Improved survival of children and adolescents with classical Hodgkin lymphoma treated on a harmonised protocol in South Africa

Author:

Geel Jennifer1ORCID,van Zyl Anel2ORCID,Plessis Jan du3ORCID,Hendricks Marc4ORCID,Goga Yasmin4ORCID,Carr Amy5ORCID,Neethling Beverley6ORCID,Hramyka Artsiom7ORCID,Omar Fareed8ORCID,Mathew Rema9ORCID,Louw Lizette10ORCID,Naidoo Thanushree1112,Ngcana Thandeka13ORCID,Schickerling Tanya14ORCID,Netshituni Vutshilo15ORCID,Madzhia Elelwani16,du Plessis Liezl17ORCID,Kelsey Tom7ORCID,Ballot Daynia E.18ORCID,Metzger Monika L.19ORCID

Affiliation:

1. Pediatric Haematology‐Oncology University of the Witwatersrand Charlotte Maxeke Johannesburg Academic Hospital Wits Donald Gordon Medical Centre Johannesburg South Africa

2. Department of Paediatrics and Child Health Faculty of Medicine and Health Sciences Stellenbosch University Tygerberg Hospital Cape Town South Africa

3. Pediatric Haematology‐Oncology University of the Free State Universitas Hospital Bloemfontein South Africa

4. Department of Paediatrics and Child Health Haematology‐Oncology Service Faculty of Health Sciences University of Cape Town Red Cross War Memorial Children's Hospital Cape Town South Africa

5. Pediatric Haematology‐Oncology University of KwaZulu‐Natal Durban Greys Hospital Pietermaritzburg South Africa

6. Pediatric Haematology‐Oncology University of KwaZulu‐Natal Durban Inkosi Albert Luthuli Hospital and Greys Hospital Pietermaritzburg South Africa

7. School of Computer Science University of St Andrews St Andrews UK

8. Pediatric Haematology‐Oncology University of Pretoria Steve Biko Academic Hospital Pretoria South Africa

9. Pediatric Haematology‐Oncology Walter Sisulu University Frere Hospital East London South Africa

10. Centre of Molecular Imaging and Theranostics Johannesburg South Africa

11. Department of Radiation Oncology University of the Witwatersrand Charlotte Maxeke Johannesburg Academic Hospital Johannesburg South Africa

12. Wits Donald Gordon Medical Centre Johannesburg South Africa

13. Pediatric Haematology‐Oncology University of the Witwatersrand Chris Hani Baragwanath Academic Hospital Wits Donald Gordon Medical Centre Johannesburg South Africa

14. Netcare Alberton Hospital Johannesburg South Africa

15. Pediatric Haematology‐Oncology, University of Limpopo Polokwane‐Mankweng Hospital Complex Polokwane South Africa

16. Pediatric Haematology‐Oncology Sefako Makgatho University Dr George Mukhari Hospital Garankuwa South Africa

17. Pediatric Haematology‐Oncology University of the Free State Kimberley Hospital Kimberley South Africa

18. School of Clinical Medicine University of the Witwatersrand Charlotte Maxeke Johannesburg Academic Hospital Johannesburg South Africa

19. Medecins sans Frontieres Geneva Switzerland

Abstract

AbstractBackgroundHistoric South African 5‐year overall survival (OS) rates for Hodgkin lymphoma (HL) from 2000 to 2010 were 46% and 84% for human immunodeficiency virus (HIV)‐positive and HIV‐negative children, respectively. We investigated whether a harmonised treatment protocol using risk stratification and response‐adapted therapy could increase the OS of childhood and adolescent HL.MethodsSeventeen units prospectively enrolled patients less than 18 years, newly diagnosed with classical HL onto a risk‐stratified, response‐adapted treatment protocol from July 2016 to December 2022. Low‐ and intermediate‐risk patients received four and six courses of adriamycin, bleomycin, vinblastine, and dacarbazine (ABVD), respectively. High‐risk patients received two courses of ABVD, followed by four courses of cyclophosphamide, vincristine, prednisone, and dacarbazine (COPDac). Those with a slow early response and bulky disease received consolidation radiotherapy. HIV‐positive patients could receive granulocyte colony‐stimulating factor and less intensive therapy if stratified as high risk, at the treating clinician's discretion. Kaplan–Meier survival analysis was performed to determine 2‐year OS and Cox regression to elucidate prognostic factors.ResultsThe cohort comprised 132 patients (19 HIV‐positive, 113 HIV‐negative), median age of 9.7 years, with a median follow‐up of 2.2 years. Risk grouping comprised nine (7%) low risk, 36 (27%) intermediate risk and 87 (66%) high risk, with 71 (54%) rapid early responders and 45 (34%) slow early responders, and 16 (12%) undocumented. Two‐year OS was 100% for low‐risk, 93% for intermediate‐risk, and 91% for high‐risk patients. OS for HIV‐negative (93%) and HIV‐positive (89%) patients were similar (p = .53). Absolute lymphocyte count greater than 0.6 × 109 predicted survival (94% vs. 83%, p = .02).ConclusionIn the first South African harmonised HL treatment protocol, risk stratification correlated with prognosis. Two‐year OS of HIV‐positive and HIV‐negative patients improved since 2010, partially ascribed to standardised treatment and increased supportive care. This improved survival strengthens the harmonisation movement and gives hope that South Africa will achieve the WHO Global Initiative for Childhood Cancer goals.

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

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