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抗逆转录病毒疗法与长春碱在HIV相关多中心Castleman病中的危及生命的相互作用。

Life-threatening interaction between antiretroviral therapy and vinblastine in HIV-associated multicentric Castleman's disease.

作者信息

Kotb Rami, Vincent Isabelle, Dulioust Anne, Peretti Delphine, Taburet Anne-Marie, Delfraissy Jean-Francois, Goujard Cécile

机构信息

Department of Internal Medicine, CHU Bicêtre, AP-HP, Le Kremlin Bicêtre, Cedex, France.

出版信息

Eur J Haematol. 2006 Mar;76(3):269-71. doi: 10.1111/j.0902-4441.2005.t01-1-EJH2435.x.

Abstract

BACKGROUND

HIV-infected patients still present a high risk of developing lymphoproliferative malignancies, despite the fact that their prognosis has been considerably improved by highly active antiretroviral therapy (HAART). Potential interactions exist between antiretroviral drugs, in particular protease inhibitors, and anti-neoplastic ones, but their impact in terms of clinical and haematological adverse events remains unclear.

METHODS

We report a case of potentially life-threatening interaction between vinblastine and antiretroviral therapy in a patient presenting with HIV-associated multicentric Castleman's disease (MCD).

RESULTS

A 55-year-old HIV-1 infected patient was diagnosed with MCD while being treated with a salvage HAART regimen consisting of zidovudine, lamivudine, abacavir, nevirapine and ritonavir-boosted lopinavir. Vinblastine was prescribed as a monotherapy at the usual dose of 6 mg/m2 (i.e. 10 mg) every 3 weeks. The first vinblastine course was performed without HAART with no adverse event. Antiretroviral therapy was resumed for the two following courses which were associated with unexpected severe digestive and haematological toxicities, and moderate renal failure. Vinblastine was then administered alone at increasing doses without toxicity. HAART was finally resumed and we assessed that a decreased vinblastine dose of 2 mg/m2 was well tolerated, with a complete response of MCD.

CONCLUSIONS

HAART regimen comprising protease inhibitors, which are potent inhibitors of cytochrome P450 and P-gp, could interfere with anti-neoplastic drugs, as demonstrated with vinblastine in our case report.

摘要

背景

尽管高效抗逆转录病毒疗法(HAART)已显著改善了人类免疫缺陷病毒(HIV)感染患者的预后,但他们仍有较高的发生淋巴增殖性恶性肿瘤的风险。抗逆转录病毒药物,尤其是蛋白酶抑制剂,与抗肿瘤药物之间可能存在相互作用,但其对临床和血液学不良事件的影响尚不清楚。

方法

我们报告了1例HIV相关多中心Castleman病(MCD)患者中长春碱与抗逆转录病毒疗法之间可能危及生命的相互作用的病例。

结果

1例55岁的HIV-1感染患者在接受由齐多夫定、拉米夫定、阿巴卡韦、奈韦拉平及利托那韦增强的洛匹那韦组成的挽救性HAART方案治疗时被诊断为MCD。长春碱按常规剂量6mg/m²(即10mg)每3周进行单药治疗。第1个长春碱疗程在未使用HAART的情况下进行,未出现不良事件。随后的2个疗程恢复了抗逆转录病毒治疗,这2个疗程均出现了意外的严重消化和血液学毒性以及中度肾衰竭。之后单独给予递增剂量的长春碱,未出现毒性反应。最终恢复了HAART,我们评估长春碱剂量降至2mg/m²时耐受性良好,MCD完全缓解。

结论

如我们病例报告中长春碱所示,包含蛋白酶抑制剂的HAART方案(蛋白酶抑制剂是细胞色素P450和P-糖蛋白的强效抑制剂)可能会干扰抗肿瘤药物。

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