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溶瘤T-VEC病毒疗法联合新辅助化疗治疗非转移性三阴性乳腺癌:一项2期试验

Oncolytic T-VEC virotherapy plus neoadjuvant chemotherapy in nonmetastatic triple-negative breast cancer: a phase 2 trial.

作者信息

Soliman Hatem, Hogue Deanna, Han Hyo, Mooney Blaise, Costa Ricardo, Lee Marie C, Niell Bethany, Williams Angela, Chau Alec, Falcon Shannon, Soyano Aixa, Armaghani Avan, Khakpour Nazanin, Weinfurtner Robert J, Hoover Susan, Kiluk John, Laronga Christine, Rosa Marilin, Khong Hung, Czerniecki Brian

机构信息

Department of Breast Oncology, Moffitt Cancer Center, Tampa, FL, USA.

Clinical Trials Office, Moffitt Cancer Center, Tampa, FL, USA.

出版信息

Nat Med. 2023 Feb;29(2):450-457. doi: 10.1038/s41591-023-02210-0. Epub 2023 Feb 9.

Abstract

Talimogene laherparepvec (T-VEC) is an oncolytic virus hypothesized to enhance triple-negative breast cancer (TNBC) responses to neoadjuvant chemotherapy (NAC). This article describes the phase 2 trial of T-VEC plus NAC (ClinicalTrials.gov ID: NCT02779855 ). Patients with stage 2-3 TNBC received five intratumoral T-VEC injections with paclitaxel followed by doxorubicin and cyclophosphamide and surgery to assess residual cancer burden index (RCB). The primary end point was RCB0 rate. Secondary end points were RCB0-1 rate, recurrence rate, toxicity and immune correlates. Thirty-seven patients were evaluated. Common T-VEC toxicities were fevers, chills, headache, fatigue and injection site pain. NAC toxicities were as expected. Four thromboembolic events occurred. The primary end point was met with an estimated RCB0 rate = 45.9% and RCB0-1 descriptive rate = 65%. The 2-year disease-free rate is equal to 89% with no recurrences in RCB0-1 patients. Immune activation during treatment correlated with response. T-VEC plus NAC in TNBC may increase RCB0-1 rates. These results support continued investigation of T-VEC plus NAC for TNBC.

摘要

talimogene laherparepvec(T-VEC)是一种溶瘤病毒,被认为可增强三阴性乳腺癌(TNBC)对新辅助化疗(NAC)的反应。本文描述了T-VEC联合NAC的2期试验(ClinicalTrials.gov标识符:NCT02779855)。2-3期TNBC患者接受5次瘤内注射T-VEC并联合紫杉醇,随后使用多柔比星和环磷酰胺,然后进行手术以评估残余癌负担指数(RCB)。主要终点是RCB0率。次要终点是RCB0-1率、复发率、毒性和免疫相关性。评估了37例患者。T-VEC常见的毒性反应为发热、寒战、头痛、疲劳和注射部位疼痛。NAC的毒性反应符合预期。发生了4例血栓栓塞事件。主要终点达到预期,估计RCB0率 = 45.9%,RCB0-1描述性率 = 65%。2年无病生存率等于89%,RCB0-1患者无复发。治疗期间的免疫激活与反应相关。TNBC中T-VEC联合NAC可能会提高RCB0-1率。这些结果支持继续研究T-VEC联合NAC用于TNBC的治疗。

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