Real-world predictors of survival in patients with limited-stage small-cell lung cancer in Manitoba, Canada.

limited-stage long-term survival performance status real world small-cell lung cancer

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2023
Historique:
received: 22 03 2023
accepted: 03 11 2023
medline: 21 12 2023
pubmed: 21 12 2023
entrez: 21 12 2023
Statut: epublish

Résumé

Although therapy for limited-stage small-cell lung cancer (LS-SCLC) is administered with curative intent, most patients relapse and eventually die of recurrent disease. Chemotherapy (CT) with concurrent radiotherapy (RT) remains the standard of care for LS-SCLC; however, this could evolve in the near future. Therefore, understanding the current prognostic factors associated with survival is essential. This real-world analysis examines factors associated with long-term survival in patients with LS-SCLC treated with CT in Manitoba, Canada. A retrospective cohort study was conducted using Manitoba Cancer Registry and CancerCare Manitoba records. Eligible patients were aged >18 years and had cytologically confirmed LS-SCLC diagnosed between January 1, 2004, and December 31, 2018, for which they received CT ± RT. Baseline patient, disease, and treatment characteristics and survival duration, characterized as short (<6 months), medium (6-24 months), and long term (>24 months), were extracted. Overall survival (OS) was estimated at one, two, and five years and assessed using Kaplan-Meier methods and Cox proportional hazards models. Over the 15-year study period, 304 patients met the eligibility criteria. Long-term survivors comprised 39.1% of the cohort; at diagnosis, this subgroup was younger, more likely to have Eastern Cooperative Oncology Group Performance Status (ECOG PS) 0, and have normal lactate dehydrogenase, sodium, and hemoglobin levels. OS estimates for the entire cohort at one, two, and five years were 66%, 38%, and 18%, respectively. In the ECOG PS 0 subgroup, OS estimates at one, two, and five years were 85%, 52%, and 24%, respectively; OS estimates were 60%, 35%, and 17%, respectively, for ECOG PS 1-2 and were 47%, 23%, and 10%, respectively, for ECOG PS 3-4. OS was significantly higher among patients with normal serum sodium and hemoglobin levels than those with abnormal levels. Univariable hazard regression models found that ECOG PS, age at diagnosis, receipt of prophylactic cranial irradiation (PCI), and thoracic RT were associated with survival. On multivariable hazard regression, ECOG PS and receipt of PCI were associated with survival. Survival for greater than two years in patients with LS-SCLC treated with CT ± RT was associated with ECOG PS and receipt of PCI.

Sections du résumé

Background UNASSIGNED
Although therapy for limited-stage small-cell lung cancer (LS-SCLC) is administered with curative intent, most patients relapse and eventually die of recurrent disease. Chemotherapy (CT) with concurrent radiotherapy (RT) remains the standard of care for LS-SCLC; however, this could evolve in the near future. Therefore, understanding the current prognostic factors associated with survival is essential.
Objective UNASSIGNED
This real-world analysis examines factors associated with long-term survival in patients with LS-SCLC treated with CT in Manitoba, Canada.
Methods UNASSIGNED
A retrospective cohort study was conducted using Manitoba Cancer Registry and CancerCare Manitoba records. Eligible patients were aged >18 years and had cytologically confirmed LS-SCLC diagnosed between January 1, 2004, and December 31, 2018, for which they received CT ± RT. Baseline patient, disease, and treatment characteristics and survival duration, characterized as short (<6 months), medium (6-24 months), and long term (>24 months), were extracted. Overall survival (OS) was estimated at one, two, and five years and assessed using Kaplan-Meier methods and Cox proportional hazards models.
Results UNASSIGNED
Over the 15-year study period, 304 patients met the eligibility criteria. Long-term survivors comprised 39.1% of the cohort; at diagnosis, this subgroup was younger, more likely to have Eastern Cooperative Oncology Group Performance Status (ECOG PS) 0, and have normal lactate dehydrogenase, sodium, and hemoglobin levels. OS estimates for the entire cohort at one, two, and five years were 66%, 38%, and 18%, respectively. In the ECOG PS 0 subgroup, OS estimates at one, two, and five years were 85%, 52%, and 24%, respectively; OS estimates were 60%, 35%, and 17%, respectively, for ECOG PS 1-2 and were 47%, 23%, and 10%, respectively, for ECOG PS 3-4. OS was significantly higher among patients with normal serum sodium and hemoglobin levels than those with abnormal levels. Univariable hazard regression models found that ECOG PS, age at diagnosis, receipt of prophylactic cranial irradiation (PCI), and thoracic RT were associated with survival. On multivariable hazard regression, ECOG PS and receipt of PCI were associated with survival.
Conclusion UNASSIGNED
Survival for greater than two years in patients with LS-SCLC treated with CT ± RT was associated with ECOG PS and receipt of PCI.

Identifiants

pubmed: 38125937
doi: 10.3389/fonc.2023.1191920
pmc: PMC10731283
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1191920

Informations de copyright

Copyright © 2023 Dawe, Rittberg, Syed, Shanahan, Moldaver, Bucher, Galloway, Reynolds, Paul, Harlos, Kim and Banerji.

Déclaration de conflit d'intérêts

DD reports advisory board attendance for Merck Canada, Novartis, Jazz Pharmaceuticals, Pfizer, and AstraZeneca, honoraria for education content from Boehringer-Ingelheim and Bristol Myers Squibb, grants from Canadian Institutes of Health Research, CancerCare Manitoba Foundation, Manitoba Medical Services Foundation, and a research grant for this project from AstraZeneca. RR reports grant funding received from AstraZeneca. SB reports advisory board attendance for AstraZeneca, Bayer, Bristol Myers Squibb, Jazz Pharmaceuticals, Merck Canada, Novartis Janssen, Pfizer, and Roche, clinical trial funding from AstraZeneca, Bayer, and Roche, grants from Canadian Institutes of Health Research, grants from CancerCare Manitoba Foundation, grants from Genome Canada, outside the submitted work. IS and MS are employees and shareholders of AstraZeneca. DM was an employee of AstraZeneca at the time of this study. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

David E Dawe (DE)

Department of Internal Medicine, University of Manitoba, Winnipeg, MB, Canada.
Department of Hematology and Medical Oncology, CancerCare Manitoba, Winnipeg, MB, Canada.
CancerCare Manitoba Research Institute, CancerCare Manitoba, Winnipeg, MB, Canada.

Rebekah Rittberg (R)

Department of Internal Medicine, University of Manitoba, Winnipeg, MB, Canada.
Department of Hematology and Medical Oncology, CancerCare Manitoba, Winnipeg, MB, Canada.

Iqra Syed (I)

AstraZeneca Canada, Mississauga, ON, Canada.

Mary Kate Shanahan (MK)

AstraZeneca Canada, Mississauga, ON, Canada.

Daniel Moldaver (D)

AstraZeneca Canada, Mississauga, ON, Canada.

Oliver Bucher (O)

Department of Epidemiology and Cancer Registry, CancerCare Manitoba, Winnipeg, MB, Canada.

Katie Galloway (K)

Department of Epidemiology and Cancer Registry, CancerCare Manitoba, Winnipeg, MB, Canada.

Kayla Reynolds (K)

Department of Cellular & Physiological Sciences, University of British Columbia, Vancouver, BC, Canada.

James T Paul (JT)

Department of Internal Medicine, University of Manitoba, Winnipeg, MB, Canada.
Department of Hematology and Medical Oncology, CancerCare Manitoba, Winnipeg, MB, Canada.

Craig Harlos (C)

Department of Internal Medicine, University of Manitoba, Winnipeg, MB, Canada.
Department of Hematology and Medical Oncology, CancerCare Manitoba, Winnipeg, MB, Canada.

Julian O Kim (JO)

Department of Radiology, University of Manitoba, Winnipeg, MB, Canada.
Department of Radiation Oncology, CancerCare Manitoba, Winnipeg, MB, Canada.

Shantanu Banerji (S)

Department of Internal Medicine, University of Manitoba, Winnipeg, MB, Canada.
Department of Hematology and Medical Oncology, CancerCare Manitoba, Winnipeg, MB, Canada.
CancerCare Manitoba Research Institute, CancerCare Manitoba, Winnipeg, MB, Canada.

Classifications MeSH