Traitement Des Carcinomes à Cellules de Merkel inopérables et/ou métastatiques Par Analogue de la Somatostatine - Etude Nationale Multicentrique Mono-bras de Phase II.
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 35
- 试验地点
- 1
- 主要终点
- Percentage of patient with positive response according to the RECIST 1.1 criteria
研究概览
简要总结
The purpose of this trial is to evaluate the efficacy of lanreotide on locally evolving and/or metastatic MCC in a national prospective multicentre phase II study (centres belonging to the skin cancer task force of the French Society of Dermatology namely "Groupe de Cancérologie Cutanée de la Société Française de Dermatologie"). This one-arm study, for which the primary endpoint is overall response to lanreotide, will follow an A'Hern plan in one step (A'Hern RP. Sample size tables for exact single-stage phase II designs. Stat Med 2001, 20:859-66) with main evaluation at 12 weeks on a population of 35 patients. The investigators make assumption that a 40% success rate at 3 months would be desirable, but if it was 20% or less the treatment would be unacceptable. It gives a trial size of 35 patients with a cut-off of 12 patients. Over 12 patients lanreotide will be considered as effective.
The lanreotide treatment (Somatuline LP 120 mg injected subcutaneously every 28 days) will be provided by IPSEN Pharma laboratory. An ancillary immunohistochemistry study on somatostatine receptors 2,3,5, dopamine receptors 1,2 and polyomavirus MCPyV will bring new data on this neuroendocrine tumour and potentially provide new therapeutic perspectives.
The results of this study may :
- determine whether somatostatin analogues may help to treat locally advanced and/or metastatic MCC;
- address whether there is a correlation between positive SPECT-CT (octreoscan) assessment and therapeutic response to lanreotide;
- evaluate the place of TEP-CT and SPECT-CT for MCC evaluation/staging;
- evaluate in future studies, with the ancillary data, other analogues or hybrid molecules;
- consider, if positive results are obtained from this study, somatostatin analogues as adjuvant treatment after surgery of primary MCC.
详细描述
The efficacy will be considered as success if patient have a positive response to lanreotide.
Primary criterion Positive response at 3 months will be defined according to the RECIST 1.1 criteria (clinical and TDM evaluation will be done at 3 months): complete response (CR) or partial response (PR) or stable disease (SD) at 3 months.
Secondary Objectives:
- Assessment of the primary criterion at M6, M9, M12, M18 and M24
- Description of the overall survival and time to progression
- Assessment of the efficacy of the following radiological exams for staging the disease: SPECT-CT and TEP-CT
- Description of the correlation of SPECT-CT results (positivity or negativity) and response to treatment, and the correlation of TEP-CT results and response to treatment
- Description of the safety and tolerability of lanreotide in this study
Population and Methods
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
- •Histologically confirmed neuroendocrine carcinoma of the skin (Merkel cell carcinoma) with inoperable local-regional disease or distant metastatic disease (stages IIIB or IV AJCC 2010), cerebral nervous system metastases will be allowed.
- •First line of treatment or more
- •Measurable disease: at least 20 mm by conventional techniques or 10 mm by spiral CT scan
- •WHO performance status ECOG 0-3
- •premenopausal patients must use effective contraception
- •No other prior malignancy within 5 years except adequately treated basal cell or squamous cell carcinoma or in situ cancer of the cervix
- •No other concurrent chemotherapy, immunotherapy or hormone therapy.
- •At least 4 weeks since adjuvant chemotherapy, 14 days since radiotherapy and 2 weeks since surgery
- •Biological functions: absolute neutrophil count at least 1000/mm3, platelet count at least 100000/mm3, haemoglobin at least 9g/dl (transfusion allowed), bilirubin no greater than 3 times upper limit of normal (ULN), SGOT and SGPT no greater than 2.5 times ULN, no untreated chronic liver disease, creatinine no greater than 1.5 times ULN, no untreated chronic renal disease, no untreated diabetes or infection
- •Written informed consent
排除标准
- •previous hypersensibility to lanreotide treatment
- •complicated and untreated cholelithiasis
- •pregnancy or breast-feeding
- •patient treated with cyclosporine
研究组 & 干预措施
Only one arm
All patients receive Lanreotide.
干预措施: Lanreotide (Drug)
结局指标
主要结局
Percentage of patient with positive response according to the RECIST 1.1 criteria
时间窗: at 3 months
Positive response will be defined according to the RECIST 1.1 criteria
次要结局
- Percentage of patient with positive response according to the RECIST 1.1 criteria(at 6, 9,12,18 and 24 months)
- Number of Participants with Adverse Events(at 3,6, 9,12,18 and 24 months)