Department of Biomedicine, University of Basel, Basel, Switzerland.
Division of Medical Oncology, University Hospital Basel, Basel, Switzerland.
Cancer Immunol Res. 2024 Jul 2;12(7):814-821. doi: 10.1158/2326-6066.CIR-23-0757.
Adoptive cell therapy (ACT) with tumor-infiltrating lymphocytes (TIL) is effective in patients with melanoma, although long-term responses seem restricted in patients who have complete remissions. Many patients develop secondary resistance to TIL-ACT but the involved mechanisms are unclear. In this study, we describe a case of secondary resistance to TIL-ACT possibly due to intratumoral heterogeneity and selection of a resistant tumor cell clone by the transferred T cells. To the best our knowledge, this is the first case of clonal selection of a pre-existing nondominant tumor cell clone; this report demonstrates the mechanism involved in secondary resistance to TIL-ACT that can potentially change current clinical practice because it advocates for T-cell collection from multiple tumor sites and analysis of tumor heterogeneity before treatment with TIL-ACT.
过继性细胞疗法(ACT)采用肿瘤浸润淋巴细胞(TIL)治疗黑色素瘤患者效果显著,但完全缓解的患者其长期应答似乎受到限制。许多患者对 TIL-ACT 产生继发性耐药,但具体机制尚不清楚。在本研究中,我们描述了一例 TIL-ACT 继发性耐药的病例,可能与肿瘤内异质性和转输 T 细胞对耐药肿瘤细胞克隆的选择有关。据我们所知,这是首例预先存在的非优势肿瘤细胞克隆的克隆选择;本报告证明了 TIL-ACT 继发性耐药的相关机制,可能会改变当前的临床实践,因为它提倡在 TIL-ACT 治疗前从多个肿瘤部位采集 T 细胞并分析肿瘤异质性。