Topical DMSO treatment for pegylated liposomal doxorubicin-induced palmar-plantar erythrodysesthesia

被引:86
作者
Lopez, AM
Wallace, L
Dorr, RT
Koff, M
Hersh, EM
Alberts, DS
机构
[1] Univ Arizona, Coll Med, Arizona Canc Ctr, Tucson, AZ 85724 USA
[2] Univ Arizona, Coll Med, Dept Med, Tucson, AZ 85724 USA
[3] Univ Arizona, Coll Med, Dept Pathol, Tucson, AZ 85724 USA
[4] Univ Arizona, Coll Med, Dept Pharmacol, Tucson, AZ 85724 USA
[5] Univ Arizona, Coll Med, Dept Toxicol, Tucson, AZ 85724 USA
关键词
chemotherapy; palmar-plantar dysesthesia; dimethylsulfoxide;
D O I
10.1007/s002800050981
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Chemotherapeutic regimens that utilize fluorouracil, cytarabine, and doxorubicin have been shown to cause a dermatologic syndrome known as hand-foot syndrome, or palmar-plantar erythrodysesthesia syndrome (PPES). Pegylated liposomal doxorubicin has proven effective in the treatment of AIDS-related Kaposi's sarcoma, ovarian cancer refractory to platinum and paclitaxel therapies, and metastatic breast cancer. In a study of the treatment of refractory epithelial cell ovarian cancers with lipozomal doxorubicin utilizing intravenous doses of 50 mg/m(2) every 3 weeks, grade 3 PPES was observed in 29% of patients (10/35) and required dose reductions and/or dose delay after a median of three therapy cycles. Methods: Current methods to prevent pegylated liposomal doxorubicin-induced PPES include dose reduction, lengthening of the drug administration interval and ultimately, drug withdrawal. Topical 99% dimethylsulfoxide (DMSO) also has shown strong activity in treating tissue extravasation reactions during intravenous administration of doxorubicin. Results: Two patients undergoing chemotherapy with pegylated liposomal doxorubicin, 50 mg/m(2) every 4 weeks, developed grade 3 PPE after three cycles. Their PPES resolved over a period of 1 to 3 weeks while receiving topical 99% DMSO four times daily for 14 days. Conclusions: While these results are promising, patients must be treated in a prospective study of this topical DMSO formulation to definitively document its therapeutic efficacy.
引用
收藏
页码:303 / 306
页数:4
相关论文
共 26 条
[1]   TOPICAL DIMETHYLSULFOXIDE FOR THE PREVENTION OF SOFT-TISSUE INJURY AFTER EXTRAVASATION OF VESICANT CYTOTOXIC DRUGS - A PROSPECTIVE CLINICAL-STUDY [J].
BERTELLI, G ;
GOZZA, A ;
FORNO, GB ;
VIDILI, MG ;
SILVESTRO, S ;
VENTURINI, M ;
DELMASTRO, L ;
GARRONE, O ;
ROSSO, R ;
DINI, D .
JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (11) :2851-2855
[2]   ADRIAMYCIN - NEW ANTICANCER DRUG WITH SIGNIFICANT CLINICAL ACTIVITY [J].
BLUM, RH ;
CARTER, SK .
ANNALS OF INTERNAL MEDICINE, 1974, 80 (02) :249-259
[3]  
COMANDONE A, 1993, ANTICANCER RES, V13, P1781
[4]  
FABIAN CJ, 1990, INVEST NEW DRUG, V8, P57
[5]   DOSE - A CRITICAL FACTOR IN CANCER-CHEMOTHERAPY [J].
FREI, E ;
CANELLOS, GP .
AMERICAN JOURNAL OF MEDICINE, 1980, 69 (04) :585-594
[6]   LIPOSOME FORMULATIONS WITH PROLONGED CIRCULATION TIME IN BLOOD AND ENHANCED UPTAKE BY TUMORS [J].
GABIZON, A ;
PAPAHADJOPOULOS, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (18) :6949-6953
[7]  
GORDON KB, 1995, CANCER, V75, P2169, DOI 10.1002/1097-0142(19950415)75:8<2169::AID-CNCR2820750822>3.0.CO
[8]  
2-H
[9]   DOSE-RESPONSE IN THE TREATMENT OF BREAST-CANCER - A CRITICAL-REVIEW [J].
HENDERSON, IC ;
HAYES, DF ;
GELMAN, R .
JOURNAL OF CLINICAL ONCOLOGY, 1988, 6 (09) :1501-1515
[10]  
James N D, 1994, Clin Oncol (R Coll Radiol), V6, P294