Timing of initiation of antiretroviral therapy in human immunodeficiency virus (HIV)--associated tuberculous meningitis

M Estee Török, Nguyen Thi Bich Yen, Tran Thi Hong Chau, Nguyen Thi Hoang Mai, Nguyen Hoan Phu, Pham Phuong Mai, Nguyen Thi Dung, Nguyen Van Vinh Chau, Nguyen Duc Bang, Nguyen Anh Tien, N H Minh, Nguyen Quang Hien, Phan Vuong Khac Thai, Doan The Dong, Do Thi Tuong Anh, Nguyen Thi Cam Thoa, Nguyen Ngoc Hai, Nguyen Ngoc Lan, Nguyen Thi Ngoc Lan, Hoang Thi Quy, Nguyen Huy Dung, Tran Tinh Hien, Nguyen Tran Chinh, Cameron Paul Simmons, Menno de Jong, Marcel Wolbers, Jeremy James Farrar, M Estee Török, Nguyen Thi Bich Yen, Tran Thi Hong Chau, Nguyen Thi Hoang Mai, Nguyen Hoan Phu, Pham Phuong Mai, Nguyen Thi Dung, Nguyen Van Vinh Chau, Nguyen Duc Bang, Nguyen Anh Tien, N H Minh, Nguyen Quang Hien, Phan Vuong Khac Thai, Doan The Dong, Do Thi Tuong Anh, Nguyen Thi Cam Thoa, Nguyen Ngoc Hai, Nguyen Ngoc Lan, Nguyen Thi Ngoc Lan, Hoang Thi Quy, Nguyen Huy Dung, Tran Tinh Hien, Nguyen Tran Chinh, Cameron Paul Simmons, Menno de Jong, Marcel Wolbers, Jeremy James Farrar

Abstract

Background: The optimal time to initiate antiretroviral therapy (ART) in human immunodeficiency virus (HIV)-associated tuberculous meningitis is unknown.

Methods: We conducted a randomized, double-blind, placebo-controlled trial of immediate versus deferred ART in patients with HIV-associated tuberculous meningitis to determine whether immediate ART reduced the risk of death. Antiretroviral drugs (zidovudine, lamivudine, and efavirenz) were started either at study entry or 2 months after randomization. All patients were treated with standard antituberculosis treatment, adjunctive dexamethasone, and prophylactic co-trimoxazole and were followed up for 12 months. We conducted intention-to-treat, per-protocol, and prespecified subgroup analyses.

Results: A total of 253 patients were randomized, 127 in the immediate ART group and 126 in the deferred ART group; 76 and 70 patients died within 9 months in the immediate and deferred ART groups, respectively. Immediate ART was not significantly associated with 9-month mortality (hazard ratio [HR], 1.12; 95% confidence interval [CI], .81-1.55; P = .50) or the time to new AIDS events or death (HR, 1.16; 95% CI, .87-1.55; P = .31). The percentage of patients with severe (grade 3 or 4) adverse events was high in both arms (90% in the immediate ART group and 89% in the deferred ART group; P = .84), but there were significantly more grade 4 adverse events in the immediate ART arm (102 in the immediate ART group vs 87 in the deferred ART group; P = .04).

Conclusions: Immediate ART initiation does not improve outcome in patients presenting with HIV-associated tuberculous meningitis. There were significantly more grade 4 adverse events in the immediate ART arm, supporting delayed initiation of ART in HIV-associated tuberculous meningitis. Clinical Trials Registration. ISRCTN63659091.

Figures

Figure 1
Figure 1
Study flow. ART, antiretroviral therapy; HIV, human immunodeficiency virus. *Patients may have more than one exclusion criterion
Figure 2
Figure 2
Kaplan-Meier survival estimates according to treatment group in all patients (A) and by Tuberculous meningitis (TBM) grade (BD). Black solid lines correspond to immediate antiretroviral therapy (ART), dashed gray lines to deferred ART.

Source: PubMed

3
Subscribe