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临床试验/NCT05123950
NCT05123950已完成不适用

Treatment Patterns and Clinical Outcomes in First Line Recurrent/Metastatic Squamous Cell Carcinoma of the Head and Neck (1L R/M SCCHN) Patients in Europe

Bristol-Myers Squibb1 个研究点 分布在 1 个国家目标入组 304 人开始时间: 2019年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
304
试验地点
1
主要终点
Distribution of demographic characteristics of 1L R/M SCCHN participants treated with nivolumab: Age

研究概览

简要总结

The purpose of this observational study is to collect real-world data that describes treatment patterns and clinical outcomes in participants with first line recurrent/metastatic squamous cell carcinoma of the head & neck (1L R/M SCCHN).

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

入选标准

  • Participants are included in Cohort 1 - Augment if they meet the following criteria:
  • Adults18 years or older
  • Diagnosis of histologically confirmed R/M SCCHN, from any of the following primary sites only: oral cavity, oropharynx, hypopharynx, and larynx between 01-Jun-2017 and 31-June-
  • Prescribed 1L treatment for R/M SCCHN
  • Treatment history and response available for medical chart abstraction from date of diagnosis until death or the end of the study in living participants
  • Have available for review one month of follow-up data available post initiation of 1L R/M SCCHN therapy
  • Informed consent form (ICF) signature/collection of living participants, as required by country regulation and local ethics committees
  • Participants are included in Cohort 1 if they meet the following criteria:
  • Adults 18 years or older
  • Diagnosis of histologically confirmed R/M SCCHN, from any of the following primary sites only: oral cavity, oropharynx, hypopharynx and larynx between 01-Jan-2014 and 31-Dec-
  • Prescribed 1L treatment for R/M SCCHN
  • Treatment history and response available for medical chart abstraction from the date of diagnosis until death or the end of the study in living participants
  • Have available for review one month of follow-up data post initiation of 1L R/M SCCHN therapy
  • Informed consent form (ICF) signature/collection of living participants, as required by country regulation and local ethics committees

排除标准

  • Participants were excluded from either cohort if they meet the following criteria:
  • Were enrolled in a cancer treatment-related clinical trial since the diagnosis of R/M SCCHN
  • Recurrent or metastatic carcinoma of the nasopharynx, squamous cell carcinoma of unknown primary site, squamous cell carcinoma that originated from the skin and salivary gland or non-squamous histologies (e.g., mucosal melanoma).

结局指标

主要结局

Distribution of demographic characteristics of 1L R/M SCCHN participants treated with nivolumab: Age

时间窗: At Baseline

Recurrent/Metastatic (R/M) Squamous Cell Carcinoma of the Head \& Neck (SCCHN)

Distribution of demographic characteristics of 1L R/M SCCHN participants treated with nivolumab: Height

时间窗: At Baseline

Distribution of demographic characteristics of 1L R/M SCCHN participants treated with nivolumab: Weight

时间窗: At Baseline

Distribution of demographic characteristics of 1L R/M SCCHN participants treated with nivolumab: Body surface area (BSA)

时间窗: At Baseline

Distribution of demographic characteristics of 1L R/M SCCHN participants treated with nivolumab: Health insurance coverage

时间窗: At Baseline

Distribution of demographic characteristics of 1L R/M SCCHN participants treated with nivolumab: Tobacco use

时间窗: At Baseline

Distribution of demographic characteristics of 1L R/M SCCHN participants treated with nivolumab: Patient comorbidities

时间窗: At Baseline

Distribution of demographic characteristics of 1L R/M SCCHN participants treated with nivolumab: Alcohol use

时间窗: At Baseline

Distribution of clinical characteristics of 1L R/M SCCHN participants treated with nivolumab: Human papillomavirus(HPV) p -16 status

时间窗: At Baseline

Distribution of clinical characteristics of 1L R/M SCCHN participants treated with nivolumab: Date of early stage diagnosis

时间窗: At Baseline

Distribution of clinical characteristics of 1L R/M SCCHN participants treated with nivolumab: Receive a platinum-based agent for early stage diagnosis

时间窗: At Baseline

Distribution of clinical characteristics of 1L R/M SCCHN participants treated with nivolumab: Receive radiation within 6 months prior to early stage diagnosis

时间窗: At Baseline

Distribution of clinical characteristics of 1L R/M SCCHN participants treated with nivolumab: Undergo related surgeries within 6 months prior to early stage diagnosis

时间窗: At Baseline

Distribution of clinical characteristics of 1L R/M SCCHN participants treated with nivolumab: Date of R/M SCCHN diagnosis

时间窗: At Baseline

Distribution of clinical characteristics of 1L R/M SCCHN participants treated with nivolumab: Specialty of diagnosing physician

时间窗: At Baseline

Distribution of clinical characteristics of 1L R/M SCCHN participants treated with nivolumab: Primary site of SCCHN at R/M diagnosis

时间窗: At Baseline

Distribution of clinical characteristics of 1L R/M SCCHN participants treated with nivolumab: Clinical stage at R/M diagnosis

时间窗: At Baseline

Distribution of clinical characteristics of 1L R/M SCCHN participants treated with nivolumab: Primary tumor stage at R/M diagnosis

时间窗: At Baseline

Distribution of clinical characteristics of 1L R/M SCCHN participants treated with nivolumab: Lymph node involvement at R/M diagnosis

时间窗: At Baseline

Distribution of clinical characteristics of 1L R/M SCCHN participants treated with nivolumab: Metastasis at R/M diagnosis

时间窗: At Baseline

Distribution of clinical characteristics of 1L R/M SCCHN participants treated with nivolumab: Histologic tumor grade at R/M diagnosis

时间窗: At Baseline

Distribution of clinical characteristics of 1L R/M SCCHN participants treated with nivolumab: Overall prognosis at R/M diagnosis

时间窗: At Baseline

Distribution of clinical characteristics of 1L R/M SCCHN participants treated with nivolumab: Platinum-based grouping

时间窗: At Baseline

Distribution of diagnostic procedures of 1L R/M SCCHN participants treated with nivolumab

时间窗: At Baseline

Distribution of treatment patterns of 1L R/M SCCHN participants treated with nivolumab: First (second, third+) Line of therapy (LOT)

时间窗: At Baseline

Distribution of treatment patterns of 1L R/M SCCHN participants treated with nivolumab: Duration of LOT

时间窗: At Baseline

Distribution of treatment patterns of 1L R/M SCCHN participants treated with nivolumab: Administration form

时间窗: At Baseline

Distribution of treatment patterns of 1L R/M SCCHN participants treated with nivolumab: Dose

时间窗: At Baseline

Distribution of treatment patterns of 1L R/M SCCHN participants treated with nivolumab: Dose changes

时间窗: At Baseline

Distribution of treatment patterns of 1L R/M SCCHN participants treated with nivolumab: Frequency of treatment regimen

时间窗: At Baseline

Distribution of treatment patterns of 1L R/M SCCHN participants treated with nivolumab: Schedule of agent administration

时间窗: At Baseline

Distribution of treatment patterns of 1L R/M SCCHN participants treated with nivolumab: Number of planned cycles

时间窗: At Baseline

Distribution of treatment patterns of 1L R/M SCCHN participants treated with nivolumab: Number of completed cycles

时间窗: At Baseline

Distribution of treatment patterns of 1L R/M SCCHN participants treated with nivolumab: Reasons for prescribing therapy

时间窗: At Baseline

Distribution of treatment patterns of 1L R/M SCCHN participants treated with nivolumab: Reasons for discontinuing therapy

时间窗: At Baseline

Distribution of treatment patterns of 1L R/M SCCHN participants treated with nivolumab: Dose delays

时间窗: At Baseline

Distribution of treatment patterns of 1L R/M SCCHN participants treated with nivolumab: Radiation performed for R/M disease

时间窗: At Baseline

Distribution of treatment patterns of 1L R/M SCCHN participants treated with nivolumab: Surgical procedures performed for R/M disease

时间窗: At Baseline

Distribution of adverse events of 1L R/M SCCHN participants treated with nivolumab

时间窗: At Baseline

Distribution of adverse events of 1L R/M SCCHN participants treated with nivolumab: Action taken

时间窗: At Baseline

Distribution of adverse events of 1L R/M SCCHN participants treated with nivolumab: Resolution

时间窗: At Baseline

Distribution of clinical outcomes of 1L R/M SCCHN participants treated with nivolumab: Response to therapy

时间窗: At Baseline

Distribution of clinical outcomes of 1L R/M SCCHN participants treated with nivolumab: Duration of response

时间窗: Up to approximately 36 months

Distribution of clinical outcomes of 1L R/M SCCHN participants treated with nivolumab: Overall survival

时间窗: Up to approximately 36 months

Distribution of clinical outcomes of 1L R/M SCCHN participants treated with nivolumab: Progression free survival

时间窗: Up to approximately 36 months

次要结局

  • Comparison of patient demographics, clinical characteristics, and treatment patterns between the Cohort 1- Augment and Cohort 1(At Baseline)
  • Comparison of time to event endpoints of OS, PFS, and DOR between Cohort 1- Augment and Cohort 1(Up to approximately 36 months)

研究者

发起方
Bristol-Myers Squibb
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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