TY - JOUR
T1 - Prognostic factors and optimal therapy for stages I–II neuroendocrine carcinomas of the uterine cervix
T2 - A multi-center retrospective study
AU - Ishikawa, Mitsuya
AU - Kasamatsu, Takahiro
AU - Tsuda, Hitoshi
AU - Fukunaga, Masaharu
AU - Sakamoto, Atsuhiko
AU - Kaku, Tsunehisa
AU - Nakanishi, Toru
AU - Hasumi, Yoko
AU - Iwata, Takashi
AU - Baba, Tsukasa
AU - Nogawa, Takayoshi
AU - Kudaka, Wataru
AU - Kaneda, Hiroshi
AU - Ono, Shigemitsu
AU - Saito, Fumitaka
AU - Taniguchi, Yoshimi
AU - Okada, Satoshi
AU - Mizuno, Mika
AU - Onda, Takashi
AU - Yaegashi, Nobuo
N1 - Funding Information:
This work was partially supported by grants from the National Cancer Center Research and Development Fund (23-A-17, 26-A-4, and 29-A-3).
Publisher Copyright:
© 2017 Elsevier Inc.
PY - 2018/1
Y1 - 2018/1
N2 - Purpose We aimed to determine appropriate treatment guidelines for patients with stages I–II high-grade neuroendocrine carcinomas (HGNEC) of the uterine cervix in a multicenter retrospective study. Patients and methods We reviewed the clinicopathological features and prognoses of 93 patients with HGNEC of International Federation of Gynecology and Obstetrics (FIGO) stages I and II. All patients were diagnosed with HGNEC by central pathological review. Results The median overall survival (OS) and disease-free survival (DFS) were 111.3 months and 47.4 months, respectively. Eighty-eight patients underwent radical surgery, and five had definitive radiotherapy. The hazard ratio (HR) for death after definitive radiotherapy to death after radical surgery was 4.74 (95% confidence interval [CI], 1.01–15.90). Of the surgery group, 18 received neoadjuvant chemotherapy. Pathological prognostic factors and optimal adjuvant therapies were evaluated for the 70 patients. Forty-one patients received adjuvant chemotherapy with etoposide–platinum (EP) or irinotecan–platinum (CPT–P). Multivariate analyses identified the invasion of lymphovascular spaces as a significant prognostic factor for both OS and DFS. Pelvic lymph node metastasis was also a prognostic factor for DFS. Adjuvant chemotherapy with an EP or CPT–P regimen appeared to improve DFS (HR = 0.27, 95% CI, 0.10–0.69). A trend toward improved OS was also observed, but was not statistically significant (HR = 0.39, 95% CI, 0.15–1.01). Conclusion Radical surgery followed by adjuvant chemotherapy with an EP or CPT–P regimen was optimal treatment for stages I and II HGNEC of the uterine cervix.
AB - Purpose We aimed to determine appropriate treatment guidelines for patients with stages I–II high-grade neuroendocrine carcinomas (HGNEC) of the uterine cervix in a multicenter retrospective study. Patients and methods We reviewed the clinicopathological features and prognoses of 93 patients with HGNEC of International Federation of Gynecology and Obstetrics (FIGO) stages I and II. All patients were diagnosed with HGNEC by central pathological review. Results The median overall survival (OS) and disease-free survival (DFS) were 111.3 months and 47.4 months, respectively. Eighty-eight patients underwent radical surgery, and five had definitive radiotherapy. The hazard ratio (HR) for death after definitive radiotherapy to death after radical surgery was 4.74 (95% confidence interval [CI], 1.01–15.90). Of the surgery group, 18 received neoadjuvant chemotherapy. Pathological prognostic factors and optimal adjuvant therapies were evaluated for the 70 patients. Forty-one patients received adjuvant chemotherapy with etoposide–platinum (EP) or irinotecan–platinum (CPT–P). Multivariate analyses identified the invasion of lymphovascular spaces as a significant prognostic factor for both OS and DFS. Pelvic lymph node metastasis was also a prognostic factor for DFS. Adjuvant chemotherapy with an EP or CPT–P regimen appeared to improve DFS (HR = 0.27, 95% CI, 0.10–0.69). A trend toward improved OS was also observed, but was not statistically significant (HR = 0.39, 95% CI, 0.15–1.01). Conclusion Radical surgery followed by adjuvant chemotherapy with an EP or CPT–P regimen was optimal treatment for stages I and II HGNEC of the uterine cervix.
KW - Adjuvant chemotherapy
KW - Cervical carcinoma
KW - Neuroendocrine carcinoma
KW - Optimal therapy
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U2 - 10.1016/j.ygyno.2017.10.027
DO - 10.1016/j.ygyno.2017.10.027
M3 - Article
C2 - 29113721
AN - SCOPUS:85032828888
SN - 0090-8258
VL - 148
SP - 139
EP - 146
JO - Gynecologic Oncology
JF - Gynecologic Oncology
IS - 1
ER -