Kass Samantha L, Linden Allison F, Jackson Patrick G, De Brito Pedro A, Atkins Michael B
Georgetown University School of Medicine, Washington, DC 20007, USA.
Department of Surgery, Georgetown University Medical Center, Washington, DC 20007, USA.
Melanoma Manag. 2015 May;2(2):115-120. doi: 10.2217/mmt.15.10. Epub 2015 May 18.
Combination BRAF/MEK inhibition has shown improved response rates and longer progression-free and overall survival for patients with -mutant metastatic melanoma. A 63-year-old female with widely metastatic V600E-mutant melanoma was treated with dabrafenib/trametinib. Ten weeks into therapy, she was treated conservatively for a partial bowel obstruction involving a lesion in the distal ileum. She presented two weeks later with CT evidence of a high-grade bowel obstruction with perforation. Emergent surgery was performed. Intraoperative inspection and pathologic analysis of the resected specimen revealed no evidence of melanoma. Seven months postoperatively she is disease free and fully functional. Rapid BRAF/MEK inhibitor-induced regression of small bowel lesions can result in bowel perforation, which is critical to distinguish from the consequences of disease progression.
BRAF/MEK联合抑制疗法已显示出对携带 - 突变的转移性黑色素瘤患者有更高的缓解率、更长的无进展生存期和总生存期。一名63岁广泛转移的V600E突变黑色素瘤女性患者接受了达拉非尼/曲美替尼治疗。治疗10周后,她因涉及回肠远端病变的部分肠梗阻接受了保守治疗。两周后,她出现CT证据显示有伴有穿孔的高位肠梗阻。进行了急诊手术。对切除标本的术中检查和病理分析未发现黑色素瘤证据。术后七个月,她无疾病且功能完全正常。BRAF/MEK抑制剂快速诱导的小肠病变消退可导致肠穿孔,这对于与疾病进展的后果进行区分至关重要。