Evidence map›Paper›PMID 40241540›Full record

ArticleHaematologica2025

Prognostic value of minimal residual disease detected by EuroFlow next-generation flow cytometry and next-generation sequencing in patients with multiple myeloma achieving complete response and receiving lenalidomide maintenance after autotransplant: a prospective comparison study.

Takeshi Yoroidaka, Hiroyuki Takamatsu, Ryota Urushihara, Mitsuhiro Itagaki, Satoshi Yoshihara, Kota Sato, Naoki Takezako, Shuji Ozaki, Kazuhito Suzuki, Kentaro Kohno and 11 more

Abstract readComparative StudyMulticenter Study
In one paragraph

Article in Haematologica, 2025. 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
–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

6 citing papers in PubMed.

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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

21 authors.

Takeshi YoroidakaDepartment of Hematology, Faculty of Medicine, Institute of Medical, Pharmaceutical, and Health Sciences, Kanazawa University, Kanazawa.
Hiroyuki TakamatsuDepartment of Hematology, Faculty of Medicine, Institute of Medical, Pharmaceutical, and Health Sciences, Kanazawa University, Kanazawa. takamaz@staff.kanazawa-u.ac.jp.
Ryota UrushiharaDepartment of Hematology, Toyama Prefectural Central Hospital, Toyama.
Mitsuhiro ItagakiDepartment of Hematology, Hiroshima Red Cross Hospital and Atomic-bomb Survivors Hospital, Hiroshima.
Satoshi YoshiharaDepartment of Respiratory Medicine and Hematology, Hyogo College of Medicine, Nishinomiya.
Kota SatoDepartment of Hematology, Japanese Red Cross Medical Center, Tokyo.
Naoki TakezakoDepartment of Hematology, Nerima Hikarigaoka Hospital, Tokyo.
Shuji OzakiDepartment of Hematology, Tokushima Prefectural Central Hospital, Tokushima.
Kazuhito SuzukiDivision of Clinical Oncology and Hematology, Department of Internal Medicine, The Jikei University School of Medicine, Tokyo.
Kentaro KohnoDepartment of Hematology, Japan Community Healthcare Organization Kyusyu Hospital, Kitakyushu.
Tsuyoshi MutaDepartment of Hematology, Hiroshima Red Cross Hospital and Atomic-bomb Survivors Hospital, Hiroshima.
Morio MatsumotoDepartment of Hematology, NHO Shibukawa Medical Center, Shibukawa.
Yasushi TerasakiDivision of Hematology, Toyama City Hospital, Toyama.
Takeshi YamashitaDepartment of Hematology, Ishikawa Prefectural Central Hospital, Kanazawa.
Shin-Ichi FuchidaDepartment of Hematology, Japan Community Health care Organization Kyoto Kuramaguchi Medical Center, Kyoto.
Jun SakamotoBio Medical Laboratories (BML), INC., Kawagoe.
Tadao IshidaDepartment of Hematology, Japanese Red Cross Medical Center, Tokyo.
Kenshi SuzukiDepartment of Hematology, Japanese Red Cross Medical Center, Tokyo.
Hirokazu MurakamiFaculty of Medical Technology and Clinical Engineering, Gunma University of Health and Welfare, Maebashi.
Brian G M DurieSamuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Outpatient Cancer Center, Los Angeles, CA.
Kazuyuki ShimizuDepartment of Hematology, Higashi Nagoya National Hospital, Nagoya.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Novel agents inducing deeper responses have improved the prognosis of patients with multiple myeloma (MM). To assess minimal residual disease (MRD) and stratify patients achieving complete response (CR), advanced technologies such as EuroFlow next-generation flow cytometry (NGF) and next-generation sequencing (NGS) are increasingly utilized. This prospective study evaluated responses in newly diagnosed MM patients undergoing autologous stem cell transplantation (ASCT) followed by lenalidomide maintenance therapy across multiple Japanese medical centers. Patients achieving CR or stringent CR within 100-365 days post-ASCT were included. MRD levels in the bone marrow were assessed using both NGF and NGS (cutoff: 1×10-5) at three time points: 100-365 days, 1 year, and 2 years post-ASCT. A total of 52 patients were analyzed. MRD levels determined by NGF and NGS showed a strong correlation (r=0.9722; P<0.0001). After a median follow-up of 3 years, the 3-year progression-free survival (PFS) and overall survival (OS) rates were 76.5% (95% confidence interval [CI]: 62.3-85.9%) and 96.2% (95% CI: 85.5-99.0%), respectively. Patients with sustained MRD negativity for >6 months demonstrated superior 3-year PFS compared to those without sustained MRD negativity, as measured by both NGF (100% vs. 67.6%; hazard ratio [HR] =0.06; 95% CI: 0.0005-0.50; P<0.007) and NGS (90.5% vs. 72.2%; HR=0.23; 95% CI: 0.06-0.94; P=0.048). These findings highlighted a strong correlation in the MRD levels assessed by NGF and NGS and validated that sustained MRD negativity was significantly associated with prolonged PFS (clinical trial registered at UMIN 000022238).

Indexed as

Flow CytometryHematopoietic Stem Cell TransplantationHigh-Throughput Nucleotide SequencingLenalidomideMultiple MyelomaNeoplasm, ResidualAdultAgedFemaleHumansMaintenance ChemotherapyMaleMiddle AgedPrognosisProspective StudiesTransplantation, AutologousLenalidomide

Identifiers

PMID40241540
PMCPMC12399965

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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.