Second primary neoplasms in 633,964 cancer patients in Sweden, 1958-1996

被引:136
作者
Dong, C [1 ]
Hemminki, K [1 ]
机构
[1] Karolinska Inst, Novum, Dept Biosci, Huddinge, Sweden
关键词
second cancer; risk assessment; follow-up study; male; female;
D O I
10.1002/ijc.1317
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The Swedish Family-Cancer Database was used to analyze concordant (same site) and discordant (different site) second primary neoplasms in 633,964 cancer patients diagnosed from 1958 to 1996. Cases of second malignant neoplasms were extracted from the Database if the diagnosis date of the first and second cancer differed by at least I month. The expected numbers of cancers were obtained by applying site-, sex-, age-, period-, residence- and socioeconomic level-specific rates in the corresponding population in the Database to the appropriate person-years at risk. The standardized incidence ratio (SIRs) of a second cancer was taken to be the ratio of observed to expected numbers of second cancers. Of all cancers, 8.5% were subsequent neoplasms (8.4% for males and 8.7% for females). Sips for both concordant and discordant subsequent cancer were elevated in patients with cancer of the upper aerodigestive tract, colon, nose, breast, other female genitals, testis, kidney, urinary, bladder. skin, nervous system. endocrine, bone, connective tissue, melanoma, lymphoma and leukemia. The risks at some concordant sites, such as nose, squamous cell skin, bone and connective tissue in both sexes, breast in males and upper aerodigestive tract and leukemia in females. were very high (> 10). At discordant sites, SIRs were less than 2 but significantly increased after all but gastric and prostatic cancer. Compared with the general population, cancer patients were at a modestly increased risk for new primary cancer after cancers at many sites, calling for attention in treatment, management and prevention. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:155 / 161
页数:7
相关论文
共 42 条
[11]   Human cancer syndromes: Clues to the origin and nature of cancer [J].
Fearon, ER .
SCIENCE, 1997, 278 (5340) :1043-1050
[12]  
Frodin JE, 1997, ACTA ONCOL, V36, P465
[13]   2ND PRIMARY TUMORS FOLLOWING RADIOTHERAPY FOR CHILDHOOD-CANCER [J].
HAWKINS, MM .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1990, 19 (05) :1297-1301
[14]   Second primary cancer after in situ and invasive cervical cancer [J].
Hemminki, K ;
Dong, CH ;
Vaittinen, P .
EPIDEMIOLOGY, 2000, 11 (04) :457-461
[15]   Familial risks in second primary breast cancer based on a family cancer database [J].
Hemminki, K ;
Vaittinen, P .
EUROPEAN JOURNAL OF CANCER, 1999, 35 (03) :455-458
[16]   Subsequent cancers after in situ and invasive squamous cell carcinoma of the skin [J].
Hemminki, K ;
Dong, CH .
ARCHIVES OF DERMATOLOGY, 2000, 136 (05) :647-651
[17]   Familial relationships in squamous cell carcinoma of the skin [J].
Hemminki, K ;
Dong, CH .
EPIDEMIOLOGY, 2000, 11 (03) :309-314
[18]   Cancer in husbands of cervical cancer patients [J].
Hemminki, K ;
Dong, CH .
EPIDEMIOLOGY, 2000, 11 (03) :347-349
[19]   Familial cancers in a nationwide family cancer database: Age distribution and prevalence [J].
Hemminki, K ;
Vaittinen, P .
EUROPEAN JOURNAL OF CANCER, 1999, 35 (07) :1109-1117
[20]   Primary cancers following squamous cell carcinoma of the skin suggest involvement of Epstein-Barr virus [J].
Hemminki, K ;
Dong, CH .
EPIDEMIOLOGY, 2000, 11 (01) :94-94