Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Weill Cornell Department of Medicine, Weill Cornell Medicine, New York, New York.
Cancer. 2019 May 1;125(9):1441-1448. doi: 10.1002/cncr.31951. Epub 2019 Jan 8.
Ampullary carcinoma (AC) is a rare gastrointestinal cancer. Pathogenic germline alterations (PGAs) in BRCA2 and potentially targetable somatic alterations (SAs) in ERBB2 and ELF3 have been previously described in AC. Memorial Sloan Kettering Cancer Center has implemented an opt-in strategy for germline testing (GT) and somatic testing (ST) for patients with AC to further evaluate the spectrum of PGAs and SAs.
Forty-five patients with pathologically confirmed AC prospectively consented with the Memorial Sloan Kettering Integrated Mutation Profiling of Actionable Cancer Targets (MSK-IMPACT) test (410-468 genes). A subset of the cohort (23 of the 45 patients) also consented to GT with MSK-IMPACT (76-88 genes). Germline data for 21 of the remaining 22 patients who had not consented to GT were obtained in a de-identified fashion without clinical correlation. Clinicopathologic features, treatment histories, and survival data for consenting patients were collected and analyzed.
Pancreaticobiliary, intestinal, and mixed features of the 2 types were the primary pathologic subtypes of AC identified in this cohort. No difference in median overall survival was found between pathologic subtypes. Eight of 44 patients (18%) were identified as harboring pathogenic mutations in BRCA2, ATM, RAD50, and MUTYH. In addition, this study found a wide spectrum of SAs in genes such as KRAS, MDM2, ERBB2, ELF3, and PIK3CA. Two patients in the cohort underwent SA-targeted therapy, and 1 had a partial radiographic response.
Mutations in multiple somatic and germline genes were identified in this cohort. Significantly, actionable targets were identified in the tumors, and broader testing for PGAs and SAs should be considered for all patients with AC.
壶腹癌(AC)是一种罕见的胃肠道癌症。BRCA2 中的致病性种系改变(PGAs)和 ERBB2 和 ELF3 中潜在的靶向治疗体细胞改变(SAs)以前在 AC 中已有描述。纪念斯隆凯特琳癌症中心对 AC 患者实施了种系检测(GT)和体细胞检测(ST)的选择加入策略,以进一步评估 PGAs 和 SAs 的范围。
45 例经病理证实的 AC 患者前瞻性同意接受纪念斯隆凯特琳综合可操作癌症靶点突变分析(MSK-IMPACT)检测(410-468 个基因)。该队列的一部分(45 例患者中的 23 例)也同意进行 MSK-IMPACT(76-88 个基因)的 GT。对其余 22 例未同意 GT 的患者中的 21 例,以去识别的方式获得了无临床关联的种系数据。对同意患者的临床病理特征、治疗史和生存数据进行了收集和分析。
该队列中确定的 AC 的主要病理亚型为胰胆管、肠型和混合型。不同病理亚型之间的中位总生存期无差异。44 例患者中有 8 例(18%)被鉴定为携带 BRCA2、ATM、RAD50 和 MUTYH 的致病性突变。此外,本研究还发现了 KRAS、MDM2、ERBB2、ELF3 和 PIK3CA 等基因中广泛存在的 SAs。该队列中有 2 例患者接受了 SAs 靶向治疗,其中 1 例有部分放射学反应。
本队列中发现了多种种系和体细胞基因的突变。重要的是,在肿瘤中鉴定出了可操作的靶点,因此所有 AC 患者都应考虑进行更广泛的 PGAs 和 SAs 检测。