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Pegfilgrastim Prophylaxis Is Effective in the Prevention of Febrile Neutropenia and Reduces Mortality in Patients Aged ≥ 75 Years with Diffuse Large B-Cell Lymphoma Treated with R-CHOP: A Prospective Cohort Study

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dc.contributor.authorJeong, SH-
dc.contributor.authorKim, SJ-
dc.contributor.authorYoon, DH-
dc.contributor.authorPark, Y-
dc.contributor.authorKang, HJ-
dc.contributor.authorKoh, Y-
dc.contributor.authorLee, GW-
dc.contributor.authorLee, WS-
dc.contributor.authorYang, DH-
dc.contributor.authorDo, YR-
dc.contributor.authorKim, MK-
dc.contributor.authorYoo, KH-
dc.contributor.authorChoi, YS-
dc.contributor.authorYun, HJ-
dc.contributor.authorYi, JH-
dc.contributor.authorJo, JC-
dc.contributor.authorEom, HS-
dc.contributor.authorKwak, JY-
dc.contributor.authorShin, HJ-
dc.contributor.authorPark, BB-
dc.contributor.authorHyun, SY-
dc.contributor.authorYi, SY-
dc.contributor.authorKwon, JH-
dc.contributor.authorOh, SY-
dc.contributor.authorKim, HJ-
dc.contributor.authorSohn, BS-
dc.contributor.authorWon, JH-
dc.contributor.authorKim, SH-
dc.contributor.authorLee, HS-
dc.contributor.authorSuh, C-
dc.contributor.authorKim, WS-
dc.date.accessioned2023-02-21T04:34:07Z-
dc.date.available2023-02-21T04:34:07Z-
dc.date.issued2022-
dc.identifier.issn1598-2998-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/24794-
dc.description.abstractPURPOSE: Febrile neutropenia (FN) can cause suboptimal treatment and treatment-related mortality (TRM) in diffuse large B-cell lymphoma (DLBCL) patients treated with rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisolone (R-CHOP).
MATERIALS AND METHODS: We conducted a prospective cohort study to evaluate the effectiveness of pegfilgrastim prophylaxis in DLBCL patients receiving R-CHOP, and we compared them with the PROCESS cohort (n=485).
RESULTS: Since January 2015, 986 patients with DLBCL were enrolled. Pegfilgrastim was administered at least once in 930 patients (94.3%), covering 90.3% of all cycles. FN developed in 137 patients (13.9%) in this cohort (23.7% in the PROCESS cohort, p<0.001), and 4.2% of all cycles (10.2% in the PROCESS cohort, p<0.001). Dose delay was less common (>/=3 days: 18.1% vs. 23.7%, p=0.015; >/=5 days: 12.0% vs. 18.3%, p=0.023) in this cohort than in the PROCESS cohort. The incidence of TRM (3.2% vs. 5.6%, p=0.047) and infection-related death (1.8% vs. 4.5%, p=0.004) was lower in this cohort than in the PROCESS cohort. The 4-year overall survival (OS) and progression-free survival (PFS) rates of the two cohorts were not different (OS: 73.0% vs. 71.9%, p=0.545; PFS: 69.5% vs. 68.8%, p=0.616). However, in patients aged >/=75 years, the 4-year OS and PFS rates were higher in this cohort than in the PROCESS cohort (OS: 49.6% vs. 33.7%, p=0.032; PFS: 44.2% vs. 30.3% p=0.047).
CONCLUSION: Pegfilgrastim prophylaxis is effective in the prevention of FN and infection-related death in DLBCL patients receiving R-CHOP, and it also improves OS in patients aged >/=75 years.
en
dc.formatapplication/pdf-
dc.language.isoen-
dc.subject.MESHAged-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols-
dc.subject.MESHCyclophosphamide-
dc.subject.MESHDoxorubicin-
dc.subject.MESHFebrile Neutropenia-
dc.subject.MESHFilgrastim-
dc.subject.MESHGranulocyte Colony-Stimulating Factor-
dc.subject.MESHHumans-
dc.subject.MESHLymphoma, Large B-Cell, Diffuse-
dc.subject.MESHPolyethylene Glycols-
dc.subject.MESHPrednisolone-
dc.subject.MESHPrednisone-
dc.subject.MESHProspective Studies-
dc.subject.MESHRituximab-
dc.subject.MESHVincristine-
dc.titlePegfilgrastim Prophylaxis Is Effective in the Prevention of Febrile Neutropenia and Reduces Mortality in Patients Aged ≥ 75 Years with Diffuse Large B-Cell Lymphoma Treated with R-CHOP: A Prospective Cohort Study-
dc.typeArticle-
dc.identifier.pmid34990525-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9582490-
dc.subject.keywordDiffuse large B-cell lymphoma-
dc.subject.keywordPegfilgrastim-
dc.subject.keywordProphylaxis-
dc.contributor.affiliatedAuthor정, 성현-
dc.contributor.affiliatedAuthor최, 윤석-
dc.type.localJournal Papers-
dc.identifier.doi10.4143/crt.2021.1168-
dc.citation.titleCancer research and treatment-
dc.citation.volume54-
dc.citation.number4-
dc.citation.date2022-
dc.citation.startPage1268-
dc.citation.endPage1277-
dc.identifier.bibliographicCitationCancer research and treatment, 54(4). : 1268-1277, 2022-
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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