TY - JOUR
T1 - Pathologic response rate after concomitant neo-adjuvant radiotherapy and chemotherapy for adenocarcinoma of the uterine cervix
T2 - A retrospective multicentric study
AU - Poujade, Olivier
AU - Morice, Philippe
AU - Rouzier, Roman
AU - Madelenat, Patrick
AU - Lecuru, Fabrice
AU - Muray, Jean Michel
AU - Mathevet, Patrice
AU - Alran, Séverine
AU - Salmon, Remy J.
AU - Reyal, Fabien
PY - 2010/7/1
Y1 - 2010/7/1
N2 - Introduction: Exclusive chemoradiotherapy (including brachytherapy) is the current standard of care for locoregionally advanced cervical cancer. The aim of the present study was to evaluate the responsiveness and to identify factors predicting the response to concomitant chemoradiotherapy before surgery in cervical adenocarcinoma. Methods: A multicentric retrospective study was done in 9 French centers. A total of 54women with cervical adenocarcinoma stage IB2 to IIIB who had undergone concurrent chemoradiation therapy followed by surgical treatment were included. The patients were stratified by histopathologic response after concomitant chemoradiotherapy (lesions smaller than 1 cm or larger). Results: The median (SD) age at diagnosis was 44.2 (12.4) years (range, 19.3Y77 years). The median (SD) follow-up duration was 30.9 (36.5) months (range, 4.1Y17 years). After clinical evaluation, the mean (SD) tumor size was 5 (1.2) cm (range, 2Y7 cm). The patients achieved a clinical complete response after concurrent chemoradiation in 18 cases (33.5%). Pathologic residual tumor was noted in 36 cases (67%); tumors smaller than 1 cm were found in 18 cases (33.5%), and lesions greater than 1 cm were observed in 18 cases (33.5%). Factors being associated with a significant decreased sensitivity to neoadjuvant chemoradiotherapy were the following: Menopause (P = 0.012), parametrial invasion (P < 0.001), lymphvascular space invasion (P = 0.003), and mucinous subtype (P = 0.001). Conclusions: Identification of predictive markers associated with incomplete response to neoadjuvant chemoradiotherapy in cervical adenocarcinoma may prove clinically useful and implement an individualized treatment plan.
AB - Introduction: Exclusive chemoradiotherapy (including brachytherapy) is the current standard of care for locoregionally advanced cervical cancer. The aim of the present study was to evaluate the responsiveness and to identify factors predicting the response to concomitant chemoradiotherapy before surgery in cervical adenocarcinoma. Methods: A multicentric retrospective study was done in 9 French centers. A total of 54women with cervical adenocarcinoma stage IB2 to IIIB who had undergone concurrent chemoradiation therapy followed by surgical treatment were included. The patients were stratified by histopathologic response after concomitant chemoradiotherapy (lesions smaller than 1 cm or larger). Results: The median (SD) age at diagnosis was 44.2 (12.4) years (range, 19.3Y77 years). The median (SD) follow-up duration was 30.9 (36.5) months (range, 4.1Y17 years). After clinical evaluation, the mean (SD) tumor size was 5 (1.2) cm (range, 2Y7 cm). The patients achieved a clinical complete response after concurrent chemoradiation in 18 cases (33.5%). Pathologic residual tumor was noted in 36 cases (67%); tumors smaller than 1 cm were found in 18 cases (33.5%), and lesions greater than 1 cm were observed in 18 cases (33.5%). Factors being associated with a significant decreased sensitivity to neoadjuvant chemoradiotherapy were the following: Menopause (P = 0.012), parametrial invasion (P < 0.001), lymphvascular space invasion (P = 0.003), and mucinous subtype (P = 0.001). Conclusions: Identification of predictive markers associated with incomplete response to neoadjuvant chemoradiotherapy in cervical adenocarcinoma may prove clinically useful and implement an individualized treatment plan.
KW - Cervical adenocarcinoma
KW - Chemoradiotherapy
KW - Neoadjuvant
KW - Surgery
UR - http://www.scopus.com/inward/record.url?scp=77956821072&partnerID=8YFLogxK
U2 - 10.1111/IGC.0b013e3181df7406
DO - 10.1111/IGC.0b013e3181df7406
M3 - Article
C2 - 20606528
AN - SCOPUS:77956821072
SN - 1048-891X
VL - 20
SP - 815
EP - 820
JO - International Journal of Gynecological Cancer
JF - International Journal of Gynecological Cancer
IS - 5
ER -