Impact assessment of implementing evidence-based de-escalation strategies in early breast cancer management in South Africa.

e12744 Background: In South Africa, where oncology resources are limited, adopting evidence-based radiation and chemotherapy de-escalation strategies may reduce patient toxicity and enhance resource efficiency. The applicability and impact of these strategies, validated in high-income countries as non-inferior in low-risk breast cancer patients, remain unknown in South Africa. Methods: We conducted a retrospective analysis of the South Africa Breast Cancer & HIV Outcomes (SABCHO) cohort drawn from five public hospitals in Gauteng and KwaZulu-Natal provinces. Patients were aged ≥18 years with stage I–III breast cancer diagnosed and treated between 2015 and 2019. Radiation de-escalation eligibility was based on CALGB 9343 and PRIME II trials, adjusted for the life expectancy in South Africa. Chemotherapy de-escalation eligibility was based on TAILORx and RXPONDER trials utilizing calculated Magee recurrence scores (MRS) in lieu of Oncotype (eligible if MRS < 18 or < 25 with mitosis score = 1). We assessed the prevalence of de-escalation eligibility, treatment receipt patterns, and compared overall survival (OS) by treatment receipt using Cox proportional hazard models and Kaplan-Meier curves. Results: Among 2,369 patients, 210 (8.6%) were eligible for radiation de-escalation and 440 (18.6%) for chemotherapy de-escalation. Of these, 26.3% received adjuvant radiation and 45.2% received chemotherapy. OS stratified by receipt of treatment did not differ significantly in either group. 5-year median OS was 94.5 months and 93.3 months in patients who received radiation and those who did not, respectively (HR 1.42, 95% CI 0.82-2.43). Median OS was 96.8 months and 98.4 months in patients who received and did not receive chemotherapy, respectively (HR 0.93, 95% CI 0.60-1.42). Conclusions: Many patients receiving adjuvant radiation and chemotherapy in this South African cohort may have been appropriate for treatment de-escalation, highlighting an opportunity to mitigate toxicity and reallocate scarce resources without reducing survival. Prospective research into the clinical impact of de-escalation strategies in South Africa is warranted. Sociodemographic and clinical characteristics of early breast cancer patients in SABCHO cohort. Characteristic Overall (N = 2369) Age, years (median [IQR]) 54.0 [44.0 – 65.0] Race Asian/Indian 190 (8.0%) Black 1915 (80.8%) Mixed 107 (4.5%) White 159 (6.7%) HIV status Positive 470 (19.8%) Overall Stage Stage I 445 (18.8%) Stage II 1225 (51.7%) Stage III 699 (29.5%) Tumor stage T0 170 (7.2%) T1 502 (21.2%) T2 933 (39.4%) T3 312 (13.2%) T4 91 (3.8%) Other/Unknown 361 (15.2%) Nodal stage N0 914 (38.6%) N1 808 (34.1%) N2 212 (8.9%) Tumor size, mm 30.0 [21.7 – 45.0] Hormone receptor (HR) Positive

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Journal
Journal of Clinical Oncology
Published
2026-05-28
DOI
https://doi.org/10.1200/jco.2026.44.16_suppl.e12744
Primary Topic
Advances in Oncology and Radiotherapy
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article
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article

Impact assessment of implementing evidence-based de-escalation strategies in early breast cancer management in South Africa.

Tendai Kwaramba, Wenlong Carl Chen, Paul Ruff, Nivashini Murugan et al.
Journal of Clinical Oncology
Advances in Oncology and Radiotherapy
article

Impact assessment of implementing evidence-based de-escalation strategies in early breast cancer management in South Africa.

Tendai Kwaramba, Wenlong Carl Chen, Paul Ruff, Nivashini Murugan, Rofhiwa Mathiba, Maureen Joffe, Charmaine Blanchard, Karishma Singh, Daniel O'Neil
article en

Abstract

e12744 Background: In South Africa, where oncology resources are limited, adopting evidence-based radiation and chemotherapy de-escalation strategies may reduce patient toxicity and enhance resource efficiency. The applicability and impact of these strategies, validated in high-income countries as non-inferior in low-risk breast cancer patients, remain unknown in South Africa. Methods: We conducted a retrospective analysis of the South Africa Breast Cancer & HIV Outcomes (SABCHO) cohort drawn from five public hospitals in Gauteng and KwaZulu-Natal provinces. Patients were aged ≥18 years with stage I–III breast cancer diagnosed and treated between 2015 and 2019. Radiation de-escalation eligibility was based on CALGB 9343 and PRIME II trials, adjusted for the life expectancy in South Africa. Chemotherapy de-escalation eligibility was based on TAILORx and RXPONDER trials utilizing calculated Magee recurrence scores (MRS) in lieu of Oncotype (eligible if MRS < 18 or < 25 with mitosis score = 1). We assessed the prevalence of de-escalation eligibility, treatment receipt patterns, and compared overall survival (OS) by treatment receipt using Cox proportional hazard models and Kaplan-Meier curves. Results: Among 2,369 patients, 210 (8.6%) were eligible for radiation de-escalation and 440 (18.6%) for chemotherapy de-escalation. Of these, 26.3% received adjuvant radiation and 45.2% received chemotherapy. OS stratified by receipt of treatment did not differ significantly in either group. 5-year median OS was 94.5 months and 93.3 months in patients who received radiation and those who did not, respectively (HR 1.42, 95% CI 0.82-2.43). Median OS was 96.8 months and 98.4 months in patients who received and did not receive chemotherapy, respectively (HR 0.93, 95% CI 0.60-1.42). Conclusions: Many patients receiving adjuvant radiation and chemotherapy in this South African cohort may have been appropriate for treatment de-escalation, highlighting an opportunity to mitigate toxicity and reallocate scarce resources without reducing survival. Prospective research into the clinical impact of de-escalation strategies in South Africa is warranted. Sociodemographic and clinical characteristics of early breast cancer patients in SABCHO cohort. Characteristic Overall (N = 2369) Age, years (median [IQR]) 54.0 [44.0 – 65.0] Race Asian/Indian 190 (8.0%) Black 1915 (80.8%) Mixed 107 (4.5%) White 159 (6.7%) HIV status Positive 470 (19.8%) Overall Stage Stage I 445 (18.8%) Stage II 1225 (51.7%) Stage III 699 (29.5%) Tumor stage T0 170 (7.2%) T1 502 (21.2%) T2 933 (39.4%) T3 312 (13.2%) T4 91 (3.8%) Other/Unknown 361 (15.2%) Nodal stage N0 914 (38.6%) N1 808 (34.1%) N2 212 (8.9%) Tumor size, mm 30.0 [21.7 – 45.0] Hormone receptor (HR) Positive

Journal of Clinical OncologyVol. 44(16_suppl)
Yale New Haven Hospital (US), University of the Witwatersrand (ZA), Johannesburg Hospital (ZA), Yale Cancer Center (US), Yale University (US)
Decent work and economic growth
Openalex Percentile: Top 5%
Advances in Oncology and Radiotherapy
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