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Geriatric risk model for older patients with diffuse large B-cell lymphoma (GERIAD): a prospective multicenter cohort study

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dc.contributor.authorYhim, HY-
dc.contributor.authorPark, Y-
dc.contributor.authorKim, JA-
dc.contributor.authorShin, HJ-
dc.contributor.authorDo, YR-
dc.contributor.authorMoon, JH-
dc.contributor.authorKim, MK-
dc.contributor.authorLee, WS-
dc.contributor.authorKim, DS-
dc.contributor.authorLee, MW-
dc.contributor.authorChoi, YS-
dc.contributor.authorJeong, SH-
dc.contributor.authorKim, KH-
dc.contributor.authorKim, J-
dc.contributor.authorLee, CH-
dc.contributor.authorSong, GY-
dc.contributor.authorYang, DH-
dc.contributor.authorKwak, JY-
dc.date.accessioned2024-07-05T01:28:06Z-
dc.date.available2024-07-05T01:28:06Z-
dc.date.issued2024-
dc.identifier.issn1226-3303-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/32614-
dc.description.abstractBackground/Aims: Optimal risk stratification based on simplified geriatric assessment to predict treatment-related toxicity and survival needs to be clarified in older patients with diffuse large B-cell lymphoma (DLBCL). Methods: This multicenter prospective cohort study enrolled newly diagnosed patients with DLBCL (≥ 65 yr) between September 2015 and April 2018. A simplified geriatric assessment was performed at baseline using Activities of Daily Living (ADL), Instrumental ADL (IADL), and Charlson’s Comorbidity Index (CCI). The primary endpoint was event-free survival (EFS). Results: The study included 249 patients, the median age was 74 years (range, 65-88), and 125 (50.2%) were female. In multivariable Cox analysis, ADL, IADL, CCI, and age were independent factors for EFS; an integrated geriatric score was derived and the patients stratified into three geriatric categories: fit (n = 162, 65.1%), intermediate-fit (n = 25, 10.0%), and frail (n = 62, 24.9%). The established geriatric model was significantly associated with EFS (fit vs. intermediate-fit, HR 2.61, p < 0.001; fit vs. frail, HR 4.61, p < 0.001) and outperformed each covariate alone or in combination. In 87 intermediate-fit or frail patients, the relative doxorubicin dose intensity (RDDI) ≥ 62.4% was significantly associated with worse EFS (HR, 2.15, 95% CI 1.30–3.53, p = 0.002). It was related with a higher incidence of grade ≥ 3 symptomatic non-hematologic toxicities (63.2% vs. 27.8%, p < 0.001) and earlier treatment discontinuation (34.5% vs. 8.0%, p < 0.001) in patients with RDDI ≥ 62.4% than in those with RDDI < 62.4%. Conclusions: This model integrating simplified geriatric assessment can risk-stratify older patients with DLBCL and identify those who are highly vulnerable to standard dose-intensity chemoimmunotherapy.-
dc.language.isoen-
dc.subject.MESHActivities of Daily Living-
dc.subject.MESHAge Factors-
dc.subject.MESHAged-
dc.subject.MESHAged, 80 and over-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols-
dc.subject.MESHComorbidity-
dc.subject.MESHDecision Support Techniques-
dc.subject.MESHDoxorubicin-
dc.subject.MESHFemale-
dc.subject.MESHFrail Elderly-
dc.subject.MESHFrailty-
dc.subject.MESHGeriatric Assessment-
dc.subject.MESHHumans-
dc.subject.MESHLymphoma, Large B-Cell, Diffuse-
dc.subject.MESHMale-
dc.subject.MESHPredictive Value of Tests-
dc.subject.MESHProgression-Free Survival-
dc.subject.MESHProspective Studies-
dc.subject.MESHRepublic of Korea-
dc.subject.MESHRisk Assessment-
dc.subject.MESHRisk Factors-
dc.subject.MESHTime Factors-
dc.titleGeriatric risk model for older patients with diffuse large B-cell lymphoma (GERIAD): a prospective multicenter cohort study-
dc.typeArticle-
dc.identifier.pmid38287501-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11076889-
dc.subject.keywordDiffuse large B-cell lymphoma-
dc.subject.keywordDose intensity-
dc.subject.keywordPrognosis-
dc.subject.keywordSimplified geriatric assessment-
dc.subject.keywordToxicity-
dc.contributor.affiliatedAuthorChoi, YS-
dc.contributor.affiliatedAuthorJeong, SH-
dc.type.localJournal Papers-
dc.identifier.doi10.3904/kjim.2023.265-
dc.citation.titleThe Korean journal of internal medicine-
dc.citation.volume39-
dc.citation.number3-
dc.citation.date2024-
dc.citation.startPage501-
dc.citation.endPage512-
dc.identifier.bibliographicCitationThe Korean journal of internal medicine, 39(3). : 501-512, 2024-
dc.identifier.eissn2005-6648-
dc.relation.journalidJ012263303-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Hematology-Oncology
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