Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/26681
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dc.contributor.authorYin, Jun-
dc.contributor.authorCohen, Romain-
dc.contributor.authorJin, Zhaohui-
dc.contributor.authorLiu, Heshan-
dc.contributor.authorPederson, Levi-
dc.contributor.authorAdams, Richard-
dc.contributor.authorGrothey, Axel-
dc.contributor.authorMaughan, Timothy S-
dc.contributor.authorVenook, Alan-
dc.contributor.authorVan Cutsem, Eric-
dc.contributor.authorPunt, Cornelis-
dc.contributor.authorKoopman, Miriam-
dc.contributor.authorFalcone, Alfredo-
dc.contributor.authorTebbutt, Niall C-
dc.contributor.authorSeymour, Matthew T-
dc.contributor.authorBokemeyer, Carsten-
dc.contributor.authorRubio, Eduardo Diaz-
dc.contributor.authorKaplan, Richard-
dc.contributor.authorHeinemann, Volker-
dc.contributor.authorChibaudel, Benoist-
dc.contributor.authorYoshino, Takayuki-
dc.contributor.authorZalcberg, John-
dc.contributor.authorAndre, Thierry-
dc.contributor.authorDe Gramont, Aimery-
dc.contributor.authorShi, Qian-
dc.contributor.authorLenz, Heinz-Josef-
dc.date2021-06-01-
dc.date.accessioned2021-06-07T06:03:57Z-
dc.date.available2021-06-07T06:03:57Z-
dc.date.issued2021-06-01-
dc.identifier.citationJournal of the National Cancer Institute 2021; 113(12)en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/26681-
dc.description.abstractUnplanned subgroup analyses from several studies have suggested primary tumor sidedness (PTS) as a potential prognostic and predictive parameter in metastatic colorectal cancer (mCRC). We aimed to investigate the impact of PTS on outcomes of mCRC patients. PTS data of 9,277 mCRC patients from 12 first-line randomized trials in the ARCAD database were pooled. Overall survival (OS) and progression-free survival (PFS) were assessed using Kaplan-Meier and Cox models adjusting for age, sex, performance status, prior radiation/chemo, and stratified by treatment arm. Predictive value was tested by interaction term between PTS and treatment (cetuximab plus chemotherapy vs. chemotherapy alone). All statistical tests were 2-sided. Compared to right-sided metastatic colorectal cancer patients (n = 2421, 26.1%), left-sided metastatic colorectal cancer patients (n = 6856, 73.9%) had better OS (median = 21.6 v 15.9 months; adjusted hazard ratio [HRadj] = 0.71, 95% confidence interval [CI] = 0.67-0.76, P<.001) and PFS (median = 8.6 v 7.5 months; HRadj = 0.80, 95% CI = 0.75-0.84, P<.001). Interaction between PTS and KRAS mutation was statistically significant (Pinteraction<.001): left-sidedness was associated with better prognosis among KRAS wild-type (WT) (OS HRadj = 0.59, 95% CI = 0.53-0.66; PFS HRadj =0.68, 95% CI = 0.61-0.75), but not among KRAS mutated tumors. Among KRAS-WT tumors, survival benefit from anti-EGFR was confirmed for left-sidedness (OS HRadj = 0.85, 95% CI = 0.75-0.97, P = .01; PFS HRadj = 0.77, 95% CI = 0.67-0.88, P<.001), but not for right-sidedness. The prognostic value of PTS is restricted to the KRAS-WT population. PTS is predictive of anti-EGFR efficacy, with a statistically significant improvement of survival for left-sidedness mCRC patients. These results suggest treatment choice in mCRC should be based on both PTS and KRAS status.en
dc.language.isoeng-
dc.titlePrognostic and Predictive Impact of Primary Tumor Sidedness for Previously Untreated Advanced Colorectal Cancer.en
dc.typeJournal Articleen
dc.identifier.journaltitleJournal of the National Cancer Instituteen
dc.identifier.affiliationUniversidad Complutense Instituto de Investigacion Sanitaria del Hospital Clinico San Carlos, Madrid, Spainen
dc.identifier.affiliationDepartment of Epidemiology, Julius Center for Health Sciences and Primary Care, University Medical Center, Utrecht University, The Netherlandsen
dc.identifier.affiliationDepartment of Medical Oncology, University Medical Center Utrecht, Utrecht University, The Netherlandsen
dc.identifier.affiliationDepartment of Oncology, University of Pisa, Italyen
dc.identifier.affiliationNational Cancer Center Hospital East, Japanen
dc.identifier.affiliationNIHR Clinical Research Network, Leeds UK. St James's Hospital, and University of Leeds, Leeds, United Kingdomen
dc.identifier.affiliationMonash University, Melbourne, Australiaen
dc.identifier.affiliationDigestive Oncology, University Hospitals Gasthuisberg Leuven and University of Leuven Leuven, Belgiumen
dc.identifier.affiliationDepartment of Oncology, Haematology and Bone Marrow Transplantation with Section of Pneumology, University Medical Center Hamburg-Eppendorf, Hamburg, Germanyen
dc.identifier.affiliationUniversity Hospital Grosshadern, Ludwig Maximilian University of Munich, Munich, Germanyen
dc.identifier.affiliationDivision of Clinical Trials and Biostatistics, Mayo Clinic, Rochester, MN, USAen
dc.identifier.affiliationDepartment of Oncology, Mayo Clinic, Rochester, MN, USAen
dc.identifier.affiliationDepartment of Gastrointestinal Onocology, Keck School of Medicine at USC, Los Angeles, CA, USAen
dc.identifier.affiliationSorbonne University, Department of Medical Oncology, Saint-Antoine Hospital, AP-HP, F-75012, Paris, Franceen
dc.identifier.affiliationInstitut Franco-Britannique, Levallois-Perret, Franceen
dc.identifier.affiliationHôpital Saint-Antoine, Paris, Franceen
dc.identifier.affiliationDepartment of Medical Oncology, Franco-British Institute, Levallois-Perret, Franceen
dc.identifier.affiliationCardiff University and Velindre Cancer Centre, Cardiff, UKen
dc.identifier.affiliationCRUK/MRC Oxford Institute for Radiation Oncology, Oxford, United Kingdom St James's Hospital, and University of Leeds, Leeds, UKen
dc.identifier.affiliationMRC Clinical Trials Unit at UCL, University College London, London, UKen
dc.identifier.affiliationWest Cancer Center and Research Institute, OneOncology, Germantown, TNen
dc.identifier.affiliationDepartment of Medicine, The University of California San Francisco, San Francisco, California, United States of America..en
dc.identifier.affiliationMedical Oncologyen
dc.identifier.doi10.1093/jnci/djab112en
dc.type.contentTexten
dc.identifier.pubmedid34061178-
local.name.researcherTebbutt, Niall C
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
crisitem.author.deptMedical Oncology-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
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