TY - JOUR
T1 - Small cell carcinoma of the uterine cervix
T2 - Clinical outcome of concurrent chemoradiotherapy with a multidrug regimen
AU - Tokunaga, Hideki
AU - Nagase, Satoru
AU - Yoshinaga, Kosuke
AU - Tanaka, Sota
AU - Nagai, Tomoyuki
AU - Kurosawa, Hiroki
AU - Kaiho-Sakuma, Michiko
AU - Toyoshima, Masafumi
AU - Otsuki, Takeo
AU - Utsunomiya, Hiroki
AU - Takano, Tadao
AU - Niikura, Hitoshi
AU - Ito, Kiyoshi
AU - Yaegashi, Nobuo
PY - 2012/12/27
Y1 - 2012/12/27
N2 - Small cell carcinoma of the uterine cervix (SCCC) is a rare subtype of cervical cancer with an aggressive behavior. Although SCCC has a worse prognosis than other histological types of uterine cervical cancer such as squamous cell carcinoma or adenocarcinoma, standard therapy for SCCC remains to be established due to its rarity. The purpose of this study was to evaluate the efficacy and toxicity of concurrent chemoradiotherapy (CCRT) using a regimen consisting of vincristine, adriamycin, and cyclophosphamide alternating with cisplatin and etoposide (VAC/PE). We analyzed a series of 9 patients with SCCC. Five patients with stage IB disease underwent radical hysterectomy followed by CCRT. Four patients with advanced stage disease received CCRT primarily. With a median follow-up duration of 47.4 months (range, 10.5 to 86.4 months), 4 out of 5 patients with stage IB disease were alive without recurrence. In 4 patients with advanced stage disease, the response rate was 75% (complete response, 1; partial response, 2; progressive disease, 1). One patient with stage IVB disease remained without recurrence for 89.5 months. At 5 years, overall survival (OS) and progression-free survival for all patients was 52% and 56%, respectively. Patients with early-stage disease had an 80% 5-year OS rate compared to 25% for patients with advanced stage disease. Although all patients developed grade 3-4 neutropenia, CCRT using VAC/PE is feasible in both the primary and adjuvant settings for SCCC. In particular, this combined modality therapy may improve both local control and survival as postoperative treatment in patients with early-stage disease.
AB - Small cell carcinoma of the uterine cervix (SCCC) is a rare subtype of cervical cancer with an aggressive behavior. Although SCCC has a worse prognosis than other histological types of uterine cervical cancer such as squamous cell carcinoma or adenocarcinoma, standard therapy for SCCC remains to be established due to its rarity. The purpose of this study was to evaluate the efficacy and toxicity of concurrent chemoradiotherapy (CCRT) using a regimen consisting of vincristine, adriamycin, and cyclophosphamide alternating with cisplatin and etoposide (VAC/PE). We analyzed a series of 9 patients with SCCC. Five patients with stage IB disease underwent radical hysterectomy followed by CCRT. Four patients with advanced stage disease received CCRT primarily. With a median follow-up duration of 47.4 months (range, 10.5 to 86.4 months), 4 out of 5 patients with stage IB disease were alive without recurrence. In 4 patients with advanced stage disease, the response rate was 75% (complete response, 1; partial response, 2; progressive disease, 1). One patient with stage IVB disease remained without recurrence for 89.5 months. At 5 years, overall survival (OS) and progression-free survival for all patients was 52% and 56%, respectively. Patients with early-stage disease had an 80% 5-year OS rate compared to 25% for patients with advanced stage disease. Although all patients developed grade 3-4 neutropenia, CCRT using VAC/PE is feasible in both the primary and adjuvant settings for SCCC. In particular, this combined modality therapy may improve both local control and survival as postoperative treatment in patients with early-stage disease.
KW - Concurrent chemoradiotherapy
KW - Neuroendocrine carcinoma
KW - Small cell carcinoma of the uterine cervix
KW - Uterine cervical cancer
KW - VAC/PE
UR - http://www.scopus.com/inward/record.url?scp=84873023559&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84873023559&partnerID=8YFLogxK
U2 - 10.1620/tjem.229.75
DO - 10.1620/tjem.229.75
M3 - Article
C2 - 23269283
AN - SCOPUS:84873023559
SN - 0040-8727
VL - 229
SP - 75
EP - 81
JO - Tohoku Journal of Experimental Medicine
JF - Tohoku Journal of Experimental Medicine
IS - 1
ER -