Evidence map›Paper›PMID 41068304›Full record

ArticleAnnals of hematology2025

Polatuzumab vedotin, rituximab, cyclophosphamide, doxorubicin, and prednisone (Pola-R-CHP) therapy in diffuse large B-cell lymphoma in patients aged 80 years or older: a real-world study.

Toshiki Yamada, Nobuhiko Nakamura, Hideko Goto, Takeshi Hara, Senji Kasahara, Kenji Fukuno, Michio Sawada, Hiroshi Nakamura, Naoki Hayase, Takayuki Goto and 6 more

Abstract readMulticenter Study
In one paragraph

Article in Annals of hematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Article
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

16 authors.

Toshiki YamadaDepartment of Hematology, Gifu Prefectural General Medical Center, Gifu, Japan.
Nobuhiko NakamuraDepartment of Hematology and Infectious Disease, Gifu University Hospital, Gifu, Japan. nakamura.nobuhiko.s1@f.gifu-u.ac.jp.ORCID http://orcid.org/0000-0003-1682-7777
Hideko GotoDepartment of Hematology, Chuno Kosei Hospital, Gifu, Japan.
Takeshi HaraDepartment of Hematology and Oncology, Matsunami General Hospital, Gifu, Japan.
Senji KasaharaDepartment of Hematology, Gifu Municipal Hospital, Gifu, Japan.
Kenji FukunoDepartment of Hematology, Japanese Red Cross Takayama Hospital, Gifu, Japan.
Michio SawadaDepartment of Hematology, Japanese Red Cross Gifu Hospital, Gifu, Japan.
Hiroshi NakamuraDepartment of Hematology and Infectious Disease, Gifu University Hospital, Gifu, Japan.
Naoki HayaseDepartment of Hematology, Gifu Prefectural General Medical Center, Gifu, Japan.
Takayuki GotoDepartment of Hematology, Gifu Municipal Hospital, Gifu, Japan.
Tomomi SuzakiDepartment of Hematology, Gifu Municipal Hospital, Gifu, Japan.
Kei FujitaDepartment of Hematology and Oncology, Matsunami General Hospital, Gifu, Japan.
Shin LeeDepartment of Hematology and Oncology, Matsunami General Hospital, Gifu, Japan.
Nobuhiro KanemuraDepartment of Hematology and Infectious Disease, Gifu University Hospital, Gifu, Japan.
Masahito ShimizuDepartment of Hematology and Infectious Disease, Gifu University Hospital, Gifu, Japan.
Hisashi TsurumiDepartment of Hematology and Oncology, Matsunami General Hospital, Gifu, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diffuse large B-cell lymphoma (DLBCL) predominantly affects older adults, with an increasing proportion of patients aged ≥ 80 years. Although the POLARIX trial demonstrated improved progression-free survival with polatuzumab vedotin (Pola) combined with R-CHP (Pola-R-CHP), its applicability to very elderly patients remains unclear. A multicenter, retrospective, cohort study was conducted at seven hospitals in Japan, enrolling 172 previously untreated DLBCL patients who initiated Pola-R-CHP between August 1, 2022 and May 1, 2024. Patients were stratified by age (< 80 vs. ≥80 years). Initial dose intensity (IDI), average relative dose intensity (ARDI), treatment efficacy, and safety outcomes were evaluated. In patients aged ≥ 80 years (n = 44), the overall response rate (ORR) was 89.5%, comparable to the 97.3% in patients aged < 80 years. However, treatment-related mortality (TRM) was higher in the older group (11.4% vs. 2.3%). In this cohort, median IDI and ARDI for doxorubicin and cyclophosphamide were markedly lower, whereas Pola dosing was relatively preserved. Higher Pola IDI was associated with an increased incidence of severe adverse events (sAEs), and a lower Geriatric Nutritional Risk Index (GNRI) was independently correlated with both reduced ORR and increased sAEs. Pola-R-CHP demonstrates promising efficacy in DLBCL patients aged ≥ 80 years. However, the increased TRM highlights the importance of cautious toxicity management. Individualized dose modifications, particularly for cytotoxic agents, and comprehensive nutritional assessments may improve treatment tolerability and outcomes in this vulnerable population.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsLymphoma, Large B-Cell, DiffuseAgedAged, 80 and overAge FactorsAntibodies, MonoclonalCyclophosphamideDoxorubicinFemaleHumansImmunoconjugatesJapanMalePrednisoneRetrospective StudiesRituximabAntibodies, MonoclonalCyclophosphamideDoxorubicinImmunoconjugatespolatuzumab vedotinPrednisoneRituximabChemotherapy dose intensityDiffuse large B-Cell lymphomaGeriatric oncologyPola-R-CHPPolatuzumab vedotin

Identifiers

PMID41068304
PMCPMC12619725

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Registered trials

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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.