Impact of Consensus Molecular Subtype on Survival in Patients With Metastatic Colorectal Cancer: Results From CALGB/SWOG 80405 (Alliance)

Author:

Lenz Heinz-Josef1,Ou Fang-Shu2,Venook Alan P.3,Hochster Howard S.4,Niedzwiecki Donna5,Goldberg Richard M.6,Mayer Robert J.7,Bertagnolli Monica M.8,Blanke Charles D.9,Zemla Tyler2,Qu Xueping10,Wirapati Pratyaksha11,Tejpar Sabine12,Innocenti Federico13,Kabbarah Omar10

Affiliation:

1. University of Southern California Norris Comprehensive Cancer Center, Los Angeles, CA

2. Mayo Clinic Cancer Center, Rochester, MN

3. University of California, San Francisco, San Francisco, CA

4. Yale Cancer Center, New Haven, CT

5. Duke University Medical Center, Durham, NC

6. West Virginia University Cancer Institute, Morgantown, WV

7. Dana-Farber Cancer Institute, Boston, MA

8. Brigham and Women’s Hospital, Boston, MA

9. Oregon Health & Science University, Portland, OR

10. Genentech, San Francisco, CA

11. Swiss Institute of Bioinformatics, Lausanne, Switzerland

12. Universitair Ziekenhuis Leuven, Leuven, Belgium

13. The University of North Carolina at Chapel Hill, Chapel Hill, NC

Abstract

PURPOSE To determine the predictive and prognostic value of the consensus molecular subtypes (CMSs) of colorectal cancer (CRC) that represent a merging of gene expression–based features largely in primary tumors from six independent classification systems and provide a framework for capturing the intrinsic heterogeneity of CRC in patients enrolled in CALGB/SWOG 80405. PATIENTS AND METHODS CALGB/SWOG 80405 is a phase III trial that compared the addition of bevacizumab or cetuximab to infusional fluorouracil, leucovorin, and oxaliplatin or fluorouracil, leucovorin, and irinotecan as first-line treatment of advanced CRC. We characterized the CMS classification using a novel NanoString gene expression panel on primary CRCs from 581 patients enrolled in this study to assess the prognostic and predictive value of CMSs in these patients. RESULTS The CMSs are highly prognostic for overall survival (OS; P < .001) and progression-free survival (PFS; P < .001). Furthermore, CMSs were predictive for both OS ( P for interaction < .001) and PFS ( P for interaction = .0032). In the CMS1 cohort, patients treated with bevacizumab had a significantly longer OS than those treated with cetuximab ( P < .001). In the CMS2 cohort, patients treated with cetuximab had a significantly longer OS than patients treated with bevacizumab ( P = .0046). CONCLUSION These findings highlight the possible clinical utility of CMSs and suggests that refinement of the CMS classification may provide a path toward identifying patients with metastatic CRC who are most likely to benefit from specific targeted therapy as part of the initial treatment.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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