Intensity-modulated radiation therapy with dose-painting for pediatric sarcomas with pulmonary metastases

被引:12
作者
Yang, Joanna C. [1 ]
Wexler, Leonard H. [2 ]
Meyers, Paul A. [2 ]
Happersett, Laura [3 ]
La Quaglia, Michael P. [4 ]
Wolden, Suzanne L. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Radiat Oncol, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Pediat, New York, NY 10065 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Med Phys, New York, NY 10065 USA
[4] Mem Sloan Kettering Canc Ctr, Dept Surg, New York, NY 10065 USA
关键词
Ewing sarcoma family tumors; intensity-modulated radiotherapy with dose-painting; pediatric sarcomas; pulmonary metastases; rhabdomyosarcoma; WHOLE LUNG IRRADIATION; WILMS-TUMOR; EWINGS-SARCOMA; IRS-IV; RHABDOMYOSARCOMA; RADIOTHERAPY; DIAGNOSIS; TRIAL;
D O I
10.1002/pbc.24502
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background We examined patterns of failure in pediatric patients with thoracic sarcoma and pulmonary metastases treated with intensity-modulated radiation therapy with dose-painting (DP-IMRT). Procedure Eleven pediatric patients, five with Ewing sarcoma family tumors (ESFT) and six with rhabdomyosarcoma (RMS), with primary thoracic tumors and pulmonary metastases underwent DP-IMRT with chemotherapy for definitive treatment. Eight patients also underwent surgery. Median time to RT was 21 (15-31) weeks. Nine patients received 45-50.4-Gy in 1.8Gy fractions to the primary tumor (n=3) or post-operative tumor bed (n=6). Two patients 4 years received 12Gy intraoperative radiation therapy and 30.6-36Gy IMRT postoperatively to the tumor bed. All patients received 14-16.8Gy in 0.54-0.88Gy fractions to the whole lungs (n=6) or hemithorax (n=5) using dose-painting technique. A representative case was re-planned with IMRT plus standard AP/PA whole lung irradiation (WLI) for dosimetric comparison. Results With 27-month median follow-up, 3-year pulmonary relapse-free survival in all patients was 61%: 80% for RMS and 40% for ESFT. Five patients (4 ESFT and 1 RMS) experienced pulmonary relapse at median 16 (9-41) months. There were no local failures. Our representative case demonstrated more homogeneous target volume coverage of the whole lungs and decreased mean dose to esophagus (15%), heart (31%), spinal cord (15%), and liver (19%) with DP-IMRT. Conclusions The treatment of children with a primary thoracic tumor and pulmonary metastases poses a significant challenge. DP-IMRT is one solution to this technical problem. Initial data from this small series suggest DP-IMRT is feasible and produces superior sparing of critical normal tissues. Pediatr Blood Cancer 2013;60:1616-1620. (c) 2013 Wiley Periodicals, Inc.
引用
收藏
页码:1616 / 1620
页数:5
相关论文
共 21 条
[1]   LATE FOLLOW-UP OF LUNG-FUNCTION AFTER WHOLE LUNG IRRADIATION FOR WILMS-TUMOR [J].
ATTARDMONTALTO, SP ;
KINGSTON, JE ;
EDEN, OB ;
PLOWMAN, PN .
BRITISH JOURNAL OF RADIOLOGY, 1992, 65 (780) :1114-1118
[2]  
Bölling T, 2008, STRAHLENTHER ONKOL, V184, P193, DOI 10.1007/s00066-008-1810-x
[3]  
CANGIR A, 1990, CANCER-AM CANCER SOC, V66, P887, DOI 10.1002/1097-0142(19900901)66:5<887::AID-CNCR2820660513>3.0.CO
[4]  
2-R
[5]   Comparative dosimetric study of two strategies of intensity-modulated radiotherapy in nasopharyngeal cancer [J].
Chen, SW ;
Yang, SN ;
Liang, JA ;
Shiau, AC ;
Lin, FJ .
MEDICAL DOSIMETRY, 2005, 30 (04) :219-227
[6]  
Dantonello TM, 2001, PEDIAT BLOOD CANC, V56, P725
[7]   Assessment of different IMRT boost delivery methods on target coverage and normal-tissue sparing [J].
Dogan, N ;
King, S ;
Emami, B ;
Mohideen, N ;
Mirkovic, N ;
Leybovich, LB ;
Sethi, A .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2003, 57 (05) :1480-1491
[8]   Results from the IRS-IV randomized trial of hyperfractionated radiotherapy in children with rhabdomyosarcoma - A report from the IRSG [J].
Donaldson, SS ;
Meza, J ;
Breneman, JC ;
Crist, WM ;
Laurie, F ;
Qualman, SJ ;
Wharam, M .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2001, 51 (03) :718-728
[9]  
Dunst J., 1993, Strahlentherapie und Onkologie, V169, P621
[10]  
GREEN DM, 1989, CANCER-AM CANCER SOC, V63, P450, DOI 10.1002/1097-0142(19890201)63:3<450::AID-CNCR2820630310>3.0.CO