Compression Therapy for HIV-Associated Kaposi Sarcoma Leg Lymphedema: Results of the Kenyan Improvised Compression for Kaposi Sarcoma Randomized Controlled Trial
dc.contributor.author | Chang, Aileen Y. | |
dc.contributor.author | Karwa, Rakhi | |
dc.contributor.author | Odhiambo, Haji | |
dc.contributor.author | Were, Phelix | |
dc.contributor.author | Fletcher, Sara L. | |
dc.contributor.author | Tonui, Edith C. | |
dc.contributor.author | Kohn, Michael A. | |
dc.contributor.author | Lee, Jeannette | |
dc.contributor.author | Chang, Di | |
dc.contributor.author | Lensing, Shelly | |
dc.contributor.author | Namaemba, Diana Flora | |
dc.contributor.author | Busakhala, Naftali | |
dc.contributor.author | Kiprono, Samson K. | |
dc.contributor.author | Maurer, Toby | |
dc.contributor.author | Goodrich, Suzanne | |
dc.contributor.author | Pastakia, Sonak D. | |
dc.contributor.department | Dermatology, School of Medicine | en_US |
dc.date.accessioned | 2023-04-26T12:53:43Z | |
dc.date.available | 2023-04-26T12:53:43Z | |
dc.date.issued | 2022 | |
dc.description.abstract | Purpose: Evaluate the effectiveness of compression while receiving chemotherapy compared with chemotherapy alone in the treatment of HIV-associated Kaposi sarcoma (KS) lymphedema. Methods: A randomized controlled trial was conducted in a single oncology clinic in western Kenya (NCT03404297). A computer-generated randomization schedule was used to allocate treatment arms. Randomized block design was used for stratification by lymphedema stage. Participants were HIV positive adults age ≥ 18 years on antiretroviral therapy with biopsy-proven KS associated with leg lymphedema and being initiated on chemotherapy. The intervention was 10 weeks of weekly clinic-based application of two-component paste compression bandages. The primary outcome was change in the Lower Extremity Lymphedema Index (LELI) score from week 0 to week 14. The secondary outcomes were change in the Lymphedema Quality of Life measure (LYMQOL) and change in the European Organisation for Research and Treatment of Cancer (EORTC) QLQ-C30 score from week 0 to week 14. Blinded outcome assessments were conducted. Results: Of 30 participants randomly assigned, 25 eligible patients (chemotherapy [control], n = 13; compression plus chemotherapy [intervention], n = 12) returned at week 14. Change in LELI, LYMQOL, and EORTC QLQ-C30 scores between week 14 and week 0 did not significantly differ by arm. The mean (standard deviation) change in LELI score was -25.9 (34.6) for the control arm compared with -13.3 (29.5) for the intervention arm, P = .340. The difference (95% CI) in the change in LELI score was -12.6 (-39.3 to 14.1). Conclusion: Future studies evaluating a 14-week change in LELI for KS lymphedema should assume a standard deviation of approximately 30. Lessons learned from this pilot trial should inform the development of a larger, multicenter trial to evaluate the effectiveness of compression for KS lymphedema. | en_US |
dc.eprint.version | Final published version | en_US |
dc.identifier.citation | Chang AY, Karwa R, Odhiambo H, et al. Compression Therapy for HIV-Associated Kaposi Sarcoma Leg Lymphedema: Results of the Kenyan Improvised Compression for Kaposi Sarcoma Randomized Controlled Trial. JCO Glob Oncol. 2022;8:e2100329. doi:10.1200/GO.21.00329 | en_US |
dc.identifier.uri | https://hdl.handle.net/1805/32600 | |
dc.language.iso | en_US | en_US |
dc.publisher | American Society of Clinical Oncology | en_US |
dc.relation.isversionof | 10.1200/GO.21.00329 | en_US |
dc.relation.journal | JCO Global Oncology | en_US |
dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 International | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
dc.source | PMC | en_US |
dc.subject | HIV infections | en_US |
dc.subject | Lymphedema | en_US |
dc.subject | Kaposi sarcoma | en_US |
dc.title | Compression Therapy for HIV-Associated Kaposi Sarcoma Leg Lymphedema: Results of the Kenyan Improvised Compression for Kaposi Sarcoma Randomized Controlled Trial | en_US |
dc.type | Article | en_US |