MétaCan
Menu
Back to cohort

P16 HEALTH-RELATED QUALITY OF LIFE FOR FRAIL TRANSPLANT-INELIGIBLE PATIENTS WITH NEWLY DIAGNOSED MULTIPLE MYELOMA TREATED WITH DARATUMUMAB, LENALIDOMIDE AND DEXAMETHASONE: SUBGROUP ANALYSIS OF MAIA TRIAL

2023· article· en· W4388738295 on OpenAlexaff
Thierry Façon, Torben Plesner, Saad Z. Usmani, Shaji Kumar, Nizar J. Bahlis, Cyrille Hulin, Robert Z. Orlowski, Hareth Nahi, Peter Mollee, Karthik Ramasamy, Murielle Roussel, Arnaud Jaccard, Michel Delforge, Lionel Karlin, Bertrand Arnulf, Ajai Chari, Huiling Pei, Neeraj Gupta, S. Kaila, K. Matt, Katharine S. Gries, Robin Carson, F. Borgsten, Katja Weisel, Aurore Perrot

Bibliographic record

VenueHemaSphere · 2023
Typearticle
Languageen
FieldMedicine
TopicMultiple Myeloma Research and Treatments
Canadian institutionsUniversity of Calgary
FundersJanssen Scientific AffairsCentre Hospitalier Universitaire de ToulouseUniversitätsklinikum Hamburg-EppendorfSyddansk UniversitetUniversité de ToulouseMemorial Sloan-Kettering Cancer CenterKarolinska InstitutetUniversity of Texas MD Anderson Cancer CenterAnkara UniversitesiUniversity of OxfordUniversité de LilleCancer Research Institute
KeywordsMedicineLenalidomideDaratumumabQuality of life (healthcare)Internal medicineMultiple myelomaPopulationDexamethasoneSubgroup analysisRandomized controlled trialSurgeryConfidence interval

Abstract

fetched live from OpenAlex

Introduction: In the primary analysis of the phase 3 MAIA trial (NCT02252172), daratumumab, lenalidomide and dexamethasone (D-Rd) improved progression-free survival (PFS) in transplant-ineligible (TIE) patients with newly diagnosed multiple myeloma (NDMM) vs Rd. With longer follow-up (median: 56.2 months), D-Rd continued to demonstrate PFS benefit, conferred an overall survival benefit, induced deeper responses, and was associated with clinically meaningful improvements in patient-reported outcomes (PROs) vs Rd. The median age of these patients was 73 years with 43.6% of patients aged ≥75 years. Consistent with the overall population, in a frailty subgroup analysis (median age: 77 years), D-Rd also demonstrated deeper responses and PFS benefit vs Rd (not reached vs 30.4 months; HR, 0.62; P = 0.003) in frail patients at a median follow-up of 36.4 months. Although, D-Rd improved clinical outcomes in these elderly frail patients, little is known about health-related quality of life (HRQoL) outcomes. In frail patients, improving HRQoL and minimizing the risk of toxicity is paramount. Here, we assess PROs in the frail patients in the MAIA trial. Methods: Patients were randomized 1:1 to D-Rd or Rd until disease progression (PD) or unacceptable toxicity. Frailty was assessed using the simplified frailty score. PROs were assessed using the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core 30-item. Questionnaires were completed at baseline, on day 1 of cycles 3, 6, 9, and 12 for year 1, and every 6 months thereafter until PD. Analyses were conducted on intent-to-treat patients. Treatment effect was assessed for change from baseline by a mixed-effects model for repeated measures. Meaningful thresholds for worsening were defined a priori based on published literature. Results: Overall, 737 patients were randomized; 341 patients were classified as frail (D-Rd, n=172; Rd, n=169). Over time, frail patients treated with D-Rd showed large reductions in pain from baseline (≥20-point change) and were greater with D-Rd than Rd. Fatigue symptoms were moderately reduced with both treatments. Increases in global health status (GHS) were consistent over time for both treatment groups. Patients treated with D-Rd showed improvements from baseline in physical functioning that were greater than Rd until cycle 42 and increases in emotional and social functioning were seen with both treatments that were numerically greater with D-Rd at several time points. Improvements in role functioning were seen with both treatments with no difference between treatments. No meaningful changes from baseline were observed in nausea and vomiting with either treatment. Median time to first worsening was longer with D-Rd than Rd for GHS. Median time to first worsening for the other functional (emotional, social, role) and symptom (nausea and vomiting) scales numerically favored D-Rd vs Rd, except cognitive functioning and fatigue. Median time to worsening of pain symptoms was not reached for D-Rd. Conclusions: Frail TIE patients with NDMM treated with D-Rd reported improvements in GHS (an overall HRQoL measure) and physical functioning, with a notable reduction in pain from baseline throughout the duration of therapy. D-Rd is not only clinically effective but also results in a sustained improvement in HRQoL for frail TIE patients with NDMM.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.024
Threshold uncertainty score0.935

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0020.000
Bibliometrics0.0000.002
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.045
GPT teacher head0.318
Teacher spread0.273 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations2
Published2023
Admission routes1
Has abstractyes

Explore more

Same venueHemaSphereSame topicMultiple Myeloma Research and TreatmentsFrench-language works237,207