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 Field | Value | Language |
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dc.contributor.author | Yin, Jun | - |
dc.contributor.author | Cohen, Romain | - |
dc.contributor.author | Jin, Zhaohui | - |
dc.contributor.author | Liu, Heshan | - |
dc.contributor.author | Pederson, Levi | - |
dc.contributor.author | Adams, Richard | - |
dc.contributor.author | Grothey, Axel | - |
dc.contributor.author | Maughan, Timothy S | - |
dc.contributor.author | Venook, Alan | - |
dc.contributor.author | Van Cutsem, Eric | - |
dc.contributor.author | Punt, Cornelis | - |
dc.contributor.author | Koopman, Miriam | - |
dc.contributor.author | Falcone, Alfredo | - |
dc.contributor.author | Tebbutt, Niall C | - |
dc.contributor.author | Seymour, Matthew T | - |
dc.contributor.author | Bokemeyer, Carsten | - |
dc.contributor.author | Rubio, Eduardo Diaz | - |
dc.contributor.author | Kaplan, Richard | - |
dc.contributor.author | Heinemann, Volker | - |
dc.contributor.author | Chibaudel, Benoist | - |
dc.contributor.author | Yoshino, Takayuki | - |
dc.contributor.author | Zalcberg, John | - |
dc.contributor.author | Andre, Thierry | - |
dc.contributor.author | De Gramont, Aimery | - |
dc.contributor.author | Shi, Qian | - |
dc.contributor.author | Lenz, Heinz-Josef | - |
dc.date | 2021-06-01 | - |
dc.date.accessioned | 2021-06-07T06:03:57Z | - |
dc.date.available | 2021-06-07T06:03:57Z | - |
dc.date.issued | 2021-06-01 | - |
dc.identifier.citation | Journal of the National Cancer Institute 2021; 113(12) | en |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/26681 | - |
dc.description.abstract | Unplanned 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.iso | eng | - |
dc.title | Prognostic and Predictive Impact of Primary Tumor Sidedness for Previously Untreated Advanced Colorectal Cancer. | en |
dc.type | Journal Article | en |
dc.identifier.journaltitle | Journal of the National Cancer Institute | en |
dc.identifier.affiliation | Universidad Complutense Instituto de Investigacion Sanitaria del Hospital Clinico San Carlos, Madrid, Spain | en |
dc.identifier.affiliation | Department of Epidemiology, Julius Center for Health Sciences and Primary Care, University Medical Center, Utrecht University, The Netherlands | en |
dc.identifier.affiliation | Department of Medical Oncology, University Medical Center Utrecht, Utrecht University, The Netherlands | en |
dc.identifier.affiliation | Department of Oncology, University of Pisa, Italy | en |
dc.identifier.affiliation | National Cancer Center Hospital East, Japan | en |
dc.identifier.affiliation | NIHR Clinical Research Network, Leeds UK. St James's Hospital, and University of Leeds, Leeds, United Kingdom | en |
dc.identifier.affiliation | Monash University, Melbourne, Australia | en |
dc.identifier.affiliation | Digestive Oncology, University Hospitals Gasthuisberg Leuven and University of Leuven Leuven, Belgium | en |
dc.identifier.affiliation | Department of Oncology, Haematology and Bone Marrow Transplantation with Section of Pneumology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany | en |
dc.identifier.affiliation | University Hospital Grosshadern, Ludwig Maximilian University of Munich, Munich, Germany | en |
dc.identifier.affiliation | Division of Clinical Trials and Biostatistics, Mayo Clinic, Rochester, MN, USA | en |
dc.identifier.affiliation | Department of Oncology, Mayo Clinic, Rochester, MN, USA | en |
dc.identifier.affiliation | Department of Gastrointestinal Onocology, Keck School of Medicine at USC, Los Angeles, CA, USA | en |
dc.identifier.affiliation | Sorbonne University, Department of Medical Oncology, Saint-Antoine Hospital, AP-HP, F-75012, Paris, France | en |
dc.identifier.affiliation | Institut Franco-Britannique, Levallois-Perret, France | en |
dc.identifier.affiliation | Hôpital Saint-Antoine, Paris, France | en |
dc.identifier.affiliation | Department of Medical Oncology, Franco-British Institute, Levallois-Perret, France | en |
dc.identifier.affiliation | Cardiff University and Velindre Cancer Centre, Cardiff, UK | en |
dc.identifier.affiliation | CRUK/MRC Oxford Institute for Radiation Oncology, Oxford, United Kingdom St James's Hospital, and University of Leeds, Leeds, UK | en |
dc.identifier.affiliation | MRC Clinical Trials Unit at UCL, University College London, London, UK | en |
dc.identifier.affiliation | West Cancer Center and Research Institute, OneOncology, Germantown, TN | en |
dc.identifier.affiliation | Department of Medicine, The University of California San Francisco, San Francisco, California, United States of America.. | en |
dc.identifier.affiliation | Medical Oncology | en |
dc.identifier.doi | 10.1093/jnci/djab112 | en |
dc.type.content | Text | en |
dc.identifier.pubmedid | 34061178 | - |
local.name.researcher | Tebbutt, Niall C | |
item.grantfulltext | none | - |
item.fulltext | No Fulltext | - |
item.cerifentitytype | Publications | - |
item.languageiso639-1 | en | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.openairetype | Journal Article | - |
crisitem.author.dept | Medical Oncology | - |
crisitem.author.dept | Olivia Newton-John Cancer Wellness and Research Centre | - |
Appears in Collections: | Journal articles |
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