Evidence map›Paper›PMID 40087879›Full record

ArticleCancer medicine2025

Real-World Outcomes of Newly Diagnosed Multiple Myeloma Patients Treated Before the Era of Anti-CD38 Antibodies: The EMMY Cohort From 2017 to 2020.

Laure Vincent, Olivier Decaux, Aurore Perrot, Bruno Royer, Thomas Chalopin, Arthur Bobin, Margaret Macro, Denis Caillot, Lionel Karlin, Caroline Jacquet and 15 more

Abstract read
In one paragraph

Article in Cancer medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

25 authors.

Laure VincentDepartment of Clinical Hematology, Montpellier University Hospital Center, Montpellier, France.
Olivier DecauxCentre Hospitalier Universitaire de Rennes - Hôpital Pontchaillou, Rennes, France.
Aurore PerrotCentre Hospitalier Universitaire de Toulouse, IUCT-Oncopole, Université de Toulouse, UPS, Service d'Hématologie, Toulouse, France.ORCID https://orcid.org/0000-0003-0131-8689
Bruno RoyerSaint Louis Hospital, Paris, France.
Thomas ChalopinCentre hospitalier universitaire de Tours, Hospital, Tours, France.
Arthur BobinCHU Poitiers, Poitiers, France.
Margaret MacroIHBN-Centre Hospitalier Universitaire Caen, France.
Denis CaillotHématologie Clinique, Centre Hospitalier Universitaire de Dijon Bourgogne, Dijon, France.
Lionel KarlinHôpital Lyon Sud, Hospices Civils de Lyon, Pierre-Bénite, France.
Caroline JacquetCHU de Nancy, Vandoeuvre Les Nancy, Vandoeuvre-les-Nancy, France.
Cécile SonntagUniversity Hospital, Hôpital Hautepierre, Strasbourg, France.
Mohamad MohtyDepartment of Haematology, Saint Antoine Hospital, Paris, France.
Laurent FrenzelDepartment of Haematology, Institut Necker, Paris, France.
Arnaud JaccardReferral Center for AL Amyloidosis, Limoges, France.
Salomon ManierHématologie, Centre Hospitalier Universitaire de Lille, Lille, France.
Laurence SanhesCentre Hospitalier Perpignan, Perpignan, France.
Driss ChaouiHôpital Victor Dupouy, Argenteuil, France.
Philippe MoreauDepartment of Haematology, Centre Hospitalier Universitaire de Nantes, Nantes, France.ORCID https://orcid.org/0000-0003-1780-8746
Ronan GarlantézecSanté publique et épidémiologie, Centre Hospitalier Universitaire de Rennes, Rennes, France.
Nathalie TexierKappa Santé, Paris, France.ORCID https://orcid.org/0000-0003-3749-254X
Chanaz LouniIFM, Paris, France.
Zakaria MaaroufIFM, Paris, France.
Herve Avet LoiseauIUCT-Oncopole Toulouse, Toulouse, France.
Cyrille HulinCentre Hospitalier Universitaire de Bordeaux, Pessac Cedex, France.ORCID https://orcid.org/0000-0002-3749-5161
Karim Belhadj MerzougUnité Hémopathies Lymphoïdes, Centre Hospitalier Universitaire Henri Mondor, Créteil, France.

Funding

AmgenBristol Myers Squibb FoundationGSKJanssen-CilagPfizerSanofiTakeda Oncology
6 · The paper itself

Abstract

AIMS/

backgroundRecent agents have profoundly reshaped the multiple myeloma (MM) landscape. Their real-world impacts need to be assessed over the long term.

methodsEMMY is a non-interventional, prospective dynamic cohort, conducted in France, since 2017, with 900 patients enrolled each year. Newly diagnosed MM (NDMM) who initiated a treatment from 2017 to 2020 are here described.

resultsA total of 1036 non-transplant eligible (NTE) patients (median age: 74.9 years) and 561 patients who received autologous stem cell transplantation (ASCT) (median age: 60.6 years) were enrolled. For ASCT patients, a shift in induction treatment from bortezomib-thalidomide-dexamethasone (VTd) (29.1%) to bortezomib-lenalidomide-dexamethasone (VRd) (55.1%) marked the period. Maintenance treatment with R after ASCT became a standard (75% of patients). In NTE patients, R-based regimens were increasingly used from 29.4% in 2017 (of whom Rd.: 17.0%, VRd: 10.6%) to 73.3% in 2020 (of whom Rd.: 21.8%, VRd: 48.5%). Median progression-free survival (mPFS) was 46.5 months (95% CI: 37.8-50.6) and 18.7 months (95% CI: 16.3-20.8) in ASCT and NTE patients, respectively. In the ASCT group, patients treated with and without R maintenance had a mPFS of 51.8 (95% CI: 44.1-NA) and 29.6 months (95% CI: 21.8-40.9), respectively. In the NTE group, the mPFS was 26.3 (95% CI: 21.9-30.9) and 14.6 months (95% CI: 11.9-17.7) in patients who received an R-based and non-R-based regimen, respectively. The estimated 48-month overall survival rates were 89% (95% CI: 84.5-92.2) and 63% (95% CI: 58.5-67.1) for ASCT and NTE patients, respectively.

conclusionsThe 2017-2020 period was marked by the expansion of R use in both NDMM ASCT and NTE patients.

Indexed as

ADP-ribosyl Cyclase 1Antineoplastic Combined Chemotherapy ProtocolsMultiple MyelomaAgedAged, 80 and overBortezomibDexamethasoneFemaleFranceHematopoietic Stem Cell TransplantationHumansLenalidomideMaleMiddle AgedProgression-Free SurvivalProspective StudiesADP-ribosyl Cyclase 1BortezomibDexamethasoneLenalidomideASCT patientsfirst‐line therapymultiple myelomaNTE patientsreal world

Identifiers

PMID40087879
PMCPMC11909396

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