Irinotecan: A new antineoplastic agent for the management of colorectal cancer

被引:23
作者
Cersosimo, RJ
机构
[1] Northeastern Univ, Bouve Coll Pharm & Hlth Sci, Boston, MA 02115 USA
[2] Vet Adm Med Ctr, Dept Med Hematol Oncol, Boston, MA USA
关键词
irinotecan; cancer; colorectal; lung;
D O I
10.1345/aph.17462
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
OBJECTIVE: To review the pharmacologic, pharmacokinetic, therapeutic, and safety aspects of irinotecan, a new antineoplastic agent, and to assess its role in the treatment of colorectal and lung cancer. DATA SOURCES: English-language articles from the MEDLINE database, January 1990-March 1998; Pharmacia & Upjohn Company; published articles and meeting abstracts. STUDY SELECTION: Studies in humans with cancer, clinical case reports, and open clinical studies were reviewed. Efficacy studies were limited to trials with at least 20 evaluable patients. DATA EXTRACTION: Relevant data were extracted from published reports and abstracts. DATA SYNTHESIS: Irinotecan is an effective agent for the treatment of advanced colorectal cancer. It demonstrates significant activity as a first-line agent and in patients with disease that is refractory to fluorouracil-containing regimens. Activity against lung cancer has also been demonstrated. Limited data indicate activity against cancers of the ovary, cervix, stomach, and in non-Hodgkin's lymphomas. Major toxicity consists of myelosuppression and diarrhea. CONCLUSIONS: Irinotecan is a useful addition to the antineoplastic drug family and offers significant efficacy for treatment of patients with fluorouracil-refractory colorectal cancer.
引用
收藏
页码:1324 / 1333
页数:10
相关论文
共 66 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]  
[Anonymous], P AM SOC CLIN ONCOL
[3]   RELATIONSHIP BETWEEN DEVELOPMENT OF DIARRHEA AND THE CONCENTRATION OF SN-38, AN ACTIVE METABOLITE OF CPT-11, IN THE INTESTINE AND THE BLOOD-PLASMA OF ATHYMIC MICE FOLLOWING INTRAPERITONEAL ADMINISTRATION OF CPT-11 [J].
ARAKI, E ;
ISHIKAWA, M ;
IIGO, M ;
KOIDE, T ;
ITABASHI, M ;
HOSHI, A .
JAPANESE JOURNAL OF CANCER RESEARCH, 1993, 84 (06) :697-702
[4]  
Armand JP, 1996, ANN ONCOL, V7, P837
[5]  
BAKER L, 1997, P AN M AM SOC CLIN, V16, pA461
[6]  
BARONE C, 1997, P AN M AM SOC CLIN, V16, pA270
[7]   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
[8]   PHASE-I AND PHARMACOKINETIC STUDY OF IRINOTECAN (CPT-11) ADMINISTERED DAILY FOR 3 CONSECUTIVE DAYS EVERY 3 WEEKS IN PATIENTS WITH ADVANCED SOLID TUMORS [J].
CATIMEL, G ;
CHABOT, GG ;
GUASTALLA, JP ;
DUMORTIER, A ;
COTE, C ;
ENGEL, C ;
GOUYETTE, A ;
MATHIEUBOUE, A ;
MAHJOUBI, M ;
CLAVEL, M .
ANNALS OF ONCOLOGY, 1995, 6 (02) :133-140
[9]   POPULATION PHARMACOKINETICS AND PHARMACODYNAMICS OF IRINOTECAN (CPT-11) AND ACTIVE METABOLITE SN-38 DURING PHASE-I TRIALS [J].
CHABOT, GG ;
ABIGERGES, D ;
CATIMEL, G ;
CULINE, S ;
DEFORNI, R ;
EXTRA, JM ;
MAHJOUBI, H ;
HERAIT, P ;
ARMAND, JP ;
BUGAT, R ;
CLAVEL, M ;
MARTY, ME .
ANNALS OF ONCOLOGY, 1995, 6 (02) :141-151
[10]  
Cohen Alfred M., 1997, P1144