Safety and efficacy of Nab-paclitaxel plus gemcitabine in patients with advanced pancreatic cancer suffering from cholestatic hyperbilirubinaemia-A retrospective analysis

被引:7
|
作者
Pelzer, Uwe [1 ]
Wislocka, Lilianna [1 ]
Juehling, Anja [1 ]
Striefler, Jana [1 ]
Klein, Fritz [2 ]
Roemmler-Zehrer, Josefine [4 ]
Sinn, Marianne [1 ]
Denecke, Tim [3 ]
Bahra, Marcus [2 ]
Riess, Hanno [1 ]
机构
[1] Charite Univ Med Berlin, Freie Univ Berlin, Humboldt Univ, Div Hematol Oncol & Tumor Immunol,Univ Berlin,Be, Berlin, Germany
[2] Charite Univ Med Berlin, Med Dept Charite, Div Surg, Berlin, Germany
[3] Charite Univ Med Berlin, Med Dept Charite, Div Radiol, Berlin, Germany
[4] Celgene GmbH, Munich, Germany
关键词
Advanced pancreatic carcinoma; Cholestasis; Hyperbilirubinaemia; Chemotherapy; Nab-paclitaxel; Gemcitabine; CLINICAL-PRACTICE; SURVIVAL;
D O I
10.1016/j.ejca.2018.06.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Treatment of patients with advanced pancreatic carcinoma (APC) and hyperbilirubinaemia is problematic because these patients were regularly excluded from clinical studies. Nanoparticle albumin-bound paclitaxel and gemcitabine (nab-P/G) is an evidence-based treatment for patients with APC. This retrospective study investigated the safety and efficacy of nab-P/G in patients with APC and cholestatic hyperbilirubinaemia. Methods: We screened our prospective database for patients with APC treated with nab-P/G at total bilirubin levels of >= 1.2 mg/dl. Patients were assigned into three groups according to their bilirubin level (A: 1.2-3 mg/di, B: >3-5 mg/di, C: >5 mg/dl). Analyses with regard to safety and survival were performed. Results: Twenty-nine of 168 patients screened between Dec 2013 and Dec 2015 fulfilled the inclusion criteria. Most patients (83%) were male; median age was 63 [41-79] years. Nab-P/G administrations in patients with an elevated bilirubin level (median, range) did not result in unexpected toxicities assessed by predefined (non-)haematological parameters. Median overall survival (mOS) for the whole group was 11.7 (95% confidence interval [CI]: 6.8-14.0) months; for A: 11.8 (95% CI: 6.5-16.5), B: 9.2 (95% CI: 1.1 - NA) months and C 11.8 (95% CI: 5.9-20.0] months (p = 0.843). Again, mOS from the first application of nab-PIG did not differ between the groups (p = 0.13). Conclusion: Nab-P/G administrations in our pts with cholestatic hyperbilirubinaemia suffering from APC were feasible and safe with respect to individualised dose administrations. A multicenter phase 1 trial in pts with hyperbilirubinaemia is started (AIO-PAK-0117) to confirm these findings in a prospective setting. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:85 / 93
页数:9
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