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乳腺癌具有免疫原性:免疫学分析与使用突变反应性自体淋巴细胞的 II 期初步临床试验

英文原题:Breast Cancers Are Immunogenic: Immunologic Analyses and a Phase II Pilot Clinical Trial Using Mutation-Reactive Autologous Lymphocytes.

PubMed 2022/02/01(内容时间) J Clin Oncol Q1 · IF 44.7(JCR 2025)

研究概要

大多数乳腺癌患者产生了针对其癌症突变表达产物的天然免疫反应。TIL 过继转移是一种高度个性化的实验性选择,在此初步试验中显示能够介导 mBrCa 患者的客观缓解,值得进一步研究。

研究思路结论见上方概要

转移性乳腺癌(mBrCa)通常是一种无法治愈的疾病,对现有免疫疗法的反应有限。本研究探讨了乳腺癌体细胞突变的免疫原性,并在转移性疾病患者中开展了一项突变反应性TIL(肿瘤浸润淋巴细胞)(TILs)的初步试验,以探索其治疗疗效。

42例对既往多线治疗耐药的mBrCa患者接受了转移病灶手术切除、TIL培养物分离、外显子组非同义肿瘤突变鉴定以及新抗原反应性免疫筛选。具有适当反应性且临床符合条件的患者被纳入一项正在进行的II期试点试验的一个队列,该试验采用选择性新抗原反应性TIL过继细胞转移,并联合短程pembrolizumab治疗(ClinicalTrials.gov标识符:NCT01174121)。

TIL 从所有 42 例 mBrCa 患者的切除病灶中分离并在培养中扩增,每位患者中位鉴定出 112 个(范围:6-563)非同义突变。42 例患者中有 28 例(67%)含有可识别至少一个免疫原性体细胞突变的 TIL(每位患者中位 3 个新抗原,范围:1-11),13 例患者表现出适合过继转移的强反应性。8 例患者仍符合临床治疗条件,6 例患者入组了富集新抗原特异性 TIL 过继细胞转移联合 pembrolizumab(4 剂)的方案。3 例患者观察到客观肿瘤消退,包括 1 例完全缓解(现已持续超过 5.5 年)和 2 例部分缓解(6 个月和 10 个月)。

展开英文摘要原文

PURPOSE: Metastatic breast cancer (mBrCa) is most often an incurable disease with only modest responses to available immunotherapies. This study investigates the immunogenicity of somatic mutations in breast cancer and explores the therapeutic efficacy in a pilot trial of mutation-reactive tumor-infiltrating lymphocytes (TILs) in patients with metastatic disease. PATIENTS AND METHODS: Forty-two patients with mBrCa refractory to previous lines of treatment underwent surgical resection of a metastatic lesion(s), isolation of TIL cultures, identification of exomic nonsynonymous tumor mutations, and immunologic screening for neoantigen reactivity. Clinically eligible patients with appropriate reactivity were enrolled into one cohort of an ongoing phase II pilot trial of adoptive cell transfer of selected neoantigen-reactive TIL, with a short course of pembrolizumab (ClinicalTrials.gov identifier: NCT01174121). RESULTS: TILs were isolated and grown in culture from the resected lesions of all 42 patients with mBrCa, and a median number of 112 (range: 6-563) nonsynonymous mutations per patient were identified. Twenty-eight of 42 (67%) patients contained TIL that recognized at least one immunogenic somatic mutation (median: 3 neoantigens per patient, range: 1-11), and 13 patients demonstrated robust reactivity appropriate for adoptive transfer. Eight patients remained clinically eligible for treatment, and six patients were enrolled on a protocol of adoptive cell transfer of enriched neoantigen-specific TIL, in combination with pembrolizumab ( 4 doses). Objective tumor regression was noted in three patients, including one complete response (now ongoing over 5.5 years) and two partial responses (6 and 10 months). CONCLUSION: Most patients with breast cancer generated a natural immune response targeting the expressed products of their cancer mutations. Adoptive transfer of TIL is a highly personalized experimental option for patients with mBrCa shown to be capable of mediating objective responses in this pilot trial and deserves further study.

论文信息

作者
Zacharakis N、Huq LM、Seitter SJ、Kim SP、Gartner JJ、Sindiri S、Hill VK、Li YF
单位
Surgery Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD.United States
文献类型
II 期临床试验 · 非美国政府资助研究 · 美国 NIH 资助研究
期刊
Journal of clinical oncology : official journal of the American Society of Clinical Oncology2022 Jun 1
原文标识
PubMed 35104158 · DOI 10.1200/JCO.21.02170