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临床试验/2024-516937-10-01
2024-516937-10-01招募中3 期

Safe Stop Trial: observational study of the STOP & GO strategy of PD-1 blockade in advanced melanoma patients upon achieving a complete or partial response

Erasmus Universitair Medisch Centrum Rotterdam (Erasmus MC)14 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2024年12月18日最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
入组人数
200
试验地点
14
主要终点
The primary endpoint of this study is the rate of ongoing responses (CR and PR) according to RECIST v1 .1 (35) at 24 months after first start of nivolumab/pembrolizumab

研究概览

简要总结

The primary objective of this study is the rate of ongoing response in patients with advanced and metastatic melanoma who discontinue first-line monotherapy with nivolumab or pembrolizumab upon achieving a CR or PR.

入排标准

年龄范围
18 years 至 65+ years(65+ Years, 18-64 Years)
接受健康志愿者

入选标准

  • Age ≥ 18 year
  • Advanced or metastatic melanoma
  • Current treatment with first-line nivolumab or pembrolizumab for advanced or metastatic melanoma; previous systemic treatment, including immunotherapy, in (neo)adjuvant setting for resectable melanoma is allowed
  • Documented target lesion(s) according to RECIST v1.1 on diagnostic CT at start of PD-1 blockade with nivolumab or pembrolizumab
  • Documented tumor response evaluation every 12±1 weeks according to RECIST v1.1 (35) using a diagnostic CT as per standard practice
  • Presence of MRI brain for the screening of brain metastases (prior to discontinuation of PD-1 blockade)
  • Willingness to discontinue nlvolumab or pembrolizumab within 6 (+1) weeks weeks after confirmation of CR or PR before the full period of 2 years therapy

排除标准

  • Concomitant systemic therapies with other anti-cancer agents, e.g. BRAF-inhibitor, anti-CTLA4 (e.g. ipilimumab), or other PD-1 blockade than nlvolumab or pembrollzumab

结局指标

主要结局

The primary endpoint of this study is the rate of ongoing responses (CR and PR) according to RECIST v1 .1 (35) at 24 months after first start of nivolumab/pembrolizumab

The primary endpoint of this study is the rate of ongoing responses (CR and PR) according to RECIST v1 .1 (35) at 24 months after first start of nivolumab/pembrolizumab

次要结局

  • 1a. Total duration of tumor response after first documented CR or PR followed by treatment interruption
  • 1 b. Duration of tumor response (CR and PR) after discontinuation of PD-1 blockade
  • 2. PFS from start of first-line monotherapy with PD-1 blockade (i.e. nivolumab or pembrolizumab) until first PD (PFS1)
  • 3a. Rate of reintroduction of monotherapy with PD-1 blockade (i.e. nivolumab or pembrolizumab) upon first PD
  • 3b. Rate of introduction of other systemic salvage therapy (i.e. other than monotherapy PD-1 blockade) upon first PD
  • 4a. Best tumor response on rechallenge with monotherapy PD-1 blockade (i.e. nivolumab or pembrolizumab)
  • 4b. Best tumor response after introduction of other systemic salvage therapy (i.e. other than monotherapy PD-1 blockade)
  • Sa. PFS after reintroduction of monotherapy PD-1 blockade (i.e. nivolumab, or pembrolizumab) (PFS2a)
  • Sb. PFS after introduction other systemic salvage therapy (i.e. other than monotherapy PD- 1 blockade) (PFS2b)
  • 6a. Total PFS (PFSTata1) defined as the period from initial start of PD-1 blockade until final PD (including period after discontinuation and (re-)introduction of nivolumab/ pembrolizumab or other salvage therapy)
  • Totale PFS gedefinieerd als de periode vanaf de eerste start van PD-1-blokkering tot de uiteindelijke PD (inclusief periode na staken en bij (her)start van nivolumab/pemprolizumab of andere systemische therapie (PFStotaal)
  • 7. Rate of grade 3-4 AEs after early discontinuation or reintroduction of nivolumab/pembrolizumab monotherapy
  • 8. Change in tumor burden since the start and after early discontinuation of PD-1 blockade
  • 9. Change in Qol after discontinuation of PD-1 blockade measured at different time point
  • 10. Change in fear of disease recurrence/progression
  • Change in productivity (paid and unpaid work) after discontinuation of PD-1 blockad
  • 12. Change in healthcare resource (within and outside the hospital) after discontinuation of PD-1 blockade
  • 13. Change in hours of informal care after discontinuation of PD-1 blockade
  • Qol at disease progression and restart of systemic therapy (when applicable)
  • 14. Verandering in Qol bij PD en herstart systemlsche theraple (indien van toepassing)

研究者

申办方类型
Hospital/Clinic/Other health care facility
责任方
Principal Investigator
主要研究者

dr. A. v.d. Veldt

Scientific

Erasmus Universitair Medisch Centrum Rotterdam (Erasmus MC)

研究点 (14)

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