Title
Author
DOI
Article Type
Special Issue
Volume
Issue
Survival outcomes of Stage IB cervical cancer treated with standard radical hysterectomy
1Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Beijing, China
DOI: 10.12892/ejgo4754.2019 Vol.40,Issue 5,October 2019 pp.810-814
Accepted: 11 June 2018
Published: 10 October 2019
*Corresponding Author(s): L. Li E-mail: lileigh@163.com
Objective: To determine risk factors of survival outcomes in patients with cervical cancer of Stage IB treated with standard hysterectomy (RH). Materials Methods: From February 2001 to November 2015, patients with cervical cancer of FIGO Stage IB were included, if they received RH of Class III or Type C1. Epidemiological and clinic-pathologic characteristics were compared to determine risk factors of overall survival (OS) and progression free survival (PFS). Results: Among 406 patients included, 371 (91.4%) had definite survival data, with recurrence rate and mortality of 17.2% and 9.4%. After a median follow-up of 48.5 (range 12-189) months, and ten-year PFS were 80% and 73%, and five- and ten-year OS were 88% and 84%, respectively. In multivariate analysis, patients with Stage IB2 (HR 2.0, 95% CI 1.2-3.2), positive vaginal margin (HR 9.2, 95% CI 2.6-33.0), or lymphatic metastasis (HR 2.0, 95% CI 1.1-3.6) had higher recurrence; patients with RH before year of 2011 (HR 2.8, 95% 1.3-6.0), Stage IB2 (HR 3.6, 95% CI 1.9-6.9) or lymphatic metastasis (HR 3.6, 95% CI 1.8-7.1) had higher mortality. Recurrent sites or post-recurrent treatment plans had no impact on the survival after recurrence. Conclusion: The prognosis of cervical cancer patients treated with RH by experienced physicians is favorable. Pathologic characters and experiences of surgeons are predictive factors of survival outcomes.
Cervical cancer; Radical hysterectomy; Recurrence; Mortality
R. Du,L. Li,S. Ma,X. Tan,S. Zhong,M. Wu. Survival outcomes of Stage IB cervical cancer treated with standard radical hysterectomy. European Journal of Gynaecological Oncology. 2019. 40(5);810-814.
[1] Jemal A., Bray F., Center M.M., Ferlay J., Ward E., Forman D.: “Global cancer statistics”. CA Cancer J. Clin., 2011, 61, 69.
[2] Chen W., Zheng R., Baade P.D., Zhang S., Zeng H., Bray F., et al.: “Cancer statistics in China, 2015”. CA Cancer J. Clin., 2016, 66, 115.
[3] Nezhat C.R., Burrell M.O., Nezhat F.R., Benigno B.B., Welander C.E.: “Laparoscopic radical hysterectomy with paraaortic and pelvic node dissection”. Am. J. Obstet. Gynecol., 1992, 166, 864.
[4] Geetha P., Nair M.K.: “Laparoscopic, robotic and open method of radical hysterectomy for cervical cancer: A systematic review“. J. Minim. Access. Surg., 2012, 8, 67.
[5] Piver M.S., Rutledge F., Smith J.P.: “Five classes of extended hysterectomy for women with cervical cancer”. Obstet. Gynecol., 1974, 44, 265.
[6] Cibula D., Abu-Rustum N.R., Benedetti-Panici P., Kohler C., Raspagliesi F., Querleu D., et al.: “New classification system of radical hysterectomy: emphasis on a three-dimensional anatomic template for parametrial resection”. Gynecol. Oncol., 2011, 122, 264.
[7] Querleu D., Morrow C.P.: “Classification of radical hysterectomy”. Lancet Oncol., 2008, 9, 297.
[8] “Common Terminology Criteria for Adverse Events (CTCAE) v4.03 Available at: http://evs.nci.nih.gov/ftp1/CTCAE/
[9] Howlader N, Noone AM, Krapcho M, Neyman N., Aminou R., Waldron W., et al.: “SEER Cancer Statistics Review, 1975-2012”. National Cancer Institute. Bethesda, MD”. Available at: www.seer. cancer. gov
[10] Sedlis A., Bundy B.N., Rotman M.Z., Lentz S.S., Muderspach L.I., Zaino R.J.: “A randomized trial of pelvic radiation therapy versus no further therapy in selected patients with stage IB carcinoma of the cervix after radical hysterectomy and pelvic lymphadenectomy: A Gynecologic Oncology Group Study”. Gynecol. Oncol., 1999, 73, 177.
[11] Ryu S.Y., Park S.I., Nam B.H., Cho C.K., Kim K., Kim B.J., et al.: “Is adjuvant chemoradiotherapy overtreatment in cervical cancer patients with intermediate risk factors?”. Int. J. Radiat. Oncol. Biol. Phys., 2011, 79, 794.
[12] atsuo K., Mabuchi S., Okazawa M., Kawano M., Kuroda H., Kamiura S., et al.: “Clinical implication of surgically treated earlystage cervical cancer with multiple high-risk factors”. J. Gynecol. Oncol., 2015, 26, 3.
[13] Peters W.A., 3rd, Liu P.Y., Barrett R.J., 2nd, Stock R.J., Monk B.J., Berek J.S., et al.: “Concurrent chemotherapy and pelvic radiation therapy compared with pelvic radiation therapy alone as adjuvant therapy after radical surgery in high-risk early-stage cancer of the cervix”. J. Clin. Oncol., 2000, 18, 1606.
[14] Fagundes H., Perez C.A., Grigsby P.W., Lockett M.A.: “Distant metastases after irradiation alone in carcinoma of the uterine cervix”. Int. J. Radiat. Oncol. Biol. Phys., 1992, 24, 197.
[15] Delgado G., Bundy B., Zaino R., Sevin B.U., Creasman W.T., Major F.: “Prospective surgical-pathological study of disease-free interval in patients with stage IB squamous cell carcinoma of the cervix: a Gynecologic Oncology Group study”. Gynecol. Oncol., 1990, 38, 352.
[16] Wright J.D., Lewin S.N., Deutsch I., Burke W.M., Sun X., Herzog T.J.: “The influence of surgical volume on morbidity and mortality of radical hysterectomy for cervical cancer”. Am. J. Obstet. Gynecol., 2011, 205, 225.e221.
[17] Chou H.H., Wang C.C., Lai C.H., Hong J.H., Ng K.K., Chang T.C., et al.: “Isolated paraaortic lymph node recurrence after definitive irradiation for cervical carcinoma”. Int. J. Radiat. Oncol. Biol. Phys., 2001, 51, 442.
[18] Jeon W., Koh H.K., Kim H.J., Wu H.G., Kim J.H., Chung H.H.: “Salvage radiotherapy for lymph node recurrence after radical surgery in cervical cancer”. J. Gynecol. Oncol., 2012, 23, 168.
[19] Tempfer C.B., Beckmann M.W.: “State-of-the-Art Treatment and Novel Agents in Local and Distant Recurrences of Cervical Cancer”. Oncol. Res. Treat., 2016, 39, 525.
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