Multiple primary cancers in families with Li-Fraumeni syndrome

被引:365
作者
Hisada, M
Garber, JE
Fung, CY
Fraumeni, JF
Li, FP
机构
[1] Harvard Univ, Sch Publ Hlth, Dana Farber Canc Inst, Div Canc Epidemiol & Control, Boston, MA 02115 USA
[2] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[3] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Radiat Oncol, Boston, MA USA
[4] NCI, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
来源
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE | 1998年 / 90卷 / 08期
关键词
D O I
10.1093/jnci/90.8.606
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Li-Fraumeni syndrome is a dominantly inherited disorder characterized by early-onset breast cancer, sarcomas, and other cancers in children and young adults, Members of families with this syndrome also develop multiple primary cancers, but the frequency is unknown. To approach this issue, we quantified the incidence of second and third primary cancers in individuals from 24 Li-Fraumeni kindreds originally diagnosed with cancer during the period from 1968 through 1986, Methods: The relative risk (RR) of subsequent cancers and 95% confidence intervals (CIs) were calculated by use of population-based incidence data from the Connecticut Cancer Registry. Kaplan-Meier analysis was used to determine the cumulative probability (+/- standard error) of subsequent cancers. Results: Among 200 Li-Fraumeni syndrome family members diagnosed with cancer, 30 (15%) developed a second cancer. Eight individuals (4%) had a third cancer, while four (2%) eventually developed a fourth cancer. Overall, the RR of occurrence of a second cancer was 5.3 (95% CI = 2.8-7.8), with a cumulative probability of second cancer occurrence of 57% (+/-10%) at 30 years after diagnosis of a first cancer. RRs of second cancers occurring in families with this syndrome were 83.0 (95% CI = 36.9-187.6), 9.7 (95% CI = 4.9-19.2), and 1.5 (95% CI = 0.5-4.2) for individuals with a first cancer at ages 0-19 years, 20-44 years, and 45 years or more, respectively. Thirty (71%) of 42 subsequent cancers in this group were component cancers of Li-Fraumeni syndrome. Conclusions: Compared with the general population, members of Li-Fraumeni syndrome families have an exceptionally high risk of developing multiple primary cancers. The excess risk of additional primary cancers is mainly for cancers that are characteristic of Li-Fraumeni syndrome, with the highest risk observed for survivors of childhood cancers. Cancer survivors in these families should be closely monitored for early manifestations of new cancers.
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页码:606 / 611
页数:6
相关论文
共 56 条
[1]   POTENTIAL IMPACT OF GENETIC TESTING ON CANCER PREVENTION TRIALS, USING BREAST-CANCER AS AN EXAMPLE [J].
BAKER, SG ;
FREEDMAN, LS .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1995, 87 (15) :1137-1144
[2]   CANCER IN THE CONTRALATERAL BREAST AFTER RADIOTHERAPY FOR BREAST-CANCER [J].
BOICE, JD ;
HARVEY, EB ;
BLETTNER, M ;
STOVALL, M ;
FLANNERY, JT .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 326 (12) :781-785
[3]  
COHEN RJ, 1976, CANCER TREAT REP, V60, P1257
[4]  
Cornelis RS, 1997, HUM MUTAT, V9, P157
[5]   Solid cancers after bone marrow transplantation [J].
Curtis, RE ;
Rowlings, PA ;
Deeg, HJ ;
Shriner, DA ;
Socie, G ;
Travis, LB ;
Horowitz, MM ;
Witherspoon, RP ;
Hoover, RN ;
Sobocinski, KA ;
Fraumeni, JF ;
Boice, JD .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 336 (13) :897-904
[6]   LONG-TERM MORTALITY AFTER A SINGLE TREATMENT COURSE WITH X-RAYS IN PATIENTS TREATED FOR ANKYLOSING-SPONDYLITIS [J].
DARBY, SC ;
DOLL, R ;
GILL, SK ;
SMITH, PG .
BRITISH JOURNAL OF CANCER, 1987, 55 (02) :179-190
[8]  
EASTON DF, 1995, AM J HUM GENET, V56, P265
[9]  
Eng C, 1997, CANCER EPIDEM BIOMAR, V6, P379
[10]   MORTALITY FROM 2ND TUMORS AMONG LONG-TERM SURVIVORS OF RETINOBLASTOMA [J].
ENG, C ;
LI, FP ;
ABRAMSON, DH ;
ELLSWORTH, RM ;
WONG, FL ;
GOLDMAN, MB ;
SEDDON, J ;
TARBELL, N ;
BOICE, JD .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (14) :1121-1128