Genetic Risk for Subsequent Neoplasms Among Long-Term Survivors of Childhood Cancer

被引：104

作者：

Wang, Zhaoming ^{[1
]}

Wilson, Carmen L. ^{[1
]}

Easton, John ^{[1
]}

Thrasher, Andrew ^{[1
]}

Mulder, Heather ^{[1
]}

Liu, Qi ^{[2
]}

Hedges, Dale J. ^{[1
]}

Wang, Shuoguo ^{[1
]}

Rusch, Michael C. ^{[1
]}

Edmonson, Michael N. ^{[1
]}

Levy, Shawn ^{[3
]}

Lanctot, Jennifer Q. ^{[1
]}

Caron, Eric ^{[1
]}

Shelton, Kyla ^{[1
]}

Currie, Kelsey ^{[1
]}

Lear, Matthew ^{[1
]}

Patel, Aman ^{[1
]}

Rosencrance, Celeste ^{[1
]}

Shao, Ying ^{[1
]}

Vadodaria, Bhavin ^{[1
]}

Yergeau, Donald ^{[1
]}

Sapkota, Yadav ^{[1
]}

Brooke, Russell J. ^{[1
]}

Moon, Wonjong ^{[1
]}

Rampersaud, Evadnie ^{[1
]}

Ma, Xiaotu ^{[1
]}

Chang, Ti-Cheng ^{[1
]}

Rice, Stephen V. ^{[1
]}

Pepper, Cynthia ^{[1
]}

Zhou, Xin ^{[1
]}

Chen, Xiang ^{[1
]}

Chen, Wenan ^{[1
]}

Jones, Angela ^{[3
]}

Boone, Braden ^{[3
]}

Ehrhardt, Matthew J. ^{[1
]}

Krasin, Matthew J. ^{[1
]}

Howell, Rebecca M. ^{[1
,4
]}

Phillips, Nicholas S. ^{[1
]}

Lewis, Courtney ^{[1
]}

Srivastava, Deokumar ^{[1
]}

Pui, Ching-Hon ^{[1
]}

Kesserwan, Chimene A. ^{[1
]}

Wu, Gang ^{[1
]}

Nichols, Kim E. ^{[1
]}

Downing, James R. ^{[1
]}

Hudson, Melissa M. ^{[1
]}

Yasui, Yutaka ^{[1
]}

Robison, Leslie L. ^{[1
]}

Zhang, Jinghui ^{[1
]}

机构：

[1] St Jude Childrens Res Hosp, 332 N Lauderdale St, Memphis, TN 38105 USA

[2] Univ Alberta, Edmonton, AB, Canada

[3] HudsonAlpha Inst Biotechnol, Huntsville, AL USA

[4] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA

来源：

JOURNAL OF CLINICAL ONCOLOGY | 2018年 / 36卷 / 20期

基金：

美国国家卫生研究院;

关键词：

5-YEAR SURVIVORS; PREDISPOSITION; RECOMMENDATIONS; SURVEILLANCE; SUSCEPTIBILITY; LEUKEMIA;

D O I：

10.1200/JCO.2018.77.8589

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

Purpose Childhood cancer survivors are at increased risk of subsequent neoplasms (SNs), but the germline genetic contribution is largely unknown. We assessed the contribution of pathogenic/likely pathogenic (P/LP) mutations in cancer predisposition genes to their SN risk. Patients and Methods Whole-genome sequencing (30-fold) was performed on samples from childhood cancer survivors who were >= 5 years since initial cancer diagnosis and participants in the St Jude Lifetime Cohort Study, a retrospective hospital-based study with prospective clinical follow-up. Germline mutations in 60 genes known to be associated with autosomal dominant cancer predisposition syndromes with moderate to high penetrance were classified by their pathogenicity according to the American College of Medical Genetics and Genomics guidelines. Relative rates (RRs) and 95% CIs of SN occurrence by mutation status were estimated using multivariable piecewise exponential regression stratified by radiation exposure. Results Participants were 3,006 survivors (53% male; median age, 35.8 years [range, 7.1 to 69.8 years]; 56% received radiotherapy), 1,120 SNs were diagnosed among 439 survivors (14.6%), and 175 P/LP mutations were identified in 5.8% (95% CI, 5.0% to 6.7%) of survivors. Mutations were associated with significantly increased rates of breast cancer (RR, 13.9; 95% CI, 6.0 to 32.2) and sarcoma (RR, 10.6; 95% CI, 4.3 to 26.3) among irradiated survivors and with increased rates of developing any SN (RR, 4.7; 95% CI, 2.4 to 9.3), breast cancer (RR, 7.7; 95% CI, 2.4 to 24.4), nonmelanoma skin cancer (RR, 11.0; 95% CI, 2.9 to 41.4), and two or more histologically distinct SNs (RR, 18.6; 95% CI, 3.5 to 99.3) among nonirradiated survivors. Conclusion The findings support referral of all survivors for genetic counseling for potential clinical genetic testing, which should be prioritized for nonirradiated survivors with any SN and for those with breast cancer or sarcoma in the field of prior irradiation.

引用

页码：2078 / +

页数：13

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