Evidence map›Paper›PMID 42035062›Full record

ArticleBMC cancer2026

Geriatric assessment-based therapy for older patients with diffuse large B-cell lymphoma: results of a two-decade clinical experience.

Hironao Nukariya, Shinsaku Washinosu, Haruna Nishimaki-Watanabe, Takashi Ichinohe, Shun Ito, Toshihide Endo, Kazuya Kurihara, Yuichi Takeuchi, Takashi Koike, Takashi Hamada and 9 more

Abstract read
In one paragraph

Article in BMC cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors.

Hironao NukariyaDivision of Hematology and Rheumatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.
Shinsaku WashinosuTumor Center, Nihon University Itabashi Hospital, 30-1 Oyaguchikamicho, Itabashi City, Tokyo, 173-8610, Japan.
Haruna Nishimaki-WatanabeDivision of Oncologic Pathology, Department of Pathology and Microbiology, Nihon University School of Medicine, Tokyo, Japan.
Takashi IchinoheDivision of Hematology and Rheumatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.
Shun ItoDivision of Hematology and Rheumatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.
Toshihide EndoDivision of Hematology and Rheumatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.
Kazuya KuriharaDivision of Hematology and Rheumatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.
Yuichi TakeuchiDivision of Hematology and Rheumatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.
Takashi KoikeDivision of Hematology and Rheumatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.
Takashi HamadaDivision of Hematology and Rheumatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.
Shimon OtakeDivision of Hematology and Rheumatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.
Hiromichi TakahashiDivision of Hematology and Rheumatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.
Masaru NakagawaDepartment of Hematology, Kasukabe Medical Center, Saitama, Japan.
Noriyoshi IriyamaDepartment of Hematology and Rheumatology, NHO Saitama Hospital, Saitama, Japan.
Daisuke TsutsumiTumor Center, Nihon University Itabashi Hospital, 30-1 Oyaguchikamicho, Itabashi City, Tokyo, 173-8610, Japan.
Akihiro UchiikeTumor Center, Nihon University Itabashi Hospital, 30-1 Oyaguchikamicho, Itabashi City, Tokyo, 173-8610, Japan.
Tatsuya HayamaTumor Center, Nihon University Itabashi Hospital, 30-1 Oyaguchikamicho, Itabashi City, Tokyo, 173-8610, Japan.
Hideki NakamuraDivision of Hematology and Rheumatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.
Katsuhiro MiuraDivision of Hematology and Rheumatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan. miura.katsuhiro@nihon-u.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTreating older patients with diffuse large B-cell lymphoma (DLBCL) is challenging due to heterogeneity in fitness and tolerance to chemotherapy with rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisolone (R-CHOP). Thus, we previously established the Age, Comorbidity, and Albumin (ACA) index for this population, a geriatric assessment comprising four categories. However, its role in treatment decision-making remains unclear.

methodsWe conducted a retrospective study in patients ≥ 65 years old with DLBCL who were treated with R-CHOP between 2015 and 2022 (post-ACA cohort), evaluating initial dose intensity (IDI), relative dose intensity (RDI), and 2-year overall survival (OS). During this period, dose intensities of cytotoxic drugs were adjusted by the multidisciplinary oncology team according to the ACA index categories (Excellent, Good, Moderate, and Poor). Then, we compared these outcomes with a historical cohort of patients receiving R-CHOP between 2001 and 2012 (pre-ACA cohort), where the dose intensities were determined by each physician’s discretion. Propensity score matching (PSM), adjusted for the International Prognostic Index and the ACA index, was used to balance baseline characteristics between the cohorts.

resultsIn the post-ACA cohort comprising 135 patients with a median age of 76 years (range: 65–91 years), the median IDI, median RDI, and 2-year OS according to the aforementioned ACA categories were 97%, 80%, 70%, and 70% (p < 0.001); 93%, 78%, 62%, and 59% (p < 0.001); and 96%, 89%, 66%, and 51% (p < 0.001), respectively. After PSM, 98 patients from the pre- and post-ACA cohorts were paired. Despite well-balanced patient demographics, granulocyte-colony stimulating factor prophylaxis was more commonly used in the post-ACA group (100% vs. 49%, p < 0.001). Consequently, the post-ACA group had higher median IDI and RDI (80% vs. 68%, p < 0.001, and 77% vs. 47%, p < 0.001, respectively) and better 2-year OS (81% vs. 66%, p = 0.014).

conclusionsThe ACA index can serve as a feasible standard-of-care framework for individualized dose intensity adjustment in older patients with DLBCL. Although this strategy organizes treatment decision-making, vulnerable patients still exhibit significantly inferior outcomes, highlighting the need for further therapeutic optimization and novel strategies.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsGeriatric AssessmentLymphoma, Large B-Cell, DiffuseAgedAged, 80 and overComorbidityCyclophosphamideDoxorubicinFemaleHumansMalePrednisonePrognosisRetrospective StudiesRituximabTreatment OutcomeCyclophosphamideDoxorubicinPrednisoneR-CHOP protocolRituximabVincristineAlbuminComorbidityDiffuse large B-cell lymphomaGeriatric assessmentOlder patientsR-CHOP

Identifiers

PMID42035062
PMCPMC13251149

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.