scholarly journals PO-0841: Kidney-sparing whole abdominal irradiation in Wilms Tumor: potential advantages of VMAT technique

2018 ◽  
Vol 127 ◽  
pp. S439-S440
Author(s):  
M.J. Chen ◽  
C.R. Leao ◽  
A.L. Carioca ◽  
R.C.P. Simoes ◽  
F.S. Belletti ◽  
...  
2020 ◽  
Vol 67 (5) ◽  
Author(s):  
Michael Jenwei Chen ◽  
Caio Raposo Leao ◽  
Roberto Campos Pereira Simoes ◽  
Fernanda Salheb Belletti ◽  
Maria Luisa Sucharski Figueiredo ◽  
...  

1990 ◽  
Vol 36 (3) ◽  
pp. 327-330 ◽  
Author(s):  
David E. Linstadt ◽  
Jeffrey L. Stern ◽  
Jeanne M. Quivey ◽  
Steven A. Leibel ◽  
Conley G. Lacey

2008 ◽  
Vol 184 (3) ◽  
pp. 145-149 ◽  
Author(s):  
Nathalie Rochet ◽  
Florian Sterzing ◽  
Alexandra Jensen ◽  
Julien Dinkel ◽  
Klaus Herfarth ◽  
...  

2014 ◽  
Vol 111 ◽  
pp. S107
Author(s):  
M. Ramos Albiac ◽  
D. Mosquera ◽  
M. Hermida-López ◽  
J. Giralt

1976 ◽  
Vol 27 (4) ◽  
pp. 449-454 ◽  
Author(s):  
T.H. Kim ◽  
A.M. Panahon ◽  
M. Friedman ◽  
J.H. Webster

1986 ◽  
Vol 9 (5) ◽  
pp. 424-428 ◽  
Author(s):  
Theodore E. Yaeger ◽  
Felipe A. Calvo ◽  
Luther W. Brady

2006 ◽  
Vol 24 (1) ◽  
pp. 36-44 ◽  
Author(s):  
Marcus E. Randall ◽  
Virginia L. Filiaci ◽  
Hyman Muss ◽  
Nick M. Spirtos ◽  
Robert S. Mannel ◽  
...  

Purpose To compare whole-abdominal irradiation (WAI) and doxorubicin-cisplatin (AP) chemotherapy in women with stage III or IV endometrial carcinoma having a maximum of 2 cm of postoperative residual disease. Patients and Methods Four hundred twenty-two patients were entered onto this trial. Of 396 assessable patients, 202 were randomly allocated to receive WAI, and 194 were allocated to receive AP. Irradiation dosage was 30 Gy in 20 fractions, with a 15-Gy boost. Chemotherapy consisted of doxorubicin 60 mg/m2 and cisplatin 50 mg/m2 every 3 weeks for seven cycles, followed by one cycle of cisplatin. Results Most patient and tumor characteristics were well balanced. The median patient age was 63 years; 50% had endometrioid tumors. Median follow-up time was 74 months. The hazard ratio for progression adjusted for stage was 0.71 favoring AP (95% CI, 0.55 to 0.91; P < .01). At 60 months, 50% of patients receiving AP were predicted to be alive and disease free when adjusting for stage compared with 38% of patients receiving WAI. The stage-adjusted death hazard ratio was 0.68 (95% CI, 0.52 to 0.89; P < .01) favoring AP. Moreover, at 60 months and adjusting for stage, 55% of AP patients were predicted to be alive compared with 42% of WAI patients. Greater acute toxicity was seen with AP. Treatment probably contributed to the deaths of eight patients (4%) on the AP arm and five patients (2%) on the WAI arm. Conclusion Chemotherapy with AP significantly improved progression-free and overall survival compared with WAI. Nevertheless, further advances in efficacy and reduction in toxicity are clearly needed.


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