Characteristics and Trends of Adult Acute Lymphoblastic Leukemia in a Large, Public Safety-Net Hospital.


Journal

Clinical lymphoma, myeloma & leukemia
ISSN: 2152-2669
Titre abrégé: Clin Lymphoma Myeloma Leuk
Pays: United States
ID NLM: 101525386

Informations de publication

Date de publication:
06 2020
Historique:
received: 13 07 2019
revised: 17 10 2019
accepted: 01 11 2019
pubmed: 23 3 2020
medline: 1 6 2021
entrez: 23 3 2020
Statut: ppublish

Résumé

Management of acute lymphoblastic leukemia (ALL) in a socioeconomically vulnerable population without ready access to a hematopoietic stem cell transplant (HCT) center and clinical trials is challenging. Data regarding the outcomes of such patients are sparse. This retrospective analysis included 90 consecutive patients with ALL who presented to Harbor-UCLA between 2003 and 2018. The primary objective was overall survival (OS), whereas secondary objectives included leukemia-free survival, toxicities of therapy, and referral for HCT and incidence of successful HCT. Most patients were male (56.7%) and Hispanic (72.2%). The median age of diagnosis was 36 years (range, 18-63 years). The median OS was 26.8 months (95% confidence interval [CI], 17.4-59.0 months). In patients who achieved complete remission with therapy, the median leukemia-free survival was 16.4 months. Fifty percent of patients experienced at least 1 episode of bacteremia, and nearly 25% of patients developed an invasive fungal infection. Thirty-six percent (n = 32) of patients were referred for HCT. The referral rate increased over time, which led to improved OS in patients who underwent evaluation at a tertiary cancer center (hazard ratio, 0.44; 95% CI, 0.21-0.89; P = .02). Patients who underwent HCT had significantly better OS compared with those who did not (OS not reached vs. 21.9 months; hazard ratio, 0.16; 95% CI, 0.04-0.68; P = .01). Risk stratification and evidence-based treatment approaches are important for patients with ALL treated in a resource-limited setting. Most patients can be induced successfully and achieve complete remission with therapy. Partnership with a cancer center with early referral for HCT can facilitate curative HCT to be performed.

Sections du résumé

BACKGROUND
Management of acute lymphoblastic leukemia (ALL) in a socioeconomically vulnerable population without ready access to a hematopoietic stem cell transplant (HCT) center and clinical trials is challenging. Data regarding the outcomes of such patients are sparse.
PATIENTS AND METHODS
This retrospective analysis included 90 consecutive patients with ALL who presented to Harbor-UCLA between 2003 and 2018. The primary objective was overall survival (OS), whereas secondary objectives included leukemia-free survival, toxicities of therapy, and referral for HCT and incidence of successful HCT.
RESULTS
Most patients were male (56.7%) and Hispanic (72.2%). The median age of diagnosis was 36 years (range, 18-63 years). The median OS was 26.8 months (95% confidence interval [CI], 17.4-59.0 months). In patients who achieved complete remission with therapy, the median leukemia-free survival was 16.4 months. Fifty percent of patients experienced at least 1 episode of bacteremia, and nearly 25% of patients developed an invasive fungal infection. Thirty-six percent (n = 32) of patients were referred for HCT. The referral rate increased over time, which led to improved OS in patients who underwent evaluation at a tertiary cancer center (hazard ratio, 0.44; 95% CI, 0.21-0.89; P = .02). Patients who underwent HCT had significantly better OS compared with those who did not (OS not reached vs. 21.9 months; hazard ratio, 0.16; 95% CI, 0.04-0.68; P = .01).
CONCLUSION
Risk stratification and evidence-based treatment approaches are important for patients with ALL treated in a resource-limited setting. Most patients can be induced successfully and achieve complete remission with therapy. Partnership with a cancer center with early referral for HCT can facilitate curative HCT to be performed.

Identifiants

pubmed: 32199763
pii: S2152-2650(19)32100-7
doi: 10.1016/j.clml.2019.11.003
pii:
doi:

Types de publication

Clinical Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e320-e327

Informations de copyright

Published by Elsevier Inc.

Auteurs

Rohan Gupta (R)

Division of Hematology and Medical Oncology, Harbor-UCLA Medical Center, Torrance, CA; Department of Hematology and Hematopoietic Cell Transplant, City of Hope National Medical Center, Duarte, CA.

Tamer Othman (T)

Department of Internal Medicine, Harbor-UCLA Medical Center, Torrance, CA.

An Uche (A)

Division of Hematology and Medical Oncology, Harbor-UCLA Medical Center, Torrance, CA.

Idoroenyi Amanam (I)

Division of Hematology and Medical Oncology, Harbor-UCLA Medical Center, Torrance, CA; Department of Hematology and Hematopoietic Cell Transplant, City of Hope National Medical Center, Duarte, CA.

Chen Chen (C)

Center for Informatics, City of Hope Cancer Center, Duarte, CA.

Larissa Celles (L)

Division of Hematology and Medical Oncology, Harbor-UCLA Medical Center, Torrance, CA.

Gregorianna Lane (G)

Division of Hematology and Medical Oncology, Harbor-UCLA Medical Center, Torrance, CA.

Matthew Mei (M)

Department of Hematology and Hematopoietic Cell Transplant, City of Hope National Medical Center, Duarte, CA.

Ibrahim Aldoss (I)

Department of Hematology and Hematopoietic Cell Transplant, City of Hope National Medical Center, Duarte, CA.

Vinod Pullarkat (V)

Department of Hematology and Hematopoietic Cell Transplant, City of Hope National Medical Center, Duarte, CA.

Phyllis Kim (P)

Division of Hematology and Medical Oncology, Harbor-UCLA Medical Center, Torrance, CA.

James Yeh (J)

Division of Hematology and Medical Oncology, Harbor-UCLA Medical Center, Torrance, CA. Electronic address: jamyeh@dhs.lacounty.gov.

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