Cited 50 times in

Minimal residual disease-based effect and long-term outcome of first-line dasatinib combined with chemotherapy for adult Philadelphia chromosome-positive acute lymphoblastic leukemia

DC Field Value Language
dc.contributor.author김수정-
dc.contributor.author김진석-
dc.date.accessioned2017-10-26T08:00:17Z-
dc.date.available2017-10-26T08:00:17Z-
dc.date.issued2016-
dc.identifier.issn0923-7534-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/152802-
dc.description.abstractBACKGROUND: The use of imatinib combined with chemotherapy has demonstrated improved outcome in adults with Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph-positive ALL). However, a substantial proportion of patients continue to die as a result of disease progression. PATIENTS AND METHODS: We assessed the minimal residual disease (MRD)-based effect and long-term outcome of first-line incorporation of dasatinib (100 mg once daily) into chemotherapy alternatively for adults with Ph-positive ALL. The primary end point was the major molecular response (MMR) rate by the end of the second dasatinib cycle. Patients with a donor proceeded to allogeneic stem cell transplantation (SCT) as early as possible. MRD monitoring was centrally evaluated by real-time quantitative polymerase chain reaction (4.5-log sensitivity) using bone marrow samples. RESULTS: Fifty-one patients (median age, 46 years) were enrolled and treated with this strategy. After the first dasatinib cycle, 50 patients (98.0%) achieved complete remission (CR). By the end of the second dasatinib cycle, 46 (93.9%) of 49 assessable patients had persistent CR, and 38 (77.6%) had MMR (32.7%) or undetectable MRD (44.9%). On the basis of the MRD kinetics by this time point, the numbers of early-stable, late, and poor molecular responders were 23 (46.9%), 15 (30.7%), and 11 (22.4%), respectively. Thirty-nine patients (76.5%) underwent allogeneic SCT in CR1. After a median follow-up of 54 months, the 4-year cumulative incidence of relapse and disease-free survival (DFS) rate for all patients were 30.0% and 52.0%, respectively, and the corresponding outcomes among those receiving allogeneic SCT in CR1 were 20.5% and 64.1%, respectively. Poor molecular responders had a higher risk of relapse and DFS than those of early-stable molecular responders. CONCLUSION: This dasatinib-based protocol was effective for achieving a good quality molecular response and durable DFS in adults with Ph-positive ALL.-
dc.description.statementOfResponsibilityrestriction-
dc.publisherOxford University Press-
dc.relation.isPartOfANNALS OF ONCOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHDasatinib/administration & dosage*-
dc.subject.MESHDisease-Free Survival-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHLeukemia, Myelogenous, Chronic, BCR-ABL Positive/epidemiology-
dc.subject.MESHLeukemia, Myelogenous, Chronic, BCR-ABL Positive/pathology-
dc.subject.MESHLeukemia, Myelogenous, Chronic, BCR-ABL Positive/therapy*-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHNeoplasm, Residual/epidemiology-
dc.subject.MESHNeoplasm, Residual/pathology*-
dc.subject.MESHPhiladelphia Chromosome-
dc.subject.MESHPrecursor Cell Lymphoblastic Leukemia-Lymphoma/epidemiology-
dc.subject.MESHPrecursor Cell Lymphoblastic Leukemia-Lymphoma/pathology-
dc.subject.MESHPrecursor Cell Lymphoblastic Leukemia-Lymphoma/therapy*-
dc.subject.MESHRemission Induction-
dc.subject.MESHStem Cell Transplantation-
dc.subject.MESHTransplantation, Homologous-
dc.subject.MESHTreatment Outcome-
dc.titleMinimal residual disease-based effect and long-term outcome of first-line dasatinib combined with chemotherapy for adult Philadelphia chromosome-positive acute lymphoblastic leukemia-
dc.typeArticle-
dc.publisher.locationEngland-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Internal Medicine-
dc.contributor.googleauthorJ.-H. Yoon-
dc.contributor.googleauthorH-Y. Yhim-
dc.contributor.googleauthorJ-Y. Kwak-
dc.contributor.googleauthorJ.-S. Ahn-
dc.contributor.googleauthorD.-H. Yang-
dc.contributor.googleauthorJ.-J. Lee-
dc.contributor.googleauthorS.-J. Kim-
dc.contributor.googleauthorJ.-S. Kim-
dc.contributor.googleauthorS. J. Park-
dc.contributor.googleauthorC.W. Choi-
dc.contributor.googleauthorH.-S. Eom-
dc.contributor.googleauthorS.-K. Park-
dc.contributor.googleauthorS.-Y. Choi-
dc.contributor.googleauthorS.-H. Kim-
dc.contributor.googleauthorD.-W. Kim-
dc.contributor.googleauthorS. Lee-
dc.identifier.doi10.1093/annonc/mdw123-
dc.contributor.localIdA00633-
dc.contributor.localIdA01017-
dc.relation.journalcodeJ00171-
dc.identifier.eissn1569-8041-
dc.identifier.pmid26951627-
dc.identifier.urlhttps://academic.oup.com/annonc/article-lookup/doi/10.1093/annonc/mdw123-
dc.subject.keywordPhiladelphia chromosome-
dc.subject.keywordacute lymphoblastic leukemia-
dc.subject.keywordallogeneic stem cell transplantation-
dc.subject.keyworddasatinib-
dc.subject.keywordminimal residual disease-
dc.contributor.alternativeNameKim, Soo Jeong-
dc.contributor.alternativeNameKim, Jin Seok-
dc.contributor.affiliatedAuthorKim, Soo Jeong-
dc.contributor.affiliatedAuthorKim, Jin Seok-
dc.citation.volume27-
dc.citation.number6-
dc.citation.startPage1081-
dc.citation.endPage1088-
dc.identifier.bibliographicCitationANNALS OF ONCOLOGY, Vol.27(6) : 1081-1088, 2016-
dc.date.modified2017-10-24-
dc.identifier.rimsid40434-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.