» Articles » PMID: 9392619

Second Primary Cancers Related to Smoking and Treatment of Small-cell Lung Cancer. Lung Cancer Working Cadre

Overview
Specialty Oncology
Date 1997 Dec 10
PMID 9392619
Citations 70
Authors
Affiliations
Soon will be listed here.
Abstract

Background: An increased risk of second primary cancers has been reported in patients who survive small-cell carcinoma of the lung. The treatment's contribution to the development of second cancers is difficult to assess, in part because the number of long-term survivors seen at any one institution is small. We designed a multi-institution study to investigate the risk among survivors of developing second primary cancers other than small-cell lung carcinoma.

Methods: Demographic, smoking, and treatment information were obtained from the medical records of 611 patients who had been cancer free for more than 2 years after therapy for histologically proven small-cell lung cancer, and person-years of follow-up were cumulated. Population-based rates of cancer incidence and mortality were used to estimate the expected number of cancers or deaths. The actuarial risk of second cancers was estimated by the Kaplan-Meier method.

Results: Relative to the general population, the risk of all second cancers among these patients (mostly non-small-cell cancers of the lung) was increased 3.5-fold. Second lung cancer risk was increased 13-fold among those who received chest irradiation in comparison to a sevenfold increase among nonirradiated patients. It was higher in those who continued smoking, with evidence of an interaction between chest irradiation and continued smoking (relative risk = 21). Patients treated with various forms of combination chemotherapy had comparable increases in risk (9.4- to 13-fold, overall), except for a 19-fold risk increase among those treated with alkylating agents who continued smoking.

Implications: Because of their substantially increased risk, survivors should stop smoking and may consider entering trials of secondary chemoprevention.

Citing Articles

The pathogenic germline ETV4 P433L mutation identified in multiple primary lung cancer affect tumor stem-like property by Wnt/β-catenin pathway.

Liu Y, Fang L, Wang Y, Fan T, Wang L, Xiao C Cell Death Dis. 2024; 15(10):738.

PMID: 39389944 PMC: 11467305. DOI: 10.1038/s41419-024-07129-z.


Bilateral synchronous double primary lung cancer: A case report.

Li J, Yin B, Liu Y, Huang H Clin Case Rep. 2024; 12(4):e8635.

PMID: 38566979 PMC: 10985937. DOI: 10.1002/ccr3.8635.


Smoking status among cancer patients by specialty: A U.S. nationwide representative analysis.

Nolazco J, Tang Y, Alkhatib K, King A, Mossanen M, Chang S Cancer Med. 2023; 12(23):21389-21399.

PMID: 37986671 PMC: 10726820. DOI: 10.1002/cam4.6684.


Multiple primary lung cancer: Updates of clinical management and genomic features.

Tian H, Bai G, Yang Z, Chen P, Xu J, Liu T Front Oncol. 2023; 13:1034752.

PMID: 36910635 PMC: 9993658. DOI: 10.3389/fonc.2023.1034752.


Treating with Epidermal Growth Factor Receptor (EGFR) Tyrosine Kinase Inhibitors (TKIs) Accompanying Lower Incidence of Second Primary Cancers.

Chou W, Shia B, Huang Y, Ho C, Chen M J Clin Med. 2022; 11(17).

PMID: 36079152 PMC: 9457496. DOI: 10.3390/jcm11175222.