Michael J Magnetta1, Anish Ghodadra1, Steven J Lahti1, Minzhi Xing2, Di Zhang3, Hyun S Kim4,5,6. 1. Division of Interventional Radiology, Department of Radiology, University of Pittsburgh, Pittsburgh, PA, USA. 2. Division of Interventional Radiology, Department of Radiology and Biomedical Imaging, Yale School of Medicine, Yale Cancer Center, 330 Cedar Street TE 2-224, New Haven, CT, 06510, USA. 3. Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA. 4. Division of Interventional Radiology, Department of Radiology, University of Pittsburgh, Pittsburgh, PA, USA. kevin.kim@yale.edu. 5. Division of Interventional Radiology, Department of Radiology and Biomedical Imaging, Yale School of Medicine, Yale Cancer Center, 330 Cedar Street TE 2-224, New Haven, CT, 06510, USA. kevin.kim@yale.edu. 6. Yale Cancer Center, Yale University School of Medicine, New Haven, CT, USA. kevin.kim@yale.edu.
Abstract
PURPOSE: To determine whether pathologic colorectal tumor KRAS mutation status is correlated with progression-free survival (PFS) by imaging after selective internal radiation therapy with Yttrium-90 (SIRT Y90) for metastatic colorectal cancer in the liver (mCRC). MATERIALS AND METHODS: This was an IRB approved, HIPAA compliant retrospective cohort study. Consecutive patients with unresectable mCRC with documented KRAS mutation status treated at a single center from 2002 to 2013 with SIRT Y90 were investigated. Treatment response was compared between KRAS wild-type (wt) and mutant (mut) using an anatomic tumor response criteria based on RECIST 1.0. Kaplan-Meier estimation and Cox regression analysis were used to measure progression-free survival (PFS) and to assess independent prognostic factors for PFS. RESULTS: 82 of 186 patients met review criteria. 33 (40.2%) patients were identified as KRAS mut. PFS was longer in KRAS wt (median 166 days [95% CI 96-258 days]) vs. mut (median 91 days [95% CI 79-104 days], p = 0.002). KRAS mut patients were 1.48 times more likely to progress at first follow-up imaging than wt (95% CI 1.06-2.08, p = 0.024). Univariate analysis identified high pre-SIRT Y90 INR, KRAS wt, any use of anti-EGFR therapy, and post-SIRT Y90 chemotherapy as prognostic factors for longer PFS. In multivariate analysis, only KRAS wt was an independent prognostic factor for longer PFS (RR: 1.80 [95% CI 1.08-2.99], p = 0.024). CONCLUSION: Longer PFS is associated with KRAS wt vs. mut following SIRT Y90.
PURPOSE: To determine whether pathologic colorectal tumorKRAS mutation status is correlated with progression-free survival (PFS) by imaging after selective internal radiation therapy with Yttrium-90 (SIRT Y90) for metastatic colorectal cancer in the liver (mCRC). MATERIALS AND METHODS: This was an IRB approved, HIPAA compliant retrospective cohort study. Consecutive patients with unresectable mCRC with documented KRAS mutation status treated at a single center from 2002 to 2013 with SIRT Y90 were investigated. Treatment response was compared between KRAS wild-type (wt) and mutant (mut) using an anatomic tumor response criteria based on RECIST 1.0. Kaplan-Meier estimation and Cox regression analysis were used to measure progression-free survival (PFS) and to assess independent prognostic factors for PFS. RESULTS: 82 of 186 patients met review criteria. 33 (40.2%) patients were identified as KRAS mut. PFS was longer in KRAS wt (median 166 days [95% CI 96-258 days]) vs. mut (median 91 days [95% CI 79-104 days], p = 0.002). KRAS mut patients were 1.48 times more likely to progress at first follow-up imaging than wt (95% CI 1.06-2.08, p = 0.024). Univariate analysis identified high pre-SIRT Y90 INR, KRAS wt, any use of anti-EGFR therapy, and post-SIRT Y90 chemotherapy as prognostic factors for longer PFS. In multivariate analysis, only KRAS wt was an independent prognostic factor for longer PFS (RR: 1.80 [95% CI 1.08-2.99], p = 0.024). CONCLUSION: Longer PFS is associated with KRAS wt vs. mut following SIRT Y90.
Authors: Kathy P Willowson; Aimee R Hayes; David L H Chan; Michael Tapner; Elizabeth J Bernard; Richard Maher; Nick Pavlakis; Stephen J Clarke; Dale L Bailey Journal: EJNMMI Res Date: 2017-05-23 Impact factor: 3.138
Authors: Meaghan S Dendy; Johannes M Ludwig; Nima Kokabi; Stacey M Stein; Jill Lacy; Howard S Hochster; Hyun S Kim Journal: Oncotarget Date: 2018-08-21