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Clinical Trial Summary

The primary purpose of this study is to determine the sensitivity of CYBRID Score for predicting in-vivo clinical response based on surgical response or RECIST 1.1 for neoadjuvant and locally advanced/metastatic patients, respectively. The secondary purposes is to determine the sensitivity of the CYBRID Score for predicting in-vivo clinical response based on surgical response or RECIST 1.1 for neoadjuvant and locally advanced/metastatic patients, respectively.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Breast Neoplasms
  • Carcinoma
  • Carcinoma, Hepatocellular
  • Carcinoma, Non-Small-Cell Lung
  • Carcinoma, Renal Cell
  • Carcinoma, Transitional Cell
  • Colorectal Neoplasms
  • Endometrial Neoplasms
  • Esophageal Neoplasms
  • Liver Neoplasms
  • Locally Advanced Bladder Urothelial Carcinoma
  • Locally Advanced Cervical Carcinoma
  • Locally Advanced Clear Cell Renal Cell Carcinoma
  • Locally Advanced Colorectal Carcinoma
  • Locally Advanced Lung Non-Small Cell Carcinoma
  • Metastatic Bladder Urothelial Carcinoma
  • Metastatic Cervical Carcinoma
  • Metastatic Clear Cell Renal Cell Carcinoma
  • Metastatic Colorectal Carcinoma
  • Metastatic Endometrial Carcinoma
  • Metastatic Esophageal Carcinoma
  • Metastatic Liver Carcinoma
  • Metastatic Lung Non-Small Cell Carcinoma
  • Metastatic Malignant Skin Neoplasm
  • Metastatic Malignant Solid Neoplasm
  • Metastatic Triple-Negative Breast Carcinoma
  • Neoplasms
  • Resectable Colorectal Carcinoma
  • Resectable Lung Non-Small Cell Carcinoma
  • Skin Neoplasms

NCT number NCT06349642
Study type Observational
Source Mayo Clinic
Contact Clinical Trials Referral Office
Phone 855-776-0015
Email mayocliniccancerstudies@mayo.edu
Status Recruiting
Phase
Start date April 24, 2024
Completion date May 2027

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