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临床试验/NCT03290820
NCT03290820尚未招募2 期

Aspirin Improve Survival of Patients With N2-3 Nasopharyngeal Carcinoma: A Phase 2 Prospective Randomized Controlled Trial

Sun Yat-sen University1 个研究点 分布在 1 个国家目标入组 184 人开始时间: 2018年1月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
184
试验地点
1
主要终点
Distant-metastasis-free survival

研究概览

简要总结

Nasopharyngeal carcinoma (NPC) is one of the most common maligancies of China. In the era of intensity-modulated radiotherapy (IMRT), the 5-year overall survival (OS) has now reached 85.0% or more. However, even after chemoradiation, the 5-year distant-metastasis rate of patients with N2-3 NPC is still 36.7%. Aspirin is proven in lab and clinical studies to have the abilities of inhibiting the inflammation which could enhance metastasis of breast and colorectal cancers. And before this study, it was discovered that regular aspirin intake might be associated with distant-metastasis-free survival (MFS) and OS independently. So this Phase 2 trial was conducted to validate the impact of aspirin on prognosis of N2-3 NPC.

详细描述

Nasopharyngeal carcinoma (NPC) is one of the most common maligancies of China. In the era of intensity-modulated radiotherapy (IMRT), the 5-year overall survival (OS) has now reached 85.0% or more. However, the prognosis of the patients with late N (N2-3) diseases remains poor. Even after chemoradiation, the 5-year distant-metastasis rate of these patients is nearly 36.7%. Additionally, these patients occupies about 30.0% of the whole NPC population. To improve the prognosis of the patients with N2-3 NPC, there is a need to explore a new, practical and effective method to eliminate the distant metastasis.

Aspirin is proven in lab and clinical studies to have the abilities of inhibiting the inflammation which could enhance metastasis of many malignant tumors, such as breast and colorectal cancers. And before this study, patients with N2-3 nonmetastatic NPC between 2008 and 2011 were retrospectively analyzed, to discovered that regular aspirin intake might be associated with distant-metastasis-free survival (MFS) and OS independently. So this Phase 2 randomized controlled trial was conducted to validate the impact of aspirin on prognosis of N2-3 NPC.

This study aim to enroll patients with T1-4N2-3M0 NPC. All the patients will be treated with IMRT and concurrent chemotherapy of the PF (Nedaplatin + 5-flurouracil) regimen. After randomization, patients in the Experimental Group will also receive daily aspirin of 75mg. The 5-year MFS is the primary endpoint. And the 5-year OS and aspirin-related toxicities are the secondary endponits.

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 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Pathologic dianosis of nasopharyngeal carcinoma
  • Stage of T1-4N2-3M0 (UICC/AJCC classification ver. 7)
  • 18-70 years old
  • Karnofsky performance score > 70

排除标准

  • Distant metastasis before or during radiotherapy
  • Severe dysfunctions of liver, kidney, lung, heart of bone marrow which are not fit for radiotherapy
  • Prior malignancies
  • Prior history of radiotherapy, chemotherapy or monoclonal antibody therapy
  • Participation of other drug trials within 3 months
  • Regular use of aspirin before dianosis
  • Contraindication or allergy of aspirin
  • Patients who are considered by the researchers not suitable to participate this trial

研究组 & 干预措施

Controlled Group

Active Comparator

The patients in the Controlled Group are allocated to receive radiotherapy and concurrent chemotherapy.

干预措施: Radiotherapy (Radiation)

Controlled Group

Active Comparator

The patients in the Controlled Group are allocated to receive radiotherapy and concurrent chemotherapy.

干预措施: Concurrent chemotherapy (Drug)

Experimental Group

Experimental

The patients in the Experimental Group are allocated to receive radiotherapy and concurrent chemotherapy plus daily aspirin.

干预措施: Radiotherapy (Radiation)

Experimental Group

Experimental

The patients in the Experimental Group are allocated to receive radiotherapy and concurrent chemotherapy plus daily aspirin.

干预措施: Concurrent chemotherapy (Drug)

Experimental Group

Experimental

The patients in the Experimental Group are allocated to receive radiotherapy and concurrent chemotherapy plus daily aspirin.

干预措施: Aspirin (Drug)

结局指标

主要结局

Distant-metastasis-free survival

时间窗: 5 years after diagnosis

The percentage of patients of a data set who survive without distant metastasis after a defined period of time from pathologic diagnosis

次要结局

  • Overall survival(5 years after diagnosis)
  • Aspirin-related toxicities(5 years after diagnosis)

研究者

发起方
Sun Yat-sen University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Yun-fei Xia

Professor

Sun Yat-sen University

研究点 (1)

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