Evidence map›Paper›PMID 38867578›Full record

ArticleHaematologica2024

Event-free survival at 36 months is a suitable endpoint for diffuse large B-cell lymphoma patients treated with immunochemotherapy: real-world evidence from the North Japan Hematology Study Group.

Koh Izumiyama, Tasuku Inao, Hideki Goto, Shinpei Harada, Hajime Senjo, Keito Suto, Junichi Hashiguchi, Reiki Ogasawara, Tomoyuki Saga, Tetsuyuki Igarashi and 14 more

Abstract read
In one paragraph

Article in Haematologica, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  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

24 authors.

Koh IzumiyamaNorth Japan Hematology Study Group (NJHSG); Blood Disorders Center, Aiiku Hospital, Sapporo. izumi5318@yahoo.co.jp.
Tasuku InaoDepartment of Biostatistics, Hokkaido University Graduate School of Medicine, Sapporo.
Hideki GotoNorth Japan Hematology Study Group (NJHSG); Department of Hematology, Hokkaido University Faculty of Medicine, Sapporo.
Shinpei HaradaNorth Japan Hematology Study Group (NJHSG); Department of Hematology, Hokkaido University Faculty of Medicine, Sapporo.
Hajime SenjoNorth Japan Hematology Study Group (NJHSG); Department of Hematology, Hokkaido University Faculty of Medicine, Sapporo.
Keito SutoNorth Japan Hematology Study Group (NJHSG); Department of Hematology, Hokkaido University Faculty of Medicine, Sapporo.
Junichi HashiguchiNorth Japan Hematology Study Group (NJHSG); Department of Hematology, Kitami Red Cross Hospital, Kitami.
Reiki OgasawaraNorth Japan Hematology Study Group (NJHSG); Department of Hematology, Sapporo Hokuyu Hospital, Sapporo.
Tomoyuki SagaNorth Japan Hematology Study Group (NJHSG); Department of Hematology, Kin-ikyo Chuo Hospital, Sapporo.
Tetsuyuki IgarashiNorth Japan Hematology Study Group (NJHSG); Department of Hematology, Tenshi Hospital, Sapporo.
Kentaro WakasaNorth Japan Hematology Study Group (NJHSG); Division of Hematology, Hokkaido P.W.F.A.C. Obihiro-Kosei General Hospital, Obihiro.
Ikumi KasaharaNorth Japan Hematology Study Group (NJHSG); Department of Hematology, Sapporo City General Hospital, Sapporo.
Yukari TakedaNorth Japan Hematology Study Group (NJHSG); Department of Hematology, Tonan Hospital, Sapporo.
Keisuke YamaguchiNorth Japan Hematology Study Group (NJHSG); Department of Hematology, Teine Keijinkai Hospital, Sapporo.
Akio ShigematsuNorth Japan Hematology Study Group (NJHSG); Department of Hematology, Kushiro Rosai Hospital, Kushiro.
Mutsumi TakahataNorth Japan Hematology Study Group (NJHSG); Department of Hematology, Sapporo-Kosei General Hospital, Sapporo.
Katsuya FujimotoNorth Japan Hematology Study Group (NJHSG); Department of Hematology, National Hospital Organization Hokkaido Cancer Center, Sapporo.
Yoshihito HaseyamaNorth Japan Hematology Study Group (NJHSG); Department of Hematology, Tonan Hospital, Sapporo.
Takahiro NagashimaNorth Japan Hematology Study Group (NJHSG); Department of Hematology, Kitami Red Cross Hospital, Kitami.
Hajime SakaiNorth Japan Hematology Study Group (NJHSG); Department of Hematology, Teine Keijinkai Hospital, Sapporo.
Yasutaka KakinokiNorth Japan Hematology Study Group (NJHSG); Department of Hematology, Asahikawa City Hospital, Asahikawa.
Mitsutoshi KurosawaNorth Japan Hematology Study Group (NJHSG); Department of Hematology, National Hospital Organization Hokkaido Cancer Center, Sapporo.
Isao YokotaDepartment of Biostatistics, Hokkaido University Graduate School of Medicine, Sapporo.
Takanori TeshimaNorth Japan Hematology Study Group (NJHSG); Department of Hematology, Hokkaido University Faculty of Medicine, Sapporo.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Information regarding follow-up duration after treatment for newly diagnosed diffuse large B-cell lymphoma (DLBCL) is important. However, a clear endpoint has yet to be established. We enrolled a total of 2,182 patients newly diagnosed with DLBCL between 2008 and 2018. The median age of the patients was 71 years. All patients were treated with rituximab- and anthracycline-based chemotherapies. Each overall survival (OS) was compared with the age- and sex-matched Japanese general population (GP) data. At a median follow-up of 3.4 years, 985 patients experienced an event and 657 patients died. Patients who achieved an event-free survival (EFS) at 36 months (EFS36) had an OS equivalent to that of the matched GP (standard mortality ratio [SMR], 1.17; P=0.1324), whereas those who achieved an EFS24 did not have an OS comparable to that of the matched GP (SMR, 1.26; P=0.0095). Subgroup analysis revealed that relatively old patients (>60 years), male patients, those with limited-stage disease, those with a good performance status, and those with low levels of soluble interleukin 2 receptor already had a comparable life expectancy to the matched GP at an EFS24. In contrast, relatively young patients had a shorter life expectancy than matched GP, even with an EFS36. In conclusion, an EFS36 was shown to be a more suitable endpoint for newly diagnosed DLBCL patients than an EFS24. Of note, younger patients require a longer EFS period than older patients in order to obtain an equivalent life expectancy to the matched GP.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsLymphoma, Large B-Cell, DiffuseAdultAgedAged, 80 and overFemaleFollow-Up StudiesHumansImmunotherapyJapanMaleMiddle AgedPrognosisRituximabTreatment OutcomeYoung AdultRituximab

Identifiers

PMID38867578
PMCPMC11532691

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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.