A Ten-Year Experience of Treating Chronic Myeloid Leukemia in Rural Rwanda: Outcomes and Insights for a Changing Landscape

Author:

Morgan Jennifer1ORCID,DeBoer Rebecca J.2ORCID,Bigirimana Jean Bosco3,Nguyen Cam4,Ruhangaza Deogratias5,Paciorek Alan2ORCID,Mugabo Fred5,Villaverde Chandler6,Nsabimana Nicaise3,Bihizimana Pascal3,Umwizerwa Aline3ORCID,Lehmann Leslie E.7,Shulman Lawrence N.8ORCID,Shyirambere Cyprien3ORCID

Affiliation:

1. Lineberger Comprehensive Cancer Center, Chapel Hill, NC

2. Helen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, CA

3. Partners In Health/Inshuti Mu Buzima, Burera District, Rwanda

4. University of Colorado, Aurora, CO

5. Republic of Rwanda Ministry of Health, Burera District, Rwanda

6. Department of Medicine, University of Washington, Seattle, WA

7. Dana-Farber/Boston Children's Hospital Cancer Center, Boston, MA

8. Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA

Abstract

PURPOSE In describing our ten-year experience with treating chronic myeloid leukemia (CML) as part of the Glivec Patient Assistance Program (GIPAP) in rural Rwanda, we evaluate (1) patient characteristics and treatment outcomes, (2) resource-adapted management strategies, and (3) the impact of diagnostic capacity development. METHODS We retrospectively reviewed all patients with BCR-ABL–positive CML enrolled in this GIPAP program between 2009 and 2018. Clinical data were analyzed using descriptive statistics, Kaplan-Meier methods, proportional hazards regression, and the Kruskal-Wallis test. RESULTS One hundred twenty-four patients were included. The median age at diagnosis was 34 (range 8-81) years. On imatinib, 91% achieved complete hematologic response (CHR) after a median of 49 days. Seven (6%) and 12 (11%) patients had primary and secondary imatinib resistance, respectively. The 3-year overall survival was 80% (95% CI, 72 to 87) for the cohort, with superior survival in imatinib responders compared with those with primary and secondary resistance. The median time from imatinib initiation to CHR was 59 versus 38 days ( P = .040) before and after in-country diagnostic testing, whereas the median time to diagnosis ( P = .056) and imatinib initiation ( P = .170) was not significantly different. CONCLUSION Coupling molecular diagnostics with affordable access to imatinib within a comprehensive cancer care delivery program is a successful long-term strategy to treat CML in resource-constrained settings. Our patients are younger and have higher rates of imatinib resistance compared with historic cohorts in high-income countries. High imatinib resistance rates highlight the need for access to molecular monitoring, resistance testing, and second-generation tyrosine kinase inhibitors, as well as systems to support drug adherence. Hematologic response is an accurate resource-adapted predictor of survival in this setting. Local diagnostic capacity development has allowed for continuous, timely CML care delivery in Rwanda.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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