Zheng Jian, Chou Joanne F, Gönen Mithat, Vachharajani Neeta, Chapman William C, Majella Doyle Maria B, Turcotte Simon, Vandenbroucke-Menu Franck, Lapointe Réal, Buettner Stefan, Groot Koerkamp Bas, Ijzermans Jan N M, Chan Chung Yip, Goh Brian K P, Teo Jin Yao, Kam Juinn Huar, Jeyaraj Prema R, Cheow Peng Chung, Chung Alexander Y F, Chow Pierce K H, Ooi London L P J, Balachandran Vinod P, Kingham T Peter, Allen Peter J, D'Angelica Michael I, DeMatteo Ronald P, Jarnagin William R, Lee Ser Yee
*Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY †Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY ‡Department of Surgery, Washington University School of Medicine, St. Louis, MO §Department of Surgery, Université de Montréal, Montreal, Quebec, Canada ¶Department of Surgery, Erasmus MC, University Medical Center, Rotterdam, The Netherlands ||Department of Hepatopancreatobiliary and Transplant Surgery, Singapore General Hospital, Singapore, Singapore **Division of Surgical Oncology, National Cancer Center, Singapore, Singapore.
Ann Surg. 2017 Oct;266(4):693-701. doi: 10.1097/SLA.0000000000002360.
This study aims to validate a previously reported recurrence clinical risk score (CRS).
Salvage transplantation after hepatocellular carcinoma (HCC) resection is limited to patients who recur within Milan criteria (MC). Predicting recurrence patterns may guide treatment recommendations.
An international, multicenter cohort of R0 resected HCC patients were categorized by MC status at presentation. CRS was calculated by assigning 1 point each for initial disease beyond MC, multinodularity, and microvascular invasion. Recurrence incidences were estimated using competing risks methodology, and conditional recurrence probabilities were estimated using the Bayes theorem.
From 1992 to 2015, 1023 patients were identified, of whom 613 (60%) recurred at a median follow-up of 50 months. CRS was well validated in that all 3 factors remained independent predictors of recurrence beyond MC (hazard ratio 1.5-2.1, all P < 0.001) and accurately stratified recurrence risk beyond MC, ranging from 19% (CRS 0) to 67% (CRS 3) at 5 years. Among patients with CRS 0, no other factors were significantly associated with recurrence beyond MC. The majority recurred within 2 years. After 2 years of recurrence-free survival, the cumulative risk of recurrence beyond MC within the next 5 years for all patients was 14%. This risk was 12% for patients with initial disease within MC and 17% for patients with initial disease beyond MC.
CRS accurately predicted HCC recurrence beyond MC in this international validation. Although the risk of recurrence beyond MC decreased over time, it never reached zero.
本研究旨在验证先前报道的复发临床风险评分(CRS)。
肝细胞癌(HCC)切除术后的挽救性移植仅限于在米兰标准(MC)内复发的患者。预测复发模式可能有助于指导治疗建议。
将国际多中心队列中接受R0切除的HCC患者按就诊时的MC状态进行分类。CRS的计算方法是,初始疾病超出MC、多结节性和微血管侵犯各计1分。使用竞争风险方法估计复发发生率,并使用贝叶斯定理估计条件复发概率。
1992年至2015年,共纳入1023例患者,其中613例(60%)复发,中位随访时间为50个月。CRS得到了很好的验证,因为所有3个因素仍然是超出MC后复发的独立预测因素(风险比1.5 - 2.1,所有P < 0.001),并且准确地对超出MC的复发风险进行了分层,5年时从19%(CRS 0)到67%(CRS 3)。在CRS为0的患者中,没有其他因素与超出MC的复发显著相关。大多数患者在2年内复发。在无复发生存2年后,所有患者在接下来5年内超出MC的累积复发风险为14%。初始疾病在MC内的患者这一风险为12%,初始疾病超出MC的患者为17%。
在这项国际验证中,CRS准确预测了超出MC的HCC复发。尽管超出MC的复发风险随时间降低,但从未降至零。