NCT06422247已完成不适用
Observational Study in Japanese Patients With Peripheral T-Cell Lymphoma Who Received Second-Line Therapy
Bristol-Myers Squibb1 个研究点 分布在 1 个国家目标入组 307 人开始时间: 2024年4月5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
- 已完成
- 发起方
- 入组人数
- 307
- 试验地点
- 1
- 主要终点
- Overall survival (OS)
研究概览
简要总结
The purpose of this study is to describe the therapeutic practices and the prognosis of patients with relapsed or refractory peripheral T-cell lymphoma in Japan
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Retrospective
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Male or female participants with a confirmed diagnosis of the specific subtypes of peripheral T-cell lymphoma (PTCL) according to The World Health Organization (WHO) classification of lymphoid neoplasm, 4th edition defined by WHO and International Agency for Research on Cancer (IARC).
- •Participates aged ≥18 years of age at diagnosis of PTCL.
- •Participates who have been treated with a systemic therapy for PTCL and have initiated a systemic therapy as a second-line therapy for relapsed or refractory PTCL between April 1, 2018 and March 31, 2023.
排除标准
- •Participates who have medical history of peripheral T-cell lymphoma (PTCL) treatment by unapproved drug in Japan as of 31 March 2024 or off-label drug for PTCL in Japan as of 31 March
- •Participates who have medical history of participation to a separately defined registration study for regulatory approval in PTCL.
- •Participates who have medical history of PTCL treatment in a separately defined clinical study with intervention by on-label regimen for PTCL.
- •Participates judged to be inappropriate for enrollment in this study by the site investigator.
研究组 & 干预措施
Relapsed or refractory peripheral T-cell lymphoma initiating second-line systemic therapy
干预措施: Systemic therapy (Drug)
结局指标
主要结局
Overall survival (OS)
时间窗: From baseline until date of death from any cause or last known alive date, assessed up to 6 years
次要结局
- Frequency of treatment regimen by treatment line(End date of each treatment-line of therapy, assessed up to 6 years)
- Time to next treatment line or death (TTNT)(From date of first-line therapy initiation until death from any cause or last known alive date, assessed up to 6 years)
- Participant baseline demographics(Baseline)
- Participant baseline clinical characteristics(Baseline)
- Participant treatment sequence from initial diagnosis(From date of initial diagnosis until death from any cause or last known alive date, assessed up to 6 years)
研究者
研究点 (1)
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