Antiviral and immunomodulatory treatment for AIDS-related primary central nervous system lymphoma: AIDS malignancies consortium pilot study 019

被引:24
作者
Aboulafia, David M.
Ratner, Lee
Miles, Steven A.
Harrington, William J., Jr.
机构
[1] Virginia Mason Med Ctr, Div Hematol, Seattle, WA 98111 USA
[2] Virginia Mason Med Ctr, Div Oncol, Seattle, WA 98111 USA
[3] Univ Washington, Div Oncol, Seattle, WA 98111 USA
[4] Univ Washington, Div Hematol, Seattle, WA 98111 USA
[5] Washington Univ, St Louis, MO USA
[6] Univ Calif Los Angeles, Jonsson Comprehens Canc Ctr, Los Angeles, CA 90024 USA
[7] Univ Miami, Sch Med, Sylvester Comprehens Canc Ctr, Coral Gables, FL 33124 USA
关键词
antiretroviral therapy; central nervous system lesions; ganciclovir; human immunodeficiency virus; interleukin-2; zidovudine;
D O I
10.3816/CLM.2006.n.017
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: A consistent association with Epstein-Barr Virus (EBV) distinguishes acquired immunodeficiency syndrome (AIDS)-related primary central nervous system lymphoma (PCNSL) from that which occurs in the general population. Recent descriptions of long-term remissions in patients with posttransplantation EBV-associated PCNSL who received EBV-specific therapy suggest some antitumor effect is anti-EBV mediated. Patients and Methods: We enrolled 4 patients with AIDS-related PCNSL into a novel antiviral and immunomodulatory protocol. An additional patient was treated in a similar fashion off protocol. Treatment consisted of intravenously administered zidovudine (1.5 g twice daily), ganciclovir (5 mg/kg twice daily), and interleukin-2 (2,000,000 U twice daily). After 2 weeks of therapy, patients were switched to oral ganciclovir (1 g 3 times daily), patient-specific, highly active, antiretroviral therapy, and subcutaneous interleukin-2 (2,000,000 U 3 times weekly). A final patient was treated with intravenous zidovudine and hydroxyurea. All 6 patients had advanced-stage AIDS as reflected by a CD4(+) T-lymphocyte cell count of < 50/mu L and a detectable human immunodeficiency virus (HIV)-1 viral RNA load (median copies, 135,000/mL; range, 2170-360,000/mL). One of 4 protocol-enrolled patients remains in complete remission with > 4 years' follow-up. Results: Three patients died from complications of progressive PCNSL. Two patients treated off protocol exhibited favorable responses and remain in complete remission at 28 months and 52 months, respectively. Grade 3/4 myelosuppression was uniformly noted, but there were no clinically significant hemorrhagic or infectious complications. Conclusion: We conclude that for patients with AIDS and PCNSL, treatments with dual efficacy against HIV and EBV merit further investigation. Our experience provides a platform for future studies.
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收藏
页码:399 / 402
页数:4
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