Complete remission of unresectable hepatocellular carcinoma on healthy liver by the combination of aggressive surgery and high-dose-intensity chemotherapy by CPT-11

被引:10
作者
Gornet, JM
Azoulay, D
Duclos-Vallée, JC
Goldwasser, F
机构
[1] Hop Paul Brousse, Serv Cancerol, F-94804 Villejuif, France
[2] Hop Paul Brousse, Ctr Hepatobiliaire, F-94804 Villejuif, France
关键词
CPT-11; hepatectomy; hepatocellular carcinoma; liver transplantation; topoisomerase I poisons;
D O I
10.1097/00001813-200009000-00009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hepatocellular carcinoma (HCC) is one of the most frequent cancers, The only curative treatment is liver transplantation or complete surgical resection; however, most patients have inoperable disease at diagnosis. To date, no cytotoxic agent has demonstrated a clinical impact on time-related parameters, especially survival, The development of new treatments of inoperable HCC patients is highly desirable, Among the new cytotoxic agents, DNA topoisomerase I poisons are those with the widest spectrum of antitumor activity, However, few data are available in HCC patients. One of the main obstacles to the use of irinotecan in HCC is the frequent alterations of liver function at diagnosis. A 48-year-old patient with a HCC that had developed within a normal liver but of very poor prognosis because of a multifocal primary tumor with a large nodule measuring 10 cm of diameter, associated with a portal thrombosis, could tolerate very intensive treatment with irinotecan using doses up to 700 mg/m(2) every 2 weeks and was responsive to treatment as measured by alpha-fetoprotein levels. Despite initial criteria of inoperability, the absence of disease progression under therapy with a follow-up of 1 year invited us to propose a liver transplant, The patient is still in post-surgical complete remission and has consolidation chemotherapy with irinotecan. This result invites us to consider the evaluation of the efficacy of topoisomerase I poisons in HCC patients and to escalate the dose of irinotecan in patients with less than grade 4 neutropenia. [(C) 2000 Lippincott Williams & Wilkins.].
引用
收藏
页码:649 / 652
页数:4
相关论文
共 19 条
[1]   PHASE-I AND PHARMACOLOGICAL STUDIES OF THE CAMPTOTHECIN ANALOG IRINOTECAN ADMINISTERED EVERY 3 WEEKS IN CANCER-PATIENTS [J].
ABIGERGES, D ;
CHABOT, GG ;
ARMAND, JP ;
HERAIT, P ;
GOUYETTE, A ;
GANDIA, D .
JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (01) :210-221
[2]   Pharmacokinetics and pharmacodynamics of irinotecan during a phase II clinical trial in colorectal cancer [J].
Canal, P ;
Gay, C ;
Dezeuze, A ;
Douillard, JY ;
Bugat, R ;
Brunet, R ;
Adenis, A ;
Herait, P ;
Lokiec, F ;
MathieuBoue, A .
JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (10) :2688-2695
[3]  
GOLDWASSER F, 1995, CANCER RES, V55, P2116
[4]  
GOLDWASSER F, 2000, P AM ASS CLIN ONCOL, V19, P840
[5]  
GOLDWASSER F, 2000, IN PRESS MANAGEMENT
[6]  
GOLDWASSER F, 2000, IN PRESS ANN ONCOL
[7]  
GOLDWASSER F, 1998, P AM ASSOC CANC RES, V39, P5056
[8]  
LEE NW, 1982, WORLD J SURG, V6, P66, DOI 10.1007/BF01656375
[9]  
Leung TWT, 1999, CLIN CANCER RES, V5, P1676
[10]  
LUPORINI G, 1993, J SURG ONCOL, P115