Villalona-Calero Miguel A, Lam Elaine, Otterson Gregory A, Zhao Weiqiang, Timmons Matthew, Subramaniam Deepa, Hade Erinn M, Gill George M, Coffey Matthew, Selvaggi Giovanni, Bertino Erin, Chao Bo, Knopp Michael V
Division of Medical Oncology, Department of Internal Medicine, Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Department of Pathology, Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Cancer. 2016 Mar 15;122(6):875-83. doi: 10.1002/cncr.29856. Epub 2015 Dec 28.
The type 3 Dearing reovirus (Reolysin) is a naturally occurring virus that preferentially infects and causes oncolysis in tumor cells with a Ras-activated pathway. It induces host immunity and cell cycle arrest and acts synergistically with cytotoxic agents.
This study evaluated Reolysin combined with paclitaxel and carboplatin in patients with metastatic/recurrent KRAS-mutated or epidermal growth factor receptor (EGFR)-mutated/amplified non-small cell lung cancer.
Thirty-seven patients were treated. Molecular alterations included 20 KRAS mutations, 10 EGFR amplifications, 3 EGFR mutations, and 4 BRAF-V600E mutations. In total, 242 cycles (median, 4; range, 1-47) were completed. The initial doses were area under the curve (AUC) 6 mg/mL/min for carboplatin, 200 mg/m(2) for paclitaxel on day 1, and 3 × 10(10) 50% tissue culture infective dose for Reolysin on days 1 to 5 of each 21-day cycle. Because of diarrhea and febrile neutropenia (in the first 2 patients), subsequent doses were reduced to 175 mg/m(2) for paclitaxel and AUC 5 mg/mL/min for carboplatin. Toxicities included fatigue, diarrhea, nausea/vomiting, neutropenia, arthralgia/myalgia, anorexia, and electrolyte abnormalities. Response Evaluation Criteria in Solid Tumors 1.0 responses included the following: partial response for 11 patients, stable disease (SD) for 20 patients, progressive disease for 4 patients, and not evaluable for 2 patients (objective response rate, 31%; 90% 1-sided lower confidence interval, 21%). Four SD patients had >40% positron emission tomography standardized uptake value reductions. The median progression-free survival, median overall survival, and 12-month overall survival rate were 4 months, 13.1 months, and 57%, respectively. Seven patients were alive after a median follow-up of 34.2 months; they included 2 patients without disease progression at 37 and 50 months.
Reolysin in combination with paclitaxel and carboplatin was well tolerated. The observed response rate suggests a benefit of the reovirus for chemotherapy. A follow-up randomized study is recommended. The proportion of patients surviving longer than 2 years (30%) suggests a second/third-line treatment effect or possibly the triggering of an immune response after tumor reovirus infiltration.
3型迪林呼肠孤病毒(Reolysin)是一种天然存在的病毒,它优先感染具有Ras激活途径的肿瘤细胞并导致其溶瘤。它可诱导宿主免疫和细胞周期停滞,并与细胞毒性药物协同作用。
本研究评估了Reolysin联合紫杉醇和卡铂用于转移性/复发性KRAS突变或表皮生长因子受体(EGFR)突变/扩增的非小细胞肺癌患者的疗效。
共治疗了37例患者。分子改变包括20例KRAS突变、10例EGFR扩增、3例EGFR突变和4例BRAF-V600E突变。总共完成了242个周期(中位数为4;范围为1-47)。初始剂量为卡铂曲线下面积(AUC)6mg/mL/min,第1天紫杉醇200mg/m²,每个21天周期的第1至5天Reolysin为3×10¹⁰ 50%组织培养感染剂量。由于腹泻和发热性中性粒细胞减少(前2例患者),随后的剂量调整为紫杉醇175mg/m²,卡铂AUC 5mg/mL/min。毒性包括疲劳、腹泻、恶心/呕吐、中性粒细胞减少、关节痛/肌痛、厌食和电解质异常。实体瘤疗效评价标准1.0的反应包括:11例患者部分缓解,20例患者疾病稳定(SD),4例患者疾病进展,2例患者不可评价(客观缓解率为31%;90%单侧下限置信区间为21%)。4例SD患者的正电子发射断层扫描标准化摄取值降低>40%。无进展生存期的中位数、总生存期的中位数和12个月总生存率分别为4个月、13.1个月和57%。中位随访34.2个月后,7例患者存活;其中包括在37个月和50个月时无疾病进展的2例患者。
Reolysin联合紫杉醇和卡铂耐受性良好。观察到的缓解率表明呼肠孤病毒对化疗有益。建议进行后续随机研究。存活超过2年的患者比例(30%)表明具有二线/三线治疗效果,或者可能是肿瘤呼肠孤病毒浸润后引发了免疫反应。