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使用mFOLFOX6联合帕尼单抗对伴有家族性腺瘤性息肉病的多发性结直肠癌不可切除肝转移进行转化治疗。

Conversion Therapy Using mFOLFOX6 With Panitumumab for Unresectable Liver Metastases From Multiple Colorectal Cancers With Familial Adenomatous Polyposis.

作者信息

Toiyama Yuji, Inoue Yasuhiro, Kitajima Takahito, Okigami Masato, Kawamura Mikio, Kawamoto Aya, Okugawa Yoshinaga, Hiro Jyunichiro, Tanaka Koji, Mohri Yasuhiko, Kusunoki Masato

机构信息

Department of Gastrointestinal and Pediatric Surgery, Division of Reparative Medicine, Institute of Life Sciences, Graduate School of Medicine, Mie University, Mie, Japan.

出版信息

Int Surg. 2014 Nov-Dec;99(6):795-801. doi: 10.9738/INTSURG-D-13-00125.1.

Abstract

A 39-year-old man received a diagnosis of unresectable multiple liver metastases from multiple colorectal cancers with familial adenomatous polyposis. After construction of an ileostomy, modified FOLFOX6 (mFOLFOX6) with panitumumab was administrated because rectal cancer and sigmoid colon cancer are KRAS wild type. The 13 courses of chemotherapy resulted in a marked reduction in the size of liver metastases and sigmoid colon cancer. Consequently, curative resection with total colectomy, ileal pouch anal anastomosis, and liver metastasis resection with radiofrequency ablation was performed. Progression of KRAS wild-type rectal cancer after chemotherapy suggested that each clone from rectal and sigmoid colon cancer might have a different sensitivity to epidermal growth factor receptor antibody. Immunohistochemical analysis revealed loss of PTEN expression in rectal cancer compared with liver metastases from sigmoid colon cancer, showing that the difference of mFOLFOX6 with panitumumab might be related to activation of the PI3K-AKT pathway.

摘要

一名39岁男性被诊断为患有家族性腺瘤性息肉病的多发性结直肠癌伴不可切除的多发性肝转移。在进行回肠造口术后,由于直肠癌和乙状结肠癌为KRAS野生型,给予了联合帕尼单抗的改良FOLFOX6(mFOLFOX6)方案化疗。13个疗程的化疗使肝转移灶和乙状结肠癌的大小显著缩小。因此,进行了全结肠切除术、回肠储袋肛管吻合术及肝转移灶射频消融根治性切除术。化疗后KRAS野生型直肠癌进展提示,直肠癌和乙状结肠癌的每个克隆对表皮生长因子受体抗体可能具有不同的敏感性。免疫组化分析显示,与乙状结肠癌肝转移灶相比,直肠癌中PTEN表达缺失,表明mFOLFOX6联合帕尼单抗的差异可能与PI3K-AKT通路的激活有关。

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