Evidence map›Paper›PMID 42728379›Full record

ArticleNature medicine2026

Teclistamab versus lenalidomide-dexamethasone in high-risk smoldering multiple myeloma: a randomized phase 2 trial.

Omar Nadeem, David M Cordas Dos Santos, Sophie Magidson, Jeffrey Matous, Eva Medvedova, Elizabeth O'Donnell, Robert A Redd, Yuxin Liu, Shonali Midha, Adam S Sperling and 22 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature medicine, 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

32 authors.

Omar Nadeem *Center for Early Detection and Interception of Blood Cancers, Dana-Farber Cancer Institute, Boston, MA, USA.ORCID http://orcid.org/0000-0002-4124-4277
David M Cordas Dos Santos *Center for Early Detection and Interception of Blood Cancers, Dana-Farber Cancer Institute, Boston, MA, USA.ORCID http://orcid.org/0000-0002-9198-8338
Sophie MagidsonCenter for Early Detection and Interception of Blood Cancers, Dana-Farber Cancer Institute, Boston, MA, USA.
Jeffrey MatousColorado Blood Cancer Institute, Denver, CO, USA.
Eva MedvedovaKnight Cancer Institute, Oregon Health and Science University, Portland, OR, USA.
Elizabeth O'DonnellCenter for Early Detection and Interception of Blood Cancers, Dana-Farber Cancer Institute, Boston, MA, USA.
Robert A ReddDepartment of Data Science, Dana-Farber Cancer Institute, Boston, MA, USA.
Yuxin LiuCenter for Early Detection and Interception of Blood Cancers, Dana-Farber Cancer Institute, Boston, MA, USA.
Shonali MidhaCenter for Early Detection and Interception of Blood Cancers, Dana-Farber Cancer Institute, Boston, MA, USA.ORCID http://orcid.org/0000-0003-4948-5507
Adam S SperlingDivision of Hematology, Stanford University, Palo Alto, CA, USA.ORCID http://orcid.org/0000-0002-9369-4413
Frances ArtersCenter for Early Detection and Interception of Blood Cancers, Dana-Farber Cancer Institute, Boston, MA, USA.
Christine DavieCenter for Early Detection and Interception of Blood Cancers, Dana-Farber Cancer Institute, Boston, MA, USA.
Caroline RicciardiCenter for Early Detection and Interception of Blood Cancers, Dana-Farber Cancer Institute, Boston, MA, USA.
Rosa ToengesCenter for Early Detection and Interception of Blood Cancers, Dana-Farber Cancer Institute, Boston, MA, USA.
Nayda BidikianCenter for Early Detection and Interception of Blood Cancers, Dana-Farber Cancer Institute, Boston, MA, USA.
Subear HusseinCenter for Early Detection and Interception of Blood Cancers, Dana-Farber Cancer Institute, Boston, MA, USA.
Jean-Baptiste AlbergeCenter for Early Detection and Interception of Blood Cancers, Dana-Farber Cancer Institute, Boston, MA, USA.
Sungjae KimCenter for Early Detection and Interception of Blood Cancers, Dana-Farber Cancer Institute, Boston, MA, USA.
Lorena Pantano-RubinoCenter for Early Detection and Interception of Blood Cancers, Dana-Farber Cancer Institute, Boston, MA, USA.
Francesco CorradoCenter for Early Detection and Interception of Blood Cancers, Dana-Farber Cancer Institute, Boston, MA, USA.
Hannah AshtonCenter for Early Detection and Interception of Blood Cancers, Dana-Farber Cancer Institute, Boston, MA, USA.
Daniel AddonizioCenter for Early Detection and Interception of Blood Cancers, Dana-Farber Cancer Institute, Boston, MA, USA.
Siham MohamedCenter for Early Detection and Interception of Blood Cancers, Dana-Farber Cancer Institute, Boston, MA, USA.
Ashlee SturtevantCenter for Early Detection and Interception of Blood Cancers, Dana-Farber Cancer Institute, Boston, MA, USA.
Marjorie MartoCenter for Early Detection and Interception of Blood Cancers, Dana-Farber Cancer Institute, Boston, MA, USA.
Amy BergeronCenter for Early Detection and Interception of Blood Cancers, Dana-Farber Cancer Institute, Boston, MA, USA.
Francesco MalfonaDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Kevin PanaroDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.ORCID http://orcid.org/0009-0004-7430-1399
Paul G RichardsonDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Jerome RitzDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.ORCID http://orcid.org/0000-0001-5526-4669
Lorenzo TrippaDepartment of Data Science, Dana-Farber Cancer Institute, Boston, MA, USA.ORCID http://orcid.org/0000-0001-5218-5666
Irene M GhobrialCenter for Early Detection and Interception of Blood Cancers, Dana-Farber Cancer Institute, Boston, MA, USA. irene_ghobrial@dfci.harvard.edu.ORCID http://orcid.org/0000-0001-7361-3092

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Teclistamab, a B cell maturation antigen-targeting bispecific antibody, has demonstrated substantial activity in relapsed multiple myeloma (MM), particularly in earlier lines of therapy, and may have higher efficacy in high-risk smoldering MM (HR-SMM) with a more functional immune system. In the randomized phase 2 ImmunoPRISM trial, we compared fixed-duration teclistamab with lenalidomide-dexamethasone (Rd) in HR-SMM. After a six-patient safety run-in, patients were randomized 2:1 to teclistamab or Rd. The primary endpoint was complete response (CR) rate. As of 26 May 2026, 59 patients were treated-45 received teclistamab and 14 received Rd. Teclistamab treatment induced a CR in 77.8% patients versus 0% with Rd, and minimal residual disease negativity at 10

Identifiers

PMID42728379

What OpenQuestion holds

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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.