Survival in early lung cancer patients treated with high dose radiotherapy is independent of pathological confirmation.


Journal

Thoracic cancer
ISSN: 1759-7714
Titre abrégé: Thorac Cancer
Pays: Singapore
ID NLM: 101531441

Informations de publication

Date de publication:
02 2019
Historique:
received: 17 10 2018
revised: 11 12 2018
accepted: 12 12 2018
pubmed: 9 1 2019
medline: 8 2 2020
entrez: 9 1 2019
Statut: ppublish

Résumé

Approximately 15% of lung cancer patients are diagnosed in early stages. Microscopic proof of disease cannot always be obtained because of comorbidity or reluctance to undergo invasive diagnostic procedures. In the current study, survival data of patients with and without pathology are compared. One hundred and sixty three patients with NSCLC I-IIb (T3 N0) treated between 2002 and 2016 were eligible: 123 (75%) had pathological confirmation of disease, whereas 40 (25%) did not. In accordance with international guidelines, both groups received radiotherapy. Comorbidity was assessed with the Charlson Comorbidity Index (CCI). The median follow-up was 28.6 months (range: 0.3-162): 66 (40%) patients are still alive, while 97 (59%) patients died: 48 (29%) cancer-related deaths and 49 (30%) from causes other than cancer. Median overall survival (OS) in patients without pathological confirmation was 58.6 months (range: 0.5-162), which did not differ from those with microscopic proof of disease (39.4 months, range: 0.3-147.5; logrank P = 0.481). Median cancer-specific survival (CSS) also did not differ at 113.4 months (range: 0.5-162) in the non-confirmation group (logrank P = 0.763) versus 51.5 months (range: 3.7-129.5) in patients with pathology. In Cox regression, a CCI of ≥ 3 was associated with poor OS (hazard ratio 2.0; range 1.2-3.4; P = 0.010) and CSS (hazard ratio 2.0; 1.0-4.0; P = 0.043). OS and CSS in early lung cancer patients depend on comorbidity rather than on pathological confirmation of disease.

Sections du résumé

BACKGROUND
Approximately 15% of lung cancer patients are diagnosed in early stages. Microscopic proof of disease cannot always be obtained because of comorbidity or reluctance to undergo invasive diagnostic procedures. In the current study, survival data of patients with and without pathology are compared.
METHODS
One hundred and sixty three patients with NSCLC I-IIb (T3 N0) treated between 2002 and 2016 were eligible: 123 (75%) had pathological confirmation of disease, whereas 40 (25%) did not. In accordance with international guidelines, both groups received radiotherapy. Comorbidity was assessed with the Charlson Comorbidity Index (CCI).
RESULTS
The median follow-up was 28.6 months (range: 0.3-162): 66 (40%) patients are still alive, while 97 (59%) patients died: 48 (29%) cancer-related deaths and 49 (30%) from causes other than cancer. Median overall survival (OS) in patients without pathological confirmation was 58.6 months (range: 0.5-162), which did not differ from those with microscopic proof of disease (39.4 months, range: 0.3-147.5; logrank P = 0.481). Median cancer-specific survival (CSS) also did not differ at 113.4 months (range: 0.5-162) in the non-confirmation group (logrank P = 0.763) versus 51.5 months (range: 3.7-129.5) in patients with pathology. In Cox regression, a CCI of ≥ 3 was associated with poor OS (hazard ratio 2.0; range 1.2-3.4; P = 0.010) and CSS (hazard ratio 2.0; 1.0-4.0; P = 0.043).
CONCLUSION
OS and CSS in early lung cancer patients depend on comorbidity rather than on pathological confirmation of disease.

Identifiants

pubmed: 30618120
doi: 10.1111/1759-7714.12966
pmc: PMC6360228
doi:

Types de publication

Clinical Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

321-329

Informations de copyright

© 2019 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd.

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Auteurs

Franz Zehentmayr (F)

Department of Radiation Oncology, Paracelsus Medical University, SALK, Salzburg, Austria.
radART, Paracelsus Medical University, Salzburg, Austria.

Martin Sprenger (M)

Postgraduate Public Health Program, Medical University of Graz, Graz, Austria.

Lukas Rettenbacher (L)

Department of Nuclear Medicine, Paracelsus Medical University, SALK, Salzburg, Austria.

Romana Wass (R)

Department of Pneumology, Paracelsus Medical University, SALK, Salzburg, Austria.

Peter Porsch (P)

Department of Pneumology, Paracelsus Medical University, SALK, Salzburg, Austria.

Gerd Fastner (G)

Department of Radiation Oncology, Paracelsus Medical University, SALK, Salzburg, Austria.

Christian Pirich (C)

Department of Nuclear Medicine, Paracelsus Medical University, SALK, Salzburg, Austria.

Michael Studnicka (M)

Department of Pneumology, Paracelsus Medical University, SALK, Salzburg, Austria.

Felix Sedlmayer (F)

Department of Radiation Oncology, Paracelsus Medical University, SALK, Salzburg, Austria.
radART, Paracelsus Medical University, Salzburg, Austria.

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