ID
Bron
Aandoening
Oncology- Metastatic renal cell carcinoma (mRCC)
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Characterize differences in the following outcomes in mRCC patients receiving 2nd targeted therapy with everolimus, sorafenib, or axitinib following a 1st targeted therapy with sunitinib or pazopanib:
<br><br>
a. OS from the initiation of 2nd targeted therapy<br>
b. Treatment duration of the 2nd targeted therapy<br>
c. PFS from the initiation of 2nd targeted therapy
Achtergrond van het onderzoek
Renal Cell Carcinoma (RCC) is a common adult malignancy worldwide. At RCC diagnosis, more than one fourth of patients present with metastatic disease, and about half of those with resectable disease eventually develop metastases. Tyrosine kinase inhibitors (TKIs) and inhibitors of the mammalian target of rapamycin (mTOR) are the current standard of care for patients with metastatic RCC (mRCC). To date, four TKIs (axitinib, sorafenib, sunitinib, and pazopanib) and two inhibitors of mTOR (temsirolimus and everolimus) have been approved for the treatment of mRCC in multiple countries, including the EU 5, Japan, Canada, and US.
TKIs can prolong overall and progression-free survival in patients with mRCC, and have been the most commonly used as 1st targeted therapy. However, almost all RCC patients eventually fail their 1st targeted therapy and experience progression. Maximizing the value of the mRCC therapeutic armamentarium will require careful selection of the next treatment. Given the growing number of treatment options, limited comparative evidence and lack of consensus on proper sequencing in mRCC, a well-conducted observational study of real-world outcomes of 2nd targeted therapy may provide valuable inputs for decision making. Commonly used 2nd targeted therapies include sorafenib, everolimus, axitinib, and temsirolimus (Market share data, Novartis data on file). In addition, an increased use of axitinib and a decreased use of temsirolimus have been observed (Market Share data on file). Thus, the current study proposes to evaluate the real-world use of everolimus, sorafenib and axitinib as 2nd targeted therapy.
Onderzoeksopzet
N/A
Onderzoeksproduct en/of interventie
N/A as we are not assigning patients into a specific treatment group
Publiek
Dony Patel
25 Basinghall Street
London EC2V 5HA
United Kingdom
+44 (0)20 7 015 2388 / +44 (0)7760 158 663
dony.patel@navigant.com
Wetenschappelijk
Dony Patel
25 Basinghall Street
London EC2V 5HA
United Kingdom
+44 (0)20 7 015 2388 / +44 (0)7760 158 663
dony.patel@navigant.com
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
• Adult patients (age ≥18 years, males and females) diagnosed with mRCC per medical chart
• The patient received 1st targeted therapy with either sunitinib or pazopanib (i.e. a TKI other than sorafenib or axitinib)
• The patient experienced disease progression during their 1st targeted therapy and subsequently initiated one of the following 2nd targeted therapies:
(1) Everolimus
(2) Sorafenib
(3) Axitinib
• The date of initiating 2nd targeted therapy was during a defined time period from the time when everolimus, sorafenib, and axitinib all became available in the local market, to 20 months (tentative, pending on sample size) prior to the data extraction time
• Treatment history and outcomes related to mRCC are available for chart review
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
• The patient used an mTOR inhibitor, bevacizumab or cytokines [IL-2, IFN- α2a] prior to initiation of the 2nd targeted therapy
• The patient used a combination therapy with ≥2 targeted agents prior to or upon the initiation of the 2nd targeted therapy
• The patient initiated the 2nd targeted therapy in an interventional trial in the mRCC setting
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
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Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL5560 |
NTR-old | NTR5681 |
Ander register | : 06-12-2014 |