Treating Nephroblastoma in Rwanda: Using International Society of Pediatric Oncology Guidelines in a Novel Oncologic Care Model

Author:

Shyirambere Cyprien1,Xu Mary Jue1,Elmore Shekinah Nefreteri1,Fadelu Temidayo1,May Leana1,Tapela Neo1,Umuhizi Denis Gilbert1,Uwizeye Frank Regis1,Driscoll Caitlin1,Muhayimana Clemence1,Hategekimana Vedaste1,Rubagumya Fidel1,Nzayisenga Ignace1,Shulman Lawrence N.1,Mpunga Tharcisse1,Lehmann Leslie E.1

Affiliation:

1. Cyprien Shyirambere, Neo Tapela, Frank Regis Uwizeye, and Ignace Nzayisenga, Inshuti Mu Buzima/Partners in Health Rwanda; Denis Gilbert Umuhizi, Clemence Muhayimana, Vedaste Hategekimana, Fidel Rubagumya, and Tharcisse Mpunga, Ministry of Health Rwanda, Kigali, Rwanda; Mary Jue Xu, Shekinah Nefreteri Elmore, Neo Tapela, Lawrence N. Shulman, and Leslie E. Lehmann, Harvard Medical School; Temidayo Fadelu, Neo Tapela, and Leslie E. Lehmann, Brigham and Women’s Hospital; Leana May and Leslie E. Lehmann,...

Abstract

Purpose Success in treating nephroblastoma in high-income countries has been transferred to some resource-constrained settings; multicenter studies report disease-free survival of greater than 70%. However, few reports present care models with rural-based components, care tasks shifted to internists and pediatricians, and data collection structured for monitoring and evaluation. Here, we report clinical outcomes and protocol compliance for patients with nephroblastoma evaluated at Butaro Cancer Center of Excellence in Rwanda. Patients and Methods This retrospective study reports the care of 53 patients evaluated between July 1, 2012, and June 30, 2014. Patients receiving less than half of their chemotherapy at Butaro Cancer Center of Excellence were excluded. Results Of the 53 patients included, 9.4% had stage I, 13.2% had stage II, 24.5% had stage III, 26.4% had stage IV, and 5.7% had stage V disease; the remaining 20.8% had unknown stage disease from inadequate work-up or unavailable surgical report. The incidence of neutropenia increased with treatment progression, and the greatest proportion of delays occurred during the surgical referral phase. At the end of the study period, 32.1% of patients (n = 17) remained alive after treatment; 24.5% (n = 13) remained alive while continuing treatment, including one patient with recurrent disease; 30.2% (n = 16) died; and 13.2% (n = 7) were lost to follow-up. Conclusion Our findings confirm that nephroblastoma can be effectively treated in resource-constrained settings. Using an approach in which chemotherapy is delivered at a rural-based center by nononcologists and data are used for routine evaluation, care can be delivered in safe, novel ways. Protocol modifications to mitigate chemotherapy toxicities and strong communication between the multidisciplinary team members will likely minimize delays and further improve outcomes in similar settings.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Oncology,Cancer Research

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