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Prognostic and Predictive Impact of Primary Tumor Sidedness for Previously Untreated Advanced Colorectal Cancer.
Yin, Jun; Cohen, Romain; Jin, Zhaohui; Liu, Heshan; Pederson, Levi; Adams, Richard; Grothey, Axel; Maughan, Timothy S; Venook, Alan; Van Cutsem, Eric; Punt, Cornelis; Koopman, Miriam; Falcone, Alfredo; Tebbutt, Niall C; Seymour, Matthew T; Bokemeyer, Carsten; Rubio, Eduardo Diaz; Kaplan, Richard; Heinemann, Volker; Chibaudel, Benoist; Yoshino, Takayuki; Zalcberg, John; Andre, Thierry; De Gramont, Aimery; Shi, Qian; Lenz, Heinz-Josef.
Affiliation
  • Yin J; Division of Clinical Trials and Biostatistics, Mayo Clinic, Rochester, MN, USA.
  • Cohen R; Department of Medical Oncology, Saint-Antoine Hospital, Paris, France.
  • Jin Z; Department of Oncology, Mayo Clinic, Rochester, MN, USA.
  • Liu H; Division of Clinical Trials and Biostatistics, Mayo Clinic, Rochester, MN, USA.
  • Pederson L; Division of Clinical Trials and Biostatistics, Mayo Clinic, Rochester, MN, USA.
  • Adams R; Cardiff University and Velindre Cancer Centre, Cardiff, UK.
  • Grothey A; West Cancer Center and Research Institute, OneOncology, Germantown, TN, USA.
  • Maughan TS; CRUK/MRC Oxford Institute for Radiation Oncology, Oxford, UK.
  • Venook A; St James's Hospital, University of Leeds, Leeds, UK.
  • Van Cutsem E; Department of Medicine, University of California San Francisco, San Francisco, CA, USA.
  • Punt C; Digestive Oncology, University Hospitals Gasthuisberg Leuven, University of Leuven, Leuven, Belgium.
  • Koopman M; Department of Epidemiology, Julius Center for Health Sciences and Primary Care, University Medical Center, the Netherlands.
  • Falcone A; Department of Medical Oncology, University Medical Center Utrecht, Utrecht University, the Netherlands.
  • Tebbutt NC; Department of Oncology, University of Pisa, Pisa, Italy.
  • Seymour MT; Department of Medical Oncology, Austin Health, Melbourne, Australia.
  • Bokemeyer C; NIHR Clinical Research Network, St James's Hospital, University of Leeds, Leeds, UK.
  • Rubio ED; Department of Oncology, Haematology and Bone Marrow Transplantation with Section of Pneumology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Kaplan R; Universidad Complutense Instituto de Investigacion Sanitaria del Hospital Clinico San Carlos, Madrid, Spain.
  • Heinemann V; MRC Clinical Trials Unit at UCL, University College London, London, UK.
  • Chibaudel B; University Hospital Grosshadern, Ludwig Maximilian University of Munich, Munich, Germany.
  • Yoshino T; Institut Franco-Britannique, Levallois-Perret, France.
  • Zalcberg J; National Cancer Center Hospital East, Tokyo, Japan.
  • Andre T; School of Public Health and Preventative Medicine, Monash University, Melbourne, Australia.
  • De Gramont A; Hôpital Saint-Antoine, Paris, France.
  • Shi Q; Department of Medical Oncology, Franco-British Institute, Levallois-Perret, France.
  • Lenz HJ; Division of Clinical Trials and Biostatistics, Mayo Clinic, Rochester, MN, USA.
J Natl Cancer Inst ; 113(12): 1705-1713, 2021 11 29.
Article in En | MEDLINE | ID: mdl-34061178
ABSTRACT

BACKGROUND:

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.

METHODS:

PTS data of 9277 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/chemotherapy, 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.

RESULTS:

Compared with 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 vs 15.9 months; adjusted hazard ratio [HRadj] = 0.71, 95% confidence interval [CI] = 0.67 to 0.76; P < .001) and PFS (median = 8.6 vs 7.5 months; HRadj = 0.80, 95% CI = 0.75 to 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 to 0.66; PFS HRadj =0.68, 95% CI = 0.61 to 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 to 0.97; P = .01; PFS HRadj = 0.77, 95% CI = 0.67 to 0.88; P < .001) but not for right-sidedness.

CONCLUSIONS:

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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Colorectal Neoplasms / Proto-Oncogene Proteins p21(ras) Type of study: Clinical_trials / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: J Natl Cancer Inst Year: 2021 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Colorectal Neoplasms / Proto-Oncogene Proteins p21(ras) Type of study: Clinical_trials / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: J Natl Cancer Inst Year: 2021 Document type: Article Affiliation country:
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