Chemotherapy versus Best Supportive Care in Advanced Biliary Tract Carcinoma: A Multi-institutional Propensity Score Matching Analysis

Purpose Although chemotherapy is recommended by various guidelines for advanced biliary tract cancer (BTC), the evidence supporting its use over best supportive care (BSC) is limited. The aim of this study was to investigate the survival benefit of chemotherapy over that of BSC in advanced BTC patients. Materials and Methods Advanced BTC patientswith a good performance status (Eastern CooperativeOncologyGroup [ECOG] 0-2) were eligible for the study. Data were retrospectively collected from four tertiary cancer centers and analyzed using propensity score matching (PSM). Of the 604 patients enrolled, 206 received BSC and 398 received chemotherapy. PSM analysis was performed using the following variables: age, ECOG status, carcinoembryonic antigen (CEA) level, white blood cell level, albumin level, total bilirubin level, and aspartate aminotransferase level. The sample size of each group was 164 patients after PSM. Median survival was compared between the two groups by using the Kaplan-Meier method, and prognostic factors were investigated using Cox proportional regression analysis. Results In post-PSM analysis, the respective median survival for the chemotherapy and BSC groups was dependent on the following prognostic factors: total population, 12.0 months vs. 7.5 months (p=0.001); locally advanced disease, 16.7 months vs. 13.4 months (p=0.490); cancer antigen 19-9 ≤ 100 IU/mL, 12.7 months vs. 10.6 months (p=0.330); and CEA ≤ 3.4 ng/mL, 17.1 months vs. 10.6 months (p=0.052). Conclusion Chemotherapy improved overall survival of patients with advanced BTC who had a good performance status. However, this survival benefit was not observed in BTC patients with locally advanced disease or with lower tumor marker. Individualized approach is needed for initiation of palliative chemotherapy in advanced BTC.

[1]  E. Vasile,et al.  Second-line chemotherapy in advanced biliary cancer progressed to first-line platinum-gemcitabine combination: a multicenter survey and pooled analysis with published data , 2015, Journal of Experimental & Clinical Cancer Research.

[2]  A. Lièvre,et al.  Second‐line chemotherapy for advanced biliary tract cancer after failure of the gemcitabine‐platinum combination: A large multicenter study by the Association des Gastro‐Entérologues Oncologues , 2015, Cancer.

[3]  Joon-Oh Park,et al.  Natural history of metastatic biliary tract cancer (BTC) patients with good performance status (PS) who were treated with only best supportive care (BSC). , 2015, Japanese journal of clinical oncology.

[4]  G. Hortobagyi,et al.  Clinical impact of delaying initiation of adjuvant chemotherapy in patients with breast cancer. , 2014, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[5]  Keda Yu,et al.  Association between delayed initiation of adjuvant CMF or anthracycline-based chemotherapy and survival in breast cancer: a systematic review and meta-analysis , 2013, BMC Cancer.

[6]  W. Mackillop,et al.  Association between time to initiation of adjuvant chemotherapy and survival in colorectal cancer: a systematic review and meta-analysis. , 2011, JAMA.

[7]  V. Sreenivas,et al.  Best supportive care compared with chemotherapy for unresectable gall bladder cancer: a randomized controlled study. , 2010, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[8]  B. Uzzan,et al.  Does delaying adjuvant chemotherapy after curative surgery for colorectal cancer impair survival? A meta-analysis. , 2010, European journal of cancer.

[9]  Myung-Hwan Kim,et al.  Natural History and Prognostic Factors of Advanced Cholangiocarcinoma without Surgery, Chemotherapy, or Radiotherapy: A Large-Scale Observational Study , 2009, Gut and liver.

[10]  M. Highley,et al.  Gemcitabine alone or in combination with cisplatin in patients with advanced or metastatic cholangiocarcinomas or other biliary tract tumours: a multicentre randomised phase II study – The UK ABC-01 Study , 2009, British Journal of Cancer.

[11]  A. Sjölander Propensity scores and M‐structures , 2009, Statistics in medicine.

[12]  J. Yuen,et al.  A meta-analysis of two randomised trials of early chemotherapy in asymptomatic metastatic colorectal cancer , 2005, British Journal of Cancer.

[13]  A. Flahault,et al.  Randomized trial of 5-fluorouracil, leucovorin and cisplatin in advanced pancreatic cancer. , 2001, Hepato-gastroenterology.

[14]  A. Cull,et al.  Chemotherapy prolongs survival in inoperable pancreatic carcinoma , 1994, The British journal of surgery.

[15]  Raymond A. Lee,et al.  An evaluation of early or delayed adjuvant chemotherapy in premenopausal patients with advanced breast cancer undergoing oophorectomy A later analysis , 1982, American journal of clinical oncology.

[16]  J. Hanley,et al.  Chemotherapy in pancreatic cancer: results of a controlled, prospective, randomised, multicentre trial. , 1980, British medical journal.

[17]  C. Lohrisch Clinical Impact of Delaying Initiation of Adjuvant Chemotherapy in Patients With Breast Cancer , 2015 .