Isolated central nervous system relapse following treatment reduction in low-risk acute lymphoblastic leukemia at the children's cancer center of lebanon

dc.contributor.authorEl-Khoury, Habib
dc.contributor.authorChahrour, Mohamad A.
dc.contributor.authorGhanem, Khaled M.
dc.contributor.authorSaifi, Omran
dc.contributor.authorTamim, Hani Mohammed
dc.contributor.authorEl-Solh, Hassan
dc.contributor.authorHamideh, Dima
dc.contributor.authorTarek, Nidale
dc.contributor.authorSaab, Raya H.
dc.contributor.authorAbboud, Miguel Raul
dc.contributor.authorMuwakkit, Samar A.
dc.contributor.departmentPediatrics and Adolescent Medicine
dc.contributor.departmentClinical Research Institute
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T12:10:59Z
dc.date.available2025-01-24T12:10:59Z
dc.date.issued2020
dc.description.abstractThe aim of this trial was to decrease the incidence of life-threatening infections by decreasing the dose and the duration of dexamethasone treatment during maintenance therapy. This was a prospective, nonrandomized trial of low-risk acute lymphoblastic leukemia patients 1 to 18 years of age who were treated at the Children's Cancer Center of Lebanon (CCCL). Patients consecutively diagnosed between 2002 and 2013 were divided into groups 1 and 2 receiving total dexamethasone doses of 1144 and 618 mg/m2, respectively. A total of 84 patients were assigned to group 1 and 33 patients to group 2. The 5-year cumulative incidence of isolated central nervous system relapse increased from (n=0% [95% confidence interval: 0%-4.4%]) in group 1 to 9.1% [95% confidence interval: 3%-23%]; P=0.021) in group 2. Decreasing cumulative dose of dexamethasone for low-risk childhood acute lymphoblastic leukemia patients aiming to avoid serious viral infections led to a significant increase in isolated central nervous system relapse. © 2020 Lippincott Williams and Wilkins. All rights reserved.
dc.identifier.doihttps://doi.org/10.1097/MPH.0000000000001785
dc.identifier.eid2-s2.0-85082515533
dc.identifier.pmid32205785
dc.identifier.urihttp://hdl.handle.net/10938/32472
dc.language.isoen
dc.publisherLippincott Williams and Wilkins
dc.relation.ispartofJournal of Pediatric Hematology/Oncology
dc.sourceScopus
dc.subjectChildhood acute lymphoblastic leukemia
dc.subjectDecreasing dexamethasone dose
dc.subjectIsolated cns relapse
dc.subjectLebanon
dc.subjectAdolescent
dc.subjectAntineoplastic combined chemotherapy protocols
dc.subjectCase-control studies
dc.subjectCentral nervous system neoplasms
dc.subjectChild
dc.subjectChild, preschool
dc.subjectDexamethasone
dc.subjectDose-response relationship, drug
dc.subjectFemale
dc.subjectFollow-up studies
dc.subjectHumans
dc.subjectIncidence
dc.subjectInfant
dc.subjectMale
dc.subjectMethotrexate
dc.subjectNeoplasm recurrence, local
dc.subjectNon-randomized controlled trials as topic
dc.subjectPrecursor cell lymphoblastic leukemia-lymphoma
dc.subjectPrognosis
dc.subjectProspective studies
dc.subjectSurvival rate
dc.subjectAsparaginase
dc.subjectCyclophosphamide
dc.subjectCytarabine
dc.subjectDaunorubicin
dc.subjectDoxorubicin
dc.subjectMercaptopurine
dc.subjectPrednisone
dc.subjectVincristine
dc.subjectAntineoplastic agent
dc.subjectAcute lymphoblastic leukemia
dc.subjectAdult
dc.subjectArticle
dc.subjectCancer risk
dc.subjectCentral nervous system disease
dc.subjectDrug dose reduction
dc.subjectDrug megadose
dc.subjectDrug withdrawal
dc.subjectHuman
dc.subjectIsolated central nervous system relapse
dc.subjectLife threat
dc.subjectLow risk patient
dc.subjectMaintenance therapy
dc.subjectMajor clinical study
dc.subjectMultiple cycle treatment
dc.subjectPediatric hospital
dc.subjectPriority journal
dc.subjectProspective study
dc.subjectTreatment duration
dc.subjectVirus infection
dc.subjectCase control study
dc.subjectCentral nervous system tumor
dc.subjectControlled clinical trial (topic)
dc.subjectDose response
dc.subjectFollow up
dc.subjectPathology
dc.subjectPreschool child
dc.subjectTumor recurrence
dc.titleIsolated central nervous system relapse following treatment reduction in low-risk acute lymphoblastic leukemia at the children's cancer center of lebanon
dc.typeArticle

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