Assessment of the Clinical Value of a Docetaxel, Cisplatin and 5-fluorouracil (DCF) Strategy Adapted to Patients for the Management of Metastatic or Locally Advanced Anal Resistant Radiochemotherapy Squamous Cell Anal Carcinoma.
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 70
- 试验地点
- 16
- 主要终点
- Progression-free survival rate
研究概览
简要总结
Squamous cell carcinoma of the anal canal (SCCA) is a rare disease and mostly diagnosed at an early stage. After standard concurrent chemoradiation (CRT) with mitomycin (MMC) and 5-fluorouracil (5FU), the disease will recur in 20% of patients. After treatment failure (including salvage surgery), cisplatin-5FU combination is the standard option but complete response is a rare event and the prognosis remains poor with most patients' death occurring in the first 12 months. Decision making for physicians in this setting is only based on retrospective studies or small phase II clinical trials including less than 20 patients. Hence, no efficient standard of care is currently available for relapsing SCCA patients who are currently treated with a palliative intent.
Between 2007 and 2013, 8 consecutive patients with advanced recurrent SCCA after CRT were treated with DCF regimen (docetaxel, cisplatin and 5-fluorouracil) in the Regional Cancer Institute of Franche Comté. After a median follow-up of 41 months, 4 patients (50%) achieved a complete response. Three patients underwent surgery of all involved metastatic sites. A pathological complete response was observed for all of them including in metastases occurring in irradiated fields, suggesting that taxane-based chemotherapy might be an effective strategy to circumvent resistance to radiotherapy (a preliminary cohort of 8 patients was published (Kim S et al Annals of oncology 2013). Furthermore, all complete responders were HPV 16, and high levels of specific T cell responses against Human Papillomavirus (HPV) HPV16-derived E6/E7 and telomerase were detected in 50% of complete responders suggesting the potential restoration of cancer immunosurveillance by this regimen.
Then, the Epitopes-HPV02 multicenter phase II study will aim to confirm the new role of taxane-based chemotherapy in SCCA patients.
详细描述
Epitopes-HPV02 study is a national multicenter open label phase II trial including 66 patients.
Patients will receive 6 cycles of DCF regimen (docetaxel 75 mg/m2 day, CDDP 75 mg/m2 and 5FU at 750 mg/m2/day for 5 days) every 3 weeks or 8 cycles of modified-DCF regimen (docetaxel 40 mg/m2 day, CDDP 40 mg/m2 day and 5-FU at 1200 mg/m2/day for 2 days) every 2 weeks, according to their clinical status.
CT scan will be planned at baseline, after 3 and after 6 cycles of DCF regimen (or after 4 and 8 cycles of modified-DCF regimen) and then every three months until disease progression or death. A Pet-scan will be performed before and after 6 cycles of DCF. Tumor assessment will be carried out according to RECIST V1.1 criteria.
This study is carried out by the University Hospital of Besançon and were approved by the independent Est-II French Committee for Protection of Persons (CPP) and by the French Health Products Safety Agency (ANSM). This study will be conducted in 17 clinical centers in France.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age ≥ 18 years
- •Performance status ECOG-WHO ≤ 1
- •histologically proved and unresectable locally advanced or metastatic squamous cell anal carcinoma
- •patient eligible to DCF regimen
- •signed written informed consent
排除标准
- •known hypersensitivity or contraindication to any of the study drugs (docetaxel, cisplatin, 5-fluorouracil).
- •previous chemotherapy for metastatic disease
- •previous chemotherapy by paclitaxel, docetaxel or navelbine
- •previous chemotherapy by cisplatin, except of concomitant radiotherapy
- •clinically significant cardiac disease
- •other malignancy within the last 3 years, except for adequately treated carcinoma in situ of the cervix or squamous carcinoma of the skin, or adequately controlled limited basal cell skin cancer.
- •simultaneous participation in another clinical study
- •pregnancy, breast-feeding or absence of adequate contraception for fertile patients
- •patient with any medical or psychiatric condition or disease which would make the patient inappropriate for entry into this study.
- •patient under guardianship, curator or under the protection of justice.
研究组 & 干预措施
DCF regimen
docetaxel 75 mg/m2 day, Cisplatin75 mg/m2 and 5Fluorouracil at 750 mg/m2/day for 5 days
干预措施: Docetaxel, Cisplatin and 5-Fluorouracil (Drug)
结局指标
主要结局
Progression-free survival rate
时间窗: 12 months after initiation of chemotherapy DCF.
Progression-free survival observed = the number of patients alive without progression at 12 months.
次要结局
- HPV-specific T cell responses measured by ELISPOT assay before and after DCF treatment(at baseline (inclusion) and 4 weeks after the end of DCF regimen)
- Overall survival(date of death from any cause (within 3 years after the initiation of the treatment))
- quality of life related to health(from the inclusion to patient death or for maximum 3 years after end of treatment)
- response rate(4 weeks after the end of DCF regimen)
- Tolerance of the DCF regimen ( Common Terminology Criteria for Adverse Events version 4.03)(from the initiation of DCF regimen to 4 weeks after the end of DCF regimen)
- Progression free survival(date of first progression of the disease (within 3 years after the initiation of the treatment))