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Published on: January 25, 2015
Second-line systemic treatment for advanced cholangiocarcinoma
Jane E Rogers1, Lindsey Law1, Van D Nguyen1
11 Pharmacy Clinical Programs, 2 Department of Gastrointestinal Medical Oncology, 3 Department of Biostatistics, UT MD Anderson Cancer Center, Houston, TX 77030, USA.
Second-line chemotherapy for advanced cholangiocarcinoma (aCC) offers a median progression-free survival of 2.7 months and a 50% disease control rate. This study suggests potential survival benefits from various second-line systemic treatments.
Area of Science:
- Oncology
- Gastroenterology
Background:
- Advanced cholangiocarcinoma (aCC) has a dismal 5-10% five-year survival rate.
- Gemcitabine plus platinum (GEM-P) is the standard first-line treatment, yielding an 8-month PFS and 11.7-month OS.
- Second-line treatment options for aCC remain less defined.
Purpose of the Study:
- To describe the outcomes of second-line systemic treatment for advanced cholangiocarcinoma (aCC) at a single institution.
- To evaluate progression-free survival (PFS) as the primary objective.
- To assess overall survival (OS) and disease control rate (DCR) as secondary objectives.
Main Methods:
- Retrospective chart review of aCC patients initiating second-line systemic treatment between 2009 and 2012.
- Classification of second-line regimens into four groups: GEM-P, gemcitabine + fluoropyrimidine (GEM-FU), other FU combination (FU-combo), and others.
- Analysis of PFS, OS, and DCR for each treatment group.
Main Results:
- Fifty-six patients with aCC were included, predominantly with intrahepatic disease.
- Second-line therapies included GEM-P (19.6%), GEM-FU (28.6%), FU-combo (37.5%), and others (14.3%).
- Median PFS was 2.7 months, median OS was 13.8 months, and DCR was 50%, with no significant survival differences between groups.
Conclusions:
- Second-line systemic therapy for aCC demonstrated a 2.7-month PFS and 50% DCR, indicating a potential survival benefit.
- Viable second-line options include GEM-FU, FU-combo, and GEM-P if not used first-line.
- Consideration of targeted therapies like erlotinib or bevacizumab in addition to chemotherapy is recommended.
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