Evidence map›Paper›PMID 39376032›Full record

ArticleCancer reports (Hoboken, N.J.)2024

Improving Health Outcomes Through Treatment Sequencing Optimization in Multiple Myeloma: A Simulation Model in Transplant-Ineligible Patients.

C Geraldes, M Neves, R Bergantim, C Silva, F Leal da Costa

Abstract read
In one paragraph

Article in Cancer reports (Hoboken, N.J.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. Article
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.

C GeraldesCentro Hospitalar Universitário de Coimbra, Coimbra, Portugal.
M NevesFundação Champalimaud, Lisboa, Portugal.
R BergantimFaculty of Medicine of the University of Porto (FMUP), Porto, Portugal; i3S - Institute for Research and Innovation in Health, University of Porto, Porto, Portugal; Cancer Drug Resistance Group, Institute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, Portugal; Department of Hematology, Centro Hospitalar Universitário de São João, Porto, Portugal.
C SilvaInstitute for Evidence-Based Health (ISBE), Lisboa, Portugal.ORCID 0009-0005-5079-1677
F Leal da CostaInstituto Português de Oncologia, Lisboa, Portugal.

Funding

Johnson & Johnson Innovative Medicines
6 · The paper itself

Abstract

objectivesPatients with multiple myeloma often require multiple treatment lines. The order in which treatments are sequenced has impact on clinical outcomes. This study aimed to estimate progression-free survival (PFS) and overall survival (OS) with common treatment sequences used in Portugal and the incremental benefit of an optimal sequence in transplant-ineligible patients with multiple myeloma.

methodsA state-transition sequential model with a five-health state conceptual structure was developed to simulate and compare survival outcomes between treatment sequences up to four lines of treatments. Data sources included randomized clinical trials and indirect treatment comparisons. A panel of Portuguese hematologists listed four most common treatment sequences and optimal sequence of choice in transplant-ineligible patients.

resultsOur simulation estimated an OS between 6.1 and 7.8 years using the most common sequences, with VMP + DRd + Pd + Kd as the most effective (7.8 years). Optimal sequence of choice (DRd + PVd + Kd + Vd) achieved OS of 9.8 years and may extend OS in 2.0-3.7 years vs. most common sequences (26%-61% increase). This benefit was mostly explained by extended PFS in the first line of treatment.

conclusionModel results demonstrate that choosing the most effective treatment upfront is crucial in delaying disease progression thus yielding better survival outcomes in transplant-ineligible patients. There was a clear survival benefit in using daratumumab-based regimens in first line. This modelling exercise highlights the need to raise awareness around the impact of sequencing strategies to improve patient's outcomes.

Indexed as

Multiple MyelomaAntineoplastic Combined Chemotherapy ProtocolsComputer SimulationHumansPortugalProgression-Free SurvivalRandomized Controlled Trials as Topicmultiple myelomaoptimizationoutcomesoverall survivalsimulationtreatment sequencing

Identifiers

PMID39376032
PMCPMC11458883

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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.