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Vemurafenib in combination with cobimetinib in relapsed and refractory extramedullary multiple myeloma harboring the BRAF V600E mutation

机译:Vemurafenib与Cobimetinib的复发和难治性髓外骨髓瘤联合,涉及BRAF V600E突变

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摘要

Abstract BRAF mutations are present in a variety of cancers and cause constitutive activation of the Ras‐Raf–MEK‐ERK signaling pathway. In cutaneous malignant melanoma, combined treatment with BRAF and MEK inhibitors is associated with high response rates and has been shown to improve progression free as well as overall survival compared to BRAF inhibition alone. In multiple myeloma, BRAF mutations are detectable only in a minority of patients. Only few data are available regarding the clinical activity of BRAF inhibitors in BRAF‐positive multiple myeloma patients, including some anecdotal reports on remarkable responses in individuals being resistant to all other available anti‐myeloma treatment approaches. We here present the first report on the combination of vemurafenib and cobimetinib in a young patient with highly resistant and rapidly progressing multiple myeloma harboring the BRAF V600E mutation who achieved a rapid and sustained response to this combination therapy.
机译:摘要BRAF突变存在于各种癌症中,并导致RAS-RAF-MEK-ERK信号通路的组成型激活。 在皮肤恶性黑色素瘤中,与BRAF和MEK抑制剂的组合处理与高反应率相关,并且已被证明与单独的BRAF抑制相比,与BRAF抑制相比,自由的渐进性和总体存活率有关。 在多种骨髓瘤中,BRAF突变仅在少数患者中可检测到。 关于BRAF阳性多发性骨髓瘤患者的BRAF抑制剂的临床活性只有很少的数据,包括一些关于个人对所有其他可用抗骨髓瘤治疗方法的非凡反应的轶事报告。 我们在这里提出了关于vemureafenib和Cobimetinib在一名年轻患者中的第一份报告,具有高度抗性和迅速进展的多发性骨髓瘤,其涉及对这种联合治疗的快速和持续反应的快速和持续反应。

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