Evidence map›Paper›PMID 41037196›Full record

ArticleInternational journal of hematology2026

Investigation of early mortality in the patients with newly diagnosed multiple myeloma: insights from a real-world cohort using J-CHAEGE-MM database.

Michihide Tokuhira, Hitomi Nakayama, Kohtaro Toyama, Motoki Takano, Noriyoshi Iriyama, Atsushi Takahata, Eriko Sato, Yasutaka Senpuku, Maho Kawakami, Keigo Okada and 17 more

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

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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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

27 authors.

Michihide TokuhiraDepartment of Hematology, Japan Community Health Care Organization, Saitama Medical Center, Saitama, Japan. m_tokuhira@icloud.com.ORCID http://orcid.org/0000-0003-3780-5331
Hitomi NakayamaDepartment of Hematology, Yokohama Municipal Citizen's Hospital, Kanagawa, Japan.
Kohtaro ToyamaDepartment of Hematology, Fujioka General Hospital, Gunma, Japan.
Motoki TakanoDepartment of Hematology, Fukushima Medical University, Fukushima, Japan.
Noriyoshi IriyamaDepartment of Hematology and Rheumatology, National Hospital Organization Saitama Hospital, Saitama, Japan.
Atsushi TakahataDepartment of Hematology, Yokosuka Kyosai Hospital, Kanagawa, Japan.
Eriko SatoDepartment of Hematology, Juntendo University Nerima Hospital, Tokyo, Japan.
Yasutaka SenpukuDepartment of Hematology, Ageo Central General Hospital, Saitama, Japan.
Maho KawakamiDepartment of Hematology, Ome Medical Center, Tokyo, Japan.
Keigo OkadaDepartment of Hematology, Ome Medical Center, Tokyo, Japan.
Keisuke TanakaDepartment of Hematology, Institute of Science Tokyo, Tokyo, Japan.
Takashi AbeDepartment of Hematology, Niigata City General Hospital, Niigata, Japan.
Yuki OsadaDepartment of Hematology, Fraternity Memorial Hospital, Tokyo, Japan.
Koh YamamotoDepartment of Hematology, Yokohama City Minato Red Cross Hospital, Kanagawa, Japan.
Junichi WatanabeDepartment of Hematology, TMG Asaka Medical Center, Saitama, Japan.
Toshiaki HayashiDepartment of Hematology, Teine Keijinkai Hospital, Hokkaido, Japan.
Yasunobu SekiguchiDepartment of Hematology, Saitama Cancer Center, Saitama, Japan.
Yuta KimuraDepartment of Hematology, Japan Community Health Care Organization, Saitama Medical Center, Saitama, Japan.
Gaku OshikawaDepartment of Hematology, Japanese Red Cross Musashino Hospital, Tokyo, Japan.
Masaru NakagawaDepartment of Hematology, Kasukabe Municipal Medical Center, Saitama, Japan.
Ken SuzukiDepartment of Hematology, Fraternity Memorial Hospital, Tokyo, Japan.
Takashi KumagaiDepartment of Hematology, Ome Medical Center, Tokyo, Japan.
Shigeo ToyotaDepartment of Hematology, Yokosuka Kyosai Hospital, Kanagawa, Japan.
Katsuhiro MiuraDivision of Hematology and Rheumatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.
Takayuki IkezoeDepartment of Hematology, Fukushima Medical University, Fukushima, Japan.
Tomonori NakazatoDepartment of Hematology, Yokohama Municipal Citizen's Hospital, Kanagawa, Japan.
Takehiko MoriDepartment of Hematology, Institute of Science Tokyo, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although novel therapeutic agents, including proteasome inhibitors, immunomodulatory drugs, and anti-CD38 monoclonal antibodies, have markedly improved outcomes in multiple myeloma (MM), the disease remains incurable and is associated with various causes of death. However, comprehensive analyses of mortality patterns, particularly early mortality, are still limited. In this study, we focused on patients who died within one year of treatment initiation (1-year group), based on data from the J-CHARGE-MM database showing that 146 out of 461 total deaths (31.7%) occurred within the first year. The most common cause of death was disease progression (43.2%), followed by infection (primarily pneumonia and sepsis), which frequently occurred within the first few months of induction therapy. Cardiac-associated events, such as heart failure and cardiac amyloidosis (including suspected cases), accounted for 14.4% of deaths, and sudden death for 7.5%. Multivariate analysis revealed that early mortality was significantly associated with age ≥ 65 years, elevated serum lactate dehydrogenase (LDH), elevated serum C-reactive protein (CRP), and poor performance status (PS ≥ 3), compared with later deaths. These findings support that early mortality in MM may be reduced through comprehensive cardiac evaluation and proactive infection prevention strategies, particularly in elderly patients with elevated CRP, elevated LDH, or poor PS.

Indexed as

Multiple MyelomaAgedAged, 80 and overCause of DeathCohort StudiesC-Reactive ProteinDatabases, FactualDisease ProgressionFemaleHumansL-Lactate DehydrogenaseMaleMiddle AgedC-Reactive ProteinL-Lactate DehydrogenaseEarly mortalityInfectionMultiple myelomaProgressive diseaseSudden death

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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.