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Phase II trial of concurrent chemoradiotherapy with L-asparaginase and MIDLE chemotherapy for newly diagnosed stage I/II extranodal NK/T-cell lymphoma, nasal type (CISL-1008)

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dc.contributor.authorYoon, DH-
dc.contributor.authorKim, SJ-
dc.contributor.authorJeong, SH-
dc.contributor.authorShin, DY-
dc.contributor.authorBae, SH-
dc.contributor.authorHong, J-
dc.contributor.authorPark, SK-
dc.contributor.authorYhim, HY-
dc.contributor.authorYang, DH-
dc.contributor.authorLee, H-
dc.contributor.authorKang, HJ-
dc.contributor.authorLee, MH-
dc.contributor.authorEom, HS-
dc.contributor.authorKwak, JY-
dc.contributor.authorLee, JH-
dc.contributor.authorSuh, C-
dc.contributor.authorKim, WS-
dc.date.accessioned2018-05-04T00:25:59Z-
dc.date.available2018-05-04T00:25:59Z-
dc.date.issued2016-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/15073-
dc.description.abstractWe designed a new treatment protocol incorporating concurrent administration of L-asparaginase (to reduce the probability of systemic progression during concurrent chemoradiotherapy (CCRT)) plus high-dose methotrexate to consolidation chemotherapy to intensify the regimen for treating localized extranodal NK/T cell lymphoma, nasal type (ENKTL). CCRT comprised radiation (36-44 Gy) with weekly cisplatin (30 mg/m2) and tri-weekly L-asparaginase (4 000 IU). Chemotherapy-MIDLE (methotrexate 3 g/m2 on day 1, etoposide 100 mg/m2 and Ifosfamide 1 000 mg/m2 on days 2-3, dexamethasone 40 mg on days 1-4, and L-asparaginase 6 000 IU/m2 on days 4, 6, 8, 10)-was repeated every 28 days for two cycles. One of the 28 patients developed distant lesions after CCRT. The final complete response rate was 82.1%. Four patients dropped out during or after their first MIDLE cycle due to toxicities (recurrent G3 hyperbilirubinemia [n = 1], G3-5 increased creatinine [n = 2], and G5 infection [n = 1]). With a median follow-up of 46 months (95% CI: 39-47 months), the estimated 3-year progression-free survival rate and overall survival rate were 74.1% and 81.5%, respectively. This MIDLE protocol may be effective for localized ENKTL. However, concurrent administration of L-asparaginase during CCRT does not seem to provide additional benefits.-
dc.language.isoen-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols-
dc.subject.MESHAsparaginase-
dc.subject.MESHChemoradiotherapy-
dc.subject.MESHCisplatin-
dc.subject.MESHDexamethasone-
dc.subject.MESHDisease Progression-
dc.subject.MESHDisease-Free Survival-
dc.subject.MESHDrug Administration Schedule-
dc.subject.MESHEtoposide-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHIfosfamide-
dc.subject.MESHKaplan-Meier Estimate-
dc.subject.MESHLymphoma, Extranodal NK-T-Cell-
dc.subject.MESHMale-
dc.subject.MESHMethotrexate-
dc.subject.MESHMiddle Aged-
dc.subject.MESHNeoplasm Staging-
dc.subject.MESHRadiotherapy Dosage-
dc.subject.MESHRadiotherapy, Conformal-
dc.subject.MESHRepublic of Korea-
dc.subject.MESHTime Factors-
dc.subject.MESHTreatment Outcome-
dc.titlePhase II trial of concurrent chemoradiotherapy with L-asparaginase and MIDLE chemotherapy for newly diagnosed stage I/II extranodal NK/T-cell lymphoma, nasal type (CISL-1008)-
dc.typeArticle-
dc.identifier.pmid27542213-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5356760/-
dc.contributor.affiliatedAuthor정, 성현-
dc.type.localJournal Papers-
dc.identifier.doi10.18632/oncotarget.11319-
dc.citation.titleOncotarget-
dc.citation.volume7-
dc.citation.number51-
dc.citation.date2016-
dc.citation.startPage85584-
dc.citation.endPage85591-
dc.identifier.bibliographicCitationOncotarget, 7(51). : 85584-85591, 2016-
dc.identifier.eissn1949-2553-
dc.relation.journalidJ019492553-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Hematology-Oncology
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