Real-world treatment patterns and clinical outcomes in patients with AML unfit for first-line intensive chemotherapy


Journal

Leukemia & lymphoma
ISSN: 1029-2403
Titre abrégé: Leuk Lymphoma
Pays: United States
ID NLM: 9007422

Informations de publication

Date de publication:
04 2022
Historique:
pubmed: 12 2 2022
medline: 21 4 2022
entrez: 11 2 2022
Statut: ppublish

Résumé

Acute myeloid leukemia (AML) predominantly affects the elderly, and prognosis declines with age. Induction chemotherapy plus consolidation therapy is standard of care for fit patients; options for unfit patients include hypomethylating agents (HMA), low-dose cytarabine (LDAC), targeted therapies, and best supportive care (BSC). This retrospective chart review evaluated clinical outcomes in unfit patients with AML who initiated first-line treatment or BSC 01/01/2015-12/31/2018. Overall survival (OS), progression-free survival (PFS), time-to-treatment failure (TTF), and response rates were assessed. Of 1762 patients, 1310 received systemic therapies: 809 HMA, 199 LDAC, and 302 other therapies; 452 received BSC. Median OS was 9.9, 7.9, 5.4, and 2.5 months for HMA, LDAC, other, and BSC, respectively. Median PFS was 7.5, 5.3, 4.1, and 2.1 months for HMA, LDAC, other, and BSC, respectively; median TTF was 4.9, 2.1, 2.2, and 2.1 months, respectively. Our findings highlight the unmet need for novel therapies for unfit patients.

Identifiants

pubmed: 35147482
doi: 10.1080/10428194.2021.2002321
doi:

Substances chimiques

Cytarabine 04079A1RDZ

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

928-938

Auteurs

Toshihiro Miyamoto (T)

Medicine and Biosystemic Science, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.

David Sanford (D)

Leukemia/Bone Marrow Transplant Program of BC, Division of Hematology, The University of British Columbia, Vancouver, BC, Canada.

Ciprian Tomuleasa (C)

Department of Hematology - Medfuture Research Center for Advanced Medicine, Ion Chiricuta Clinical Cancer Center, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Hui-Hua Hsiao (HH)

Department of Internal Medicine, Division of Hematology-Oncology, Kaohsiung Medical University Hospital and Kaohsiung Medical University, Kaohsiung, Taiwan.

Leonardo José Enciso Olivera (LJE)

Instituto Nacional de Cancerología, Bogotá, Colombia.

Anoop Kumar Enjeti (AK)

Calvary Mater Newcastle, University of Newcastle and New South Wales Health Pathology, Waratah, Australia.

Alberto Gimenez Conca (A)

Section of Hematology, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina.

Teresa Bernal Del Castillo (TBD)

Servicio de Hematología y Hemoterapia, University Hospital Central de Asturias, ISPA, IUOPA, Oviedo, Spain.

Larisa Girshova (L)

Federal State Budgetary Institution 'Almazov National Medical Research Centre' of the Ministry of Health of the Russian Federation, St. Petersburg, Russia.

Maria Paola Martelli (MP)

Department of Medicine and Surgery - Section of Hematology and Clinical Immunology, Perugia University, 'Santa Maria della Misericordia' Hospital, Perugia, Italy.

Birol Guvenc (B)

Department of Hematology, Faculty of Medicine, Cukurova University, Adana, Turkey.

Alexander Delgado (A)

AbbVie, Inc., Singapore, Singapore.

Yinghui Duan (Y)

AbbVie, Inc., North Chicago, IL, USA.

Belen Garbayo Guijarro (B)

AbbVie, Inc., Madrid, Spain.

Cynthia Llamas (C)

AbbVie, Inc., North Chicago, IL, USA.

Je-Hwan Lee (JH)

Department of Hematology, University of Ulsan College of Medicine and Asan Medical Center, Seoul, Republic of Korea.

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Classifications MeSH