Combination of etoposide, idarubicin, cyclophosphamide, vincristine, prednisone and bleomycin (VICOP-B) in the treatment of advanced cutaneous T-cell lymphoma

被引:27
作者
Fierro, M
Doveil, GC
Quaglino, P
Savoia, P
Verrone, A
Bernengo, MG
机构
[1] Clinica Dermatologica I, Dell’Università di Torino
关键词
antineoplastic agents; cutaneous T-cell lymphoma; idarubicin; VICOP-B regimen;
D O I
10.1159/000246116
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Response of cutaneous T-cell lymphoma (CTCL) to systemic chemotherapy is unsatisfactory: despite an initially high response rate (RR), duration is always short-lived. Objective: To investigate the capability of a third-generation regimen including idarubicin in improving RR and response duration in CTCL patients. Methods: Twenty-five patients with advanced CTCL (stages IIB and IV) were treated with a 12-week polychemotherapeutic regimen (VICOP-B), which foresees the use of idarubicin in association with etoposide, cyclophosphamide, vincristine, prednisone and bleomycin., Results: The overall objective RR was 80% (36% complete response), The mycosis fungoides (MF) RR was 84%, with a median duration of 8.7 months, The pleomorphic-lymphoma RR was higher (100%), but the corresponding response duration was shorter (median: 3 months), No responses were documented in Sezary syndrome. Conclusion: VICOP-B regimen is effective and feasible as first-line chemotherapy in advanced MF, with or without extracutaneous involvement.
引用
收藏
页码:268 / 272
页数:5
相关论文
共 21 条
[11]   A RANDOMIZED TRIAL COMPARING COMBINATION ELECTRON-BEAM RADIATION AND CHEMOTHERAPY WITH TOPICAL THERAPY IN THE INITIAL TREATMENT OF MYCOSIS-FUNGOIDES [J].
KAYE, FJ ;
BUNN, PA ;
STEINBERG, SM ;
STOCKER, JL ;
IHDE, DC ;
FISCHMANN, AB ;
GLATSTEIN, EJ ;
SCHECHTER, GP ;
PHELPS, RM ;
FOSS, FM ;
PARLETTE, HL ;
ANDERSON, MJ ;
SAUSVILLE, EA .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 321 (26) :1784-1790
[12]   NCAM (CD56)-POSITIVE MALIGNANT-LYMPHOMA [J].
KERN, WF ;
SPIER, CM ;
MILLER, TP ;
GROGAN, TM .
LEUKEMIA & LYMPHOMA, 1993, 12 (1-2) :1-&
[13]   MYCOSIS-FUNGOIDES AND THE SEZARY-SYNDROME - A REVIEW OF PATHOGENESIS, DIAGNOSIS, AND THERAPY [J].
KUZEL, TM ;
ROENIGK, HH ;
ROSEN, ST .
JOURNAL OF CLINICAL ONCOLOGY, 1991, 9 (07) :1298-1313
[14]   THE ROLE OF PENTOSTATIN IN THE TREATMENT OF T-CELL MALIGNANCIES - ANALYSIS OF RESPONSE RATE IN 145 PATIENTS ACCORDING TO DISEASE SUBTYPE [J].
MERCIECA, J ;
MATUTES, E ;
DEARDEN, C ;
MACLENNAN, K ;
CATOVSKY, D .
JOURNAL OF CLINICAL ONCOLOGY, 1994, 12 (12) :2588-2593
[15]  
MILLER AB, 1981, CANCER, V47, P207, DOI 10.1002/1097-0142(19810101)47:1<207::AID-CNCR2820470134>3.0.CO
[16]  
2-6
[17]   MACOP-B AND VACOP-B IN DIFFUSE LARGE CELL LYMPHOMAS AND MOPP ABV IN HODGKINS-DISEASE [J].
OREILLY, SE ;
HOSKINS, P ;
KLIMO, P ;
CONNORS, JM .
ANNALS OF ONCOLOGY, 1991, 2 :17-23
[18]   CLINICAL PHARMACOKINETICS OF IDARUBICIN [J].
ROBERT, J .
CLINICAL PHARMACOKINETICS, 1993, 24 (04) :275-288
[19]   HISTOPATHOLOGIC STAGING AT INITIAL DIAGNOSIS OF MYCOSIS-FUNGOIDES AND THE SEZARY SYNDROME - DEFINITION OF 3 DISTINCTIVE PROGNOSTIC GROUPS [J].
SAUSVILLE, EA ;
EDDY, JL ;
MAKUCH, RW ;
FISCHMANN, AB ;
SCHECHTER, GP ;
MATTHEWS, M ;
GLATSTEIN, E ;
IHDE, DC ;
KAYE, F ;
VEACH, SR ;
PHELPS, R ;
OCONNOR, T ;
TREPEL, JB ;
COTELINGAM, JD ;
GAZDAR, AF ;
MINNA, JD ;
BUNN, PA .
ANNALS OF INTERNAL MEDICINE, 1988, 109 (05) :372-382
[20]  
WINKLER CF, 1986, J CLIN ONCOL, V4, P1094, DOI 10.1200/JCO.1986.4.7.1094