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Assessment of Bone Biomarkers for TKI Response in RCC With Bone Metastases, HRQoL and Comparison of Imaging Techniques

Terminated
Conditions
Renal Cell Carcinoma
Registration Number
NCT02747173
Lead Sponsor
Spanish Oncology Genito-Urinary Group
Brief Summary

Prospective observational study to assess bone predictive biomarkers for TKI response in RCC patients with bone metastasis and HRQoL with TKI in these patients as well as the sensitivity and specificity of whole body magnetic resonance versus bone scintigraphy and versus CT in the assessment of metastatic lesions at bone level and at other sites.

Detailed Description

Prospective observational study to assess:

* Bone predictive biomarkers for tyrosine kinase inhibitor (TKI) response in renal cell carcinoma (RCC) patients with bone metastasis - Health Related Quality of Life (HRQoL) with TKI

* Comparison of the sensitivity and specificity of whole body magnetic resonance versus bone scintigraphy and versus Computerized tomography (CT) in the assessment of metastatic lesions at bone level and at other sites.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
4
Inclusion Criteria
  • Diagnosis of a stage IV renal cell carcinoma with confirmed presence of bone metastases, subsidiary of treatment with an TKI in first line
  • 18 years old or more
  • Life expectancy > 12 weeks
  • Eastern Cooperative Oncology Group Performance Status (ECOG PS): 0 - 2
  • Capability of understanding the study and completing the numerical pain scale, diary of analgesics and Quality of Life forms
  • Patient who has given informed consent
  • Adequate renal, hepatic and hematologic functions
Exclusion Criteria
  • Pregnancy, breastfeeding or fertile patients who do not use adequate contraceptive methods
  • Non-clear cell histology
  • Non irradiated brains metastases
  • Symptomatic brain metastases
  • Inability to undergo any of the medical tests of the study
  • A history of breast cancer or melanoma. Other tumors are accepted as long as the patients has been for at least 5 years free of disease
  • Synchronic diagnosis of another neoplasm
  • Presence of an active infection
  • Any decompensated disease or metabolic disorder
  • Cardiac events or pulmonary embolism in the 12 months previous to inclusion

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Assess bone biomarkers in response to TKIEvery 3 months until an average of 12 months

Assess the predictive value to TKI of bone biomarkers (bone formation BAP, P1NP, OPG and osteocalcin, and bone resorption biomarkers CTX) in patients with RCC with bone metastases.

Secondary Outcome Measures
NameTimeMethod
Objective response rateAn average of 12 months

Assess the efficacy of TKI in patients with RCC with bone metastases.

Change and correlation of magnetic resonance and CT results in the assessment of global disease response to TKI. Using RECIST and MASS criteriaEvery 3 months until an average of 12 months

Compare globally the magnetic resonance and CT results in the assessment of disease response to TKI using RECIST and MASS criteria

Efficacy of TKI in the improvement of pain produced by bone metastases throughout the study periodevery week until an average of 12 months

Assess the efficacy of TKI in the improvement of pain produced by bone metastases assessing the use of analgesics.

Measurements in time of bone metastases in RCC using whole body magnetic resonance and bone scintigraphyEvery 3 months until an average of 12 months

Comparison of the sensibility and specificity of whole body magnetic resonance and bone scintigraphy in the detection of metastases and response assessment of bone metastases in RCC

Quality of life of patients with RCC and bone metastases throughout the study period using FACT-BPEvery 3 months until an average of 12 months

Assess the quality of life of patients with RCC and bone metastases using the FACT-BP questionnaire

Assessment osteonecrosis of the jaw with use of biphosphonates or denosumab throughout the study periodevery week until an average of 12 months

Risk of osteonecrosis of the jaw with use of biphosphonates or denosumab

Progression free survivalAn average of 12 months

Assess the efficacy of TKI in patients with RCC with bone metastases.

Quality of life of patients with RCC and bone metastases throughout the study period using the FSI-15Every 3 months until an average of 12 months

Assess the quality of life of patients with RCC and bone metastases using the 15 item Functional Assessment of Cancer Therapy-Kidney Symptom Index (FKSI-15)

Efficacy of TKI in the improvement of pain produced by bone metastases throughout the study period using the NPR scaleevery week until an average of 12 months

Assess the efficacy of TKI in the improvement of pain produced by bone metastases using the Numeric Pain Rating Scale

Trial Locations

Locations (12)

Hospital Universitario central de Asturias

🇪🇸

Oviedo, Asturias, Spain

Hospital de Donostia

🇪🇸

San Sebastián, Guipuzcoa, Spain

Complejo Hospitalario Univ de Santiago de Compostela

🇪🇸

Santiago de Compostela, La Coruña, Spain

Hospital de Navarra

🇪🇸

Pamplona, Navarra, Spain

Complejo Hospitalario Univ de Vigo

🇪🇸

Vigo, Pontevedra, Spain

Consorcio Hospitalario Parc Tauli

🇪🇸

Barcelona, Spain

Complejo Hospitalario de León

🇪🇸

Leon, Spain

Hospital Univ Lucus Augusti

🇪🇸

Lugo, Spain

Complejo Hospitalario de Ourense

🇪🇸

Ourense, Spain

Instituto Valenciano de Oncologia

🇪🇸

Valencia, Spain

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Hospital Universitario central de Asturias
🇪🇸Oviedo, Asturias, Spain

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