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Author's reply to: Identification of EGFR mutations in lung sarcomatoid carcinomas

✍ Scribed by Antoine Italiano


Publisher
John Wiley and Sons
Year
2010
Tongue
French
Weight
69 KB
Volume
128
Category
Article
ISSN
0020-7136

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✦ Synopsis


We have read with great interest the comments of Leone et al. 1 indicating that they have analyzed a series of 23 cases of lung sarcomatoid carcinomas (SC) and found 2 cases harboring an EGFR mutation. At the time of this writing, 78 cases 1- 7 and 58 cases 1,2,6 of SC have been screened for EGFR and KRAS genes mutation, respectively. EGFR mutations were found in 8 cases. 1,[3][4][5]7 Strikingly, all these mutations but 2 were found in Asian patients. [3][4][5]7 Moreover, in 3 of these cases, EGFR mutations were detected in adenocarcinomatous component, but not in sarcomatoid component. 7 KRAS mutations were found in 18 cases (31%). 1,2,6 All of them were Caucasian patients. When considering only Caucasian patients (n ΒΌ 58), EGFR mutation appears to be a very rare event in SC (3.5%), whereas KRAS mutation is more frequent than in other typical nonsmall cell lung cancer (mainly adenocarcinomas). Altogether, these pooled data confirm our findings 2 and suggest that most patients with lung SC are not likely to benefit from anti-EGFR therapies.


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## Abstract ## Background Somatic mutations in the tyrosine kinase domain of the epidermal growth factor receptor (EGFR) are involved in tumorigenesis and response to targeted therapies in distinct cancer types. Squamous cell carcinomas of the head and neck (HNSCC) show an incidence of EGFR mutati