Second primary cancers related to smoking and treatment of small-cell lung cancer

被引:163
作者
Tucker, MA
Murray, N
Shaw, EG
Ettinger, DS
Mabry, M
Huber, MH
Feld, R
Shepherd, FA
Johnson, DH
Grant, SC
Aisner, J
Johnson, BE
机构
[1] NCI,GENET EPIDEMIOL BRANCH,DIV CANC EPIDEMIOL & GENET,BETHESDA,MD 20892
[2] BRITISH COLUMBIA CANC AGCY,VANCOUVER,BC V5Z 4E6,CANADA
[3] MAYO CLIN,ROCHESTER,MN
[4] JOHNS HOPKINS ONCOL CTR,BALTIMORE,MD
[5] RHONE POULENC RORER,NORRISTOWN,PA
[6] PRINCESS MARGARET HOSP,TORONTO,ON M4X 1K9,CANADA
[7] TORONTO HOSP,TORONTO,ON,CANADA
[8] VANDERBILT UNIV,SCH MED,NASHVILLE,TN 37212
[9] MEM SLOAN KETTERING CANC CTR,NEW YORK,NY 10021
[10] INST CANC RES,NEW BRUNSWICK,NJ
[11] NCI,NAVY MED ONCOL BRANCH,BETHESDA,MD 20892
关键词
D O I
10.1093/jnci/89.23.1782
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 mas 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.
引用
收藏
页码:1782 / 1788
页数:7
相关论文
共 28 条
[1]   LONG-TERM SURVIVAL AND TOXICITY IN SMALL-CELL LUNG-CANCER - EXPANDED SOUTHWEST-ONCOLOGY-GROUP EXPERIENCE [J].
ALBAIN, KS ;
CROWLEY, JJ ;
LIVINGSTON, RB .
CHEST, 1991, 99 (06) :1425-1432
[2]  
BOICE JD, 1986, NEW ENGL J MED, V314, P119
[3]  
BOICE JD, 1996, NIH PUBL
[4]   INCREASED INCIDENCE OF ACUTE NONLYMPHOCYTIC LEUKEMIA FOLLOWING THERAPY IN PATIENTS WITH SMALL CELL-CARCINOMA OF THE LUNG [J].
CHAK, LY ;
SIKIC, BI ;
TUCKER, MA ;
HORNS, RC ;
COX, RS .
JOURNAL OF CLINICAL ONCOLOGY, 1984, 2 (05) :385-390
[5]   BREAST-CANCER AFTER TREATMENT OF HODGKINS-DISEASE [J].
HANCOCK, SL ;
TUCKER, MA ;
HOPPE, RT .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (01) :25-31
[6]   FACTORS AFFECTING LATE MORTALITY FROM HEART-DISEASE AFTER TREATMENT OF HODGKINS-DISEASE [J].
HANCOCK, SL ;
TUCKER, MA ;
HOPPE, RT .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1993, 270 (16) :1949-1955
[7]   THE INCIDENCE OF 2ND PRIMARY TUMORS IN LONG-TERM SURVIVORS OF SMALL-CELL LUNG-CANCER [J].
HEYNE, KH ;
LIPPMAN, SM ;
LEE, JJ ;
LEE, JS ;
HONG, WK .
JOURNAL OF CLINICAL ONCOLOGY, 1992, 10 (10) :1519-1524
[8]   2ND PRIMARY MALIGNANCIES IN SMALL-CELL LUNG-CANCER - A MAJOR CONSEQUENCE OF MODEST SUCCESS [J].
IHDE, DC ;
TUCKER, MA .
JOURNAL OF CLINICAL ONCOLOGY, 1992, 10 (10) :1511-1513
[9]  
IHDE DC, 1993, CANCER PRINCIPLES PR, P723
[10]   LUNG-CANCER RISK AND RADIATION-DOSE AMONG WOMEN TREATED FOR BREAST-CANCER [J].
INSKIP, PD ;
STOVALL, M ;
FLANNERY, JT .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1994, 86 (13) :983-988