Article Data

  • Views 1757
  • Dowloads 129

Original Research

Open Access

Effects and toxicity of neoadjuvant chemotherapy preoperative followed by adjuvant chemoradiation in small cell neuroendocrine cervical carcinoma

  • Z.M. Yin1
  • A.J. Yu1
  • M.J. Wu1
  • J. Fang1
  • L.F. Liu1
  • J.Q. Zhu1
  • H. Yu1,*,

1 Department of Gynecologic Oncology (State Key Laboratory of Radiation Oncology Treatment), The Zhejiang Cancer Hospital, Hangzhou, China

DOI: 10.12892/ejgo2723.2015 Vol.36,Issue 3,June 2015 pp.326-329

Published: 10 June 2015

*Corresponding Author(s): H. Yu E-mail: ayuhua@126.com

Abstract

Objective: To determine the efficacy and toxicity of a combined–modality regimen of neoadjuvant chemotherapy (NACT) before primary radical surgery followed by adjuvant chemoradiation in small cell neuroendocrine cervical cancer (SCNEC) patients. Materials and Methods: The study was approved by the ethics committee of the present hospital. The records of 23 SCNEC patients who received NACT before primary radical surgery were reviewed at the Zhejiang Cancer Hospital between January 1998 and May 2010. All patients received one to four cycles of NACT and two to eight cycles of chemotherapy (NACT and adjuvant chemotherapy) on the basis of platinum, 17 (73.9%) patients received NACT using a regimen consisting of etoposide and cisplatin (EP). Eighteen (85.7%) patients received adjuvant chemotherapy using a regimen consisting of PE and EP. Kaplan-Meier and Cox regression methods were used for analyses. Results: Of the 23 eligible patients, 18 had Stages I-IIA, five had Stages IIB- IIIB disease. Twelve patients (52.2%) developed grade 3 and 4 neutropenia. Fourteen patients (60.9%) developed grade 3 and 4 anemia. The majority of grade 3 and 4 neutropenia and non-hematologic toxicities were usually self-limited. Three patients (13.0%) who postoperative pathology showed pathologic complete response (CR) had better prognosis than those did not show pathologic CR; the median survival was 69.5 months (range, 51.1–177.1), 54.5 months (range: 7.3–81.5), respectively. In univariate analysis, lymphovascular space invasion (LSI) ( p = 0.013), and deep stromal invasion (DSI) ( p = 0.001) were considered poor prognostic factors. With a median follow-up for surviving patients was 40.8 months (range, 7–177), 12 patients recurred, 11 of which had died. The estimated three- and five-year overall survival (OS) rates for all patients were 55.8% and 39.9%, respectively. Conclusion: NACT before primary radical surgery followed by adjuvant chemoradiation or chemotherapy was well tolerated and seems to be effective for early stage SCNEC patients. Prospective clinical study is necessary and we hope that this research’s results help to design a prospective clinical study.

Keywords

Neuroendocrine carcinoma; Neoadjuvant chemotherapy; Small cell; Uterine cervix.

Cite and Share

Z.M. Yin,A.J. Yu,M.J. Wu,J. Fang,L.F. Liu,J.Q. Zhu,H. Yu. Effects and toxicity of neoadjuvant chemotherapy preoperative followed by adjuvant chemoradiation in small cell neuroendocrine cervical carcinoma. European Journal of Gynaecological Oncology. 2015. 36(3);326-329.

References

[1] Tsunoda S., Jobo T., Aria M., Imai M., Kanai T., Tamura T., et al.: “Small-cell carcinoma of the uterine cervix: a clinicopathologic study of 11 cases”. Int. J. Gynecol. Cancer, 2005, 15, 295.

[2] Chung H.H., Jang M.J., Jung K.W., Won Y.J., Shin H.R., Kim J.W., et al.: “Cervical cancer incidence and survival in Korea: 1993-2002”. Int. J. Gynecol. Cancer, 2006, 16, 1833.

[3] Crowder S., Tuller E.: “Small cell carcinoma of the female genital tract”. Semin. Oncol., 2007, 34, 57.

[4] Viswanathan A.N., Deavers M.T., Jhing A., Ramirez P.T., Levenback C., Eifel P.J.: “Small cell neuroendocrine carcinoma of the cervix: outcome and patterns of recurrence”. Gynecol. Oncol., 2004, 93, 27.

[5] Chan J.K., Loizzi V., Burger R.A., Rutgers J., Monk B.J.: “Prognostic factors in neuroendocrine small cell cervical carcinoma: a multivariate analysis”. Cancer, 2003, 97, 568.

[6] Chen J., Macdonald O.K., Gaffney D.K.: “Incidence, mortality, and prognostic factors of small cell carcinoma of the cervix”. Obstet. Gynecol., 2008, 111, 1394.

[7] Lan-Fang L., Hai-Yan S., Zuo-Ming Y., Jian-Qing Z., Ya-Qing C.: “Small cell neuroendocrine carcinoma of the cervix: analysis of the prognosis and role of radiation therapy for 43 cases”. Eur. J. Gynaecol. Oncol., 2012, 33, 68.

[8] Bermudez A., Vighi S., Garcia A., Sardi J.: “Neuroendocrine cervical carcinoma: a diagnostic and therapeutic challenge”. Gynecol. Oncol., 2001, 82, 32.

[9] Lee J.M., Lee K.B., Nam J.H., Ryu S.Y., Bae D.S., Park J.T., et al.: “Prognostic factors in FIGO stage IB–IIA small cell neuroendocrine carcinoma of the uterine cervix treated surgically: results of a multicenter retrospective Korean study”. Ann. Oncol., 2008, 19, 321.

[10] Crowder S., Tuller E.: “Small cell carcinoma of the female genital tract”. Semin. Oncol., 2007, 34, 57.

[11] Hoskins P.J., Swenerton K.D., Pike J.A., Lim P., Aquino-Parsons C., Wong F., Lee N.: “Small-cell carcinoma of the cervix: fourteen years of experience at a single institution using a combined-modality regimen of involved-field irradiation and platinum-based combination chemotherapy”. J. Clin. Oncol., 2003, 21, 3495.

[12] Sheets E.E., Berman M.L., Hrountas C.K. Liao S.Y., DiSaia P.J.: “Surgically treated, early-stage neuroendocrine small-cell cervical carcinoma”. Obstet. Gynecol., 1988, 71, 10.

[13] Sevin B.U., Method M.W., Nadji M., Lu Y., Averette H.A.: “Efficacy of radical hysterectomy as treatment for patients with small cell carcinoma of the cervix”. Cancer, 1996, 77, 1489.

[14] Bermudez A., Vighi S., Garcia A., Sardi J.: “Neuroendocrine cervical carcinoma: a diagnostic and therapeutic challenge”. Gynecol. Oncol., 2001, 82, 32.

[15] Cohen J.G., Kapp D.S., Shin J.Y., Urban R., Sherman A.E., Chen L.M., et al.: “Small cell carcinoma of the cervix: treatment and survival outcomes of 188 patients”. Am. J. Obstet. Gynecol., 2010, 203, 347.

[16] Tian W.J., Zhang M.Q., Shui R.H.: “Prognostic factors and treatment comparison in early-stage small cell carcinoma of the uterine cervix”. Oncol. Lett., 2012, 3, 125.

Submission Turnaround Time

Top