Treatment of AIDS-related primary central nervous system lymphoma with zidovudine, ganciclovir, and interleukin 2

被引:48
作者
Raez, L
Cabral, L
Cai, JP
Landy, H
Sfakianakis, G
Byrne, GE
Hurley, J
Scerpella, E
Jayaweera, D
Harrington, WJ
机构
[1] Univ Miami, Jackson Mem Hosp, Sch Med, Div Hematol Oncol, Miami, FL 33136 USA
[2] Univ Miami, Jackson Mem Hosp, Sch Med, Dept Med, Miami, FL 33136 USA
[3] Univ Miami, Jackson Mem Hosp, Sch Med, Dept Neurol Surg, Miami, FL 33136 USA
[4] Univ Miami, Jackson Mem Hosp, Sch Med, Dept Radiol,Div Nucl Med, Miami, FL 33136 USA
[5] Univ Miami, Jackson Mem Hosp, Sch Med, Dept Pathol, Miami, FL 33136 USA
[6] Univ Miami, Jackson Mem Hosp, Sch Med, Div Infect Dis, Miami, FL 33136 USA
关键词
D O I
10.1089/088922299310809
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
AIDS-related primary central nervous system lymphoma (AIDS PCNSL) is a rapidly fatal disease. Conventional therapeutic modalities offer little and new approaches are needed. Previous work has shown that zidovudine (AZT) in combination with other agents is active in retroviral lymphomas, Epstein-Barr virus (EBV) is detected in tumor tissue and cerebrospinal fluid of AIDS PCNSL patients. In a preliminary in vitro study we found that an Epstein-Barr virus-positive B cell line underwent apoptosis on coculture with AZT, This effect was accentuated by the addition of ganciclovir (GCV). We treated five patients with AIDS PCNSL with a regimen consisting of parenteral zidovudine (1.6 g twice daily), ganciclovir (5 mg/kg twice daily), and interleukin 2 (2 million units twice daily), Four of five had an excellent response. Two patients are alive and free of disease 22 and 13 months later; another responded on two separate occasions, 5 months apart, and the last patient responded with a 70-80% regression of tumor but could not be maintained on therapy owing to myelosuppression, We conclude that parenteral zidovudine, ganciclovir, and interleukin 2 is an active combination for AIDS-related central nervous system lymphoma.
引用
收藏
页码:713 / 719
页数:7
相关论文
共 30 条
[1]   Phenotypic and functional analysis of Fas (CD95) expression in primary central nervous system lymphoma of patients with acquired immunodeficiency syndrome [J].
Baiocchi, RA ;
Khatri, VP ;
Lindemann, MJ ;
Ross, ME ;
Papoff, G ;
Caprio, AJ ;
Caprio, TV ;
Fenstermaker, R ;
Ruberti, G ;
Bernstein, ZP ;
Caligiuri, MA .
BLOOD, 1997, 90 (05) :1737-1746
[2]  
BASELGA J, 1993, CANCER, V71, P2332, DOI 10.1002/1097-0142(19930401)71:7<2332::AID-CNCR2820710726>3.0.CO
[3]  
2-P
[4]   PRIMARY CENTRAL-NERVOUS-SYSTEM LYMPHOMAS - NATURAL-HISTORY AND RESPONSE TO RADIATION-THERAPY IN 55 PATIENTS WITH ACQUIRED-IMMUNODEFICIENCY-SYNDROME [J].
BAUMGARTNER, JE ;
RACHLIN, JR ;
BECKSTEAD, JH ;
MEEKER, TC ;
LEVY, RM ;
WARA, WM ;
ROSENBLUM, ML .
JOURNAL OF NEUROSURGERY, 1990, 73 (02) :206-211
[5]   PROLONGED ADMINISTRATION OF LOW-DOSE INTERLEUKIN-2 IN HUMAN IMMUNODEFICIENCY VIRUS-ASSOCIATED MALIGNANCY RESULTS IN SELECTIVE EXPANSION OF INNATE IMMUNE EFFECTORS WITHOUT SIGNIFICANT CLINICAL TOXICITY [J].
BERNSTEIN, ZP ;
PORTER, MM ;
GOULD, M ;
LIPMAN, B ;
BLUMAN, EM ;
STEWART, CC ;
HEWITT, RG ;
FYFE, G ;
POIESZ, B ;
CALIGIURI, MA .
BLOOD, 1995, 86 (09) :3287-3294
[6]   HIGH EXPRESSION OF LATENT MEMBRANE-PROTEIN-1 OF EPSTEIN-BARR-VIRUS AND BCL-2 ONCOPROTEIN IN ACQUIRED IMMUNODEFICIENCY SYNDROME-RELATED PRIMARY BRAIN LYMPHOMAS [J].
CAMILLERIBROET, S ;
DAVI, F ;
FEUILLARD, J ;
BOURGEOIS, C ;
SEILHEAN, D ;
HAUW, JJ ;
RAPHAEL, M .
BLOOD, 1995, 86 (02) :432-435
[7]   Immunophenotypic and molecular analyses of acquired immune deficiency syndrome-related and Epstein-Barr virus associated lymphomas: Comparative study [J].
Carbone, A ;
Dolcetti, R ;
Gloghini, A ;
Maestro, R ;
Vaccher, E ;
DiLuca, D ;
Tirelli, U ;
Boiocchi, M .
HUMAN PATHOLOGY, 1996, 27 (02) :133-146
[8]  
CHAMBERLAIN MC, 1994, CANCER, V73, P1728, DOI 10.1002/1097-0142(19940315)73:6<1728::AID-CNCR2820730629>3.0.CO
[9]  
2-8
[10]   Minimally invasive diagnosis of acquired immunodeficiency syndrome-related primary central nervous system lymphoma [J].
Cingolani, A ;
De Luca, A ;
Larocca, LM ;
Ammassari, A ;
Scerrati, M ;
Antinori, A ;
Ortona, L .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1998, 90 (05) :364-369