As-Needed Vs Immediate Etoposide Chemotherapy in Combination With Antiretroviral Therapy for Mild-to-Moderate AIDS-Associated Kaposi Sarcoma in Resource-Limited Settings: A5264/AMC-067 Randomized Clinical Trial

被引:28
作者
Hosseinipour, Mina C. [1 ,2 ]
Kang, Minhee [3 ]
Krown, Susan E. [4 ]
Bukuru, Aggrey [5 ]
Umbleja, Triin [3 ]
Martin, Jeffrey N. [6 ]
Orem, Jackson [7 ]
Godfrey, Catherine [8 ]
Hoagland, Brenda [9 ]
Mwelase, Noluthando [10 ]
Langat, Deborah [11 ]
Nyirenda, Mulinda [12 ]
MacRae, John [13 ]
Borok, Margaret [4 ,14 ]
Samaneka, Wadzanai [14 ]
Moses, Agnes [1 ,2 ,4 ]
Mngqbisa, Rosie [15 ]
Busakhala, Naftali [16 ]
Martinez-Maza, Otoniel [4 ,17 ]
Ambinder, Richard [4 ,18 ]
Dittmer, Dirk P. [2 ,4 ]
Nokta, Mostafa [19 ]
Campbell, Thomas B. [20 ]
机构
[1] UNC Project, Lilongwe, Malawi
[2] Univ N Carolina, Sch Med, Chapel Hill, NC 27515 USA
[3] Harvard TH Chan Sch Publ Hlth, Ctr Biostat AIDS Res, Boston, MA USA
[4] AIDS Malignancy Consortium, New York, NY USA
[5] Joint Clin Res Ctr, Kampala, Uganda
[6] Univ Calif San Francisco, San Francisco, CA 94143 USA
[7] Uganda Canc Inst, Kampala, Uganda
[8] NIAID, HIV Res Branch, TRP, DAIDS,NIH, Rockville, MD USA
[9] Fiocruz MS, INI Evandro Chagas, Rio De Janeiro, Brazil
[10] Univ Witwatersrand, Johannesburg, South Africa
[11] Kenya Govt Med Res Ctr, Walter Reed Project, Kericho, Kenya
[12] Univ Malawi, Coll Med, Johns Hopkins Project, Blantyre, Malawi
[13] IMPACTA Peru, Lima, Peru
[14] Univ Zimbabwe, Harare, Zimbabwe
[15] Enhancing Care Fdn, DICRS, Durban, South Africa
[16] Moi Univ, Eldoret, Kenya
[17] Univ Calif Los Angeles, Los Angeles, CA USA
[18] Johns Hopkins Univ, Baltimore, MD USA
[19] NCI, Bethesda, MD 20892 USA
[20] Univ Colorado, Sch Med, Aurora, CO USA
关键词
Kaposi sarcoma; HIV; etoposide; chemotherapy; antiretroviral therapy; ORAL ETOPOSIDE; RISK-FACTORS; COMPETING RISK; MORTALITY; AFRICA; ADULTS; OUTCOMES; MALAWI; IMPACT; COHORT;
D O I
10.1093/cid/ciy044
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Mild-to-moderate AIDS-associated Kaposi sarcoma (KS) often responds to antiretroviral therapy (ART) alone; the role of chemotherapy is unclear. We assessed the impact of immediate vs as-needed oral etoposide (ET) among human immunodeficiency virus (HIV)-infected individuals with mild-to-moderate KS initiating ART. Methods. Chemotherapy-naive, HIV type 1-infected adults with mild-to-moderate KS initiating ART in Africa and South America were randomized to ART (tenofovir/emtricitabine/efavirenz) alone (chemotherapy "as-needed" arm) vs ART plus up to 8 cycles of oral ET (immediate arm). Participants with KS progression on ART alone received ET as part of the as-needed strategy. Primary outcome was ordinal as follows: failure, stable, and response at 48 weeks. Secondary outcomes included time to initial KS progression, KS-associated immune reconstitution inflammatory syndrome (KS-IRIS), and KS response. Results. Of 190 randomized participants (as-needed=94, immediate=96), the majority were men (71%) and African (93%). Failure (53.8% vs 56.6%), stable (16.3% vs 10.8%), and response (30% vs 32.5%) did not differ between arms (as-needed vs immediate) among those with week 48 data potential (N=163, P=.91). Time to KS progression (P=.021), KS-IRIS (P=.003), and KS response (P=.003) favored the immediate arm. Twenty-five participants died (13%). Mortality, adverse events, CD4+ T-cell changes, and HIV RNA suppression were similar at 48 weeks. Conclusions. Among HIV-infected adults with mild-to-moderate KS, immediate ET provided early, nondurable clinical benefits. By 48 weeks, no clinical benefit was observed compared to use of ET as needed. Mortality was high and tumor response was low.
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收藏
页码:251 / 260
页数:10
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