首页> 外文期刊>Case Reports in Oncological Medicine >Response to Ipilimumab/Nivolumab Rechallenge and BRAF Inhibitor/MEK Inhibitor Rechallenge in a Patient with Advanced Metastatic Melanoma Previously Treated with BRAF Targeted Therapy and Immunotherapy
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Response to Ipilimumab/Nivolumab Rechallenge and BRAF Inhibitor/MEK Inhibitor Rechallenge in a Patient with Advanced Metastatic Melanoma Previously Treated with BRAF Targeted Therapy and Immunotherapy

机译:对Ipilimumab / Nivolumab重新检查和BRAF抑制剂/ MEK抑制剂在患者中重新检查,所述患者预先用BRAF靶向治疗和免疫治疗治疗

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Little is known about the optimal sequencing of targeted therapy and immunotherapy in the treatment of patients with BRAFV600-mutated metastatic melanoma. BRAF/MEK inhibition often has the benefit of rapid disease regression; however, resistance is frequently seen with long-term use. Treatment with immune checkpoint inhibitors offers the potential for long-term response but displays a lower rate of objective response. The benefit of synergy between therapies is apparent; however, there is limited data regarding optimal sequencing in the treatment of advanced melanoma. We present the case of a 62-year-old gentleman with advanced BRAFV600-mutated melanoma who followed an unconventional treatment path. After progressing on single-agent vemurafenib, he had response to multiple modalities of immunotherapy before progression. After, he had a substantial response to multiple BRAF/MEK inhibitor rechallenges before developing resistance. The patient is now stable after a retrial of combination immunotherapy. Our case illustrates that with the right sequencing of therapy, meaningful clinical responses can be elicited with rechallenging of targeted therapy and immunotherapy in metastatic melanoma.
机译:关于靶向治疗和免疫疗法的最佳测序众所周知,治疗Brafv600突变转移性黑素瘤的患者。 BRAF / MEK抑制往往具有快速疾病回归的益处;然而,长期使用经常看到抗性。用免疫检查点抑制剂治疗提供了长期响应的潜力,但显示了较低的客观反应速度。在疗法之间的效益是明显的;然而,在治疗晚期黑色素瘤的最佳测序存在有限的数据。我们提出了一个62岁的绅士,具有高级Brafv600-突变黑色素瘤的紧随统治治疗路径​​。在单孕vemurafenib上进行后,他在进展之前对多种免疫疗法的响应进行了反应。之后,他在发育抗性之前对多BRAF / MEK抑制剂重组进行了重大反应。患者在联合免疫疗法重新调用后稳定。我们的病例说明,随着治疗的正确测序,可以引发有意义的临床反应,并在转移性黑色素瘤中的靶向治疗和免疫疗法引发。

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