Dose rate correction in medium dose rate brachytherapy for carcinoma cervix

Citation
Fd. Patel et al., Dose rate correction in medium dose rate brachytherapy for carcinoma cervix, RADIOTH ONC, 49(3), 1998, pp. 317-323
Citations number
14
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging","Onconogenesis & Cancer Research
Journal title
RADIOTHERAPY AND ONCOLOGY
ISSN journal
01678140 → ACNP
Volume
49
Issue
3
Year of publication
1998
Pages
317 - 323
Database
ISI
SICI code
0167-8140(199812)49:3<317:DRCIMD>2.0.ZU;2-5
Abstract
Purpose: To establish the magnitude of brachytherapy dose reduction require d for stage IIB and III carcinoma cervix patients treated by external radia tion and medium dose rate (MDR) brachytherapy at a dose rate of 220 +/- 10 cGy/h at point A. Materials and methods: In study-I, at the time of MDR brachytherapy applica tion at a dose rate of 220 +/- 10 cGy/h at point A, patients received eithe r 3060 cGy, a 12.5% dose reduction (MDR-12.5), or 2450 cGy, a 30% dose redu ction (MDR-30), to point A and they were compared to a group of previously treated LDR patients who received 3500 cGy to point A at a dose rate of 55- 65 cGy/h. Study-II was a prospective randomized trial and patients received either 2450 cGy, a 30% dose reduction (MDR-II (30)) or 2800 cGy, a 20% dos e reduction (MDR-II (20), at point A. Patients were evaluated for local con trol of disease and morbidity. Results: In study-I the 5-year actuarial local control rate in the MDR-30 a nd MDR-12.5 groups was 71.7 +/- 10% and 70.5 +/- 10%, respectively, compare d to 63.4 +/- 10% in the LDR group. However, the actuarial morbidity tall g rades) in the MDR-12.5 group was 58.5 +/- 14% as against 34.9 +/- 9% in the LDR group (P < 0.05). Similarly, the grade III and IV morbidity also in th e MDR-12.5 group was 12.5 +/- 9% as against 5.3 +/- 5% in the LDR group (P < 0.05). No statistically significant difference in morbidity was seen betw een the MDR-30 and LDR groups. In study-II the 3-year actuarial local contr ol rate in the MDR-II (30) and MDR-II (20) groups was 66.6 +/- 10% and 74.8 +/- 9%, respectively. There was a significant correlation between the rect al BED received and the percentage of patients developing rectal morbidity. Only 10% of patients receiving a rectal BED of (100 < 120) Gy(3) developed complication as against 62.5% of those receiving a rectal BED of (140 < 16 0) Gy(3) (chi(2) = 46.43; P < 0.001). Conclusion: We suggest that at a dose rate of 220 +/- 10 cGy/h at point A t he brachytherapy dose reduction factor should be around 30%, as suggested b y radiobiological data, to keep the morbidity as low as possible without co mpromising the local control rates. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.