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KRAS Genotypes and Outcome in Patients With Chemotherapy-Refractory Metastatic Colorectal Cancer Treated With Cetuximab

Chen Mao, MD; Jin-Ling Tang, MD, PHD
JAMA. 2011;305(6):564-566. doi:10.1001/jama.2011.86.
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To the Editor: Dr De Roock and colleagues1 studied the effect of KRAS p.G13D mutation on cetuximab efficacy in chemotherapy-refractory metastatic colorectal cancer. The authors concluded that patients with KRAS p.G13D-mutated tumors have longer overall survival and progression-free survival than patients with other KRAS -mutated tumors.

In vitro data2 suggest that KRAS p.G13D mutation and other KRAS mutations may have different biological effects. However, most studies evaluate the effect of KRAS mutations as a whole on cetuximab efficacy, estimating a mean effect that depends on the relative proportions of p.G13D and other mutations.34 De Roock et al compared p.G13D mutation with other KRAS mutations and with wild-type KRAS. However, the authors did not present data for the comparison between other KRAS mutations and wild-type KRAS. It would be interesting to know, in comparison with wild-type KRAS tumors, whether the clinical outcomes for patients with p.G13D mutations are better than for patients with other KRAS mutations.

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References

February 9, 2011
Eeonora Zaccarelli, MD; Silverio Tomao, MD; Giovanni Codacci-Pisanelli, MD
JAMA. 2011;305(6):564-566. doi:10.1001/jama.2011.87.
February 9, 2011
Kohei Shitara, MD; Tomoya Yokota, MD; Kei Muro, MD
JAMA. 2011;305(6):564-566. doi:10.1001/jama.2011.85.
February 9, 2011
Sabine Tejpar, MD, PhD; Wendy De Roock, MD, PhD; Derek Jonker, MD
JAMA. 2011;305(6):564-566. doi:10.1001/jama.2011.88.
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