Defining the Role of Adjuvant Radiotherapy for Biliary Tract Cancers: A Site-Specific Propensity-Matched Analysis

被引:0
|
作者
Seo, Yongwoo David [1 ]
Acidi, Belkacem [1 ]
Newton, Andrew [2 ]
Haddad, Antony [1 ]
Chiang, Yi-Ju [1 ]
Coelho, Rainna [3 ]
Newhook, Timothy E. [1 ]
Tzeng, Ching-Wei D. [1 ]
Chun, Yun Shin [1 ]
Ludmir, Ethan B. [4 ]
Koay, Eugene J. [4 ]
Javle, Milind [5 ]
Vauthey, Jean Nicolas [1 ]
Cao, Hop S. Tran [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Surg Oncol, Houston, TX 77030 USA
[2] Ochsner Hlth, Dept Surg Oncol, New Orleans, LA 70112 USA
[3] Univ Houston, Dept Surg, HCA Houston Healthcare, Houston, TX 77204 USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Radiat Oncol, Houston, TX 77030 USA
[5] Univ Texas MD Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, Houston, TX 77030 USA
关键词
biliary tract cancer; adjuvant therapy; chemoradiotherapy; liver cancer; CURATIVE-INTENT RESECTION; PERIHILAR CHOLANGIOCARCINOMA; CONCURRENT CAPECITABINE; RADIATION-THERAPY; PHASE-II; RECURRENCE; GEMCITABINE;
D O I
10.3390/cancers17030494
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Biliary tract cancers (BTCs) have distinct tumor biology but share a poor prognosis, with a 5-year-survival-rate of 5-19%. Surgical resection is the only potential cure, but recurrences are common. The role of adjuvant radiotherapy (XRT) remains unclear. Methods: Using the National Cancer Database (2006-2018), we analyzed resected non-metastatic BTCs. Patients who survived beyond 90 days post-surgery were included, while those with R2 resections or neoadjuvant therapy were excluded. Propensity matching was performed based on predictors of adjuvant radiation, age, and sex. Survival outcomes were compared between no adjuvant therapy, chemotherapy alone, and XRT +/- chemotherapy. Results: Among 21,275 patients, including 5308 intrahepatic cholangiocarcinoma (IHC), 2689 perihilar cholangiocarcinoma (PHC), 3092 distal cholangiocarcinoma (DCC), and 10,186 gallbladder cancer (GBC) cases, adjuvant XRT did not improve survival for IHC. For PHC and DCC, XRT improved survival over no adjuvant therapy (PHC: 31.2 vs. 26.3 months, p = 0.004; DCC: 33.7 vs. 27.0 months, p = 0.015) but not over chemotherapy alone. For GBC, XRT significantly improved survival compared to both no adjuvant therapy and chemotherapy (30.2 vs. 26.6 and 24.6 months; p = 0.05 and p = 0.001). Conclusions: XRT provides a survival benefit for GBC, especially in node-positive and R1-resected patients. For PHC and DCC, XRT improves outcomes compared to no therapy, but its benefit over chemotherapy is uncertain. No benefit was observed for IHC.
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页数:11
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