TY - JOUR
T1 - Preoperative brachytherapy of early-stage cervical cancer
T2 - A multicenter study by the SFRO brachytherapy group
AU - Ka, Kanta
AU - Cordoba, Abel
AU - Cagetti, Leonel Varela
AU - Schiappa, Renaud
AU - Kissel, Manon
AU - Escande, Alexandre
AU - Casabianca, Laurence Gonzague
AU - Buchalet, Chloe
AU - Gouy, Sebastien
AU - Morice, Philippe
AU - Narducci, Fabrice
AU - Martinez, Carlos
AU - Jauffret, Camille
AU - Lambaudie, Eric
AU - Delpech, Yann
AU - Laas, Enora
AU - Gaillard, Thomas
AU - Hannoun-Levi, Jean Michel
AU - Espenel, Sophie
AU - Chargari, Cyrus
N1 - Publisher Copyright:
© 2024
PY - 2024/9/1
Y1 - 2024/9/1
N2 - Objective: To report the results of a multicenter cohort of preoperative brachytherapy (PBT) for treatment of early-stage cervical cancer (ESCC). Methods: A retrospective analysis was conducted among five French comprehensive cancer centers on behalf of the SFRO Brachytherapy Group to examine the outcome of patients with ESCC who received PBT between 2001 and 2019 because of adverse prognostic factors (tumor size >2 cm, presence of lymphovascular invasion, adenocarcinoma).Brachytherapy was followed 4–8 weeks later by surgery. Local relapse free, distant metastasis-free survival, disease-free, and overall survival and adverse effects were examined. Uni- and multivariate analyses were conducted looking for oncological prognostic factors. Results: A total of 451 patients were identified, with a mean tumor size of 24.7 mm. Adenocarcinoma accounted for 43.5% of cases, and lympho-vascular space invasion (LVSI) was present in 15.7%. A complete histological response was observed in 69.6%. With a mean follow-up of 75.4 months, DFS, LRFS, and OS rates at five years were 88% [95% CI (84–91), 98% [95% CI (96–99), and 92% [95% CI (87–95)], respectively. At the last follow-up, 8.2% of patients had died, including 31 (6.8%) from cervical cancer. Severe side effects range from 1.1% to 2%. At multivariate analysis, adenocarcinoma histological type, tumor size ≥2 cm, and the presence of residual tumors were prognosticators for DFS and DMFS. Conclusion: PBT shows excellent oncological outcomes in this cohort of patients with adverse histoprognostic factors. Favorable survival rates and low complications rates were observed, supporting this strategy in the management of ESCC.
AB - Objective: To report the results of a multicenter cohort of preoperative brachytherapy (PBT) for treatment of early-stage cervical cancer (ESCC). Methods: A retrospective analysis was conducted among five French comprehensive cancer centers on behalf of the SFRO Brachytherapy Group to examine the outcome of patients with ESCC who received PBT between 2001 and 2019 because of adverse prognostic factors (tumor size >2 cm, presence of lymphovascular invasion, adenocarcinoma).Brachytherapy was followed 4–8 weeks later by surgery. Local relapse free, distant metastasis-free survival, disease-free, and overall survival and adverse effects were examined. Uni- and multivariate analyses were conducted looking for oncological prognostic factors. Results: A total of 451 patients were identified, with a mean tumor size of 24.7 mm. Adenocarcinoma accounted for 43.5% of cases, and lympho-vascular space invasion (LVSI) was present in 15.7%. A complete histological response was observed in 69.6%. With a mean follow-up of 75.4 months, DFS, LRFS, and OS rates at five years were 88% [95% CI (84–91), 98% [95% CI (96–99), and 92% [95% CI (87–95)], respectively. At the last follow-up, 8.2% of patients had died, including 31 (6.8%) from cervical cancer. Severe side effects range from 1.1% to 2%. At multivariate analysis, adenocarcinoma histological type, tumor size ≥2 cm, and the presence of residual tumors were prognosticators for DFS and DMFS. Conclusion: PBT shows excellent oncological outcomes in this cohort of patients with adverse histoprognostic factors. Favorable survival rates and low complications rates were observed, supporting this strategy in the management of ESCC.
KW - Adenocarcinoma
KW - Cervical cancer
KW - Preoperative brachytherapy
KW - Prognostic factors
KW - Surgery
UR - http://www.scopus.com/inward/record.url?scp=85196960040&partnerID=8YFLogxK
U2 - 10.1016/j.ygyno.2024.06.010
DO - 10.1016/j.ygyno.2024.06.010
M3 - Article
C2 - 38941964
AN - SCOPUS:85196960040
SN - 0090-8258
VL - 188
SP - 90
EP - 96
JO - Gynecologic Oncology
JF - Gynecologic Oncology
ER -