Evidence map›Paper›PMID 39753553›Full record

Trial reportNature communications2025

Deeper response predicts better outcomes in high-risk-smoldering-myeloma: results of the I-PRISM phase II clinical trial.

Omar Nadeem, Michelle P Aranha, Robert Redd, Michael Timonian, Sophie Magidson, Elizabeth D Lightbody, Jean-Baptiste Alberge, Luca Bertamini, Ankit K Dutta, Habib El-Khoury and 12 more

Registry-linked trialAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02916771 (Phase II Trial of Combination of Ixazomib and Lenalidomide and Dexamethasone in Smoldering Multiple Myeloma), which is not on this map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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.

NCT02916771 phase2completednot on this map

Phase II Trial of Combination of Ixazomib and Lenalidomide and Dexamethasone in Smoldering Multiple Myeloma

TypeinterventionalSponsorDana-Farber Cancer InstituteRan2016 to 2025Enrolled61ConditionsSmoldering Multiple MyelomaArmsIxazomib, Lenalidomide, Dexamethasone
3 · Its place in the literature

Who cites it

11 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

22 authors.

Omar Nadeem *Center for Early Detection and Interception of Blood Cancers, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA. omar_nadeem@dfci.harvard.edu.
Michelle P Aranha *Center for Early Detection and Interception of Blood Cancers, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.ORCID 0000-0002-8230-5726
Robert ReddDepartment of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA, USA.ORCID 0000-0002-1329-5288
Michael TimonianCenter for Early Detection and Interception of Blood Cancers, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.ORCID 0000-0002-1014-3502
Sophie MagidsonCenter for Early Detection and Interception of Blood Cancers, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.ORCID 0009-0007-4225-135X
Elizabeth D LightbodyCenter for Early Detection and Interception of Blood Cancers, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Jean-Baptiste AlbergeCenter for Early Detection and Interception of Blood Cancers, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.ORCID 0000-0002-4218-7294
Luca BertaminiCenter for Early Detection and Interception of Blood Cancers, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Ankit K DuttaCenter for Early Detection and Interception of Blood Cancers, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Habib El-KhouryCenter for Early Detection and Interception of Blood Cancers, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Mark BustorosCenter for Early Detection and Interception of Blood Cancers, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.ORCID 0000-0002-4652-5449
Jacob P LaubachCenter for Early Detection and Interception of Blood Cancers, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Giada BianchiAmyloidosis Program, Division of Hematology, Brigham and Women's Hospital and Dana Farber Cancer Institute, Boston, MA, USA.
Elizabeth O'DonnellCenter for Early Detection and Interception of Blood Cancers, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Ting WuBroad Institute of MIT and Harvard, Boston, MA, USA.
Junko TsujiBroad Institute of MIT and Harvard, Boston, MA, USA.
Kenneth C AndersonCenter for Early Detection and Interception of Blood Cancers, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.ORCID 0000-0002-6418-0886
Gad GetzHarvard Medical School, Boston, MA, USA.
Lorenzo TrippaDepartment of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA, USA.
Paul G RichardsonCenter for Early Detection and Interception of Blood Cancers, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Romanos Sklavenitis-PistofidisCenter for Early Detection and Interception of Blood Cancers, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Irene M GhobrialCenter for Early Detection and Interception of Blood Cancers, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA. irene_ghobrial@dfci.harvard.edu.ORCID 0000-0001-7361-3092

Funding

Molecular Prediction of Myeloma Initiation Molecular Prediction of Myeloma InitiationR35CA263817 · NCI · DANA-FARBER CANCER INST · PI Irene M. Ghobrial · 2022 to 2026
$5.1M
Cancer Research UKNCI NIH HHS R35 CA263817U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) R35CA263817
6 · The paper itself

Abstract

Early therapeutic intervention in high-risk smoldering multiple myeloma (HR-SMM) has shown benefits, however, no studies have assessed whether biochemical progression or response depth predicts long-term outcomes. The single-arm I-PRISM phase II trial (NCT02916771) evaluated ixazomib, lenalidomide, and dexamethasone in 55 patients with HR-SMM. The primary endpoint, median progression-free survival (PFS), was not reached (NR) (95% CI: 57.7-NR, median follow-up 50 months). The secondary endpoint, biochemical PFS, was 48.6 months (95% CI: 39.9-NR) and coincided with or preceded SLiM-CRAB in eight patients. For additional secondary objectives, the overall response rate was 93% with 31% achieving complete response (CR) and 45% very good partial response (VGPR) or better. CR correlated strongly with the absence of SLiM-CRAB and biochemical progression. MRD-negativity (10

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBoron CompoundsDexamethasoneGlycineLenalidomideSmoldering Multiple MyelomaAdultAgedAged, 80 and overDisease ProgressionFemaleHumansMaleMiddle AgedMultiple MyelomaProgression-Free SurvivalBoron CompoundsDexamethasoneGlycineixazomibLenalidomide

Identifiers

PMID39753553
PMCPMC11698957

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Registered trials

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.