Multisite 11-year experience of less-intensive vs intensive therapies in acute myeloid leukemia

Author:

Sorror Mohamed L.12ORCID,Storer Barry E.34,Fathi Amir T.5ORCID,Brunner Andrew5,Gerds Aaron T.6ORCID,Sekeres Mikkael A.6,Mukherjee Sudipto6,Medeiros Bruno C.7,Wang Eunice S.8,Vachhani Pankit8ORCID,Shami Paul J.9,Peña Esteban9,Elsawy Mahmoud110,Adekola Kehinde11ORCID,Luger Selina12,Baer Maria R.13,Rizzieri David14ORCID,Wildes Tanya M.15,Koprivnikar Jamie16,Smith Julie17,Garrison Mitchell17,Kojouri Kiarash18,Leisenring Wendy3ORCID,Onstad Lynn3,Nyland Jennifer E.19ORCID,Becker Pamela S.120ORCID,McCune Jeannine S.121ORCID,Lee Stephanie J.12ORCID,Sandmaier Brenda M.12ORCID,Appelbaum Frederick R.12,Estey Elihu H.120

Affiliation:

1. Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA;

2. Division of Medical Oncology, Department of Medicine, University of Washington School of Medicine, Seattle, WA;

3. Clinical Statistics Program, Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA;

4. Department of Biostatistics, University of Washington School of Public Health, Seattle, WA;

5. Massachusetts General Hospital, Harvard Medical School, Boston, MA;

6. Leukemia & Myeloid Disorders Program, Cleveland Clinic, Cleveland, OH;

7. Division of Hematology, Department of Medicine, Stanford University, Stanford, CA;

8. Roswell Park Cancer Institute, Buffalo, NY;

9. Division of Hematology and Hematologic Malignancies, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT;

10. Division of Hematology, Department of Medicine, Dalhousie University, Halifax, NS, Canada;

11. Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL;

12. Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA;

13. Greenebaum Comprehensive Cancer Center, University of Maryland, Baltimore, MD;

14. Division of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, NC;

15. Division of Oncology, Washington University School of Medicine, St Louis, MO;

16. John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, NJ;

17. Confluence Health/Wenatchee Valley Hospital and Clinic, Wenatchee, WA;

18. Skagit Valley Hospital, Mount Vernon, WA;

19. Penn State College of Medicine, Hershey, PA;

20. Division of Hematology, Department of Medicine, University of Washington School of Medicine, Seattle, WA; and

21. Department of Population Sciences, City of Hope, Duarte, CA

Abstract

Abstract Less-intensive induction therapies are increasingly used in older patients with acute myeloid leukemia (AML). Using an AML composite model (AML-CM) assigning higher scores to older age, increased comorbidity burdens, and adverse cytogenetic risks, we defined 3 distinct prognostic groups and compared outcomes after less-intensive vs intensive induction therapies in a multicenter retrospective cohort (n = 1292) treated at 6 institutions from 2008 to 2012 and a prospective cohort (n = 695) treated at 13 institutions from 2013 to 2017. Prospective study included impacts of Karnofsky performance status (KPS), quality of life (QOL), and physician perception of cure. In the retrospective cohort, recipients of less-intensive therapies were older and had more comorbidities, more adverse cytogenetics, and worse KPS. Less-intensive therapies were associated with higher risks of mortality in AML-CM scores of 4 to 6, 7 to 9, and ≥10. Results were independent of allogeneic transplantation and similar in those age 70 to 79 years. In the prospective cohort, the 2 groups were similar in baseline QOL, geriatric assessment, and patient outcome preferences. Higher mortality risks were seen after less-intensive therapies. However, in models adjusted for age, physician-assigned KPS, and chance of cure, mortality risks and QOL were similar. Less-intensive therapy recipients had shorter length of hospitalization (LOH). Our study questions the survival and QOL benefits (except LOH) of less-intensive therapies in patients with AML, including those age 70 to 79 years or with high comorbidity burdens. A randomized trial in older/medically infirm patients is required to better assess the value of less-intensive and intensive therapies or their combination. This trial was registered at www.clinicaltrials.gov as #NCT01929408.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference53 articles.

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3