HODGKIN LYMPHOMA IN CHILDREN: A 16-YEAR EXPERIENCE AT THE CHILDREN’S WELFARE TEACHING HOSPITAL OF BAGHDAD, IRAQ.
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Published:2024-06-29
Issue:1
Volume:16
Page:e2024053
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ISSN:2035-3006
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Container-title:Mediterranean Journal of Hematology and Infectious Diseases
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language:
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Short-container-title:Mediterr J Hematol Infect Dis
Author:
Testi Anna Maria,Al-Jadiry Mazin Faisal,Moleti Maria Luisa,Uccini Stefania,Al-Darraij Amir Fadhil,Al-Saeed Raghad Majid,Ghali Hasanein Habeeb,Sabhan Ahmed Hatem,Fadhil Samaher Abdulrazzaq,Al-Badri Safaa Abdulelah,Alsaadawi Adil Rabeea,Hameedi Ameer Dh,Shanshal Manhal Hashim,Al-Agele Yasir Saadoon,Al-Saffar Fatimah Abdul Ridha,Yaseen Nihal Khalid,Piciocchi Alfonso,Marsili Giovanni,Al-Hadad Salma Abbas
Abstract
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.
Publisher
Hematology Section, Dept. of Radiological Science and Hematology, Catholic University, Rome, Italy