Pulmonary large cell neuroendocrine carcinoma (LCNEC): a population-based study addressing recent molecular-genetic advances and emerging therapeutic approaches.


Journal

Clinical and experimental medicine
ISSN: 1591-9528
Titre abrégé: Clin Exp Med
Pays: Italy
ID NLM: 100973405

Informations de publication

Date de publication:
Nov 2023
Historique:
received: 07 02 2023
accepted: 05 04 2023
medline: 2 11 2023
pubmed: 16 4 2023
entrez: 15 4 2023
Statut: ppublish

Résumé

Large cell neuroendocrine carcinoma (LCNEC) of the lung is a rare, aggressive cancer most commonly found in the lungs but not exclusively, with a worse prognosis than non-small cell lung carcinomas. Currently, LCNEC patients are treated using small cell and non-small cell protocols. This study aims to use the SEER database to identify demographic, clinical, pathological, and therapeutic factors affecting the prognosis and survival of patients with LCNEC of the lung. Demographic, clinical, and management data of patients with lung LCNEC were extracted from the SEER database for the period 2000-2018. In the USA, LCNEC has a higher incidence in elderly white men: M:F ratio = 1.2:1, Caucasian: 83.3%, mean age: 67 ± 10.2 years. The most common treatment modality was chemotherapy only: 29.2%, followed by surgery: 21.5% (but in this group the statuses of chemotherapy were unknown), and combination surgery/chemotherapy: 8.8%. The overall and cause-specific 5-year survival was 17.5% (95% CI 16.3-18.8) and 21.9% (95% CI 20.5-23.4), respectively. By treatment, the best 5-year survival was for surgery alone (48%), followed by multimodality therapy (chemo + surgery + radiation) at 35% (95% CI 27-43). Age > 60 years, male gender, size > 7 cm, and nodal and liver metastasis were independent risk factors associated with increased mortality. Lung LCNEC is an aggressive neoplasm most common in older white males that presents at an advanced stage despite small primary tumors. Most patients die within 2 years. The best predictor of survival is surgery with chemotherapy. Given its dismal prognosis, new treatment guidelines are needed for this aggressive cancer.

Sections du résumé

BACKGROUND BACKGROUND
Large cell neuroendocrine carcinoma (LCNEC) of the lung is a rare, aggressive cancer most commonly found in the lungs but not exclusively, with a worse prognosis than non-small cell lung carcinomas. Currently, LCNEC patients are treated using small cell and non-small cell protocols. This study aims to use the SEER database to identify demographic, clinical, pathological, and therapeutic factors affecting the prognosis and survival of patients with LCNEC of the lung.
METHODS METHODS
Demographic, clinical, and management data of patients with lung LCNEC were extracted from the SEER database for the period 2000-2018.
RESULTS RESULTS
In the USA, LCNEC has a higher incidence in elderly white men: M:F ratio = 1.2:1, Caucasian: 83.3%, mean age: 67 ± 10.2 years. The most common treatment modality was chemotherapy only: 29.2%, followed by surgery: 21.5% (but in this group the statuses of chemotherapy were unknown), and combination surgery/chemotherapy: 8.8%. The overall and cause-specific 5-year survival was 17.5% (95% CI 16.3-18.8) and 21.9% (95% CI 20.5-23.4), respectively. By treatment, the best 5-year survival was for surgery alone (48%), followed by multimodality therapy (chemo + surgery + radiation) at 35% (95% CI 27-43). Age > 60 years, male gender, size > 7 cm, and nodal and liver metastasis were independent risk factors associated with increased mortality.
CONCLUSION CONCLUSIONS
Lung LCNEC is an aggressive neoplasm most common in older white males that presents at an advanced stage despite small primary tumors. Most patients die within 2 years. The best predictor of survival is surgery with chemotherapy. Given its dismal prognosis, new treatment guidelines are needed for this aggressive cancer.

Identifiants

pubmed: 37060529
doi: 10.1007/s10238-023-01071-8
pii: 10.1007/s10238-023-01071-8
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3947-3955

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer Nature Switzerland AG.

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Auteurs

Jaffar Khan (J)

Department of Pathology, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.

Abdul Qahar Khan Yasinzai (AQK)

Bolan Medical College, Quetta, Pakistan.

Sabrina Matosz (S)

Georgia Cancer Center, Medical College of Georgia, Augusta University, Augusta, GA, 30912, USA.

Marjan Khan (M)

Department of Medicine, Marshfield Clinic, Marshfield, WI, USA.

Saleh Heneidi (S)

Molecular Pathology Laboratory, Cedars-Sinai Medical Center, Los Angeles, CA, 90048, USA.

Hector Mesa (H)

Department of Pathology, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.

Aman Chauhan (A)

Department of Hematology and Oncology, University of Kentucky, Lexington, USA.

Jaydira Del Rivero (J)

Division of Hematology and Oncology, National Cancer Institute, NIH, Bethesda, MD, 20892, USA.

Nagla Abdel Karim (NA)

Inova Schar Cancer Institute, Department of Medicine, University of Virginia, Fairfax, VA, 22031, USA.

Asad Ullah (A)

Department of Pathology and Laboratory Medicine, Vanderbilt University Medical Center, Vanderbilt University, Nashville, TN, 37232, USA. drasadkhankakar@gmail.com.

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