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低剂量甲氨蝶呤、博来霉素、阿霉素、环磷酰胺、长春新碱、地塞米松联合扎西他滨用于获得性免疫缺陷综合征相关淋巴瘤患者。随时间推移对人类免疫缺陷病毒及血清白细胞介素-6水平的影响。

Low dose methotrexate, bleomycin, doxorubicin, cyclophosphamide, vincristine, and dexamethasone with zalcitabine in patients with acquired immunodeficiency syndrome-related lymphoma. Effect on human immunodeficiency virus and serum interleukin-6 levels over time.

作者信息

Levine A M, Tulpule A, Espina B, Boswell W, Buckley J, Rasheed S, Stain S, Parker J, Nathwani B, Gill P S

机构信息

Department of Medicine, Division of Hematology, University of Southern California School of Medicine, Los Angeles, USA.

出版信息

Cancer. 1996 Aug 1;78(3):517-26. doi: 10.1002/(SICI)1097-0142(19960801)78:3<517::AID-CNCR20>3.0.CO;2-0.

Abstract

BACKGROUND

Use of multiagent chemotherapy has been associated with complete remission (CR) in approximately 50% of patients with newly diagnosed acquired immunodeficiency syndrome (AIDS)-lymphoma, although additional AIDS-related complications may occur. Both chemotherapy and antiretroviral therapy were employed in an attempt to ascertain if the combination was safe, and associated with changes in human immunodeficiency virus (HIV) p24 antigen levels during the course of treatment.

METHODS

Low dose methotrexate, bleomycin, doxorubicin, cyclophosphamide, vincristine, and dexamethasone(M-BACOD) chemotherapy and zalcitabine (ddC) were employed in 28 patients. Since both vincristine and zalcitabine may cause peripheral neuropathy, a Phase I/II study design was employed. Serum was analyzed for immune complex dissociated (ICD) HIV p24 antigen and interleukin (IL)-6 levels during therapy.

RESULTS

CR was achieved in 14 of 25 patients (56%), with partial response (PR) in 5 (20%). CRs were equivalent in patients with good or poor prognostic indicators, including a history of AIDS prior to lymphoma (CR = 60%); and/or CD4 lymphocytes < 200/mm3 (CR = 53%). Five patients with a CR subsequently relapsed (36%); median survival of CR patients was 29.2 months (4.1-61+), whereas that of all of the treated patients was 8.1 months. No significant peripheral neuropathy or other toxicity was observed. Serum ICD p24 antigen levels either fell (7/14) or remained consistently negative (2/14) in 9 of 14 patients (64%), whereas 36% experienced an increase. Elevated serum IL-6 levels at diagnosis were associated with systemic "B" symptoms (P = 0.023), whereas changes in IL-6 correlated with response to therapy over time (P = 0.006).

CONCLUSIONS

Combination antineoplastic and zalcitabine antiretroviral therapy may be safely administered to patients with AIDS-related lymphoma, resulting in CR in 56%, lack of significant neurotoxicity, and favorable effect on HIV p24 antigen in 50%. Elevation of serum IL-6 is associated with systemic "B" symptoms, whereas changes in serum IL-6 may correlate with response.

摘要

背景

多药联合化疗可使约50%新诊断的获得性免疫缺陷综合征(AIDS)相关淋巴瘤患者达到完全缓解(CR),不过可能会出现其他与AIDS相关的并发症。采用化疗和抗逆转录病毒疗法,以确定两者联合是否安全,以及在治疗过程中是否与人类免疫缺陷病毒(HIV)p24抗原水平的变化相关。

方法

28例患者采用低剂量甲氨蝶呤、博来霉素、阿霉素、环磷酰胺、长春新碱和地塞米松(M-BACOD)化疗及扎西他滨(ddC)。由于长春新碱和扎西他滨均可引起周围神经病变,故采用I/II期研究设计。在治疗期间分析血清中免疫复合物解离(ICD)的HIV p24抗原和白细胞介素(IL)-6水平。

结果

25例患者中有14例(56%)达到CR,5例(20%)部分缓解(PR)。预后指标良好或不良的患者CR率相当,包括淋巴瘤发病前有AIDS病史者(CR = 60%);和/或CD4淋巴细胞<200/mm3者(CR = 53%)。5例CR患者随后复发(36%);CR患者的中位生存期为29.2个月(4.1 - 61 +),而所有接受治疗患者的中位生存期为8.1个月。未观察到明显的周围神经病变或其他毒性。14例患者中有9例(64%)血清ICD p24抗原水平下降(7/14)或一直保持阴性(2/14),而36%的患者升高。诊断时血清IL-6水平升高与全身“B”症状相关(P = 0.023),而IL-6的变化与治疗反应随时间的变化相关(P = 0.006)。

结论

联合抗肿瘤和扎西他滨抗逆转录病毒疗法可安全用于AIDS相关淋巴瘤患者,56%的患者达到CR,无明显神经毒性,50%的患者对HIV p24抗原有良好影响。血清IL-6升高与全身“B”症状相关,而血清IL-6的变化可能与治疗反应相关。

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