FIGO 2018 stage IB2 (2-4 cm) Cervical cancer treated with Neo-adjuvant chemotherapy followed by fertility Sparing Surgery (CONTESSA); Neo-Adjuvant Chemotherapy and Conservative Surgery in Cervical Cancer to Preserve Fertility (NEOCON-F). A PMHC, DGOG, GCIG/CCRN and multicenter study

被引:55
作者
Plante, Marie [1 ]
van Trommel, Nienke [2 ,3 ]
Lheureux, Stephanie [4 ]
Oza, Amit M. [5 ]
Wang, Lisa [4 ]
Sikorska, Karolina [6 ]
Ferguson, Sarah Elizabeth [7 ]
Han, Kathy [8 ]
Amant, Frederic [9 ,10 ]
机构
[1] Ctr Hosp Univ Quebec, Obstet & Gynecol, Quebec City, PQ G1R 2J6, Canada
[2] Netherlands Canc Inst, Gynecol Oncol, Amsterdam, Netherlands
[3] Ctr Gynecol Oncol Amsterdam, Gynecol Oncol, Amsterdam, Netherlands
[4] Princess Margaret Consortium, Drug Dev Program, Toronto, ON, Canada
[5] Princess Margaret Hosp, Dept Med, Ctr Canc, Toronto, ON, Canada
[6] Netherlands Canc Inst, Dept Biostat, Amsterdam, Netherlands
[7] Princess Margaret Hosp, Gynecol Oncol, Ctr Canc, Toronto, ON, Canada
[8] Princess Margaret Hosp, Ctr Canc, Toronto, ON, Canada
[9] Netherlands Canc Inst, Amsterdam, Netherlands
[10] Univ Amsterdam, Med Ctr, Gynecol Oncol, Amsterdam, Netherlands
关键词
ABDOMINAL RADICAL TRACHELECTOMY; LYMPH-NODE BIOPSY; PREGNANCY OUTCOMES; RANDOMIZED-TRIAL; PHASE-II; PACLITAXEL; CARCINOMA; CISPLATIN; HYSTERECTOMY; CARBOPLATIN;
D O I
10.1136/ijgc-2019-000398
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background There are limited data regarding the optimal management of pre-menopausal women with cervical lesions measuring 2-4 cm who desire to preserve fertility. Primary objectives To evaluate the feasibility of preserving fertility. Study hypothesis Neo-adjuvant chemotherapy will be effective in reducing the size of the tumor and will enable fertility-sparing surgery without compromising oncologic outcome. Trial design Pre-menopausal women diagnosed with stage International Federation of Gynecology and Obstetrics (FIGO) IB2, 2-4 cm cervical cancer who wish to preserve fertility will receive three cycles of platinum/paclitaxel chemotherapy. Patients with complete/partial response will undergo fertility-sparing surgery. Patients will be followed for 3 years to monitor outcome. Patients with suboptimal response (residual lesion >= 2 cm) will receive definitive radical hysterectomy and/or chemoradiation. Major eligibility criteria Patients must have histologically confirmed invasive cervical cancer, 2-4 cm lesion, by clinical examination and magnetic resonance imaging (MRI), negative node, and pre-menopausal (<= 40 years old). Following three cycles of neo-adjuvant chemotherapy, patients must achieve a complete/partial response (residual lesion <2 cm). Exclusion criteria include high-risk histology, tumor extension to uterine corpus/isthmus (as per MRI), and suboptimal response/progression following neo-adjuvant chemotherapy. Primary endpoints Assess the rate of functional uterus defined as successful fertility-sparing surgery and no adjuvant therapy. Sample size A total of 90 evaluable patients will be needed to complete the study. Estimated dates for completing accrual and presenting results Expected complete accrual in 2022 with presentation of results by 2025.
引用
收藏
页码:969 / 975
页数:7
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