跳至主要内容
临床试验/NCT04949282
NCT04949282招募中不适用

SEPTRALU, Spanish Series of Patients Treated With the Radionuclide Lutetium177

Sociedad Española de Medicina Nuclear e Imagen Molecular20 个研究点 分布在 1 个国家目标入组 5,000 人开始时间: 2021年5月10日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
5,000
试验地点
20
主要终点
Progression Free Survival (PFS)

研究概览

简要总结

This study aims to pool the clinical experience of Spanish centers treating patients with 177Lu-DOTATATE to evaluate the efficacy, tolerance, and safety of the drug in routine clinical practice and to learn about the profiles of patients and tumors treated and the results in each type of patient and tumor.

详细描述

Patient data will be collected from medical records after obtaining consent and retrospectively.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Written informed consent must be obtained prior to any data collection.
  • Patients must be diagnosed with unresectable or metastatic, progressive, somatostatin receptor positive tumour
  • Aged ≥18 years.

排除标准

  • 未提供

研究组 & 干预措施

Lutathera

干预措施: Lutetium [177Lu] oxodotreotide/dotatate (Device)

结局指标

主要结局

Progression Free Survival (PFS)

时间窗: Up to 12 months

Defined as the time, in months, from Lutathera® treatment initiation to the date of first objective tumour progression, determined according to Response Evaluation Criteria in Solid Tumours (RECIST) Criteria, Version 1.1, or death due to any cause, whichever comes first.

Overall survival (OS)

时间窗: Up to 12 months

Defined as the time, in months, from Lutathera® treatment initiation to the date of death due to any cause.

Overall response rate (ORR)

时间窗: Up to 12 months

Is determined by imaging technique according to RECIST criteria v1.1 and is defined as the proportion of treated patients who achieve a best overall response of partial response (PR) or complete response (CR) according to RECIST 1.1

次要结局

  • Prognostic factors(Up to 12 months)
  • Adverse Events (AEs)(Up to 12 months)
  • Areas for improvement care(Up to 12 months)
  • Characteristics of the population .(Up to 12 months)
  • Health-related Quality of Life (HRQoL)(Up to 12 months)

研究者

发起方
Sociedad Española de Medicina Nuclear e Imagen Molecular
申办方类型
Other
责任方
Sponsor

研究点 (20)

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