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Durable complete responses off all treatment in patients with metastatic malignant melanoma after sequential immunotherapy followed by a finite course of BRAF inhibitor therapy

机译:序贯免疫治疗后一定疗程的BRAF抑制剂治疗后,转移性恶性黑色素瘤患者所有治疗的持久完全反应

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We report 3cases of durable complete response (CR) in patients with BRAF-mutated metastatic melanoma who were initially treated unsuccessfully with sequential immunotherapies (high dose interleukin 2followed by ipilimumab with or without concurrent radiation therapy). After progression during or post immunotherapy, these patients were given BRAF inhibitor therapy and developed rapid CRs. Based on the concomitant presence of autoimmune manifestations (including vitiligo and hypophysitis), we postulated that there was a synergistic effect between the prior immune therapy and the BRAF targeting agents. Accordingly, the inhibitors were gradually weaned off beginning at 3months and were stopped completely at 9-12months. The three patients remain well and in CR off of all therapy at up to 15months radiographic follow-up. The institution of the BRAF therapy was associated with development of severe rheumatoid-like arthritis in 2patients which persisted for months after discontinuation of therapy, suggesting it was not merely a known toxicity of BRAF inhibitors (arthralgias). On immunologic analysis, these patients had high levels of non-T-regulatory, CD4 positive effector phenotype T-cells, which persisted after completion of therapy. Of note, we had previously reported a similar phenomenon in patients with metastatic melanoma who failed high dose interleukin-2 and were then placed on a finite course of temozolomide with rapid complete responses that have remained durable for many years after discontinuation of temozolomide. We postulate that a finite course of cytotoxic or targeted therapy specific for melanoma given after apparent failure of prior immunotherapy can result in complete and durable remissions that may persist long after the specific cytotoxic or targeted agents have been discontinued suggesting the existence of sequence specific synergism between immunotherapy and these agents. Here, we discuss these cases in the context of the literature on synergy between conventional or targeted cytotoxic therapy and immunotherapy in cancer treatment.
机译:我们报告了BRAF突变的转移性黑色素瘤患者的3例持久完全反应(CR),这些患者最初未接受序贯免疫疗法(高剂量白介素2继之以ipilimumab联合或不联合放射治疗)。在免疫治疗期间或之后进展后,这些患者接受了BRAF抑制剂治疗并出现了快速CR。基于自身免疫表现(包括白癜风和垂体炎)的同时存在,我们推测先前的免疫治疗与BRAF靶向药物之间存在协同作用。因此,抑制剂从3个月开始逐渐断奶,并在9-12个月完全停止。 3例患者在长达15个月的影像学随访中均保持良好状态,并且在所有治疗中均未发生CR。 BRAF治疗的实施与2名患者中严重的类风湿性关节炎的发展有关,这种疾病在停止治疗后持续了数月,这表明BRAF不仅是已知的BRAF抑制剂毒性(关节痛)。通过免疫学分析,这些患者具有高水平的非T调节性CD4阳性效应表型T细胞,在治疗完成后仍持续存在。值得注意的是,我们先前曾报道过转移性黑素瘤患者发生类似现象,该患者在大剂量白介素2失败后被置于有限剂量的替莫唑胺疗程中,快速完全反应,在停用替莫唑胺后仍可维持多年。我们假设先前免疫治疗的明显失败后针对黑素瘤进行的有限细胞毒性或靶向治疗疗程可能会导致完全和持久的缓解,这种缓解可能会在特定细胞毒性或靶向药物停用后持续很长时间,这表明两者之间存在序列特异性协同作用免疫疗法和这些药物。在这里,我们在有关常规或靶向细胞毒性治疗与癌症治疗中免疫治疗之间协同作用的文献中讨论这些病例。

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