CONTINUOUS-INFUSION OF VINCRISTINE, IFOSFAMIDE AND EPIRUBICIN OVER 6 WEEKS IN TREATMENT-RESISTANT ADVANCED BREAST-CANCER

被引:4
作者
GURNEY, H
HARNETT, P
STUARTHARRIS, R
KEFFORD, R
机构
[1] Department of Medical Oncology and Palliative Care, Westmead Hospital
关键词
BREAST CANCER; INFUSIONAL CHEMOTHERAPY;
D O I
10.1016/0959-8049(95)00384-U
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
28 patients with recurrent advanced breast cancer were treated with a salvage regimen consisting of vincristine, epirubicin and ifosfamide/mesna (VIE). All patients had poor prognostic characteristics defined as relapse within 12 months of chemotherapy or as relapse within a radiotherapy field. Chemotherapy was infused continuously through a central venous catheter using a portable pump. Ifosfamide (3 g/m(2)) mixed with mesna (3 g/m(2)) was infused for 7 days followed by epirubicin (50 mg/m(2)) mixed with vincristine (1.5 mg/m(2)) over a further seven days and alternated for a total of 6 weeks. 9 of the 28 patients (32%) responded to VIE (six partial and three complete responses). This included 6 of the 18 patients (33%) who had previously received doxorubicin or mitoxantrone, 6 of the 17 patients (35%) who had an inoperable in-field relapse after radiotherapy for locally advanced cancer, and 5 of the 21 patients (24%) relapsing within 6 months of previous chemotherapy. Median duration of response and overall survival were 3.7 and 6.9 months, respectively. Myelotoxicity was mild. One patient had neutropenic sepsis, 3 patients had grade 3 nausea and vomiting and one patient developed paralytic ileus attributed to vincristine. Central venous catheter complications occurred in 12 of 33 catheters requiring removal in 6. Continuous infusional chemotherapy using vincristine, epirubicin and ifosfamide achieves a 32% overall response rate in treatment-resistant advanced breast cancer, and is associated with minimal toxicity and a short treatment period. VIE may be a suitable alternative to conventional chemotherapy.
引用
收藏
页码:1773 / 1777
页数:5
相关论文
共 29 条
[1]  
AHMANN FR, 1987, CANCER, V59, P239, DOI 10.1002/1097-0142(19870115)59:2<239::AID-CNCR2820590211>3.0.CO
[2]  
2-C
[3]  
BEIJNEN J H, 1985, Journal of Parenteral Science and Technology, V39, P220
[4]   STABILITY OF INTRAVENOUS ADMIXTURES OF DOXORUBICIN AND VINCRISTINE [J].
BEIJNEN, JH ;
NEEF, C ;
MEUWISSEN, OJAT ;
RUTTEN, JJMH ;
ROSING, H ;
UNDERBERG, WJM .
AMERICAN JOURNAL OF HOSPITAL PHARMACY, 1986, 43 (12) :3022-3027
[5]  
BOYAGES J, 1987, INT J RADIAT ONCOL, V14, P71
[6]   RESULTS OF SALVAGE HORMONAL-THERAPY AND SALVAGE CHEMOTHERAPY IN WOMEN FAILING ADJUVANT CHEMOTHERAPY AFTER MASTECTOMY FOR BREAST-CANCER [J].
BUCKNER, JC ;
INGLE, JN ;
EVERSON, LK ;
OFALLON, JR ;
CULLINAN, SA ;
AHMANN, DL ;
KROOK, JE ;
PFEIFLE, DM .
BREAST CANCER RESEARCH AND TREATMENT, 1989, 13 (02) :135-142
[7]   IFOSFAMIDE BY CONTINUOUS INFUSION TO PREVENT ENCEPHALOPATHY [J].
CERNY, T ;
CASTIGLIONE, M ;
BRUNNER, K ;
KUPFER, A ;
MARTINELLI, G ;
LIND, M .
LANCET, 1990, 335 (8682) :175-175
[8]   TREATMENT OF ESTROGEN RECEPTOR-NEGATIVE OR HORMONALLY REFRACTORY BREAST-CANCER WITH DOUBLE HIGH-DOSE CHEMOTHERAPY INTENSIFICATION AND BONE-MARROW SUPPORT [J].
DUNPHY, FR ;
SPITZER, G ;
BUZDAR, AU ;
HORTOBAGYI, GN ;
HORWITZ, LJ ;
YAU, JC ;
SPINOLO, JA ;
JAGANNATH, S ;
HOLMES, F ;
WALLERSTEIN, RO ;
BOHANNAN, PA ;
DICKE, KA .
JOURNAL OF CLINICAL ONCOLOGY, 1990, 8 (07) :1207-1216
[9]  
GREGORY WM, 1993, P AM SOC CLIN ONCOL, V12, P57
[10]   ESCALATING DRUG DELIVERY IN CANCER-CHEMOTHERAPY - A REVIEW OF CONCEPTS AND PRACTICE .2. [J].
GURNEY, H ;
DODWELL, D ;
THATCHER, N ;
TATTERSALL, MHN .
ANNALS OF ONCOLOGY, 1993, 4 (02) :103-115