Park Se Jun, Shin Kabsoo, Hong Tae Ho, Lee Sung Hak, Kim In-Ho, Kim Younghoon, Lee MyungAh
Division of Medical Oncology, Department of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul St. Mary's Hospital, Seoul 06591, Republic of Korea.
Cancer Research Institute, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea.
Cancers (Basel). 2024 Aug 3;16(15):2756. doi: 10.3390/cancers16152756.
Adenocarcinoma of the ampulla of Vater (AAC) is a rare malignancy with heterogeneous tumors arising from various histologic subtypes, necessitating new therapeutic strategies. This study examines epidermal growth factor receptor (EGFR), human epidermal growth factor receptor 2 (HER2), and c-Met expression in AAC, given their potential as druggable targets. Among 87 patients who underwent curative resection, EGFR overexpression was found in 87.4%, HER2 in 11.5%, and c-Met in 50%. EGFR overexpression was more common in the pancreatobiliary subtype ( = 0.018) and associated with a higher histologic grade ( = 0.008). HER2 did not correlate with clinicopathological features, while c-Met was more common in node-negative groups ( = 0.004) and often co-expressed with EGFR ( = 0.049). EGFR-positive patients had worse disease-free (HR = 2.89; 95% CI, 1.35-6.20; = 0.061) and overall survival (HR = 6.89; 95% CI, 2.94-16.2; = 0.026) than EGFR-negative patients. HER2-positive AAC showed a trend towards shorter survival, although not statistically significant, and c-Met had no impact on survival outcomes. In the context of systemic disease, survival outcomes did not vary according to EGFR, HER2, and c-Met expression, but the HER2-positive group showed a trend towards inferior progression-free survival (HR = 1.90; 95% CI, 0.56-6.41; = 0.166). This study underscores the potential of EGFR, HER2, and c-Met as targets for personalized therapy in AAC, warranting further research to evaluate targeted treatments.
壶腹腺癌(AAC)是一种罕见的恶性肿瘤,其肿瘤具有异质性,起源于多种组织学亚型,因此需要新的治疗策略。鉴于表皮生长因子受体(EGFR)、人表皮生长因子受体2(HER2)和c-Met作为可成药靶点的潜力,本研究检测了它们在AAC中的表达情况。在87例行根治性切除术的患者中,EGFR过表达率为87.4%,HER2为11.5%,c-Met为50%。EGFR过表达在胰胆管亚型中更为常见(P = 0.018),且与更高的组织学分级相关(P = 0.008)。HER2与临床病理特征无相关性,而c-Met在无淋巴结转移组中更为常见(P = 0.004),且常与EGFR共表达(P = 0.049)。EGFR阳性患者的无病生存期(HR = 2.89;95%CI,1.35 - 6.20;P = 0.061)和总生存期(HR = 6.89;95%CI,2.94 - 16.2;P = 0.026)均较EGFR阴性患者差。HER2阳性的AAC患者生存期有缩短趋势,但无统计学意义,c-Met对生存结局无影响。在全身性疾病的情况下,生存结局并不因EGFR、HER2和c-Met的表达而有所不同,但HER2阳性组的无进展生存期有较差趋势(HR = 1.90;95%CI,0.56 - 6.41;P = 0.166)。本研究强调了EGFR、HER2和c-Met作为AAC个性化治疗靶点的潜力,值得进一步研究以评估靶向治疗。