pembrolizumab, radiation therapy, and surgery versus radiation therapy and surgery for stage III soft tissue sarcoma of the extremity (SU2C-SARC032): an open-label, randomised clinical trial

Background

Approximately half of patients with localised, high-risk soft tissue sarcoma of the extremity develop metastases. We aimed to assess whether the addition of pembrolizumab to preoperative radiotherapy and surgery would improve disease-free survival.

Methods

We completed an open-label, randomised clinical trial in patients with grade 2 or 3, stage III undifferentiated pleomorphic sarcoma or dedifferentiated or pleomorphic liposarcoma of the extremity and limb girdle. Patients were enrolled at 20 academic institutions in Australia, Canada, Italy, and the USA. Patients were randomly assigned to preoperative radiotherapy then surgery (control group) or preoperative pembrolizumab with radiotherapy (initiated 1–14 days after the first dose of pembrolizumab) then surgery and postoperative pembrolizumab (experimental group). Pembrolizumab (200 mg intravenously every 3 weeks) was administered as three neoadjuvant cycles (before, during, and after radiotherapy) and 14 or less adjuvant cycles. Primary endpoint was disease-free survival. This study is registered with ClincialTrials.gov (NCT03092323).

Findings

Between Nov 18, 2017, and Nov 14, 2023, 143 participants were randomly assigned to treatment. A modified intention-to-treat analysis of 127 patients with median follow-up of 43 months showed that the experimental group (n=64) had significantly longer disease-free survival than the control group (n=63; log-rank one-sided p=0·035; hazard ratio [HR] 0·61; 90% CI 0·39–0·96). The 2-year disease-free survival increased by 15% with addition of pembrolizumab: 52% (90% CI 42–64) and 67% (90% CI 58–78) for the control and experimental groups, respectively. Disease-free survival was similarly improved with pembrolizumab for the intention-to-treat patient population (HR 0·61 [90% CI 0·39–0·95]). Grade 3 or higher adverse events occurred more frequently in the experimental group (56%) than the control group (31%).

Interpretation

Addition of pembrolizumab to preoperative radiotherapy and surgery improves disease-free survival for patients with stage III undifferentiated pleomorphic sarcoma and pleomorphic or dedifferentiated liposarcoma of the extremity, which establishes a promising new treatment option for these patients.

Funding

Stand Up to Cancer and Merck Sharp & Dohme.
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