Management of chemotherapy-induced adverse effects in the treatment of colorectal cancer

被引:56
作者
Jansman, FGA
Sleijfer, DT
de Graaf, JC
Coenen, JLLM
Brouwers, JRBJ
机构
[1] Isala Klin, Dept Clin Pharmacol, Zwolle, Netherlands
[2] Univ Groningen Hosp, Dept Med Oncol, Groningen, Netherlands
[3] Isala Klin, Dept Med Oncol, Zwolle, Netherlands
[4] Univ Groningen, Sch Pharm, GUIDE Res Inst, Groningen, Netherlands
[5] Gen Hosp De Tjongerschans, Dept Clin Pharm, Heerenveen, Netherlands
关键词
D O I
10.2165/00002018-200124050-00002
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
The anticancer agents fluorouracil, raltitrexed, irinotecan and oxaliplatin show limited efficacy in the treatment of colorectal cancer and may be associated with substantial toxicity. Therefore, the prevention and reduction of chemotherapy-induced adverse effects is of major significance, in accordance with the increasing concern for the quality of life of patients with cancer. Therapeutic drug monitoring of fluorouracil and chronomodulation of fluorouracil and oxaliplatin. have been effective in reducing the incidence and gravity of adverse effects in several clinical trials. However, these concepts have not been implemented in clinical practice yet. At the present time, dose adaptation and supportive measures are the main tools for toxicity control in the treatment of colorectal cancer. In this review, supportive measures for alleviation of the adverse effects of fluorouracil. raltitrexed. irinotecan and oxaliplatin, respectively, are described, based on study results. The main adverse effects of these agents are myelosuppression, oral mucositis, diarrhoea, acute cholinergic syndrome, nausea and emesis, neurotoxicity, hand-foot syndrome and other cutaneous adverse effects, ocular toxicity, cardiotoxicity, small bowel toxicity, asthenia. elevated liver transaminase levels and alopecia. The incidence and gravity of these adverse effects are more or less related to the agent and administration schedule involved. The supportive measures and recommendations include the use of specific drugs, alterations of administration schedule and several nonpharmacological methods. In addition, guidelines for dosage adjustments when toxicity occurs are presented. For optimal management of adverse effects. patients should be considered individually, while patients, nurses and physicians should cooperate to identify and treat adverse effects in an early stage of their development.
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收藏
页码:353 / 367
页数:15
相关论文
共 120 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]   IRINOTECAN (CPT-11) HIGH-DOSE ESCALATION USING INTENSIVE HIGH-DOSE LOPERAMIDE TO CONTROL DIARRHEA [J].
ABIGERGES, D ;
ARMAND, JP ;
CHABOT, GG ;
DACOSTA, L ;
FADEL, E ;
COTE, C ;
HERAIT, P ;
GANDIA, D .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1994, 86 (06) :446-449
[3]  
AlTweigeri T, 1996, CANCER, V78, P1359, DOI 10.1002/(SICI)1097-0142(19961001)78:7<1359::AID-CNCR1>3.0.CO
[4]  
2-G
[5]  
*AM SOC HLTH SYST, 2000, AHFS DRUG INF 2000, P933
[6]   CPT-11 (irinotecan) addition to bimonthly, high-dose leucovorin and bolus and continuous-infusion 5-fluorouracil (FOLFIRI) for pretreated metastatic colorectal cancer [J].
André, T ;
Louvet, C ;
Maindrault-Goebel, F ;
Couteau, C ;
Mabro, M ;
Lotz, JP ;
Gilles-Amar, V ;
Krulik, M ;
Carola, E ;
Izrael, V ;
de Gramont, A .
EUROPEAN JOURNAL OF CANCER, 1999, 35 (09) :1343-1347
[7]   Multicenter phase II study of bimonthly high-dose leucovorin, fluorouracil infusion, and oxaliplatin for metastatic colorectal cancer resistant to the same leucovorin and fluorouracil regimen [J].
André, T ;
Bensmaine, MA ;
Louvet, C ;
François, E ;
Lucas, V ;
Desseigne, F ;
Beerblock, K ;
Bouché, O ;
Carola, E ;
Merrouche, Y ;
Morvan, F ;
Dupon-André, G ;
de Gramont, A .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (11) :3560-3568
[8]   Bimonthly high-dose leucovorin, 5-fluorouracil infusion and oxaliplatin (FOLFOX3) for metastatic colorectal cancer resistant to the same leucovorin and 5-fluorouracil regimen [J].
André, T ;
Louvet, C ;
Raymond, E ;
Tournigand, C ;
de Gramont, A .
ANNALS OF ONCOLOGY, 1998, 9 (11) :1251-1253
[9]  
[Anonymous], 1996, J CLIN ONCOL, V14, P1957
[10]  
[Anonymous], 1994, J CLIN ONCOL, V12, P2471