Johnston Christine, Harrington Robert, Jain Rupali, Schiffer Joshua, Kiem Hans-Peter, Woolfrey Ann
Department of Medicine, University of Washington, Seattle, Washington; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Department of Medicine, University of Washington, Seattle, Washington.
Biol Blood Marrow Transplant. 2016 Jan;22(1):149-56. doi: 10.1016/j.bbmt.2015.08.006. Epub 2015 Aug 8.
The ability to continue combination antiretroviral therapy (cART) in human immunodeficiency virus (HIV)-infected patients undergoing hematopoietic cell transplantation (HCT) for treatment of hematologic malignancies is likely a critical factor in preventing the establishment of an HIV reservoir in transplanted stem cells. Thus, we studied the feasibility of continued antiretroviral therapy in our HIV-infected patients undergoing autologous or allogeneic transplantation. All HIV-infected adults undergoing HCT for hematologic malignancy at Fred Hutchinson Cancer Research Center between 2006 and 2014 were included; most were enrolled in a prospective clinical study to monitor HIV reservoirs after transplantation (NCT00968630 and NCT00112593). Non-nucleotide reverse transcriptase inhibitor or integrase-strand inhibitor-anchored antiretroviral therapy regimens were continued or selected before HCT by infectious disease physicians. Plasma HIV RNA was measured every other day for the first 2 weeks after transplantation and then every 2 weeks. Missed doses of cART and reasons for changing the cART regimen during the post-transplantation hospitalization were documented through review of inpatient pharmacy records. Seven autologous and 8 allogeneic transplantations were performed. In 9 transplantations, the cART regimen was not altered after HCT and no doses were missed. In 2 patients who required alterations in their cART regimen because of development of acute renal failure (n = 1) and small bowel obstruction (n = 1) after HCT, enfuvirtide was used as a bridging component of the regimen. Plasma HIV RNA remained suppressed during the first 28 days in 12 of 15 transplantations, and no patients had a plasma HIV RNA >1000 copies/mL during long-term follow up. Non-nucleotide reverse transcriptase inhibitor- and integrase-strand inhibitor-based cART are safe and effective in HIV-infected persons during the peri-HCT period. Most patients undergoing HCT were able to continue cART without missed doses. Sustained HIV viremia and emergence of resistance were not detected.
对于因血液系统恶性肿瘤而接受造血细胞移植(HCT)的人类免疫缺陷病毒(HIV)感染患者,能够继续进行联合抗逆转录病毒治疗(cART)可能是预防HIV储库在移植干细胞中建立的关键因素。因此,我们研究了在接受自体或异体移植的HIV感染患者中继续进行抗逆转录病毒治疗的可行性。纳入了2006年至2014年间在弗雷德·哈钦森癌症研究中心因血液系统恶性肿瘤接受HCT的所有HIV感染成人;大多数患者参加了一项前瞻性临床研究,以监测移植后的HIV储库(NCT00968630和NCT00112593)。在HCT前,传染病医生继续使用或选择基于非核苷类逆转录酶抑制剂或整合酶链转移抑制剂的抗逆转录病毒治疗方案。移植后前2周每隔一天测量血浆HIV RNA,之后每2周测量一次。通过查阅住院药房记录,记录移植后住院期间cART漏服剂量及更改cART方案的原因。共进行了7例自体移植和8例异体移植。在9例移植中,HCT后cART方案未改变,也没有漏服剂量。在2例因HCT后出现急性肾衰竭(1例)和小肠梗阻(1例)而需要更改cART方案的患者中,恩夫韦肽被用作方案的桥接成分。15例移植中的12例在最初28天内血浆HIV RNA持续被抑制,长期随访期间没有患者的血浆HIV RNA>1000拷贝/mL。基于非核苷类逆转录酶抑制剂和整合酶链转移抑制剂的cART在HCT围手术期对HIV感染患者安全有效。大多数接受HCT的患者能够继续cART且无漏服剂量。未检测到持续性HIV病毒血症和耐药性的出现。