1. Final report of a prospective randomized study on thoracic radiotherapy target volume for limited‐stage small cell lung cancer with radiation dosimetric analyses
- Author
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Ming Chen, Fang Peng, Chang Yu, Yun Fan, Min Fang, Yong Bao, Yiping Zhang, Wei Hong, Peng cheng Chen, Hui neng Zhu, Zheng bo Song, Jin Wang, Yu Jin Xu, Qi xun Chen, Qiang Zhao, Liang Zhu, Ying Jin, You hua Jiang, Bai qiang Dong, Wei Min Mao, Hong lian Ma, Xin Min Yu, Li Zhang, Hua rong Tang, Xin ming Zhou, Wen yong Sun, Ying Guo, Xiaoling Xu, Yue Kong, Xiao Hu, M. Chen, and Jin shi Liu
- Subjects
Cancer Research ,medicine.diagnostic_test ,business.industry ,medicine.medical_treatment ,Induction chemotherapy ,Hilum (biology) ,medicine.disease ,law.invention ,Radiation therapy ,03 medical and health sciences ,0302 clinical medicine ,medicine.anatomical_structure ,Oncology ,Randomized controlled trial ,law ,Positron emission tomography ,030220 oncology & carcinogenesis ,Medicine ,030212 general & internal medicine ,business ,Supraclavicular fossa ,Lung cancer ,Nuclear medicine ,Etoposide ,medicine.drug - Abstract
Background The thoracic radiotherapy (TRT) target volume for limited-stage small-cell lung cancer (SCLC) has been controversial for decades. In this report, the final results of a prospective randomized trial on the TRT target volume before and after induction chemotherapy are presented. Methods After 2 cycles of etoposide and cisplatin, patients arm were randomized to receive TRT to the postchemotherapy or prechemotherapy tumor volume in a study arm and a control arm. Involved-field radiotherapy was received in both arms. TRT consisted of 1.5 grays (Gy) twice daily in 30 fractions to up to a total dose of 45 Gy. Lymph node regions were contoured, and intentional and incidental radiation doses were recorded. Results The study was halted early because of slow accrual. Between 2002 and 2017, 159 and 150 patients were randomized to the study arm or the control arm, respectively; and 21.4% and 19.1% of patients, respectively, were staged using positron emission tomography/computed tomography (P = .31). With a median follow-up of 54.1 months (range, 19.9-165.0 months) in survivors, the 3-year local/regional progression-free probability was 58.2% and 65.5% in the study and control arms, respectively (P = .44), and the absolute difference was -7.3% (95% CI, -18.2%, 3.7%). In the study and control arms, the median overall survival was 21.9 months and 26.6 months, respectively, and the 5-year overall survival rate was 22.8% and 28.1%, respectively (P = .26). Grade 3 esophagitis was observed in 5.9% of patients in the study arm versus 15.5% of those in the control arm (P = .01). The isolated out-of-field failure rate was 2.6% in the study arm versus 4.1% in the control arm (P = .46), and all such failures were located in the supraclavicular fossa or contralateral hilum. The regions 7, 3P, 4L, 6, 4R, 5, and 2L received incidental radiation doses >30 Gy. Conclusions TRT could be limited to the postchemotherapy tumor volume, and involved-field radiotherapy could be routinely applied for limited-stage SCLC.
- Published
- 2019