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日本的家族性和遗传性胰腺癌。

Familial and hereditary pancreatic cancer in Japan.

机构信息

Division of Genetic Medicine Promotion and Endoscopy, Shizuoka Cancer Center, Shimonagakubo, Nagaizumi, Suntogun, Shizuoka, 411-8777, Japan.

Department of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital, Tokyo, 104-0045, Japan.

出版信息

Fam Cancer. 2024 Aug;23(3):365-372. doi: 10.1007/s10689-024-00395-y. Epub 2024 May 11.

Abstract

As in Western countries, familial pancreatic cancer accounts for 5-7% of pancreatic cancer (PC) in Japan. Opportunities for diagnosing hereditary pancreatic cancer (HPC) are increasing owing to the coverage of companion diagnostics and cancer genomic profiling by national health insurance in patients with unresectable or recurrent PC refractory to standard chemotherapies. HPC is recognized in 7% of PCs and 15% of familial pancreatic cancer, including germline variants of BRCA1/2, ATM, PALB2, APC, and mismatch repair genes. Individuals with 5-fold or greater inherited risks of PC are recommended to undergo pancreatic surveillance according to Japanese guidelines. The imaging modalities for this surveillance include endoscopic ultrasound, magnetic resonance cholangiopancreatography, abdominal ultrasound, and enhanced computed tomography. Currently, a nationwide prospective surveillance study is ongoing in Japan. Platinum-based chemotherapy is an effective pancreatic cancer treatment in patients with variants of homologous recombination repair genes (BRCA1/2 and PALB2); however, the use of platinum regimens solely based on familial/personal cancer history remains controversial. The efficacy of olaparib maintenance therapy, as confirmed by the POLO study, has significantly impacted the clinical treatment of advanced PC patients in Japan. Since the initiation of precision cancer medicine in 2019, genetic medicine for PC patients has expanded in Japan.

摘要

与西方国家一样,家族性胰腺癌约占日本胰腺癌(PC)的 5-7%。由于国家健康保险涵盖了无法切除或复发性 PC 标准化疗耐药患者的伴随诊断和癌症基因组分析,诊断遗传性胰腺癌(HPC)的机会正在增加。HPC 在 7%的 PCs 和 15%的家族性胰腺癌中得到认可,包括 BRCA1/2、ATM、PALB2、APC 和错配修复基因的种系变异。根据日本指南,建议具有 5 倍或更高 PC 遗传风险的个体进行胰腺监测。该监测的影像学方式包括内镜超声、磁共振胰胆管成像、腹部超声和增强计算机断层扫描。目前,日本正在进行一项全国性的前瞻性监测研究。铂类化疗是同源重组修复基因(BRCA1/2 和 PALB2)变异患者有效的胰腺癌治疗方法;然而,仅基于家族/个人癌症史使用铂类方案仍存在争议。POLO 研究证实奥拉帕利维持治疗的疗效,这对日本晚期 PC 患者的临床治疗产生了重大影响。自 2019 年精准癌症医学启动以来,日本 PC 患者的遗传医学得到了扩展。

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