» Articles » PMID: 27799952

Tolerance and Efficacy of Preoperative Intracavitary HDR Brachytherapy in IB and IIA Cervical Cancer

Overview
Date 2009 Mar 1
PMID 27799952
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: The aim of this work is to analyze the efficacy and tolerance of preoperative intracavitary HDR brachytherapy (HDR-BT) in patients with IB and IIA cervical cancer.

Material And Methods: 139 patients with cervical cancer IB-IIA with preoperative HDR-BT, out of which 60 patients with cervical cancer IB (43.2%) and 79 with IIA (56.8%) were treated since 1996 to 2002. In preoperative BT total dose to point A ranged from 30-45 Gy in 6-9 fractions twice a week. The fraction dose was 4-5 Gy at point A. Six weeks after BT all patients underwent radical Wertheim-Meigs hysterectomy. Patients with disadvantageous risk factors or with positive specimen histology had a complementary therapy: external-beam radiotherapy (EBRT) given to the whole pelvic volume in daily fractions of 2 Gy up to total dose of 36-52 Gy (20 patients) or EBRT with cisplatin-based chemotherapy with the dose of 30-40 mg/m in 5-7 fractions given weekly (7 patients) or chemotherapy (6 patients). Acute and late radiation toxicity was evaluated according to EORTC/RTOG.

Results: In postoperative specimen histopathology the number of 114 women (82%) had tumor-free specimen within brachytherapy target (in cervix and cavity), 96 women (60.1%) had tumor-free specimen both in and outside brachytherapy target (lymph nodes, parametra, adnexis). The 5-year and 10-year DFS were 93.8% and 88% for IB and 89.7% and 64.7% for IIA respectively. 7.9% of patients developed acute toxicity both in rectum and bladder (only in I and II grade of EORTC/RTOG). Late severe complication occurred in rectum in 2.2% of patients and in bladder 1.4%.

Conclusions: 1. Preoperative HDR-BT in patients with IB and IIA cervical cancer is an effective and well tolerated therapy with acceptable rate of side effects. 2. Preoperative HDR-BT followed by surgery in a group without risk factors is a sufficient treatment option with no additional adjuvant therapy requirement.

Citing Articles

Pathologic complete remission after preoperative high-dose-rate brachytherapy in patients with operable cervical cancer: preliminary results of a prospective randomized multicenter study.

Vizkeleti J, Vereczkey I, Frohlich G, Varga S, Horvath K, Pulay T Pathol Oncol Res. 2014; 21(2):247-56.

PMID: 25011515 DOI: 10.1007/s12253-014-9815-5.


The dosimetric impact of vaginal balloon-packing on intracavitary high-dose-rate brachytherapy for gynecological cancer.

Rockey W, Bhatia S, Jacobson G, Kim Y J Contemp Brachytherapy. 2013; 5(1):17-22.

PMID: 23634151 PMC: 3635049. DOI: 10.5114/jcb.2013.34449.

References
1.
Fowler J, Lindstrom M . Loss of local control with prolongation in radiotherapy. Int J Radiat Oncol Biol Phys. 1992; 23(2):457-67. DOI: 10.1016/0360-3016(92)90768-d. View

2.
Chung H, Kang S, Cho J, Kim J, Park N, Song Y . Can preoperative MRI accurately evaluate nodal and parametrial invasion in early stage cervical cancer?. Jpn J Clin Oncol. 2007; 37(5):370-5. DOI: 10.1093/jjco/hym036. View

3.
Nag S, Orton C, Young D, Erickson B . The American brachytherapy society survey of brachytherapy practice for carcinoma of the cervix in the United States. Gynecol Oncol. 1999; 73(1):111-8. DOI: 10.1006/gyno.1998.5334. View

4.
Lyng H, Sundfor K, Trope C, Rofstad E . Disease control of uterine cervical cancer: relationships to tumor oxygen tension, vascular density, cell density, and frequency of mitosis and apoptosis measured before treatment and during radiotherapy. Clin Cancer Res. 2000; 6(3):1104-12. View

5.
Barranger E, Coutant C, Cortez A, Uzan S, Darai E . Sentinel node biopsy is reliable in early-stage cervical cancer but not in locally advanced disease. Ann Oncol. 2005; 16(8):1237-42. DOI: 10.1093/annonc/mdi245. View