Pediatric randomized trial EORTC CLG 58951: Outcome for adolescent population with acute lymphoblastic leukemia
Autor: | Yves Bertrand, Pierre-Simon Rohrlich, Laura Olivier-Gougenheim, Hélène Cavé, Barbara De Moerloose, Anne Uyttebroeck, Alina Ferster, Stefan Suciu, Carine Domenech, Chloé Arfeuille, Geneviève Plat, N Sirvent |
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Přispěvatelé: | Hospices Civils de Lyon (HCL), AP-HP Hôpital universitaire Robert-Debré [Paris], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), European Organization for Research and Treatment of Cancer (EORTC), EORTC, Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier), Université de Montpellier (UM), CHU Toulouse [Toulouse], Hôpital Universitaire des Enfants Reine Fabiola [Bruxelles, Belgique] (HUDERF), Universiteit Gent = Ghent University [Belgium] (UGENT), University Hospitals Leuven [Leuven], Centre Hospitalier Universitaire de Nice (CHU Nice) |
Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
Male
Cancer Research Pediatrics MESH: Remission Induction MESH: Combined Modality Therapy Lymphoblastic Leukemia genetic abnormalities law.invention chemistry.chemical_compound 0302 clinical medicine Randomized controlled trial law Antineoplastic Combined Chemotherapy Protocols Medicine Young adult MESH: Treatment Outcome education.field_of_study Remission Induction Hematopoietic Stem Cell Transplantation clinical trial [SDV.MHEP.HEM]Life Sciences [q-bio]/Human health and pathology/Hematology Hematology General Medicine Precursor Cell Lymphoblastic Leukemia-Lymphoma Prognosis Combined Modality Therapy 3. Good health MESH: Antineoplastic Combined Chemotherapy Protocols MESH: Maintenance Chemotherapy Treatment Outcome Oncology 030220 oncology & carcinogenesis outcome Female medicine.medical_specialty Asparaginase Population [SDV.CAN]Life Sciences [q-bio]/Cancer acute lymphoblastic leukemia MESH: Prognosis Maintenance Chemotherapy 03 medical and health sciences Humans education MESH: Hematopoietic Stem Cell Transplantation MESH: Adolescent MESH: Precursor Cell Lymphoblastic Leukemia-Lymphoma MESH: Humans business.industry Cancer medicine.disease MESH: Male Adolescent population Clinical trial chemistry adolescent business MESH: Female 030215 immunology |
Zdroj: | Hematological Oncology Hematological Oncology, Wiley, 2020, 38 (5), pp.763-772. ⟨10.1002/hon.2791⟩ |
ISSN: | 0278-0232 1099-1069 |
DOI: | 10.1002/hon.2791⟩ |
Popis: | International audience; Over the years, the prognosis of adolescents treated for acute lymphoblastic leukemia (ALL) has improved. However, this age group still represents a challenge with an overall survival (OS) of 60% compared to 85% in younger children. Herein, we report the outcome of adolescents treated in the European Organisation for Research and Treatment of Cancer (EORTC) 58951 clinical trial. EORTC 58951 clinical trial included patients with de novo ALL between 1998 and 2008. For this study, we analyzed data of all adolescents between 15 and under 18. Data from 97 adolescents were analyzed, 70 had B-lineage and 27 had T-lineage ALL. The 8-year event-free survival (EFS) and OS for the B-cell precursor ALL cases were 72.3% (59.4%-81.7%) and 80.8% (67.4%-89.1%), respectively. For the T-lineage, the 8-year EFS and OS were 57.4% (36.1%-74.0%) and 59.0% (36.1%-76.2%), respectively. "B-other" ALL, defined as BCP-ALL lacking any known recurrent genetic abnormalities were more frequent in our adolescent population (52.8%) than in younger children (27.1%). Outcome of adolescents in the EORTC 58951 study is supporting the findings that adolescents have better outcome in pediatric compared to adults' trials. Nevertheless, in pediatric studies, adolescents still have a worse prognosis than younger children. Despite the fact that specific unfavorable characteristics may be linked to the adolescent population, a careful study and characterization of adolescents "B-other" genetic abnormalities in ALL is critical to improve the outcome of this population. |
Databáze: | OpenAIRE |
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