跳至主要内容
临床试验/NCT01381601
NCT01381601已完成不适用

Incidence, Prevalence, and Symptom Burden Associated With Advanced Renal Cell Carcinoma in Commercially Insured Population (Pharmetrics)

GlaxoSmithKline0 个研究点目标入组 1 人开始时间: 2011年3月最近更新:
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
入组人数
1
主要终点
New and existing claims of metastatic renal cell carcinoma across multiple years

研究概览

简要总结

Information on the prevalence of advanced/metastatic renal cell carcinoma and its symptom burden is limited in commercially insured adult patients. Additionally, limited information exists on economic burden of adverse events associated with treatments for advanced/metastatic renal cell carcinoma. An objective of the current study is to estimate the incidence, prevalence, and symptom burden associated with advanced/metastatic RCC in a US "real-world" setting. Another objective is to quantify the economic burden of severe adverse events with agents used in management of first line advanced/metastatic RCC (sunitinib, sorafenib, bevacizumab, and pazopanib). This study will employ a retrospective cohort design. Analyses of health insurance claims data from a large commercially insured population will be employed in the current study. Study subjects will consist of all persons, aged ≥18 years, with evidence of advanced RCC between January 1, 2000 and December 31, 2009; these persons will be identified based in part on case-ascertainment algorithms. Analyses will be directed at estimating annual rates of incidence and prevalence of advanced/metastatic RCC, as well as symptom burden and costs of common severe adverse events associated with treatments used in management of advanced/metastatic RCC (sunitinib, sorafenib, bevacizumab, and pazopanib).

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 64 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • two or more medical encounters with a diagnosis of kidney cancer (ICD-9-CM 189.0) or malignant neoplasm of the renal pelvis (189.1), and
  • two or more medical encounters with a diagnosis of distant secondary malignant neoplasm (ICD-9-CM 197.XX-199.0, excluding 198.0 [kidney metastasis]) on different days <120 days apart (the date of the earliest such encounter will be designated the "index date").

排除标准

  • evidence of receipt of chemotherapeutic agents indicated or used in the treatment of advanced TCC, or
  • evidence of cystoscopy, biopsy of the bladder, or radical cystectomy
  • evidence of any other primary cancer

研究组 & 干预措施

Severe adverse event claims in subjects with metastatic RCC

Presence or absence of common severe treatment related adverse events (based on existence of claims) in patients with metastatic RCC. Common severe adverse event defined as Grade 3 or higher with >=5% frequency of occurence as reported in product label.

干预措施: Targeted agents indicated in management of advanced/metastatic RCC (sunitinib, sorafenib, bevacizumab, and pazopanib) (Drug)

结局指标

主要结局

New and existing claims of metastatic renal cell carcinoma across multiple years

时间窗: 2000 - 2009 (up to 10 years)

Identifying new and existing claims (based on claims based case-ascertainment algorithm) of metastatic renal cell carcinoma across multiple years

Cost associated with management of common severe adverse events related to 1st line treatments used in metastatic renal cell carcinoma

时间窗: 2000 - 2009 (up to 10 years)

Quantifying economic burden associated with management of common severe adverse events (defined as grade 3 and above adverse events occurring \>= 5% as per product label) related to agents used in 1st line metastatic RCC (sunitinib, sorafenib, bevacizumab, and pazopanib). Adverse events will be identified based on product labels.

次要结局

  • Quantify symptom burden associated with metastatic renal cell carcinoma(2000 - 2009 (up to 10 years))

研究者

申办方类型
Industry
责任方
Sponsor

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