Literature DB >> 24963044

The ethics of a proposed study of hematopoietic stem cell transplant for children with "less severe" sickle cell disease.

Robert S Nickel1, Jeanne E Hendrickson2, Ann E Haight1.   

Abstract

Hematopoietic stem cell transplant (HSCT) is the only cure for sickle cell disease (SCD). HSCT using an HLA-identical sibling donor is currently an acceptable treatment option for children with severe SCD, with expected HSCT survival >95% and event-free survival >85%. HSCT for children with less severe SCD (children who have not yet suffered overt disease complications or only had mild problems) is controversial. It is important to consider the ethical issues of a proposed study comparing HLA-identical sibling HSCT to best supportive care for children with less severe SCD. In evaluating the principles of nonmaleficence, respect for individual autonomy, and justice, we conclude that a study of HLA-identical sibling HSCT for all children with SCD, particularly hemoglobin SS and Sβ(0)-thalassemia disease, is ethically sound. Future work should explore the implementation of a large trial to help determine whether HSCT is a beneficial treatment of children with less severe SCD.
© 2014 by The American Society of Hematology.

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Year:  2014        PMID: 24963044     DOI: 10.1182/blood-2014-05-575209

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  8 in total

Review 1.  Curative therapies: Allogeneic hematopoietic cell transplantation from matched related donors using myeloablative, reduced intensity, and nonmyeloablative conditioning in sickle cell disease.

Authors:  Gregory M T Guilcher; Tony H Truong; Santosh L Saraf; Jacinth J Joseph; Damiano Rondelli; Matthew M Hsieh
Journal:  Semin Hematol       Date:  2018-04-25       Impact factor: 3.851

Review 2.  How I treat sickle cell disease with hematopoietic cell transplantation.

Authors:  Elizabeth O Stenger; Shalini Shenoy; Lakshmanan Krishnamurti
Journal:  Blood       Date:  2019-12-19       Impact factor: 22.113

Review 3.  Pediatric sickle cell disease: past successes and future challenges.

Authors:  Emily Riehm Meier; Angeli Rampersad
Journal:  Pediatr Res       Date:  2016-10-05       Impact factor: 3.756

4.  Sickle cell disease: an international survey of results of HLA-identical sibling hematopoietic stem cell transplantation.

Authors:  Eliane Gluckman; Barbara Cappelli; Francoise Bernaudin; Myriam Labopin; Fernanda Volt; Jeanette Carreras; Belinda Pinto Simões; Alina Ferster; Sophie Dupont; Josu de la Fuente; Jean-Hugues Dalle; Marco Zecca; Mark C Walters; Lakshmanan Krishnamurti; Monica Bhatia; Kathryn Leung; Gregory Yanik; Joanne Kurtzberg; Nathalie Dhedin; Mathieu Kuentz; Gerard Michel; Jane Apperley; Patrick Lutz; Bénédicte Neven; Yves Bertrand; Jean Pierre Vannier; Mouhab Ayas; Marina Cavazzana; Susanne Matthes-Martin; Vanderson Rocha; Hanadi Elayoubi; Chantal Kenzey; Peter Bader; Franco Locatelli; Annalisa Ruggeri; Mary Eapen
Journal:  Blood       Date:  2016-12-13       Impact factor: 22.113

Review 5.  Sickle Cell Disease: Advances in Treatment.

Authors:  Renée V Gardner
Journal:  Ochsner J       Date:  2018

Review 6.  Hematopoietic stem cell transplantation in sickle cell disease: patient selection and special considerations.

Authors:  Monica Bhatia; Sujit Sheth
Journal:  J Blood Med       Date:  2015-07-10

7.  A Child as a Donor for Hematopoietic Stem Cell Transplantation: Bioethical Justification-A Case Study on Sickle Cell Disease.

Authors:  Andrea Z Pereira; Ricardo Hellman; Nelson Hamerschlak; Andrea Kondo; Polianna Mara Rodrigues de Souza; Wilson Leite Pedreira; Luiz Fernando Alves Lima Mantovani; Eduardo Juan Troster; Henrique Grunspun; Marco Aurélio Scarpinella Bueno
Journal:  Case Rep Hematol       Date:  2017-02-23

8.  Awareness and Acceptance of Hematopoietic Stem Cell Transplantation for Sickle Cell Disease in Jazan Province, Saudi Arabia.

Authors:  Eman Hurissi; Alaa Hakami; Jawahir Homadi; Fatimah Kariri; Ethar Abu-Jabir; Rahaf Alamer; Raghad Mobarki; Abdulaziz A Jaly; Edrous Alamer; Abdulaziz H Alhazmi
Journal:  Cureus       Date:  2022-01-07
  8 in total

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