Evidence map›Paper›PMID 37486974›Full record

ArticleBlood cancer discovery2023

Time-Dependent Prognostic Value of Serological and Measurable Residual Disease Assessments after Idecabtagene Vicleucel.

Bruno Paiva, Irene Manrique, Julie Rytlewski, Timothy Campbell, Christian C Kazanecki, Nathan Martin, Larry D Anderson, Jesús G Berdeja, Sagar Lonial, Noopur S Raje and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Blood cancer discovery, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
9.0field-weighted citation impact, top 2% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 9 institutions in 4 countries.

Bruno PaivaClinica Universidad de Navarra (CUN), Centro de Investigacion Medica Aplicada (CIMA), Instituto de Investigacion Sanitaria de Navarra (IDISNA), CIBER-ONC number CB16/12/00369, Pamplona, Spain.ORCID 0000-0003-1977-3815
Irene ManriqueClinica Universidad de Navarra (CUN), Centro de Investigacion Medica Aplicada (CIMA), Instituto de Investigacion Sanitaria de Navarra (IDISNA), CIBER-ONC number CB16/12/00369, Pamplona, Spain.ORCID 0009-0002-6092-1891
Julie RytlewskiBristol Myers Squibb, Seattle, Washington.ORCID 0000-0001-5244-6790
Timothy CampbellBristol Myers Squibb, San Francisco, California.ORCID 0000-0002-3538-8784
Christian C KazaneckiBristol Myers Squibb, Seattle, Washington.ORCID 0009-0009-0020-6133
Nathan MartinBristol Myers Squibb, Seattle, Washington.ORCID 0009-0002-2658-0958
Larry D AndersonMyeloma, Waldenström's, and Amyloidosis Program, Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, Texas.ORCID 0000-0002-6531-9595
Jesús G BerdejaSarah Cannon Research Institute and Tennessee Oncology, Nashville, Tennessee.ORCID 0000-0003-4362-0376
Sagar LonialEmory School of Medicine, Atlanta, Georgia.ORCID 0000-0002-8322-9323
Noopur S RajeMassachusetts General Hospital, Boston, Massachusetts.ORCID 0000-0003-3066-1275
Yi LinMayo Clinic, Rochester, Minnesota.ORCID 0000-0002-1556-6416
Philippe MoreauCentre Hospitalier Universitaire de Nantes, Nantes, France.ORCID 0000-0003-1780-8746
Jesús F San-MiguelClinica Universidad de Navarra (CUN), Centro de Investigacion Medica Aplicada (CIMA), Instituto de Investigacion Sanitaria de Navarra (IDISNA), CIBER-ONC number CB16/12/00369, Pamplona, Spain.ORCID 0000-0002-9183-4857
Nikhil C MunshiThe LeBow Institute for Myeloma Therapeutics and Jerome Lipper Multiple Myeloma Center, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.ORCID 0000-0002-7344-9795
Shari M KaiserBristol Myers Squibb, Seattle, Washington.ORCID 0009-0003-8337-9123
Bristol-Myers Squibb (Germany) · DENavarre Institute of Health Research · ESCentre Hospitalier Universitaire de Nantes · FRDana-Farber Cancer Institute · USEmory University · USMassachusetts General Hospital · USMayo Clinic · USSouthwestern Medical Center · USTennessee Oncology · US

Funding

Project 4: Targeting Resistance to T-Cell Directed Therapy in Multiple MyelomaP50CA186781 · NCI · MAYO CLINIC ARIZONA · PI Peter Leif Bergsagel · 2015 to 2026
$25.5M
NCI NIH HHS P50 CA186781
6 · The paper itself

Abstract

The role of measurable residual disease (MRD) in multiple myeloma patients treated with chimeric antigen receptor (CAR) T cells is uncertain. We analyzed MRD kinetics during the first year after idecabtagene vicleucel (ide-cel) infusion in 125 relapsed/refractory multiple myeloma patients enrolled in KarMMa. At month 1 after ide-cel, there were no differences in progression-free survival (PFS) between patients in less than complete response (CR) versus those in CR; only MRD status was predictive of significantly different PFS at this landmark. In patients with undetectable MRD at 3 months and beyond, PFS was longer in those achieving CR versus <CR. Persistent MRD in the 10-6 logarithmic range and reappearance of normal plasma cells in MRD-negative patients were associated with inferior PFS. This study unveils different prognostic implications of serological and MRD response dynamics after ide-cel and suggests the potential value of studying the reappearance of normal plasma cells as a surrogate of loss of CAR T-cell functionality. SIGNIFICANCE: This is one of the first studies evaluating the impact of CR and MRD dynamics after CAR T therapy in relapsed/refractory multiple myeloma. These data help interpret the prognostic significance of serological and MRD responses at early and late time points after CAR T-cell infusion. See related commentary by Landgren and Kazandjian, p. 346 . This article is featured in Selected Articles from This Issue, p. 337.

Indexed as

Multiple MyelomaNeoplasms, Plasma CellReceptors, Chimeric AntigenHumansImmunotherapy, AdoptiveNeoplasm, ResidualPrognosisidecabtagene vicleucelReceptors, Chimeric Antigen

Identifiers

PMID37486974
PMCPMC10472177
OpenAlexW4385191703

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.