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临床试验/NCT05679583
NCT05679583招募中2 期

Preoperative Stereotactic Body Radiation Therapy in Patients With Resectable Pancreatic Cancer: A Prospective Phase II Study

Yonsei University1 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2022年9月26日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
招募中
入组人数
25
试验地点
1
主要终点
R0 rate

研究概览

简要总结

Pancreatic cancer is a cancer with a poor prognosis and a high mortality rate. The prognosis of surgically resectable pancreatic cancer is better than that of unresectable pancreatic cancer. But the prognosis is still poor enough to report a 2-year disease-free survival rate of 47.0% despite the application of standard treatment. Preoperative chemotherapy or radiotherapy for pancreatic cancer has been performed for a long time, especially for locally advanced pancreatic cancer. However, there are very few studies on the application of preoperative chemotherapy or radiotherapy for borderline resectable or resectable pancreatic cancer. The PREOPANC trial is a representative randomized study to investigate the effect of preoperative chemo/radiation therapy in borderline resectable or resectable pancreatic cancer. As a result, the overall survival, progression-free survival, local control, and distant control rates were significantly superior in preoperative therapy group. However, when only patients with resectable pancreatic cancer were analyzed separately, there was no significant difference in overall survival rate or complete resection rate. In 2020, retrospective propensity score matching analysis using the national cancer database revealed that the addition of preoperative stereotactic body radiation therapy (SBRT) showed a significant increase in overall survival rate rather than preoperative chemotherapy alone. In addition, SBRT also showed a significant increase in overall survival rather than conventional fractionated RT. In summary, the current standard treatment for resectable pancreatic cancer is surgical resection, but a higher survival rate can be expected when preoperative therapy is added. However, there is no study that focused on the role of preoperative SBRT. Therefore, this study aims to confirm the effectiveness of adding preoperative SBRT alone in resectable pancreatic cancer.

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
20 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Histologically diagnosed adenocarcinoma of the pancreas
  • •Resectable pancreatic cancer at the time of diagnosis
  • •Resectable pancreatic cancer refers to cases in which all of the following conditions are met:
  • •If the tumor does not reach the superior mesenteric vein or portal vein, or even if it does, it reaches within 180°
  • •If the tumor does not reach the superior mesenteric artery, celiac artery, or common hepatic artery
  • •In the absence of distant metastases 3) Patients aged 20 years or older at the time of diagnosis 4) General performance status is 0-2 based on the Eastern Cooperative Oncology Group (ECOG) standard 5) Patients who voluntarily decided to participate in this clinical study and signed the written informed consent

排除标准

  • •If there is a history of radiation exposure to the abdomen
  • •Pancreatic cancer that cannot be resected
  • •When accompanied by distant metastasis
  • •Patients who are currently judged to be difficult to undergo surgery based on general performance status, bone marrow, and kidney function tests
  • •Patients with active or uncontrolled infection
  • •Patients with uncontrolled heart disease
  • •Pregnant or lactating women
  • •Patients with a history of malignant tumor excluding skin epithelial carcinoma, except for malignant melanoma, stage 0 cervical cancer, and early thyroid cancer
  • •Patients who have been treated for malignant tumors and have been cured for more than 5 years can participate in the study

研究组 & 干预措施

Preoperative SBRT arm

Experimental

Patients with resectable pancreatic cancer will receive preoperative SBRT 2 to 4 weeks before surgery. And 4 weeks after surgery, adjuvant CTx will be administered for 6 months.

干预措施: Preoperative Stereotactic body radiation therapy (SBRT), Pancreatic resection, Adjuvant Chemotherapy (Radiation)

结局指标

主要结局

R0 rate

时间窗: 2 weeks after the surgical resection

R0 resection is defined as the resection margin more than 1 mm away from the tumor on histological findings after pancreatic cancer surgery. The R0 rate refers to the proportion of patients showing R0 resection, based on all patients.

次要结局

  • Local control rate(Patient follow-up will be performed 3 months after the surgery and then at 6-month intervals thereafter. Follow-up will be conducted for a total of 2 years.)
  • Tumor recurrence(Patient follow-up will be performed 3 months after the surgery and then at 6-month intervals thereafter. Follow-up will be conducted for a total of 2 years.)
  • Quality of life (based on EORTC QLQ-C30)(Patient follow-up will be performed 3 months after the surgery and then at 6-month intervals thereafter. Follow-up will be conducted for a total of 2 years.)
  • Disease-free survival(Patient follow-up will be performed 3 months after the surgery and then at 6-month intervals thereafter. Follow-up will be conducted for a total of 2 years.)
  • Quality of life (based on FACT-Hep)(Patient follow-up will be performed 3 months after the surgery and then at 6-month intervals thereafter. Follow-up will be conducted for a total of 2 years.)
  • Treatment related acute/chronic toxicity (based on CTCAE ver 5.0)(Patient follow-up will be performed 3 months after the surgery and then at 6-month intervals thereafter. Follow-up will be conducted for a total of 2 years.)
  • Overall survival rate(Patient follow-up will be performed 3 months after the surgery and then at 6-month intervals thereafter. Follow-up will be conducted for a total of 2 years.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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