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临床试验/NCT01628211
NCT01628211招募中2 期

Randomized Phase 2 Study Comparing Second Look Laparoscopy to Standard Follow up in Patients With no Radiologic Evidence of Disease at 6 Months After Complete Resection of Colorectal Mucinous Carcinoma

National Cancer Institute, Naples1 个研究点 分布在 1 个国家目标入组 140 人开始时间: 2012年4月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
140
试验地点
1
主要终点
overall survival

研究概览

简要总结

The purpose of this study is to evaluate whether a second-look laparoscopy, followed by peritonectomy, hyperthermic intraperitoneal chemotherapy (HIPEC) or systemic chemotherapy in case of peritoneal carcinosis, improves the overall survival of patients who have had radical resection of mucinous colorectal cancer.

详细描述

Patients will be entered into the study after radical resection of mucinous colorectal cancer, and reevaluated by CT scan after 6 months. Patients with no evidence of disease will be randomized to receive either standard follow up, or to have a second look laparoscopy to evaluate for peritoneal carcinosis. After laparoscopy, those patients who do not have peritoneal carcinosis will continue with standard follow up. Patients with peritoneal carcinosis diagnosed by laparoscopy will be treated according to their peritoneal carcinosis index (PCI). For patients with PCI > 20, systemic chemotherapy will be given according to Italian Association of Medical Oncology (AIOM) guidelines. Patients with PCI < 20 will undergo peritonectomy and then receive intravenous chemotherapy immediately followed by HIPEC.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Histologic diagnosis colorectal adenocarcinoma
  • Mucinous histotype
  • Stage I-III
  • Radical (R0) surgical resection of primary tumor
  • CT scan with contrast showing no evidence of disease recurrence 6 months after primary surgery
  • Age ≥ 18 ≤ 65 years
  • Performance Status ECOG ≤1
  • Normal hepatic, renal and hematologic function
  • Adjuvant chemotherapy permitted
  • Signed informed consent

排除标准

  • Residual disease after surgical resection of primary tumor
  • Distant metastasis
  • Active systemic infection
  • Chronic cardiovascular illness that would contraindicate abdominal dilatation with pneumoperitoneum
  • Concomitant or previous malignancy with 5 years of surgical resection of primary tumor (except for adequately treated non-melanoma skin cancer and in situ cervical cancer)
  • Pregnancy or lactation
  • Refusal or incapability of providing informed consent
  • Impossibility of complying with study schedules and follow-up

研究组 & 干预措施

Second look laparoscopy

Experimental

Second look laparoscopy to evaluate for and treat peritoneal carcinosis

干预措施: Laparoscopy (Procedure)

Second look laparoscopy

Experimental

Second look laparoscopy to evaluate for and treat peritoneal carcinosis

干预措施: peritonectomy (Procedure)

Second look laparoscopy

Experimental

Second look laparoscopy to evaluate for and treat peritoneal carcinosis

干预措施: Folinic Acid (Drug)

Second look laparoscopy

Experimental

Second look laparoscopy to evaluate for and treat peritoneal carcinosis

干预措施: 5-Fluorouracil (Drug)

Second look laparoscopy

Experimental

Second look laparoscopy to evaluate for and treat peritoneal carcinosis

干预措施: Oxaliplatin (Drug)

Second look laparoscopy

Experimental

Second look laparoscopy to evaluate for and treat peritoneal carcinosis

干预措施: systemic chemotherapy (Drug)

结局指标

主要结局

overall survival

时间窗: two years

次要结局

  • overall survival(five years)
  • changes in quality of life(6 months)
  • worst grade adverse event per patient(7 months)
  • number of patients with peritoneal carcinosis diagnosed at laparoscopy in the experimental arm(6 months)
  • list of therapies and clinical outcomes of patients who had radiologic evidence of disease within 6 months after initial surgery(two years)
  • number of patients with radiologic evidence of disease after initial surgery(6 months)

研究者

发起方
National Cancer Institute, Naples
申办方类型
Other
责任方
Sponsor

研究点 (1)

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