Evidence map›Paper›PMID 37905989›Full record

ArticleBlood advances2023

Preferences for potential benefits and risks for gene therapy in the treatment of sickle cell disease.

Juan Marcos Gonzalez Sepulveda, Jui-Chen Yang, Shelby D Reed, Ting-Hsuan Lee, Xinyi Ng, Sarah Stothers, Telba Irony, Martin Ho, Jennifer A Rothman, Sherif Badawy and 5 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
8.7field-weighted citation impact, top 2% of its field
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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 5 institutions in 2 countries.

Juan Marcos Gonzalez SepulvedaDuke University School of Medicine, Durham, NC.ORCID 0000-0002-5386-0907
Jui-Chen YangDuke Clinical Research Institute, Durham, NC.
Shelby D ReedDuke University School of Medicine, Durham, NC.
Ting-Hsuan LeeCenter for Biologics Evaluation and Research, Office of Biostatistics and Pharmacovigilance, US Food and Drug Administration, Rockville, MD.
Xinyi NgCenter for Biologics Evaluation and Research, Office of Biostatistics and Pharmacovigilance, US Food and Drug Administration, Rockville, MD.
Sarah StothersCenter for Biologics Evaluation and Research, Office of Biostatistics and Pharmacovigilance, US Food and Drug Administration, Rockville, MD.
Telba IronyCenter for Biologics Evaluation and Research, Office of Biostatistics and Pharmacovigilance, US Food and Drug Administration, Rockville, MD.
Martin HoCenter for Biologics Evaluation and Research, Office of Biostatistics and Pharmacovigilance, US Food and Drug Administration, Rockville, MD.
Jennifer A RothmanDuke University School of Medicine, Durham, NC.ORCID 0000-0003-1582-2886
Sherif BadawyLurie Children's Hospital of Chicago, Chicago, IL.
Carolyn RowleyCayenne Wellness Center, Burbank, CA.
Jane LittleDivision of Hematology, The University of North Carolina, Chapel Hill, NC.
Nirmish R ShahDuke University School of Medicine, Durham, NC.ORCID 0000-0002-7506-0935
Kaiwen LiDuke University School of Medicine, Durham, NC.
Marilyn J TelenDuke University School of Medicine, Durham, NC.ORCID 0000-0003-3809-1780
Duke University · USCenter for Biologics Evaluation and Research · USCalifornia Wellness Foundation · USNorthwestern University · USUniversity of North Carolina at Chapel Hill · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective of this study is to quantify benefit-risk tradeoffs pertaining to potential gene therapies among adults and parents/caregivers of children with sickle cell disease (SCD). A discrete-choice experiment survey was developed in which respondents selected their preferred treatment alternatives in a series of experimentally controlled pairs of hypothetical gene therapies and a "no gene therapy" option. Gene therapy alternatives were defined based on the chance of eliminating SCD symptoms, expected increases in life expectancy they could offer, treatment-related risk of death, and potential increases in lifetime cancer risk. Respondents made selections based on their current disease severity and in the context of expectations of worsened disease. Three clinical sites and 1 patient organization recruited 174 adult patients and 109 parents of children with SCD to complete the survey. Adult and parent respondents were generally willing to choose gene therapies, but the adults required higher expected levels of efficacy (ie, higher chance of eliminating symptoms) than parents to choose gene therapies that conferred mortality risks of ≥10%. When adults and parents of children with less severe symptoms were asked to consider scenarios of higher levels of disease severity, the increased risk tolerance, and the lowest acceptable level of efficacy for gene therapies with mortality risks dropped by >50%. Baseline SCD symptoms are a major driver of gene therapy acceptability. Adults and parents of patients with milder symptoms may prefer other treatment options; however, an expectation of symptoms deterioration triggers strong reassessment of the acceptable benefit-risk balance of this novel technology.

Indexed as

Anemia, Sickle CellAdultChildGenetic TherapyHumansParentsRisk AssessmentSurveys and Questionnaires

Identifiers

PMID37905989
PMCPMC10726244
OpenAlexW4388033885

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.