Andrea Cercek,Michael B Foote,Benoit Rousseau,J Joshua Smith,Jinru Shia,Jenna Sinopoli,Jill Weiss,Melissa Lumish,Lindsay Temple,Miteshkumar Patel,Callahan Wilde,Leonard B Saltz,Guillem Argiles,Zsofia Stadler,Oliver Artz,Steven Maron,Geoffrey Ku,Ping Gu,Yelena Y Janjigian,Daniela Molena,Gopa Iyer,Jonathan Coleman,Wassim Abida,Seth Cohen,Kevin Soares,Mark Schattner,Vivian E Strong,Rona Yaeger,Philip Paty,Marina Shcherba,Ryan Sugarman,Paul B Romesser,Alice Zervoudakis,Avni Desai,Neil H Segal,Imane El Dika,Maria Widmar,Iris Wei,Emmanouil Pappou,Gerard Fumo,Santiago Aparo,Mithat Gonen,Marc Gollub,Vetri S Jayaprakasham,Tae-Hyung Kim,Julio Garcia Aguilar,Martin Weiser,Luis A Diaz
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Whether this approach can be extended to all early-stage dMMR solid tumors, regardless of tumor site, is unknown.\r\n\r\nMETHODS\r\nWe conducted a phase 2 study in which patients with stage I, II, or III dMMR solid tumors that were amenable to curative-intent surgery were treated with neoadjuvant dostarlimab, a programmed cell death 1 (PD-1) blocking agent, for 6 months. The response to treatment was assessed in two cohorts: patients in cohort 1 had dMMR, locally advanced rectal cancer, and patients in cohort 2 had dMMR nonrectal solid tumors. Patients with a clinical complete response could elect to proceed with nonoperative management; those with residual disease were to undergo resection. In this analysis, the primary end point, assessed in cohort 1, was a sustained clinical complete response at 12 months. Recurrence-free survival and safety were evaluated.\r\n\r\nRESULTS\r\nA total of 117 patients were included in the analysis. In cohort 1, all 49 patients who completed treatment had a clinical complete response and elected to proceed with nonoperative management. A total of 37 patients had a sustained clinical complete response at 12 months, a finding that met the criterion for efficacy. In cohort 2, a total of 35 of 54 patients who completed treatment had a clinical complete response, and 33 elected to proceed with nonoperative management. Among the 103 patients who completed treatment across both cohorts, 84 had a clinical complete response, and 82 did not undergo surgery. Among the 117 total patients, recurrence-free survival at 2 years was 92% (95% confidence interval, 86 to 99); the median follow-up for recurrence was 20.0 months (range, 0 to 60.8). The majority of patients (95%) had reversible, grade 1 or 2 adverse events (60%) or had no adverse events (35%). 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In cohort 1, all 49 patients who completed treatment had a clinical complete response and elected to proceed with nonoperative management. A total of 37 patients had a sustained clinical complete response at 12 months, a finding that met the criterion for efficacy. In cohort 2, a total of 35 of 54 patients who completed treatment had a clinical complete response, and 33 elected to proceed with nonoperative management. Among the 103 patients who completed treatment across both cohorts, 84 had a clinical complete response, and 82 did not undergo surgery. Among the 117 total patients, recurrence-free survival at 2 years was 92% (95% confidence interval, 86 to 99); the median follow-up for recurrence was 20.0 months (range, 0 to 60.8). The majority of patients (95%) had reversible, grade 1 or 2 adverse events (60%) or had no adverse events (35%). 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引用次数: 0
摘要
背景:在错配修复缺陷(dMMR)、局部晚期直肠癌患者中,新辅助检查点阻断消除了大部分患者的手术需求。该方法是否可以推广到所有早期dMMR实体瘤,无论肿瘤部位如何,目前尚不清楚。方法:我们进行了一项2期研究,在该研究中,适用于治愈意图手术的I、II或III期dMMR实体瘤患者接受新辅助dostarlimab(一种程序性细胞死亡1 (PD-1)阻断剂)治疗6个月。对治疗的反应分为两个队列进行评估:队列1患者患有dMMR,局部晚期直肠癌,队列2患者患有dMMR非直肠实体瘤。临床完全缓解的患者可以选择继续非手术治疗;有残余病变者行切除。在该分析中,在队列1中评估的主要终点是12个月时的持续临床完全缓解。评估无复发生存期和安全性。结果共纳入117例患者。在队列1中,所有49名完成治疗的患者均有临床完全缓解,并选择继续进行非手术治疗。总共有37名患者在12个月时有持续的临床完全缓解,这一发现符合疗效标准。在队列2中,54例完成治疗的患者中有35例临床完全缓解,33例选择继续非手术治疗。在两个队列中完成治疗的103例患者中,84例临床完全缓解,82例未接受手术。在117例患者中,2年无复发生存率为92%(95%可信区间,86 - 99);复发的中位随访时间为20.0个月(范围0 ~ 60.8个月)。大多数患者(95%)有可逆的1级或2级不良事件(60%)或无不良事件(35%)。在任何患者的治疗期间或治疗后,治疗性切除的选择都没有受到损害。结论:在早期dMMR实体瘤患者中,新辅助PD-1阻断导致了高比例的患者器官保存。(由Swim Across America和其他机构资助;ClinicalTrials.gov号码:NCT04165772)。
Nonoperative Management of Mismatch Repair-Deficient Tumors.
BACKGROUND
Among patients with mismatch repair-deficient (dMMR), locally advanced rectal cancer, neoadjuvant checkpoint blockade eliminated the need for surgery in a high proportion of patients. Whether this approach can be extended to all early-stage dMMR solid tumors, regardless of tumor site, is unknown.
METHODS
We conducted a phase 2 study in which patients with stage I, II, or III dMMR solid tumors that were amenable to curative-intent surgery were treated with neoadjuvant dostarlimab, a programmed cell death 1 (PD-1) blocking agent, for 6 months. The response to treatment was assessed in two cohorts: patients in cohort 1 had dMMR, locally advanced rectal cancer, and patients in cohort 2 had dMMR nonrectal solid tumors. Patients with a clinical complete response could elect to proceed with nonoperative management; those with residual disease were to undergo resection. In this analysis, the primary end point, assessed in cohort 1, was a sustained clinical complete response at 12 months. Recurrence-free survival and safety were evaluated.
RESULTS
A total of 117 patients were included in the analysis. In cohort 1, all 49 patients who completed treatment had a clinical complete response and elected to proceed with nonoperative management. A total of 37 patients had a sustained clinical complete response at 12 months, a finding that met the criterion for efficacy. In cohort 2, a total of 35 of 54 patients who completed treatment had a clinical complete response, and 33 elected to proceed with nonoperative management. Among the 103 patients who completed treatment across both cohorts, 84 had a clinical complete response, and 82 did not undergo surgery. Among the 117 total patients, recurrence-free survival at 2 years was 92% (95% confidence interval, 86 to 99); the median follow-up for recurrence was 20.0 months (range, 0 to 60.8). The majority of patients (95%) had reversible, grade 1 or 2 adverse events (60%) or had no adverse events (35%). The option for curative resection was not compromised during or after treatment in any of the patients.
CONCLUSIONS
Among patients with early-stage dMMR solid tumors that were amenable to curative-intent surgery, neoadjuvant PD-1 blockade led to organ preservation in a high proportion of patients. (Funded by Swim Across America and others; ClinicalTrials.gov number, NCT04165772.).
期刊介绍:
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