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R-CHOP chemoimmunotherapy followed by autologous transplantation for the treatment of diffuse large B-cell lymphoma

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dc.contributor.authorLee, Hong Ghi-
dc.contributor.authorChoi, Yunsuk-
dc.contributor.authorKim, Sung-Yong-
dc.contributor.authorKim, Inho-
dc.contributor.authorKim, Yeo-Kyeoung-
dc.contributor.authorKim, Yang Soo-
dc.contributor.authorLee, Ho Sup-
dc.contributor.authorKim, Seok Jin-
dc.contributor.authorKim, Jeong-A-
dc.contributor.authorPark, Byeong-Bae-
dc.contributor.authorPark, Jinny-
dc.contributor.authorShim, Hyeok-
dc.contributor.authorEom, Hyeon Seok-
dc.contributor.authorLee, Junglim-
dc.contributor.authorPark, Sung Kyu-
dc.contributor.authorCheong, June-Won-
dc.contributor.authorPark, Keon Woo-
dc.date.accessioned2022-07-16T04:26:09Z-
dc.date.available2022-07-16T04:26:09Z-
dc.date.created2021-05-13-
dc.date.issued2014-06-
dc.identifier.issn2287-979X-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/159779-
dc.description.abstractBackground: We investigated factors that influence outcomes in diffuse large B-cell lymphoma (DLBCL) patients treated with rituximab combined with the CHOP regimen (R-CHOP) followed by upfront autologous stem cell transplantation (Auto-SCT). Methods: We retrospectively evaluated survival differences between subgroups based on the age-adjusted International Prognostic Index (aaIPI) and revised-IPI (R-IPI) at diagnosis, disease status, and positron emission tomographic/computerized tomographic (PET/CT) status at transplantation in 51 CD20-positive DLBCL patients treated with R-CHOP followed by upfront Auto-SCT. Results: Patients had either stage I/II bulky disease (5.9%) or stage III/IV disease (94.1%). The median patient age at diagnosis was 47 years (range, 22-66 years); 53.3% and 26.7% had high-intermediate and high risks according to aaIPI, respectively. At the time of Auto-SCT, 72.5% and 27.5% experienced complete (CR) and partial remission (PR) after R-CHOP, respectively. The median time from diagnosis to Auto-SCT was 7.27 months (range, 3.4-13.4 months). The 5-year overall (OS) and progression-free survival (PFS) were 77.3% and 72.4%, respectively. The 5-year OS and PFS rates according to aaIPI, R-IPI, and PET/CT status did not differ between the subgroups. More importantly, the 5-year OS and PFS rates of the patients who achieved PR at the time of Auto-SCT were not inferior to those of the patients who achieved CR (P=0.223 and 0.292, respectively). Conclusion: Survival was not influenced by the aaIPI and R-IPI at diagnosis, disease status, or PET/CT status at transplantation, suggesting that upfront Auto-SCT might overcome unfavorable outcomes attributed to PR after induction chemoimmunotherapy.-
dc.language영어-
dc.language.isoen-
dc.publisherKorean Society of Hematology-
dc.titleR-CHOP chemoimmunotherapy followed by autologous transplantation for the treatment of diffuse large B-cell lymphoma-
dc.typeArticle-
dc.contributor.affiliatedAuthorPark, Byeong-Bae-
dc.identifier.doi10.5045/br.2014.49.2.107-
dc.identifier.scopusid2-s2.0-84903534435-
dc.identifier.bibliographicCitationBlood Research, v.49, no.2, pp.107 - 114-
dc.relation.isPartOfBlood Research-
dc.citation.titleBlood Research-
dc.citation.volume49-
dc.citation.number2-
dc.citation.startPage107-
dc.citation.endPage114-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.identifier.kciidART001882811-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.subject.keywordPluscyclophosphamide-
dc.subject.keywordPlusdoxorubicin-
dc.subject.keywordPlusfluorodeoxyglucose f 18-
dc.subject.keywordPlusprednisolone-
dc.subject.keywordPlusrituximab-
dc.subject.keywordPlusvincristine-
dc.subject.keywordPlusadult-
dc.subject.keywordPlusaged-
dc.subject.keywordPlusarticle-
dc.subject.keywordPlusautologous stem cell transplantation-
dc.subject.keywordPluscancer combination chemotherapy-
dc.subject.keywordPluscancer grading-
dc.subject.keywordPluscancer immunotherapy-
dc.subject.keywordPluscancer radiotherapy-
dc.subject.keywordPluscancer recurrence-
dc.subject.keywordPluscancer regression-
dc.subject.keywordPluscancer risk-
dc.subject.keywordPluscancer survival-
dc.subject.keywordPluscause of death-
dc.subject.keywordPluscomputer assisted emission tomography-
dc.subject.keywordPluscontrolled study-
dc.subject.keywordPlusfemale-
dc.subject.keywordPlusfollow up-
dc.subject.keywordPlushuman-
dc.subject.keywordPlusInternational Prognostic Index-
dc.subject.keywordPluslactic acidosis-
dc.subject.keywordPluslarge cell lymphoma-
dc.subject.keywordPlusmajor clinical study-
dc.subject.keywordPlusmale-
dc.subject.keywordPlusoutcome assessment-
dc.subject.keywordPlusoverall survival-
dc.subject.keywordPluspneumonia-
dc.subject.keywordPlusprogression free survival-
dc.subject.keywordPlusretrospective study-
dc.subject.keywordPlussurvival rate-
dc.subject.keywordAuthorAutologous transplantation-
dc.subject.keywordAuthorDiffuse large B-cell lymphoma-
dc.subject.keywordAuthorHematopoietic stem cell transplantation-
dc.subject.keywordAuthorRituximab-
dc.subject.keywordAuthorSurvival analysis-
dc.identifier.urlhttps://synapse.koreamed.org/articles/1092131-
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