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Intensified First Cycle of Rituximab Plus Eight Cycles of Cyclophosphamide, Doxorubicin, Vincristine, and Prednisolone with Rituximab Chemotherapy for Advanced-Stage or Bulky Diffuse Large B-Cell Lymphoma: A Multicenter Phase II Consortium for Improving Survival of Lymphoma (CISL) Study

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dc.contributor.authorKim, Yu Ri-
dc.contributor.authorKim, Jin Seok-
dc.contributor.authorKim, Won Seog-
dc.contributor.authorEom, Hyeon Seok-
dc.contributor.authorYang, Deok-Hwan-
dc.contributor.authorBae, Sung Hwa-
dc.contributor.authorKim, Hyo Jung-
dc.contributor.authorLee, Jae Hoon-
dc.contributor.authorOh, Suk-Joong-
dc.contributor.authorYoon, Sung -Soo-
dc.contributor.authorKwak, Jae-Yong-
dc.contributor.authorChoi, Chul Won-
dc.contributor.authorKim, Min Kyoung-
dc.contributor.authorOh, Sung Young-
dc.contributor.authorKang, Hye Jin-
dc.contributor.authorNam, Seung Hyun-
dc.contributor.authorShim, Hyeok-
dc.contributor.authorPark, Joon Seong-
dc.contributor.authorMun, Yeung-Chul-
dc.contributor.authorSuh, Cheolwon-
dc.date.accessioned2023-12-15T15:10:32Z-
dc.date.available2023-12-15T15:10:32Z-
dc.date.issued2023-10-
dc.identifier.issn1598-2998-
dc.identifier.issn2005-9256-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/89611-
dc.description.abstractPurpose This phase II, open-label, multicenter study aimed to investigate the efficacy and safety of a rituximab intensification for the 1st cycle with every 21-day of rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisolone (R-CHOP-21) among patients with previously untreated advanced-stage or bulky diffuse large B-cell lymphoma (DLBCL).Materials and Methods Ninety-two patients with stage III/IV or bulky DLBCL from 21 institutions were administered 8 cycles of R -CHOP-21 with an additional one dose of rituximab intensification on day 0 of the 1st cycle (RR-CHOP). The primary endpoint was a complete response (CR) rate after 3 cycles of chemotherapy.Results Among the 92 DLBCL patients assessed herein, the response rate after 3 cycles of chemotherapy was 88.0% (38.0% CR+50.0% partial response [PR]). After the completion of 8 cycles of chemotherapy, the overall response rate was observed for 68.4% (58.7% CR+9.8% PR). The 3-year progression-free survival rate was 64.0%, and the 3-year overall survival rate was 70.4%. Febrile neutropenia was one of the most frequent >= grade 3 adverse events (40.0%) and five treatment-related deaths occurred. Compared with the clinical outcomes of patients who received R-CHOP chemotherapy as a historical control, the interim CR rate was higher in male patients with RR-CHOP (20.5% vs. 48.8%, p=0.016).Conclusion Rituximab intensification on days 0 to the 1st cycle of the standard 8 cycles R-CHOP-21 for advanced DLBCL yielded favorable response rates after the 3 cycles of chemotherapy and acceptable toxicities, especially for male patients (ClinicalTrials.gov ID: NCT01054781).-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherKOREAN CANCER ASSOCIATION-
dc.titleIntensified First Cycle of Rituximab Plus Eight Cycles of Cyclophosphamide, Doxorubicin, Vincristine, and Prednisolone with Rituximab Chemotherapy for Advanced-Stage or Bulky Diffuse Large B-Cell Lymphoma: A Multicenter Phase II Consortium for Improving Survival of Lymphoma (CISL) Study-
dc.typeArticle-
dc.identifier.wosid001087738400028-
dc.identifier.doi10.4143/crt.2023.271-
dc.identifier.bibliographicCitationCANCER RESEARCH AND TREATMENT, v.55, no.4, pp 1355 - 1362-
dc.identifier.kciidART003005746-
dc.description.isOpenAccessY-
dc.identifier.scopusid2-s2.0-85175118829-
dc.citation.endPage1362-
dc.citation.startPage1355-
dc.citation.titleCANCER RESEARCH AND TREATMENT-
dc.citation.volume55-
dc.citation.number4-
dc.type.docTypeArticle-
dc.publisher.location대한민국-
dc.subject.keywordAuthorRituximab-
dc.subject.keywordAuthorDiffuse large B -cell lymphoma-
dc.subject.keywordAuthorR -CHOP-
dc.subject.keywordAuthorResponse-
dc.subject.keywordPlusCHOP-LIKE CHEMOTHERAPY-
dc.subject.keywordPlusDOSE-DENSE RITUXIMAB-
dc.subject.keywordPlusRANDOMIZED CONTROLLED-TRIAL-
dc.subject.keywordPlusNON-HODGKIN-LYMPHOMA-
dc.subject.keywordPlusYOUNG-PATIENTS-
dc.subject.keywordPlusR-CHOP-
dc.subject.keywordPlusELDERLY-PATIENTS-
dc.subject.keywordPlusMALE GENDER-
dc.subject.keywordPlusDLBCL-
dc.subject.keywordPlusOPTIMIZATION-
dc.relation.journalResearchAreaOncology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
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