1 Pharmacy Clinical Programs, 2 Department of Gastrointestinal Medical Oncology, 3 Department of Biostatistics, UT MD Anderson Cancer Center, Houston, TX 77030, USA.
J Gastrointest Oncol. 2014 Dec;5(6):408-13. doi: 10.3978/j.issn.2078-6891.2014.072.
Gemcitabine plus platinum (GEM-P) combination chemotherapy is standard treatment for first-line advanced cholangiocarcinoma (aCC). GEM-P first-line therapy reports a progression-free survival (PFS) of 8 months and overall survival (OS) of 11.7 months. Treatment in the second-line setting is less clear. Five-year survival for aCC remains dismal at 5-10%. The purpose of this study was to describe the outcomes with second-line systemic treatment at our institution.
This study was a single institution retrospective chart review of aCC patients who initiated second-line systemic treatment during 1/1/2009 to 12/31/2012. The primary objective was to evaluate PFS with second-line systemic treatment. Secondary objectives were OS and disease control rate. Second-line systemic regimens were classified into four treatment groups: GEM-P, gemcitabine + fluoropyrimidine (GEM-FU), other FU combination (FU-combo), and others.
Fifty-six patients were included and the majority had intrahepatic aCC. A total of 80% received first-line gemcitabine-based therapy. Second-line therapy consisted of GEM-P (19.6%), GEM-FU (28.6%), FU-combo (37.5%), and others (14.3%). Median PFS was 2.7-month (95% CI, 2.3-3.8 months) with a median OS of 13.8 months (95% CI, 12-19.3 months) and a disease control rate of 50%. No significant difference in survival was identified between the four treatment groups.
This study revealed a 2.7-month PFS, 50% disease control rate, and potential survival benefit with second-line treatment. Options for second-line systemic therapy include GEM-FU, FU-combo, GEM-P if not given in the first-line setting. Targeted therapy with erlotinib or bevacizumab could be considered in addition to chemotherapy.
吉西他滨联合铂类(GEM-P)联合化疗是一线晚期胆管癌(aCC)的标准治疗方法。GEM-P 一线治疗报告无进展生存期(PFS)为 8 个月,总生存期(OS)为 11.7 个月。二线治疗方案则不太明确。aCC 的 5 年生存率仍然很差,为 5-10%。本研究旨在描述我们机构二线全身治疗的结果。
这是一项单中心回顾性图表研究,纳入了 2009 年 1 月 1 日至 2012 年 12 月 31 日期间开始二线全身治疗的 aCC 患者。主要目的是评估二线全身治疗的 PFS。次要目标是 OS 和疾病控制率。二线全身治疗方案分为 4 个治疗组:GEM-P、吉西他滨+氟尿嘧啶(GEM-FU)、其他 FU 联合(FU-combo)和其他。
共纳入 56 例患者,大多数为肝内 aCC。共有 80%的患者接受了一线基于吉西他滨的治疗。二线治疗包括 GEM-P(19.6%)、GEM-FU(28.6%)、FU-combo(37.5%)和其他(14.3%)。中位 PFS 为 2.7 个月(95%CI,2.3-3.8 个月),中位 OS 为 13.8 个月(95%CI,12-19.3 个月),疾病控制率为 50%。4 个治疗组之间的生存无显著差异。
本研究显示二线治疗的 PFS 为 2.7 个月,疾病控制率为 50%,具有潜在的生存获益。二线全身治疗的选择包括 GEM-FU、FU-combo,如果一线未使用 GEM-P,则可选用 GEM-P。除化疗外,还可以考虑厄洛替尼或贝伐珠单抗等靶向治疗。