Home LiteratureArticle Details
PMID: 9392619 Published · ppublish English Journal Article Multicenter Study Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Second primary cancers related to smoking and treatment of small-cell lung cancer. Lung Cancer Working Cadre.

Journal of the National Cancer Institute ·Vol. 89 ·No. 23 ·1997-12-03 ·Pages 1782-8

Tucker MA, Murray N, Shaw EG, Ettinger DS, Mabry M, Huber MH, Feld R, Shepherd FA, Johnson DH, Grant SC, Aisner J, Johnson BE

Abstract

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

MeSH Terms
Actuarial Analysis Antineoplastic Agents/adverse effects Carcinoma, Small Cell/drug therapy,radiotherapy Female Humans Lung Neoplasms/drug therapy,radiotherapy Male Neoplasms, Second Primary/etiology Radiotherapy/adverse effects Risk Smoking/adverse effects
Chemicals
Antineoplastic Agents
Authors & Affiliations
12 authors, click to expand affiliations / ORCID
Tucker M A
Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD 20892, USA. tuckerp@epndce.nci.nih.gov
Murray N
Shaw E G
Ettinger D S
Mabry M
Huber M H
Feld R
Shepherd F A
Johnson D H
Grant S C
Aisner J
Johnson B E
Article Info
Journal
Journal of the National Cancer Institute
Abbr.
J Natl Cancer Inst
ISSN
0027-8874
Published
1997-12-03
Pages
1782-8
Language
English
Region
United States
NLM ID
7503089
Subset
IM
Corrections
CommentIn
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com