Research Article

Concordance of KRAS/BRAF Mutation Status in Metastatic Colorectal Cancer before and after Anti-EGFR Therapy

Table 2

Overview of the clinical patient data. 20 of 21 patients show concordance of the KRAS (exon 2, Gly 12/13) and BRAF (exon 15, V600E) mutation status between samples of primary CRCs and/or corresponding metastases before and after combined cetuximab therapy. In one case (#4), the primary CRC had a mutated KRAS gene (Gly12Asp), while the liver metastasis biopsied after combined cetuximab therapy showed a genotype. BRAF mutation status in this case was concordant between the samples gathered before and after anti-EGFR therapy.

Case no.Sex/AgeDate and localisation of tumor manifestaionKRAS Gly12/13 (exon2)BRAF V600E (exon15)Anti-EGFR therapy

1M/51 y09/05 primary CRCGly12ValWT01/07–04/07 Folfiri/Cetuximab (PD)
11/07 small bowel metastasisGly12ValWTdead 05/08

2M/71 y11/02 soft tissueGly12CysWT09/04–08/05 Folfiri/Cetuximab (PR)
03/06 mesocolon transversum metastasisGly12CysWT

3M/46 y03/07 primary CRCWTWT08/07–06/08 Folfiri/Cetuximab (PR)
02/09 peritoneal carcinosisWTWT

4M/68 y11/06 primary CRCGly12AspWT04/07–02/08 Fufox/Cetuximab(PR)
03/08 liver metastasisWTWT

5F/56 y07/08 primary CRCGly12AspWT07/08–09/08 Fufox/Cetuximab (PD)
12/08 peritoneal carcinosisGly12AspWTdead 12/08

6M/71 y12/05 primary CRCGly12ValWT01/06–07/06 Folfiri/Cetuximab (PD)
12/06 liver metastasisGly12ValWTdead 04/08

7F/58 y01/08 primary CRCWTWT04/08–07/08 Folfiri/Cetuximab (PD)
07/08 peritoneal carcinosisWTWTdead 07/08

8F/44 y11/07 primary CRCWTWT05/08–03/09 Folfox/Cetuximab (PR)
12/08 peritoneal carcinosisWTWT

9F/66 y02/04 primary CRCGly12SerWT07/06–09/06 Folfox/Cetuximab (PR)
11/05 + 04/06 liver metastasisGly12SerWT07/06–09/06 Folfox/Cetuximab (PD)
11/06 lung metastasisGly12SerWT09/06-11/06 Folfiri/Avastin (PD)

10M/77 y11/05 primary CRCGly13AspWT12/05–09/06 Folfox + Cetuximab (PD)
07/06 lymph nodeGly13AspWT10/06–02/07 Folfiri + Avastin (PD) dead 05/07

11M/63 y05/07primary CRCWTWT05/07–07/08 Folfiri/Cetuximab (PR)
01/08 liver metastasisWTWT10/08–05/09 Folfox (PR)
06/09 liver metastasisWTWT

12M/67 y07/07 liver metastasisWTWT08/07–04/08 Folfox/Cetuximab (PR)
01/08 liver metastasisWTWT

13M/59 y09/07 primary CRCWTWT
10/07 liver metastasisWTWT11/07–03/08 Folfiri/Cetuximab (PR)
05/08 liver metastasisWTWT

14M/61 y07/02 primary CRCWTWT10/07–07/08 Folfox/Cetuximab (PR)
05/04 liver metastasisWTWT
07/08 peritoneal carcinosisWTWTSince 12/08 Folfox (PR)

15F/68 y09/05 primary CRCWTV600E10/05–02/06 Folfox (PD)
05/06 soft tissueWTV600E03/06–08/06 Folfiri/Cetuximab (PR)
01/07 soft tissueWTV600E01/07–05/07 Cetuximab/Irinotecon (PD) dead 06/07

16M/75 y07/00 primary CRCGly12AspWT
07/03 lung metastasisGly12AspWT08/03–07/04 Folfox (PD)
08/03 liver metastasis08/04–08/05 Folfiri (PD)
08/05 liver metastasisGly12AspWT08/05–04/06 Folfiri/Cetuximab (PD) 04/06–02/07 Cetuximab+CPT-11(PD)02/07–04/07 Panitumumab (PD)
04/07 ascitesGly12AspWTdead 05/07

17M/69 y06/02 primary CRCGly13AspWT06/02–09/02 Folfox (PR) 06/03–12/03 Folfox (PR) 07/04–01/06 Folfiri (PD) 03/06–05/06 Cetuximab + CPT-11 (PD) 09/06–02/07 Folfox (PD)
07/07 mesocolon metastasisGly13AspWTdead 09/07

18M/75 y01/04 primary CRCGly12AspWT06/07–10/07 Capecitabine/Cetximab (PD)
01/08 peritoneal carcinosisGly12AspWTdead 03/08

19F/61 y07/08 primary CRCWTWT07/08–03/09 Folfiri/Cetuximab (PR)
05/09 liver metastasisWTWT

20M/56 y05/08 primary CRCWTWT06/08-12/08 Folfox/Cetuximab (PR)
06/09 lung metastasisWTWT

21M/72 y09/08 primary CRCWTWT10/08-02/09 Folfiri/Cetuximab (PR)
01/09 liver metastasisWTWT

Response evaluation (according to RECIST criteria): PD: progressive disease; SD: stable disease; PR: partial remission; CR: complete remission.