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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, YR-
dc.contributor.authorKim, JS-
dc.contributor.authorKim, WS-
dc.contributor.authorEom, HS-
dc.contributor.authorYang, DH-
dc.contributor.authorBae, SH-
dc.contributor.authorKim, HJ-
dc.contributor.authorLee, JH-
dc.contributor.authorOh, SJ-
dc.contributor.authorYoon, SS-
dc.contributor.authorKwak, JY-
dc.contributor.authorChoi, CW-
dc.contributor.authorKim, MK-
dc.contributor.authorOh, SY-
dc.contributor.authorKang, HJ-
dc.contributor.authorNam, SH-
dc.contributor.authorShim, H-
dc.contributor.authorPark, JS-
dc.contributor.authorMun, YC-
dc.contributor.authorSuh, C-
dc.contributor.authorKorean Society of Hematology Lymphoma Working Party-
dc.date.accessioned2023-12-11T05:42:45Z-
dc.date.available2023-12-11T05:42:45Z-
dc.date.issued2023-
dc.identifier.issn1598-2998-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/32045-
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 5 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.
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dc.language.isoen-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols-
dc.subject.MESHCyclophosphamide-
dc.subject.MESHDoxorubicin-
dc.subject.MESHHumans-
dc.subject.MESHLymphoma, Large B-Cell, Diffuse-
dc.subject.MESHMale-
dc.subject.MESHPrednisolone-
dc.subject.MESHRituximab-
dc.subject.MESHTreatment Outcome-
dc.subject.MESHVincristine-
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.pmid36996864-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10582534-
dc.subject.keywordDiffuse large B-cell lymphoma-
dc.subject.keywordR-CHOP-
dc.subject.keywordResponse-
dc.subject.keywordRituximab-
dc.contributor.affiliatedAuthorPark, JS-
dc.type.localJournal Papers-
dc.identifier.doi10.4143/crt.2023.271-
dc.citation.titleCancer research and treatment-
dc.citation.volume55-
dc.citation.number4-
dc.citation.date2023-
dc.citation.startPage1355-
dc.citation.endPage1362-
dc.identifier.bibliographicCitationCancer research and treatment, 55(4). : 1355-1362, 2023-
dc.identifier.eissn2005-9256-
dc.relation.journalidJ015982998-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Hematology-Oncology
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