Cohen Romain, Pudlarz Thomas, Garcia-Larnicol Marie-Line, Vernerey Dewi, Dray Xavier, Clavel Léa, Jary Marine, Piessen Guillaume, Zaanan Aziz, Aparicio Thomas, Louvet Christophe, Tournigand Christophe, Chibaudel Benoist, Tougeron David, Guimbaud Rosine, Benouna Jaafar, Adenis Antoine, Sokol Harry, Borg Christophe, Duval Alex, Svrcek Magali, André Thierry
AP-HP, Sorbonne Université, hôpital Saint-Antoine, department of medical oncology, 75012 Paris, France.
AP-HP, hôpital Saint-Antoine, Department of medical oncology, 75012 Paris, France.
Bull Cancer. 2020 Apr;107(4):438-446. doi: 10.1016/j.bulcan.2019.11.016. Epub 2020 Feb 10.
Perioperative chemotherapy is the standard strategy for localized gastric cancers. Nevertheless, this strategy seems to be inefficient, if not deleterious, for patients with tumors harboring microsatellite instability (MSI) and/or mismatch repair deficiency (dMMR), a tumor phenotype predictive for the efficacy of immune checkpoint inhibitors (ICKi).
The GERCOR NEONIPIGA single-arm phase II study (NCT04006262; EUDRACT 2018-004712-22) aims at evaluating the efficacy of a peri-operative strategy with nivolumab and ipilimumab in neoadjuvant setting, then nivolumab alone after surgery for patients with resectable MSI/dMMR gastric cancer.
Main inclusion criteria are: gastric and oesogastric junction adenocarcinoma (GOA), T2-T4, all N stage and M0, MSI/dMMR. Patients will be treated with nivolumab 240mg Q2W, 6 infusions, and ipilimumab 1mg/kg Q6W, 2 infusions in neoadjuvant setting. Following surgery, patients with TRG 1-2-3 (Mandard tumor regression grade), acceptable tolerance of neoadjuvant treatment and postoperative ECOG performance status 0-1, will be treated with adjuvant nivolumab 480mg Q4W, 9 infusions.
The primary endpoint is pathological complete response rate (pCR-R). Based on a Fleming design, with α=5% and β=20%, 27 patients have to be evaluated (H0=5%; H1=20%). Secondary endpoints include disease-free survival, overall survival and safety.
This study is planned to include 32 patients to evaluate the pCR-R with the combination of nivolumab and ipilimumab in neoadjuvant setting for MSI/dMMR localized GOA. The MSI/MMR status should be systematically assessed on diagnostic biopsies of all GOA. If it meets its primary endpoint, the GERCOR NEONIPIGA study might mark a turning point in the management of localized MSI/dMMR GOA patients.
围手术期化疗是局部胃癌的标准治疗策略。然而,对于存在微卫星不稳定性(MSI)和/或错配修复缺陷(dMMR)的肿瘤患者,这种策略似乎效率不高,甚至可能有害,而MSI/dMMR是一种可预测免疫检查点抑制剂(ICKi)疗效的肿瘤表型。
GERCOR NEONIPIGA单臂II期研究(NCT04006262;EUDRACT 2018-004712-22)旨在评估纳武利尤单抗联合伊匹木单抗在新辅助治疗中的围手术期策略的疗效,然后对可切除的MSI/dMMR胃癌患者术后单独使用纳武利尤单抗。
主要纳入标准为:胃和食管胃交界腺癌(GOA)、T2-T4、所有N分期和M0、MSI/dMMR。患者在新辅助治疗中接受纳武利尤单抗240mg,每2周一次,共6次输注,以及伊匹木单抗1mg/kg,每6周一次,共2次输注。术后,肿瘤退缩分级(TRG)为1-2-3级(曼德尔肿瘤退缩分级)、新辅助治疗耐受性可接受且术后东部肿瘤协作组(ECOG)体能状态为0-1的患者,将接受辅助纳武利尤单抗480mg,每4周一次,共9次输注。
主要终点是病理完全缓解率(pCR-R)。基于弗莱明设计,α=5%,β=20%,必须评估27例患者(H0=5%;H1=20%)。次要终点包括无病生存期、总生存期和安全性。
本研究计划纳入32例患者,以评估纳武利尤单抗联合伊匹木单抗在新辅助治疗中对MSI/dMMR局部GOA患者的pCR-R。所有GOA的诊断活检均应系统评估MSI/MMR状态。如果达到主要终点,GERCOR NEONIPIGA研究可能会成为局部MSI/dMMR GOA患者治疗管理的一个转折点。