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临床试验/NCT01318447
NCT01318447终止2 期

International, Phase II Study of CyberKnife® for Hepatic Metastases From Colorectal Cancer

Accuray Incorporated7 个研究点 分布在 3 个国家目标入组 15 人开始时间: 2011年1月最近更新:
适应症

试验速览

阶段
2 期
状态
终止
入组人数
15
试验地点
7
主要终点
Local recurrence-free survival

研究概览

简要总结

This prospective, multicenter study is intended to establish the efficacy and toxicity of treating unresectable colorectal liver metastases with accurately administered radiation using the CyberKnife stereotactic radiosurgery system.

详细描述

Colorectal cancer is the fourth most commonly diagnosed malignant disease worldwide, with an estimated 1,023,000 new cases and 529,000 deaths each year. The liver is the most frequent site of metastatic spread from colorectal cancer, 25% of colorectal cancer patients will have liver metastases at the time of initial colorectal resection and more than 50% of colorectal cancer patients will develop liver metastases during the course of the disease.

The current standard of care and only potential curative therapy for colorectal liver metastases is liver resection of the metastatic lesions. Surgical resection provides long term survival in patients with colorectal carcinoma (CRC) liver metastases. In a report of 1001 patients with metastatic colorectal cancer from Memorial Sloan-Kettering Cancer Center in NY, USA, surgical resection of liver metastases resulted in 3- and 5-year survival rates of 37% and 22%, respectively. Advances in pre- and intra-operative imaging and chemotherapy during recent years have increased overall survival up to 60% at 5 years after liver resection. However, 80-90% of liver metastases are unresectable at the time of diagnosis usually due to tumor location, multifocality, inadequate functional hepatic reserve or the patient's overall condition. For those patients, harboring unresectable liver metastases, alternative treatment approaches include neoadjuvant chemotherapy, local ablation therapy and stereotactic radiation therapy.

The recent availability of neoadjuvant chemotherapeutic agents has increased the response rates and doubled the median overall survival time for metastatic colorectal cancer from 10 to 20 months. Recent studies have demonstrated that neoadjuvant therapy allows 12.5% of patients with unresectable CRC liver metastases to be significantly downstaged and eligible for hepatic resection.

For unresectable CRC liver metastases, local ablative therapies are widely applied. Local ablative treatment refers to a variety of intervention techniques that specifically target tumors to directly destroy them. Numerous methods of ablation have been developed including cryoablation, percutaneous ethanol injection, radiofrequency ablation (RFA) and stereotactic radiation therapy. The most widely employed non-radiation based local ablative treatment is RFA which induces thermal ablation by passing high-frequency alternating current through the tumor utilizing electrodes that are placed within the tumor and surrounding tissue. RFA can be applied percutaneously under ultrasonic guidance or directly during laparoscopy or open laparotomy. Local recurrence rates of 44.4% at 18 months were reported by Solbiati et al. for CRC liver metastases with a median diameter of 2.6 cm. For tumors greater than 4 cm the local recurrence rate was 68%. RFA has an overall 3-year survival rate of 28-46% and a 5-year survival rate of 25%. However, patients with advanced hepatic decompensation, large tumors (3 to 5 cm), or multifocal tumors are generally considered poor candidates for RFA.

Conventional radiation therapy has been shown useful for palliation of hepatic capsular pain, but historically it has played a minor role in the treatment of patients with unresectable liver metastases. This can be attributed chiefly to the low tolerance of the whole liver to radiation. The liver was thought to be a relatively radiosensitive organ and with whole liver irradiation, it was difficult to achieve the radiation doses necessary to eradicate gross tumors without causing radiation induced liver disease. Partial liver irradiation has shown some promise. Limiting irradiation to only one-third of the liver through three-dimensional (3D) conformal radiotherapy techniques, including intensity modulated radiotherapy (IMRT), several studies have shown that partial liver irradiation is safe with doses up to 50-72.6 Gy. However, further dose escalation with conventional radiation therapy techniques risks injury to adjacent abdominal organs.

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

入选标准

  • Male or Female
  • Hepatic metastases from histologically confirmed colorectal adenocarcinoma
  • 3 hepatic lesions or less present
  • Cumulative size of hepatic lesions between 1 and 10 cm
  • Treatment determined by the liver/GI tumor board or equivalent organization at the participating site
  • Metastatic disease not amenable to surgery as assessed by the panel (including a surgeon) or patient who refuses surgery
  • Patient must be able to undergo contrast enhanced CT for planning
  • Age >= 18 years old
  • Performance Status (ECOG) ≤ 2
  • Minimum of 6 months between the initial diagnosis of the disease and the first hepatic metastasis
  • Minimum of 4 weeks between prior chemotherapy or targeted therapy and the first CyberKnife session
  • Total bilirubin ≤ 3 times the upper limit of normal, ASAT and ALAT ≤ 5 times the upper limit of normal
  • Albumin >= 36 g/L and lymphocytes >= 700/mm3
  • No contraindication to fiducials implantation, hemostasis problems shall be corrected before implantation
  • Life expectancy >= 3 months
  • Patient affiliated with a health insurance system. Applicable for French patients only.
  • Patient having signed the informed consent

排除标准

  • Prior abdominal radiation therapy
  • Any evidence of visible intra-hepatic bile duct dilatation on pre-treatment images
  • Extrahepatic metastases
  • Current evidence of ascitis
  • Renal insufficiency (creatinine clearance < 45 ml/min)
  • Known allergy to gold
  • Pregnant or lactating woman
  • Prior history of other cancer except basocellular carcinoma and in situ cervix carcinoma
  • Patient already enrolled in another therapeutic clinical trial
  • Inability to comply with follow-up visits for geographical, social or psychological reasons

结局指标

主要结局

Local recurrence-free survival

时间窗: 12 months

Local hepatic control (non progression: complete response, partial response or stable disease) will be assessed according to Response Evaluation Criteria In Solid Tumors (RECIST) 1.1. Local recurrence-free survival time is calculated as the time between the date of first treatment session and the date of the first local recurrence. Patients alive who never experienced local recurrence at the time of analysis are censored at the date of the last follow-up visit. Patients who die from causes other than local recurrence at the time of analysis are censored at the date of death.

次要结局

  • Recurrence-free survival(3, 6, 9, 12, 18 and 24 months)
  • Overall survival(3, 6, 9, 12, 18 and 24 months)
  • Acute and long term toxicity(3, 6, 9, 12, 18 and 24 months)
  • Quality of Life(3, 6, 9, 12, 18 and 24 months)
  • Correlation of response as assessed by Response Evaluation Criteria In Solid Tumors (RECIST) 1.1 and Positron Emission Tomography (PET) Response Criteria in Solid Tumors (PERCIST)(6, 18 and 24 months)
  • Local recurrence-free survival(3, 6, 9, 18 and 24 months)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (7)

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