Normothermic Intraperitoneal Chemotherapy - Long Term in Peritoneal Metastases From Colorectal Cancer - Feasibility Study (NIPEC-OXA)
试验速览
- 阶段
- 1 期
- 发起方
- 入组人数
- 20
- 试验地点
- 1
- 主要终点
- Number of Participants with Adverse Events after Intraperitoneal Chemotherapy Administration (NIPEC-OXA)
研究概览
简要总结
Feasibility study regarding 20 Patients with peritoneal metastases from colorectal cancer treated with cytoreductive surgery and HIPEC and subsequently with 4 courses of normothermic intraperitoneal chemotherapy - long term (NIPEC-OXA) with oxaliplatin.
详细描述
Primary endpoint: to determine if the administration of additional i.p. chemotherapy for a period of 9 weeks after completed CRS and HIPEC is a safe procedure to be used in the future in a formal randomised trial. The toxicity of the chemotherapy given through i.p. during NIPEC-OXA courses will be analysed throughout the entire treatment period and a subsequent 3-month follow-up period.
Secondary endpoints:
- Intra-abdominal chemotherapy drug distribution 7-14 days after CRS and HIPEC and before the 4th NIPEC-OXA course
- Surgical complications after CRS, HIPEC and NIPEC-OXA until 3 months after the last NIPEC-OXA course
- Disease-free survival (DFS)
- Overall survival (OS)
Exploratory endpoint: quality of life
Estimated date of first patient enrolled: 3rd quarter of 2021 Anticipated recruitment period: 1,5 years Estimated treatment completion date of last patient: 1st quarter of 2023 Expected treatment duration per patient: 9 weeks Expected follow-up period per patient: 3 months after the last NIPEC-OXA procedure
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 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age 18 - 75 years
- •Able to provide written, informed consent regarding expected cooperation during treatment and follow-up according to ICH GCP, and national/local regulations
- •Histologically verified CRC
- •Histologically verified and/or radiologically/clinically suspected PM from CRC
- •Synchronous or metachronous PM from CRS
- •If neoadjuvant oxaliplatin-containing chemotherapy is administrated, patients with absence of progressive disease (assessed by CT)
- •In metachronous cases: if adjuvant oxaliplatin-containing chemotherapy, the interval between oxaliplatin- containing adjuvant chemotherapy and diagnosis of PM must be >6 months
- •Intraperitoneal tumour burden amenable to CRC and HIPEC with Peritoneal Cancer Index (PCI40) ≤ 20, assessed at the time of surgery
- •Absence of other metastatic sites, i.e. liver, lungs, central lymph nodes
- •Completeness of Cytoreduction (CC) score of 0 is required
- •Eastern Cooperative Oncology Group (ECOG) Performance Status either 0 or 141
- •Women of childbearing potential (WOCBP), defined as all women physiologically capable of becoming pregnant, should have a negative urine- or serum pregnancy test within 72 hours prior to receiving the 1st dose of study medication. If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required.
- •WOCBP should be willing to use 1 highly effective method of birth control or be surgically sterile, or abstain from heterosexual activity for the course of the study through 120 days after the last dose of study medication.
- •Men in a sexual relationship with a WOCBP must agree to use a condom starting with the 1st dose of study therapy through 120 days after the last dose of study therapy. In case of female partner of child-bearing potential, the female partner should use 1 highly effective contraception method as defined in section 5.1.5 - "Other considerations".
排除标准
- •Has a history of hypersensitivity to oxaliplatin or to any of the excipients listed in the SmPC section 6.1
- •Has myelosuppression before starting treatment, ie number of neutrophils granulocytes <1.0 x 109/l and/or number of platelets <75 x 109/l
- •Has peripheral sensitive neuropathy with functional outcomes before starting treatment
- •Has severe renal impairment (creatinine clearance < 30 ml min) (see the SmPC section 5.2).
- •Concurrent or previous diagnosis of invasive cancer within 5 years
- •Psychiatric or addictive disorder or other medical condition that would preclude the patient from meeting the trial requirements
- •Participation in another cancer clinical trial
- •Patients who, according to current guidelines will be offered i.v. adjuvant therapy
- •Significant cardiac or other medical illness that would limit activity or survival, such as severe congestive heart failure, unstable angina, or serious cardiac arrhythmia
- •Alcohol or drug abuse
- •Any reason why, in the opinion of the investigator, the patient should not participate
- •Has a known history of Human Immunodeficiency Virus (HIV)
- •Has known active Hepatitis B (e.g., HBsAg reactive) or Hepatitis C (e.g., HCV RNA [qualitative] is detected)
- •Is pregnant or breastfeeding, or expecting to conceive or father children within the project duration of the trial, starting with the screening visit through 120 days after the last dose of trial treatment.
研究组 & 干预措施
NIPEX-OXA arm
20 patients treated with NIPEC-OXA after CRS and HIPEC.
干预措施: Oxaliplatin (Drug)
结局指标
主要结局
Number of Participants with Adverse Events after Intraperitoneal Chemotherapy Administration (NIPEC-OXA)
时间窗: Throughout the entire treatment period, including a 3-month follow-up
Common Terminology Criteria for Adverse Events v. 5
Number of Participants with Surgical Complications after CRS, HIPEC and NIPEC-OXA
时间窗: Throughout the entire treatment period, including a 3-month follow-up
Clavien-Dindo classification
次要结局
- Number of Participants with Optimal, Suboptimal and Missing Fluid Distribution in the Abdomen Injected Through 2 I.P. Catheters(7-14 days after CRS and HIPEC and before the 4th NIPEC-OXA course)
研究者
Mariusz Goscinski
Principal Investigator
Oslo University Hospital