Mediterranean Journal of Hematology and Infectious Diseases (Jun 2024)

HODGKIN LYMPHOMA IN CHILDREN: A 16-YEAR EXPERIENCE AT THE CHILDREN’S WELFARE TEACHING HOSPITAL OF BAGHDAD, IRAQ

  • Anna Maria Testi,
  • Mazin Faisal Al-Jadiry,
  • Maria Luisa Moleti,
  • Stefania Uccini,
  • Amir Fadhil Al-Darraij,
  • Raghad Majid Al-Saeed,
  • Hasanein Habeeb Ghali,
  • Ahmed Hatem Sabhan,
  • Samaher Abdulrazzaq Fadhil,
  • Safaa Abdulelah Al-Badri,
  • Adil Rabeea Alsaadawi,
  • Ameer Dh Hameedi,
  • Manhal Hashim Shanshal,
  • Yasir Saadoon Al-Agele,
  • Fatimah Abdul Ridha Al-Saffar,
  • Nihal Khalid Yaseen,
  • Alfonso Piciocchi,
  • Giovanni Marsili,
  • Salma Abbas Al-Hadad

DOI
https://doi.org/10.4084/MJHID.2024.053
Journal volume & issue
Vol. 16, no. 1

Abstract

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Background. Childhood Hodgkin lymphoma (HL) is an eminently curable disease. Good outcomes can be achieved even in resource-limited settings and increasingly, the focus is on limiting long-term toxicity. Contemporary treatment incorporates a risk-stratified, response-adapted approach using multiagent chemotherapy with/without low-dose radiotherapy. Many developing countries continue to use ABVD-based regimens due to limited acute toxicity, cost, and ease of delivery. Objective. We herein report the outcomes of childhood HL diagnosed and treated in an Iraqi single-center over a 16 years period. Methods. Children ≤14 years with biopsy-proven HL were enrolled. Most patients received ABVD chemotherapy or COPP/ABV when Dacarbazine was unavailable. Radiotherapy was not available. Results. Three hundred-three children were consecutively newly diagnosed with HL; 284 were considered eligible for the retrospective analysis (treatment refusals 9; deaths before therapy 5; initially diagnosed of non-Hodgkin lymphoma 5). ABVD scheme was administered to 184 children (65%), COPP/ABV to 83 (29%), other schemes to the remaining 17 patients. Complete response (CR) was achieved in 277 (98%); 4 (1.4%) showed disease progression and 1 stable disease. Four patients in CR abandoned therapy and were in CR at the time of analysis, 2 died from infection. Relapse occurred in 42 patients (15%). The 15-year OS and EFS are 89.7% and 70.3%, respectively. Conclusion. In this single-center, over a 16-year period, almost 90% of children suffering from HL survive, despite the numerous limitations in diagnostic procedures, shortage of chemotherapy, no radiotherapy facilities, absence of effective second-line treatments and finally therapy abandonment for social and financial reasons.

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