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Intrahepatic Cholangiocarcinoma: Recurrence Patterns, Genomics, and Survival

医学 切除术 内科学 肿瘤科 佐剂 总体生存率 胃肠病学 阶段(地层学) 免疫组织化学 生存分析 外科 辅助治疗 存活率 回顾性队列研究 放射科 癌症
作者
Pratik Chandra,Yi Song,Esther N Drill,Alice Chia-Chi Wei,Nancy E. Kemeny,Andrea Cercek,Louise Catherine Connell,James J. Harding,Ghassan K. Abou‐Alfa,Wungki Park,T. Peter Kingham,Kevin C. Soares,Vinod P. Balachandran,Jeffrey A. Drebin,Michael Ian D'Angelica,Eileen Mary O'Reilly,Bas Groot Koerkamp,William R. Jarnagin
出处
期刊:JCO precision oncology [Lippincott Williams & Wilkins]
卷期号:9 (9): e2500402-e2500402 被引量:2
标识
DOI:10.1200/po-25-00402
摘要

PURPOSE The impact of first recurrence site on outcome after resection of intrahepatic cholangiocarcinoma (IHC) is ill-defined, as are the genomic underpinnings of recurrence and outcomes. METHODS Resected patients with IHC at two institutions with genomic data were included. Sites of first recurrence (SOFR) were classified as liver only (LO), extrahepatic (EH) only, or simultaneous liver and extrahepatic (SIM). Overall survival (OS) was calculated from the time of recurrence. RESULTS Between 1993 and 2021, 318 patients met inclusion criteria; 232 (73%) recurred. SOFR were LO = 93 (40%), EH = 80 (34%), and SIM = 59 (26%). Median OS from recurrence was similar in the LO (33 [26, 42] months) and EH groups (33 [23, 46] months) but much lower in SIM (12 [9.8, 18] months; P < .001). Moderate/poor tumor differentiation, lymphovascular invasion, N1 disease, perineural invasion, and time to recurrence (all P < .05) were associated with SIM; only positive resection margin predicted LO ( P = .007). No individual genomic or pathway alterations predicted SOFR; however, for all recurrers, TP53 mut (n = 51, 22%; hazard ratio [HR], 2.0 [1.4 to 2.9]; P = .002), CDKN2A del (n = 34, 15%; HR, 3.4 [95% CI, 2.2 to 5.3]; P < .001), CDKN2B (n = 25, 11%; HR, 3.2 [95% CI, 2.0 to 5.0]; P < .001), and KRAS mut (n = 25, 11%; HR, 2.5 [95% CI, 1.6 to 4.0]; P = .002) were associated with worse OS. On multivariable analysis, SIM (HR, 2.5 [95% CI, 1.7 to 3.5]; P < .001), N1 status (HR, 1.8 [95% CI, 1.2 to 2.6]; P = .004), and alterations in the high-risk genotype (TP53 mut , CDKN2A del or KRAS mut ; n = 84, 36%; HR, 2.4 [95% CI, 1.7 to 3.3]; P < .001) were independent predictors of poor OS. CONCLUSION Recurrence after resection of IHC is common, and the liver was the most common site (66%). Clinicopathologic and genomic factors had limited ability to predict SOFR. Although LO and EH were associated with similar OS, SIM recurrences had dramatically worse OS. Adjuvant strategies targeting liver recurrence may improve outcomes after resection of IHC.

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