Literature DB >> 34735685

Treatment decision-making in sickle cell disease patients.

A Booth1, V Bonham2, M Porteus3, K E Ormond4,5.   

Abstract

Sickle cell disease (SCD) is a blood disorder with few treatment options currently available. However, in recent years, there has been much progress toward developing new therapies and curative treatments to help patients with SCD. Stem cell transplant remains the only approved curative treatment for SCD, but new clinical trials are being initiated using gene therapy and gene editing. We surveyed patients with sickle cell disease (N=9) about attitudes toward stem cell transplant, gene therapy to add a new healthy gene, gene editing to up-regulate fetal hemoglobin, or gene editing to correct the point mutation. The participants read a fact sheet that included objective information on each curative treatment. When asked which curative treatment each participant would choose, all four options were selected at least once. The most highly selected treatment was gene correction gene editing (N=4). Participants generally agreed that the four treatment options are beneficial but were more mixed in their thoughts on whether the options are dangerous. Reasons for selecting a particular curative treatment were variable, but the most selected reasons were perception of a cure (N=4) or decreased severity (N=4), and not needing a donor (N=4). We are at the beginning stages of understanding how patients with SCD make decisions about curative treatments. Currently, patients may be interested in any of the four possibilities for curative treatments, with gene correction gene editing as the most popular choice. Reasons for choosing one treatment over another are mixed.
© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  CRISPR; Curative treatments; Decision-making; Gene editing; Gene therapy; Sickle cell disease

Year:  2021        PMID: 34735685      PMCID: PMC8799810          DOI: 10.1007/s12687-021-00562-z

Source DB:  PubMed          Journal:  J Community Genet        ISSN: 1868-310X


  17 in total

Review 1.  Fetal hemoglobin in sickle cell anemia.

Authors:  Idowu Akinsheye; Abdulrahman Alsultan; Nadia Solovieff; Duyen Ngo; Clinton T Baldwin; Paola Sebastiani; David H K Chui; Martin H Steinberg
Journal:  Blood       Date:  2011-04-13       Impact factor: 22.113

Review 2.  Gene therapy for sickle cell disease: An update.

Authors:  Selami Demirci; Naoya Uchida; John F Tisdale
Journal:  Cytotherapy       Date:  2018-05-30       Impact factor: 5.414

3.  Gene Therapy for Sickle Cell Disease Shows Promise.

Authors:  Rita Rubin
Journal:  JAMA       Date:  2019-01-29       Impact factor: 56.272

4.  Therapy preference and decision-making among patients with severe sickle cell anemia and their families.

Authors:  Jane Hankins; Pamela Hinds; Sara Day; Yvonne Carroll; Chin-Shang Li; Patricia Garvie; Winfred Wang
Journal:  Pediatr Blood Cancer       Date:  2007-06-15       Impact factor: 3.167

5.  Induction of fetal hemoglobin synthesis by CRISPR/Cas9-mediated editing of the human β-globin locus.

Authors:  Chiara Antoniani; Vasco Meneghini; Annalisa Lattanzi; Tristan Felix; Oriana Romano; Elisa Magrin; Leslie Weber; Giulia Pavani; Sara El Hoss; Ryo Kurita; Yukio Nakamura; Thomas J Cradick; Ante S Lundberg; Matthew Porteus; Mario Amendola; Wassim El Nemer; Marina Cavazzana; Fulvio Mavilio; Annarita Miccio
Journal:  Blood       Date:  2018-03-08       Impact factor: 22.113

Review 6.  Hematopoietic stem cell transplantation for patients with sickle cell disease: progress and future directions.

Authors:  Courtney D Fitzhugh; Allistair A Abraham; John F Tisdale; Matthew M Hsieh
Journal:  Hematol Oncol Clin North Am       Date:  2014-09-29       Impact factor: 3.722

Review 7.  Systematic review: Hydroxyurea for the treatment of adults with sickle cell disease.

Authors:  Sophie Lanzkron; John J Strouse; Renee Wilson; Mary Catherine Beach; Carlton Haywood; HaeSong Park; Catherine Witkop; Eric B Bass; Jodi B Segal
Journal:  Ann Intern Med       Date:  2008-05-05       Impact factor: 25.391

Review 8.  Blood and marrow transplantation for sickle cell disease: overcoming barriers to success.

Authors:  Javier Bolaños-Meade; Robert A Brodsky
Journal:  Curr Opin Oncol       Date:  2009-03       Impact factor: 3.645

9.  Hematopoietic stem-cell transplantation for sickle cell disease: current evidence and opinions.

Authors:  Shalini Shenoy
Journal:  Ther Adv Hematol       Date:  2013-10

10.  Patient Perspectives on Gene Transfer Therapy for Sickle Cell Disease.

Authors:  Heather Strong; Monica J Mitchell; Alana Goldstein-Leever; Lisa Shook; Punam Malik; Lori E Crosby
Journal:  Adv Ther       Date:  2017-07-17       Impact factor: 3.845

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