Department of Radiation Oncology, Severance Hospital, Yonsei Cancer Center, Yonsei University College of Medicine, 50-1, Yonsei-ro, Seodaemun-gu, Seoul, 03722, Korea.
Department of Radiation Oncology, CHA Bundang Medical Center, CHA University School of Medicine, Seongnam, Korea.
J Cancer Res Clin Oncol. 2021 Aug;147(8):2435-2445. doi: 10.1007/s00432-021-03524-7. Epub 2021 Jan 20.
The objective of this study was to investigate the benefits of adjuvant treatment for patients with resected perihilar cholangiocarcinoma (PHC).
Between 2001 and 2017, 196 patients with PHC adenocarcinoma underwent curative resection. The patients were divided into four groups according to adjuvant treatment type: surgery alone (S; N = 90), surgery with chemotherapy (S+CTx; N = 67), surgery with radiotherapy (S+RTx; N = 18), and surgery with chemoradiotherapy (S+ CRTx; N = 21).
The median follow-up duration of the surviving patients was 58 months. The 5-year rate of overall survival (OS) was 32%. In multivariate analysis, receiving S+CTx and S+CRTx were significant prognostic factors for OS. In subgroup analyses of the R1 resection patients, the S+CRTx group showed better OS than the S group (p < 0.05). In subgroup analyses of the stage III-IVA patients with a negative resection margin, the S+CTx and S+CRTx groups showed superior OS than the S group (p < 0.05).
Our data suggest that adjuvant chemoradiotherapy might be considered for PHC patients with R1 resection. Adjuvant chemotherapy or chemoradiotherapy is suggested for stage III-IVA patients with R0 resection. The results of this study require validation through further prospective studies.
本研究旨在探讨辅助治疗对可切除肝门部胆管癌(PHC)患者的获益。
2001 年至 2017 年间,196 例 PHC 腺癌患者接受了根治性切除术。根据辅助治疗类型,患者分为四组:单纯手术组(S;N=90)、手术联合化疗组(S+CTx;N=67)、手术联合放疗组(S+RTx;N=18)和手术联合放化疗组(S+CRTx;N=21)。
存活患者的中位随访时间为 58 个月。5 年总生存率(OS)为 32%。多因素分析显示,接受 S+CTx 和 S+CRTx 是 OS 的显著预后因素。在 R1 切除患者的亚组分析中,S+CRTx 组的 OS 优于 S 组(p<0.05)。在阴性切缘的 III-IVA 期患者的亚组分析中,S+CTx 和 S+CRTx 组的 OS 优于 S 组(p<0.05)。
我们的数据表明,对于 R1 切除的 PHC 患者,辅助放化疗可能是一种考虑。对于 R0 切除的 III-IVA 期患者,建议进行辅助化疗或放化疗。本研究结果需要进一步的前瞻性研究来验证。