Evidence map›Paper›PMID 40862742›Full record

ReviewCells2025

Preventing Skeletal-Related Events in Newly Diagnosed Multiple Myeloma.

Benjamin Massat, Patrick Stiff, Fatema Esmail, Estefania Gauto-Mariotti, Patrick Hagen

Abstract readReview
In one paragraph

Review in Cells, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
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

5 authors.

Benjamin MassatDivision of Hematology and Oncology, Department of Medicine, Loyola University Medical Center, Maywood, IL 60153, USA.ORCID 0009-0009-7760-5730
Patrick StiffDivision of Hematology and Oncology, Department of Medicine, Loyola University Medical Center, Maywood, IL 60153, USA.
Fatema EsmailDivision of Hematology and Oncology, Department of Medicine, Loyola University Medical Center, Maywood, IL 60153, USA.
Estefania Gauto-MariottiDivision of Hematology and Oncology, Department of Medicine, Loyola University Medical Center, Maywood, IL 60153, USA.
Patrick HagenDivision of Hematology and Oncology, Department of Medicine, Loyola University Medical Center, Maywood, IL 60153, USA.ORCID 0000-0003-3428-1667

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the increasing number of novel therapies to treat newly diagnosed multiple myeloma (NDMM), preventing skeletal-related events (SREs) remains a challenge. This review summarizes the mechanistic causes of myeloma bone disease, data supporting the use of bisphosphonates and RANKL inhibitors, and the optimal management of preventing SREs in NDMM patients. Both zoledronic acid (ZA) and denosumab are acceptable treatment options with comparable safety and efficacy profiles. However, in patients who are candidates for autologous stem cell transplant (ASCT), denosumab may be preferred over ZA due to a progression-free survival (PFS) benefit observed in post hoc analyses when used with proteasome inhibitor-based regimens. The optimal duration of bone-directed therapy is unclear, but it is typically given for two years. Supportive care should include dental evaluation at baseline, annually, and if symptoms appear, given the risk for jaw osteonecrosis with both ZA and denosumab. Both drugs should be held in the setting of dental work. Patients should receive adequate calcium and vitamin D supplementation. Supportive procedures such as cement augmentation, radiation, and orthopedic surgery can also help treat compression fractures, uncontrolled pain, cord compression, and pathologic fractures. We conclude with our approach for managing SREs and a review of novel therapies and targets.

Indexed as

Bone Density Conservation AgentsBone DiseasesDenosumabDiphosphonatesMultiple MyelomaDisease ManagementHumansRANK LigandZoledronic AcidBone Density Conservation AgentsDenosumabDiphosphonatesRANK LigandTNFSF11 protein, humanZoledronic Aciddenosumabmultiple myelomaskeletal-related eventszoledronic acid

Identifiers

PMID40862742
PMCPMC12384113

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.