TY - JOUR
T1 - Impact of consensus molecular subtype on survival in patients with metastatic colorectal cancer
T2 - Results from CALGB/SWOG 80405 (Alliance)
AU - Lenz, Heinz Josef
AU - Ou, Fang Shu
AU - Venook, Alan P.
AU - Hochster, Howard S.
AU - Niedzwiecki, Donna
AU - Goldberg, Richard M.
AU - Mayer, Robert J.
AU - Bertagnolli, Monica M.
AU - Blanke, Charles D.
AU - Zemla, Tyler
AU - Qu, Xueping
AU - Wirapati, Pratyaksha
AU - Tejpar, Sabine
AU - Innocenti, Federico
AU - Kabbarah, Omar
N1 - Funding Information:
Supported by National Cancer Institute grants U10CA180821 and U10CA180882 (Alliance for Clinical Trials in Oncology), U10CA180790 (Mayo Clinic), U10CA180791 (Memorial Sloan Kettering),
Publisher Copyright:
© 2019 American Society of Clinical Oncology.
PY - 2019/8/1
Y1 - 2019/8/1
N2 - 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 firstline 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.
AB - 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 firstline 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.
UR - http://www.scopus.com/inward/record.url?scp=85068908806&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85068908806&partnerID=8YFLogxK
U2 - 10.1200/JCO.18.02258
DO - 10.1200/JCO.18.02258
M3 - Article
C2 - 31042420
AN - SCOPUS:85068908806
SN - 0732-183X
VL - 37
SP - 1876
EP - 1885
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 22
ER -