Quidde Julia, Azémar Marc, Bokemeyer Carsten, Arnold Dirk, Stein Alexander
University Medical Center Hamburg-Eppendorf, Department of Oncology, Hematology, Bone Marrow Transplantation with Section Pneumology, Hubertus Wald Tumor Center, Martinistraße 52, 20246 Hamburg, Germany.
Tumor Biology Center Freiburg, Freiburg, Germany.
Ther Adv Med Oncol. 2016 May;8(3):144-52. doi: 10.1177/1758834016637585. Epub 2016 Mar 17.
Treatment of patients with severe liver dysfunction including hyperbilirubinemia secondary to liver metastases of gastrointestinal (GI) cancer is challenging. Regimen of oxaliplatin and fluoropyrimidine (FP)/folinic acid (FA) ± a monoclonal antibody (moAb), represents a feasible option considering the pharmacokinetics. Clinical data on the respective dosage and tolerability are limited and no recommendations are available.
Consecutive patients with severe hyperbilirubinemia [>2 × upper limit of the normal range (ULN) and >2.4 mg/dl] due to liver metastases of GI cancer without options for drainage receiving oxaliplatin, FP/FA ± moAb were analyzed. To collect further data a review of the literature was performed.
A total of 12 patients were identified between 2011 and 2015. At treatment start, median bilirubin level was 6.1 mg/dl (>5 × ULN, range 2.7-13.6). The majority of patients (n = 11) received dose-reduced regimen with oxaliplatin (60-76%) and FP/FA (0-77%), rapidly escalating to full dose regimen. During treatment, bilirubin levels dropped more than 50% within 8 weeks or normalized within 12 weeks in 6 patients (responders). Median overall survival was 5.75 months (range 1.0-16.0 months) but was significantly prolonged in responders compared to nonresponders [9.7 and 3.0 months, p = 0.026 (two-sided test); 95% confidence interval (CI): 1.10-10.22]. In addition, case reports or series comprising a further 26 patients could be identified. Based on the obtained data a treatment algorithm was developed.
Treatment with oxaliplatin, FP/FA ± moAb is feasible and may derive relevant benefits in patients with severe liver dysfunction caused by GI cancer liver metastases without further options of drainage.
治疗包括因胃肠道(GI)癌肝转移继发高胆红素血症在内的严重肝功能不全患者具有挑战性。考虑到药代动力学,奥沙利铂与氟嘧啶(FP)/亚叶酸(FA)±单克隆抗体(moAb)的方案是一种可行的选择。关于各自剂量和耐受性的临床数据有限,且尚无相关建议。
对因GI癌肝转移导致严重高胆红素血症[>2倍正常范围上限(ULN)且>2.4mg/dl]且无引流选择而接受奥沙利铂、FP/FA±moAb治疗的连续患者进行分析。为收集更多数据,进行了文献综述。
2011年至2015年共确定了12例患者。治疗开始时,胆红素中位数水平为6.1mg/dl(>5倍ULN,范围2.7 - 13.6)。大多数患者(n = 11)接受了奥沙利铂(60 - 76%)和FP/FA(0 - 77%)剂量减少的方案,并迅速升级为全剂量方案。治疗期间,6例患者(反应者)的胆红素水平在8周内下降超过50%或在12周内恢复正常。总生存期中位数为5.75个月(范围1.0 - 16.0个月),但反应者的总生存期明显长于无反应者[9.7和3.0个月,p = 0.026(双侧检验);95%置信区间(CI):1.10 - 10.22]。此外,还可识别出另外26例患者的病例报告或系列研究。基于所获得的数据制定了一种治疗算法。
对于因GI癌肝转移导致严重肝功能不全且无进一步引流选择的患者,使用奥沙利铂、FP/FA±moAb进行治疗是可行的,且可能带来相关益处。