The sulfhydryl containing compounds WR-2721 and glutathione as radio- and chemoprotective agents. A review, indications for use and prospects

被引:100
作者
Hospers, GAP
Eisenhauer, EA
de Vries, EGE
机构
[1] Univ Groningen Hosp, Dept Internal Med, Div Med Oncol, NL-9700 RB Groningen, Netherlands
[2] Queens Univ, NCIC Clin Trials Grp, Kingston, ON, Canada
关键词
WR-2721; glutathione; chemoprotection;
D O I
10.1038/sj.bjc.6690404
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Radio- and chemotherapy for the treatment of malignancies are often associated with significant toxicity. One approach to reduce the toxicity is the concomitant treatment with chemoprotective agents. This article reviews two sulfhydryl compounds, namely the agent WR-2721 (amifostine), a compound recently registered for use in human in many countries, and the natural occurring compound glutathione (GSH). GSH is not registered as a chemoprotective agent. WR-2721 is an aminothiol prodrug and has to be converted to the active compound WR-1065 by membrane-bound alkaline phosphatase. WR-1065 and GSH both act as naturally occurring thiols. No protective effect on the tumour has been found when these compounds are administered intravenously. There is even in vitro evidence for an increased anti-tumour effect with mafosfamide after pretreatment with WR-2721, and in vivo after treatment with carboplatin and paclitaxel. Randomized clinical studies have shown that WR-2721 and GSH decrease cisplatin-induced nephrotoxicity and that WR-2721 reduces radiation radiotherapy-induced toxicity. Side-effects associated with WR-2721 are nausea, vomiting and hypotension, GSH has no side-effects. An exact role of WR-2721 and GSH as chemoprotectors is not yet completely clear. Future studies should examine the protective effect of these drugs on mucositis, cardiac toxicity, neuro- and ototoxicity, the development of secondary neoplasms and their effect on quality of life.
引用
收藏
页码:629 / 638
页数:10
相关论文
共 85 条
[1]   HIGH-DOSE INTRAVENOUS GLUTATHIONE IN MAN - PHARMACOKINETICS AND EFFECTS ON CYST(E)INE IN PLASMA AND URINE [J].
AEBI, S ;
ASSERETO, R ;
LAUTERBURG, BH .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1991, 21 (01) :103-110
[2]   Intraperitoneal cisplatin plus intravenous cyclophosphamide versus intravenous cisplatin plus intravenous cyclophosphamide for stage III ovarian cancer [J].
Alberts, DS ;
Liu, PY ;
Hannigan, EV ;
OToole, R ;
Williams, SD ;
Young, JA ;
Franklin, EW ;
ClarkePearson, DL ;
Malviya, VK ;
DuBeshter, B ;
Adelson, MD ;
Hoskins, WJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (26) :1950-1955
[3]   CISPLATIN-ASSOCIATED NEUROTOXICITY - CAN IT BE PREVENTED [J].
ALBERTS, DS ;
NOEL, JK .
ANTI-CANCER DRUGS, 1995, 6 (03) :369-383
[4]   TOPICAL APPLICATION OF WR-2721 ACHIEVES HIGH-CONCENTRATIONS IN THE RECTAL WALL [J].
BENJOSEF, E ;
MESINA, J ;
SHAW, LM ;
BONNER, HS ;
SHAMSA, F ;
PORTER, AT .
RADIATION RESEARCH, 1995, 143 (01) :107-110
[5]   CARBOPLATIN COMBINED WITH AMIFOSTINE, A BONE-MARROW PROTECTANT, IN THE TREATMENT OF NON-SMALL-CELL LUNG-CANCER - A RANDOMIZED PHASE-II STUDY [J].
BETTICHER, DC ;
ANDERSON, H ;
RANSON, M ;
MEELY, K ;
OSTER, W ;
THATCHER, N .
BRITISH JOURNAL OF CANCER, 1995, 72 (06) :1551-1555
[6]   Neurotoxicity of cisplatin +/- reduced glutathione in the first-line treatment of advanced ovarian cancer [J].
Bogliun, G ;
Marzorati, L ;
Marzola, M ;
Miceli, MD ;
Cantu, MG ;
Cavaletti, G .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 1996, 6 (05) :415-419
[7]  
BRIZEL D, 1998, P AM SOC CLIN ONCOL, V17
[8]  
Budd GT, 1996, SEMIN ONCOL, V23, P49
[9]  
BUDD GT, 1996, P AM SOC CLIN ONCOL, V15
[10]   Selective cytoprotection with amifostine in concurrent radiochemotherapy for head and neck cancer [J].
Buntzel, J ;
Kuttner, K ;
Frohlich, D ;
Glatzel, M .
ANNALS OF ONCOLOGY, 1998, 9 (05) :505-509