Understanding clinical practice and survival outcomes in patients with unresectable stage III non-small-cell lung cancer in a single centre in Quebec.


Journal

Current oncology (Toronto, Ont.)
ISSN: 1718-7729
Titre abrégé: Curr Oncol
Pays: Switzerland
ID NLM: 9502503

Informations de publication

Date de publication:
10 2020
Historique:
entrez: 11 11 2020
pubmed: 12 11 2020
medline: 21 9 2021
Statut: ppublish

Résumé

A retrospective cohort study considered patients 18 or more years of age diagnosed between January 2007 and May 2018 with unresectable stage iii non-small-cell lung cancer (nsclc) who received combined chemoradiation (crt). Survival was analyzed using the Kaplan-Meier method to determine median overall (os) and progression-free survival (pfs) and the associated 95% confidence intervals (cis). Cox regression analysis was performed to identify factors prognostic for survival, including age, sex, smoking status, Eastern Cooperative Oncology Group performance status (ecog ps), histology, treatment type, tumour size, and nodal status. Of 226 patients diagnosed with unresectable stage iii disease, 134 (59%) received combined crt. Mean age was 63 years; most patients were white, were current smokers, had an ecog ps of 0 or 1, and had nonsquamous histology. Median pfs was 7.03 months (95% ci: 5.6 months to 8.5 months), and os for the cohort was 18.7 months (95% ci: 12.4 months to 24.8 months). Of those patients, 78% would have been eligible for durvalumab consolidation therapy. Univariate analysis demonstrated a significant os benefit ( Combined crt has been the standard treatment for unresectable stage iii nsclc. In our study, a trend of better survival was seen for ccrt compared with scrt. Factors predictive of survival in patients with stage iii disease treated with crt were tumour size and nodal station. Most patients with stage iii disease would potentially be eligible for durvalumab maintenance therapy based on the eligibility criteria from the pacific trial. The use and effectiveness of novel treatments will have to be further studied in our real-world patient population and similar populations elsewhere.

Identifiants

pubmed: 33173385
doi: 10.3747/co.27.6241
pii: conc-27-e459
pmc: PMC7606053
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e459-e466

Informations de copyright

2020 Multimed Inc.

Déclaration de conflit d'intérêts

CONFLICT OF INTEREST DISCLOSURES We have read and understood Current Oncology’s policy on disclosing conflicts of interest, and we declare the following interests: MH and RNW are employees of AstraZeneca Canada. The remaining authors have no conflicts to disclose.

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Auteurs

J Agulnik (J)

Peter Brojde Lung Cancer Centre, Sir Mortimer B. Davis Jewish General Hospital, McGill University, Montreal, QC.

G Kasymjanova (G)

Peter Brojde Lung Cancer Centre, Sir Mortimer B. Davis Jewish General Hospital, McGill University, Montreal, QC.

C Pepe (C)

Peter Brojde Lung Cancer Centre, Sir Mortimer B. Davis Jewish General Hospital, McGill University, Montreal, QC.

M Hurry (M)

AstraZeneca Canada, Mississauga, ON.

R N Walton (RN)

AstraZeneca Canada, Mississauga, ON.

L Sakr (L)

Peter Brojde Lung Cancer Centre, Sir Mortimer B. Davis Jewish General Hospital, McGill University, Montreal, QC.

V Cohen (V)

Peter Brojde Lung Cancer Centre, Sir Mortimer B. Davis Jewish General Hospital, McGill University, Montreal, QC.

M Lecavalier (M)

Peter Brojde Lung Cancer Centre, Sir Mortimer B. Davis Jewish General Hospital, McGill University, Montreal, QC.

D Small (D)

Peter Brojde Lung Cancer Centre, Sir Mortimer B. Davis Jewish General Hospital, McGill University, Montreal, QC.

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