MétaCan
Menu
← Back to cohort
Record W4405039231 · doi:10.1182/blood-2024-208803

Patient Preferences on Clinical Decision-Making in Myeloma: A 747-Patient Survey

2024· article· en· W4405039231 on OpenAlexaff
Ghulam Rehman Mohyuddin, Rajshekhar Chakraborty, Katherine Berger, Ryan Winborg, Mason S. Barnes, Jorge Arturo Hurtado Martínez, Jay R. Hydren, Douglas W Sborov, Amandeep Godara, Brian McClune, Christopher M. Booth, Edward R. Scheffer Cliff

Bibliographic record

VenueBlood · 2024
Typearticle
Languageen
FieldMedicine
TopicMultiple Myeloma Research and Treatments
Canadian institutionsQueen's University
Fundersnot available
KeywordsMultiple myelomaMedicineClinical decision makingFamily medicineInternal medicine

Abstract

fetched live from OpenAlex

Introduction: The advent of many novel myeloma treatments has increased the complexity of decision making for doctors and patients. Multiple available treatment options (some longstanding and others newly approved) lead to improved surrogate outcomes such as progression-free survival (PFS) but have not been shown to extend overall survival (OS). To better understand the priorities that underpin myeloma patients' preferences and guide their treatment decisions, we surveyed patients with myeloma about four different treatment scenarios, each with similar OS but substantially different surrogate outcomes. Methods: The HealthTree® Cure Hub by the HealthTree Foundation is the largest online portal designed to help people with plasma cell dyscrasias navigate their disease. Using this platform, we conducted a 4-question survey to investigate patient preferences. Question 1 presented the choice of a 3 drug versus a 4 drug option for newly diagnosed myeloma. Both options provided patients with a similar quality of life and 4-year OS, but the 4-drug option improved PFS (84% vs 67% at 4 years, similar to the PERSEUS trial), with increased risk of infection and neutropenia. We did not use the term “PFS” but rather described the concept in simple terms. Question 2 assumed a good response to induction therapy and presented a choice of a one-time treatment to deepen remission (analogous to melphalan autograft), or a continuation of the induction treatment once weekly for 4 additional months. The one-time treatment had a high likelihood of causing 3 months of decreased quality of life due to short term side effects. This one-time treatment increased the PFS at 5 years from 65% to 81% with no change in 5 year OS (similar to the DETERMINATION trial). Question 3 presented a choice between 1 drug or 2 drug maintenance. The 2 drug option increased 3 year PFS from 65% to 75% (similar to the FORTE trial), with similar 3 year OS. The 2 drug option had greater risks and side effects, such as those seen with the addition of carfilzomib (increased blood pressure, fevers, and cardiac toxicity). Question 4 presented the option of a treatment for multiply relapsed disease that improved PFS by 2 months and increased the likelihood of side effects but did not improve OS. The IRB-approved survey was open from April-May 2024. Statistics were assessed descriptively with Chi squares performed for between-group comparisons. Results: 747 responses were obtained. The median age of participants was 66 years (interquartile range 60-71), and most participants were female (59%) and white (91%). Of those who provided complete diagnostic information (405/747), 83% have MM and 17% have MM precursor conditions. No statistically significant differences were seen between the responses of those of have MM and those who have MM precursors. Further subset analysis will be presented at the meeting. In the 3 drug versus 4 drug scenario, 51% of participants chose 4 drug induction, and 49% chose the three drug option. For the one-time consolidation versus 4 months of weekly therapy to deepen response, 47% of participants chose a one-time treatment with 3 months of side effects, and 53% of participants chose the 4-month treatment option. 84% of participants chose 1 drug maintenance with shorter PFS compared to just 16% who chose 2 drug maintenance, with greater risks and side effects but a 10-month longer PFS. When evaluating an option for multiply relapsed disease that improved PFS but had no impact on OS, 93% of participants chose not to receive this treatment. Conclusion: Our analysis demonstrates substantial heterogeneity in patient preferences and priorities when choosing between treatments that improve PFS but not OS. For induction regimens (triplet versus quadruplet) and the use of a one-time intervention analogous to transplant to deepen response, approximately half of patients chose each option in both cases. In comparison, when evaluating long-term maintenance therapy with 2 drugs vs a single drug, or when evaluating options for multiply relapsed disease that improve PFS but not OS, the vast majority of patients choose the less toxic option that offers similar OS, even when PFS is inferior. These results provide guidance to other patients, clinicians (especially when counseling patients), industry, and regulators on patient preferences for therapies in newly diagnosed myeloma, facilitating patient-centered clinical trial design and drug development in future.

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 machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.005
metaresearch head score (Gemma)0.017
Version: metacan-v3-hybrid-931329e0061cValidation 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 score0.005
Threshold uncertainty score0.029

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0050.017
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.001
Bibliometrics0.0010.001
Science and technology studies0.0010.001
Scholarly communication0.0020.002
Open science0.0000.001
Research integrity0.0010.002
Insufficient payload (model declined to judge)0.0040.001

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 head0.073
GPT teacher head0.399
Teacher spread0.326 · 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 source (direct Gemma or distilled Codex), 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

Citations3
Published2024
Admission routes1
Has abstractyes

Explore more

Same venueBlood→Same topicMultiple Myeloma Research and Treatments→French-language works237,207→