Second cancer risk after primary cancer treatment with three-dimensional conformal, intensity-modulated, or proton beam radiation therapy

被引:119
|
作者
Xiang, Michael [1 ,2 ]
Chang, Daniel T. [1 ]
Pollom, Erqi L. [1 ,2 ]
机构
[1] Stanford Univ, Dept Radiat Oncol, 875 Blake Wilbur Dr,Room CC-G236A, Stanford, CA 94305 USA
[2] Palo Alto Vet Affairs Hosp, Palo Alto, CA USA
关键词
neoplasms; proton therapy; radiotherapy; conformal; intensity-modulated; second primary; X-RAY THERAPY; PROSTATE-CANCER; SECONDARY CANCERS; CHILDHOOD-CANCER; DOSE-RESPONSE; SOLID CANCERS; RADIOTHERAPY; MALIGNANCIES; NEOPLASMS; OUTCOMES;
D O I
10.1002/cncr.32938
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background The comparative risks of a second cancer diagnosis are uncertain after primary cancer treatment with 3-dimensional conformal radiotherapy (3DCRT), intensity-modulated radiotherapy (IMRT), or proton beam radiotherapy (PBRT). Methods Pediatric and adult patients with a first cancer diagnosis between 2004 and 2015 who received 3DCRT, IMRT, or PBRT were identified in the National Cancer Database from 9 tumor types: head and neck, gastrointestinal, gynecologic, lymphoma, lung, prostate, breast, bone/soft tissue, and brain/central nervous system. The diagnosis of second cancer was modeled using multivariable logistic regression adjusting for age, follow-up duration, radiotherapy (RT) dose, chemotherapy, sociodemographic variables, and other factors. Propensity score matching also was used to balance baseline characteristics. Results In total, 450,373 patients were identified (33.5% received 3DCRT, 65.2% received IMRT, and 1.3% received PBRT) with median follow-up of 5.1 years after RT completion and a cumulative follow-up period of 2.54 million person-years. Overall, the incidence of second cancer diagnosis was 1.55 per 100 patient-years. In a comparison between IMRT versus 3DCRT, there was no overall difference in the risk of second cancer (adjusted odds ratio [OR], 1.00; 95% CI, 0.97-1.02; P = .75). By comparison, PBRT had an overall lower risk of second cancer versus IMRT (adjusted OR, 0.31; 95% CI, 0.26-0.36; P < .0001). Results within each tumor type generally were consistent in the pooled analyses and also were maintained in propensity score-matched analyses. Conclusions The risk of a second cancer diagnosis was similar after IMRT versus 3DCRT, whereas PBRT was associated with a lower risk of second cancer risk. Future work is warranted to determine the cost-effectiveness of PBRT and to identify the population best suited for this treatment.
引用
收藏
页码:3560 / 3568
页数:9
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