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재발성/불응성 소아 급성림프모구백혈병 환자의 치료 경향 및 성적에 대한 다기관 후향적 관찰 연구

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dc.contributor.author유건희-
dc.contributor.author정낙균-
dc.contributor.author조빈-
dc.contributor.author강형진-
dc.contributor.author신희영-
dc.contributor.author임호준-
dc.contributor.author서종진-
dc.contributor.author임영탁-
dc.contributor.author유철주-
dc.contributor.author김순기-
dc.contributor.author전인상-
dc.contributor.author국훈-
dc.contributor.author구홍회-
dc.date.available2020-02-27T20:43:59Z-
dc.date.created2020-02-12-
dc.date.issued2017-
dc.identifier.issn2233-5250-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/6776-
dc.description.abstractBackground: Although the overall survival of childhood acute lymphoblastic leukemia (ALL) approaches 85-90%, the prognosis of relapsed or refractory (R/R) ALL is grave. This study aimed to identify the treatment pattern, treatment response, and overall survival of these patients. Methods: We reviewed data of 64 patients with R/R ALL whose initial diagnosis of ALL had been made between 1 and 21 years of age. Patients who received clofarabine as part of an induction regimen were excluded. Relapsed patients were limited to those who relapsed after ≥2 prior induction regimens. Treatment patterns, response rates, and overall survival were analyzed. Results: Patients’ median age was 15.0 years (range, 6.0-25.0) at the diagnosis of R/R ALL. The most frequently used agents other than steroid were vincristine (54.0%), cytarabine (44.6%), and idarubicin (36.5%), while L-asparaginase was used in only one patient. The complete remission (CR) and overall response (OR) rates were 38.1 and 42.9%, respectively. Sixteen patients (25.4%) underwent allogeneic hematopoietic stem cell transplantation (HSCT). The 5-year overall survival was 6.7%. The survival of patients with HSCT was significantly higher compared with those without HSCT (35.2% vs 0%, P=0.0097). Among 14 patients who achieved CR or CR without platelet recovery (CRp) before HSCT, the 3-year survival was 46.9%. Conclusion: The survival of Korean patients with R/R childhood ALL was dismal despite a reasonable CR rate, whereas that of those who received HSCT after CR or CRp was excellent. More treatment options are needed to improve the overall outcome of R/R childhood ALL.-
dc.language한국어-
dc.language.isoko-
dc.publisher대한소아혈액종양학회-
dc.relation.isPartOfClinical Pediatric Hematology-Oncology-
dc.title재발성/불응성 소아 급성림프모구백혈병 환자의 치료 경향 및 성적에 대한 다기관 후향적 관찰 연구-
dc.title.alternativeA Multicenter Retrospective Analysis on the Treatment Pattern and Outcome in Relapsed/Refractory Childhood Acute Lymphoblastic Leukemia-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass2-
dc.identifier.doi10.15264/cpho.2017.24.2.101-
dc.identifier.bibliographicCitationClinical Pediatric Hematology-Oncology, v.24, no.2, pp.101 - 106-
dc.identifier.kciidART002276355-
dc.citation.endPage106-
dc.citation.startPage101-
dc.citation.titleClinical Pediatric Hematology-Oncology-
dc.citation.volume24-
dc.citation.number2-
dc.contributor.affiliatedAuthor전인상-
dc.subject.keywordAuthorChildhood-
dc.subject.keywordAuthorAcute lymphoblastic leukemia-
dc.subject.keywordAuthorRelapsed-
dc.subject.keywordAuthorRefractory-
dc.description.journalRegisteredClasskci-
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