Evidence map›Paper›PMID 40176408›Full record

SynthesisCancer reports (Hoboken, N.J.)2025

Efficacy and Safety of Quadruplet Therapy in Newly Diagnosed Transplant-Eligible Multiple Myeloma: A Systematic Review and Meta-Analysis.

Aneeta Channar, Syed Arsalan Ahmed Naqvi, Muhammad Ali Khan, Arifa Bibi, Akshat Saxena, Nikita Tripathi, Ahmad Iftikhar, Ammad Raina, Kaneez Zahra Rubab Khakwani, Irbaz Bin Riaz and 1 more

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in Cancer reports (Hoboken, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
  2. 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

11 authors.

Aneeta ChannarDivision of Hematology and Medical Oncology, Mayo Clinic, Phoenix, Arizona, USA.ORCID 0009-0001-2698-0946
Syed Arsalan Ahmed NaqviDivision of Hematology and Medical Oncology, Mayo Clinic, Phoenix, Arizona, USA.
Muhammad Ali KhanDivision of Hematology and Medical Oncology, Mayo Clinic, Phoenix, Arizona, USA.
Arifa BibiDivision of Hematology and Medical Oncology, Mayo Clinic, Phoenix, Arizona, USA.
Akshat SaxenaDivision of Hematology and Medical Oncology, Mayo Clinic, Phoenix, Arizona, USA.
Nikita TripathiDivision of Hematology and Medical Oncology, Mayo Clinic, Phoenix, Arizona, USA.
Ahmad IftikharThe University of Arizona, Tucson, Arizona, USA.
Ammad RainaCanyon Vista Medical Center, Sierra Vista, Arizona, USA.
Kaneez Zahra Rubab KhakwaniThe University of Arizona, Tucson, Arizona, USA.
Irbaz Bin RiazDivision of Hematology and Medical Oncology, Mayo Clinic, Phoenix, Arizona, USA.
Muhammad HusnainThe University of Arizona, Tucson, Arizona, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe treatment landscape for multiple myeloma continues to evolve. Recently, the addition of anti-CD38 monoclonal antibodies (mAbs) to the triplet regimen, comprising a proteasome inhibitor, an immunomodulatory agent, and a steroid, for transplant-eligible newly diagnosed multiple myeloma (TENDMM) has shown promising results.

aimsTo evaluate the overall efficacy and safety of quadruplet therapy with an anti-CD38 mAb compared to a triplet regimen.

methodsA systematic search of Medline, Scopus, and EMBASE databases from inception to July 2024 identified relevant randomized controlled trials (RCTs). Efficacy and safety outcomes were derived using random-effects meta-analysis. Summarized outcomes include hazard ratios (HR) for progression-free survival (PFS) and overall survival (OS), odds ratios (OR) for response rates, measurable residual disease (MRD) negativity rate, and grade 3 or higher adverse events (G ≥ 3 AEs).

resultsFive RCTs involving 2963 patients were included. A statistically significant PFS was observed for quadruplet therapy when compared to the triplet regimen (HR 0.44; 95% Confidence Interval [CI] 0.35-0.56). PFS benefit was consistent for the standard risk (SR) group (HR 0.38; 95% CI 0.27-0.52) and high risk (HiR) group (HR 0.62; 95% CI 0.41-0.92). No statistically significant benefit was observed for OS (HR 0.55; 95% CI 0.28-1.08). A statistically significant benefit was observed for the overall response rate (OR 1.77; 95% CI 1.02-3.06) and MRD negativity rate (OR 2.67; 95% CI 1.79-3.99). No significant differences were observed for G ≥ 3 AE (OR 1.21; 95% CI 0.92-1.58), lymphopenia (OR 1.09; 95% CI 0.62-1.89), and anemia (OR 1.06; 95% CI 0.83-1.37). However, a significantly increased risk was observed for all-grade thrombocytopenia (OR 1.64; 95% CI 1.37-1.97), neutropenia (OR 2.24; 95% CI 1.67-3.02) and infections (OR 1.88; 95% CI 1.07-3.31).

conclusionQuadruplet therapy demonstrated a favorable efficacy and safety profile, with consistent benefit across subgroups. The findings support its potential as the new standard of care for TENDMM.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsMultiple MyelomaHumansProgression-Free SurvivalProteasome InhibitorsRandomized Controlled Trials as TopicProteasome Inhibitorsanti‐CD38 antibodydaratumumabisatuximabmultiple myeloma

Identifiers

PMID40176408
PMCPMC11965703

What OpenQuestion holds

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Registered trials

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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.