Evidence map›Paper›PMID 41947863›Full record

ArticleEJHaem2026

Treatment Discontinuation After Achieving MRD Negativity in Multiple Myeloma in the Pre-BCMA Era: A Prospective, Single-Centre Study.

Kota Sato, Kenshi Suzuki, Shotaro Sugita, Ukyo Kondo, Miyu Watanabe, Moe Yogo, Tomomi Takei, Mizuki Ogura, Yu Abe, Taku Kikuchi and 2 more

Abstract read
In one paragraph

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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Kota SatoDepartment of Hematology Japanese Red Cross Medical Center Shibuya-ku Tokyo Japan.ORCID https://orcid.org/0000-0001-9239-6003
Kenshi SuzukiDepartment of Hematology Japanese Red Cross Medical Center Shibuya-ku Tokyo Japan.
Shotaro SugitaDepartment of Hematology Japanese Red Cross Medical Center Shibuya-ku Tokyo Japan.
Ukyo KondoDepartment of Hematology Japanese Red Cross Medical Center Shibuya-ku Tokyo Japan.
Miyu WatanabeDepartment of Hematology Japanese Red Cross Medical Center Shibuya-ku Tokyo Japan.
Moe YogoDepartment of Hematology Japanese Red Cross Medical Center Shibuya-ku Tokyo Japan.
Tomomi TakeiDepartment of Hematology Japanese Red Cross Medical Center Shibuya-ku Tokyo Japan.
Mizuki OguraDepartment of Hematology Japanese Red Cross Medical Center Shibuya-ku Tokyo Japan.
Yu AbeDepartment of Hematology Japanese Red Cross Medical Center Shibuya-ku Tokyo Japan.
Taku KikuchiDepartment of Hematology Japanese Red Cross Medical Center Shibuya-ku Tokyo Japan.
Nobuhiro TsukadaDepartment of Hematology Japanese Red Cross Medical Center Shibuya-ku Tokyo Japan.
Tadao IshidaDepartment of Hematology Japanese Red Cross Medical Center Shibuya-ku Tokyo Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Minimal/measurable residual disease (MRD) negativity in multiple myeloma (MM) is associated with favourable outcomes; nonetheless, evidence supporting treatment discontinuation remains limited. We evaluated the feasibility of discontinuing antimyeloma therapy in patients with MRD negativity. Methods: We analysed 41 patients who discontinued therapy after achieving MRD negativity at the 10 Results: The 2- and 3-year treatment-free survival (TFS) rates were 71.2% (95% CI, 54.0-83.0) and 67.9% (95% CI, 50.1-80.4), respectively, with the median not reached. Among the 34 patients with > 2 years of follow-up, 19 (55.9%) maintained MRD negativity at 2 years. High-risk cytogenetic abnormalities were associated with shorter TFS, whereas a BM normal plasma cell proportion ≥ 0.003% at discontinuation was associated with prolonged TFS. Conclusions: Treatment discontinuation may be feasible in selected patients with MM who achieve and sustain MRD negativity, particularly in those without high-risk cytogenetics or with normal plasma cell recovery in the BM.

Indexed as

autologous stem cell transplantationhigh‐risk cytogenetic abnormalitiesminimal/measurable residual diseasemultiple myelomatreatment‐free survival

Identifiers

PMID41947863
PMCPMC13051898

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