Rodrigo J A, Hicks L K, Cheung M C, Song K W, Ezzat H, Leger C S, Boro J, Montaner J S G, Harris M, Leitch H A
Division of Hematology, St. Paul's Hospital and the University of British Columbia, Vancouver, BC, Canada V6T 1Z4.
Adv Hematol. 2012;2012:735392. doi: 10.1155/2012/735392. Epub 2011 Nov 14.
Background. The outcome of HIV-associated non-Hodgkin lymphoma (NHL) has improved substantially in the highly active antiretroviral therapy (HAART) era. However, HIV-Burkitt lymphoma (BL), which accounts for up to 20% of HIV-NHL, has poor outcome with standard chemotherapy. Patients and Methods. We retrospectively reviewed HIV-BL treated in the HAART era with the Magrath regimen (CODOX-M/IVAC±R) at four Canadian centres. Results. Fourteen patients with HIV-BL received at least one CODOX-M/IVAC±R treatment. Median age at BL diagnosis was 45.5 years, CD4 count 375 cells/mL and HIV viral load (VL) <50 copies/mL. Patients received PCP prophylaxis and G-CSF, 13 received HAART with chemotherapy and 10 rituximab. There were 63 episodes of toxicity, none fatal, including: bacterial infection, n = 20; grade 3-4 hematologic toxicity, n = 14; febrile neutropenia, n = 7; oral thrush; and ifosfamide neurological toxicity, n = 1 each. At a median followup of 11.7 months, 12 (86%) patients are alive and in remission. All 10 patients who received HAART, chemotherapy, and rituximab are alive. CD4 counts and HIV VL 6 months following BL therapy completion (n = 5 patients) were >250 cells/mL and undetectable, respectively, in 4. Conclusion. Intensive chemotherapy with CODOX-M/IVAC±R yielded acceptable toxicity and good survival rates in patients with HIV-associated Burkitt lymphoma receiving HAART.
背景。在高效抗逆转录病毒治疗(HAART)时代,与HIV相关的非霍奇金淋巴瘤(NHL)的预后有了显著改善。然而,占HIV-NHL高达20%的HIV-伯基特淋巴瘤(BL),采用标准化疗预后较差。患者与方法。我们回顾性分析了加拿大四个中心在HAART时代采用Magrath方案(CODOX-M/IVAC±R)治疗的HIV-BL患者。结果。14例HIV-BL患者接受了至少一次CODOX-M/IVAC±R治疗。BL诊断时的中位年龄为45.5岁,CD4细胞计数为375个/mL,HIV病毒载量(VL)<50拷贝/mL。患者接受了肺孢子菌肺炎预防和粒细胞集落刺激因子(G-CSF),13例在化疗时接受了HAART,10例接受了利妥昔单抗治疗。共有63次毒性发作,无致命情况,包括:细菌感染,n = 20;3-4级血液学毒性,n = 14;发热性中性粒细胞减少,n = 7;口腔念珠菌病;以及异环磷酰胺神经毒性,各n = 1。中位随访11.7个月时,12例(86%)患者存活且处于缓解状态。所有接受HAART、化疗和利妥昔单抗治疗的10例患者均存活。BL治疗完成后6个月(n = 5例患者)的CD4细胞计数和HIV VL分别为>250个/mL和检测不到。结论。对于接受HAART的HIV相关伯基特淋巴瘤患者,采用CODOX-M/IVAC±R进行强化化疗产生了可接受的毒性和良好的生存率。