Evidence map›Paper›PMID 38548963›Full record

Observational studyInternational journal of hematology2024

Primary analysis of a prospective cohort study of Japanese patients with plasma cell neoplasms in the novel drug era (2016-2021).

Hirohiko Shibayama, Mitsuhiro Itagaki, Hiroshi Handa, Akihiro Yokoyama, Akio Saito, Satoru Kosugi, Shuichi Ota, Makoto Yoshimitsu, Yasuhiro Tanaka, Shingo Kurahashi and 20 more

Open access · hybridAbstract readObservational Study
In one paragraph

Observational study in International journal of hematology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
3.2field-weighted citation impact, top 8% of its field
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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
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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

30 authors at 20 institutions in 1 country.

Hirohiko ShibayamaDepartment of Hematology, NHO Osaka National Hospital, 2-1-14 Hoenzaka Chuo-ku, Osaka City, Osaka, 540-0006, Japan. shibayama.hirohiko.ec@mail.hosp.go.jp.ORCID http://orcid.org/0000-0003-4014-2815
Mitsuhiro ItagakiDepartment of Hematology, Hiroshima Red Cross Hospital, Hiroshima, Japan.
Hiroshi HandaDepartment of Hematology, Gunma University, Gunma, Japan.
Akihiro YokoyamaDepartment of Hematology, NHO Tokyo Medical Center, Tokyo, Japan.
Akio SaitoDepartment of Hematology, NHO Shibukawa Medical Center, Gunma, Japan.
Satoru KosugiDepartment of Hematology, Toyonaka Municipal Hospital, Osaka, Japan.
Shuichi OtaDepartment of Hematology, Sapporo Hokuyu Hospital, Hokkaido, Japan.
Makoto YoshimitsuDepartment of Hematology and Rheumatology, Kagoshima University, Kagoshima, Japan.
Yasuhiro TanakaDepartment of Hematology, Shinko Hospital, Hyogo, Japan.
Shingo KurahashiDepartment of Hematology and Oncology, Toyohashi Municipal Hospital, Aichi, Japan.
Shin-Ichi FuchidaDepartment of Hematology, JCHO Kyoto Kuramaguchi Medical Center, Kyoto, Japan.
Masaki IinoDepartment of Hematology, Yamanashi Prefectural Central Hospital, Yamanashi, Japan.
Takayuki ShimizuDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
Yukiyoshi MoriuchiDepartment of Hematology, Sasebo City General Hospital, Nagasaki, Japan.
Kohtaro ToyamaDepartment of Hematology, Fujioka General Hospital, Gunma, Japan.
Kinuko MitaniDepartment of Hematology and Oncology, Dokkyo Medical University, Tochigi, Japan.
Yutaka TsukuneDepartment of Hematology, Juntendo University School of Medicine, Tokyo, Japan.
Akiko KadaClinical Research Center, NHO Nagoya Medical Center, Aichi, Japan.
Hideto TamuraDivision of Diabetes, Endocrinology and Hematology, Department of Internal Medicine, Dokkyo Medical University Saitama Medical Center, Saitama, Japan.
Masahiro AbeDepartment of Hematology, Kawashima Hospital, Tokushima, Japan.
Hiromi IwasakiDepartment of Hematology, NHO Kyushu Medical Center, Fukuoka, Japan.
Junya KurodaDivision of Hematology and Oncology, Department of Medicine, Kyoto Prefecture University of Medicine, Kyoto, Japan.
Hiroyuki TakamatsuDepartment of Hematology, Kanazawa University, Kanazawa, Japan.
Kazutaka SunamiDepartment of Hematology, NHO Okayama Medical Center, Okayama, Japan.
Masahiro KizakiDepartment of Hematology, Saitama Medical Center, Saitama Medical University, Saitama, Japan.
Tadao IshidaDepartment of Hematology, Japanese Red Cross Medical Center, Tokyo, Japan.
Toshiki SaitoClinical Research Center, NHO Nagoya Medical Center, Aichi, Japan.
Itaru MatsumuraDepartment of Hematology and Rheumatology, Kindai University, Osaka, Japan.
Koichi AkashiDepartment of Medicine and Biosystemic Science, Kyushu University, Fukuoka, Japan.
Shinsuke IidaDepartment of Hematology and Oncology, Nagoya City University Institute of Medical and Pharmaceutical Sciences, 1 Kawasumi, Mizuho-Cho, Mizuho-ku, Nagoya City, Aichi, 467-8601, Japan. iida@med.nagoya-cu.ac.jp.
Nagoya Medical Center · JPSocial Insurance Saitama Chuo Hospital · JPDokkyo Medical University · JPGunma University · JPJapanese Red Cross Hiroshima College of Nursing · JPJapanese Red Cross Medical Center · JPJuntendo University · JPKagoshima University · JPKanazawa University · JPKeio University · JPKindai University · JPKyoto Medical Center · JPKyushu University · JPNagoya City University · JPNational Kyushu Medical Center · JPOkayama Medical Center · JPOsaka National Hospital · JPSapporo Hokuyu Hospital · JPSasebo City General Hospital · JPShinko Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The emergence of novel drugs has significantly improved outcomes of patients with plasma cell neoplasms (PCN). The Japanese Society of Hematology conducted a prospective observational study in newly diagnosed PCN patients between 2016 and 2021. The analysis focused on 1385 patients diagnosed with symptomatic PCN between 2016 and 2018. The primary endpoint was the 3-year overall survival (OS) rate among patients requiring treatment (n = 1284), which was 70.0% (95%CI 67.4-72.6%). Approximately 94% of these patients received novel drugs as frontline therapy. The 3-year OS rate was 90.3% (95%CI 86.6-93.1%) in the 25% of patients who received upfront autologous stem cell transplantation (ASCT), versus just 61.4% (95%CI 58.0-64.6%) in those who did not receive upfront ASCT. The only unfavorable prognostic factor that affected OS in ASCT recipients was an age of 65 or higher. For patients who did not receive ASCT, independent unfavorable prognostic factors included frontline treatment with conventional chemotherapies, international staging system score of 2/3, extramedullary tumors, and Freiberg comorbidity index of 2/3. This study unequivocally demonstrates that use of novel drugs improved OS in Japanese myeloma patients, and underscores the continued importance of upfront ASCT as the standard of care in the era of novel drugs.

Indexed as

Neoplasms, Plasma CellAdultAgedAged, 80 and overAntineoplastic AgentsEast Asian PeopleFemaleHematopoietic Stem Cell TransplantationHumansJapanMaleMiddle AgedMultiple MyelomaPrognosisProspective StudiesSurvival RateAntineoplastic AgentsNovel drug eraPlasma cell neoplasms (PCN)Prospective cohort studyThree-year overall survival rate

Identifiers

PMID38548963
PMCPMC11136844
OpenAlexW4393316194

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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.