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Chemotherapy in the Setting of Severe Liver Dysfunction in Patients with Metastatic Colorectal Cancer.转移性结直肠癌患者严重肝功能不全时的化疗
Case Rep Oncol Med. 2015;2015:420159. doi: 10.1155/2015/420159. Epub 2015 May 21.
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Severe liver dysfunction and safe use of 5-fluorouracil leucovorin and oxaliplatin in one patient with metastatic colorectal carcinoma.1例转移性结直肠癌患者的严重肝功能不全与5-氟尿嘧啶、亚叶酸钙和奥沙利铂的安全使用
J Cancer Res Ther. 2014 Jul-Sep;10(3):745-8. doi: 10.4103/0973-1482.136034.
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Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012.全球癌症发病与死亡:GLOBOCAN 2012 数据源、方法与主要模式。
Int J Cancer. 2015 Mar 1;136(5):E359-86. doi: 10.1002/ijc.29210. Epub 2014 Oct 9.
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FOLFIRI combined with bevacizumab as first-line treatment for metastatic colorectal cancer patients with hyperbilirubinemia after UGT1A1 genotyping.在进行UGT1A1基因分型后,FOLFIRI联合贝伐单抗作为伴有高胆红素血症的转移性结直肠癌患者的一线治疗方案。
Med Princ Pract. 2014;23(5):478-81. doi: 10.1159/000358799. Epub 2014 Mar 8.
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Safety and efficacy of FOLFOX followed by cetuximab for metastatic colorectal cancer with severe liver dysfunction.奥沙利铂联合西妥昔单抗治疗严重肝功能不全的转移性结直肠癌的安全性和有效性。
J Natl Compr Canc Netw. 2014 Feb;12(2):155-60. doi: 10.6004/jnccn.2014.0016.
6
[A case of metastatic colorectal cancer with icterus due to multiple liver metastases treated effectively by FOLFOX plus bevacizumab].[1例因多发肝转移导致黄疸的转移性结直肠癌经FOLFOX联合贝伐单抗治疗有效]
Gan To Kagaku Ryoho. 2013 Aug;40(8):1115-8.
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Pilot study to assess toxicity and pharmacokinetics of docetaxel in patients with metastatic breast cancer and impaired liver function secondary to hepatic metastases.评估多西他赛对转移性乳腺癌且因肝转移导致肝功能受损患者的毒性和药代动力学的初步研究。
J Oncol Pharm Pract. 2014 Apr;20(2):120-9. doi: 10.1177/1078155213480536. Epub 2013 May 14.
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ESMO Consensus Guidelines for management of patients with colon and rectal cancer. a personalized approach to clinical decision making.ESMO 结肠癌和直肠癌患者管理共识指南。 个体化临床决策方法。
Ann Oncol. 2012 Oct;23(10):2479-2516. doi: 10.1093/annonc/mds236.
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Cetuximab pharmacokinetics influences progression-free survival of metastatic colorectal cancer patients.西妥昔单抗药代动力学影响转移性结直肠癌患者的无进展生存期。
Clin Cancer Res. 2011 Oct 1;17(19):6329-37. doi: 10.1158/1078-0432.CCR-11-1081. Epub 2011 Sep 27.
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FOLFOX plus cetuximab for a patient with metastatic colorectal cancer with icterus due to multiple liver metastases.FOLFOX方案联合西妥昔单抗用于一名因多发肝转移导致黄疸的转移性结直肠癌患者。
Gan To Kagaku Ryoho. 2011 Jul;38(7):1205-8.

胃肠道恶性肿瘤肝转移继发高胆红素血症患者的治疗方法:病例系列及文献综述

Treatment approach in patients with hyperbilirubinemia secondary to liver metastases in gastrointestinal malignancies: a case series and review of literature.

作者信息

Quidde Julia, Azémar Marc, Bokemeyer Carsten, Arnold Dirk, Stein Alexander

机构信息

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.

出版信息

Ther Adv Med Oncol. 2016 May;8(3):144-52. doi: 10.1177/1758834016637585. Epub 2016 Mar 17.

DOI:10.1177/1758834016637585
PMID:27239232
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4872252/
Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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.

CONCLUSION

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.

摘要

背景

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。

方法

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。

结果

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。

结论

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。