Abstract | OBJECTIVE: METHODS: The total number of irinotecan-refractory mCRC patients studied was 118. Among them, 117 and 107 patients were screened for KRAS mutations and genetic polymorphisms of FcγRIIa-131H/R and FcγRIIIa-158V/F, respectively. The association of FcγR polymorphisms and KRAS mutations with clinical outcome was analyzed. RESULTS: KRAS mutations were found in 33 patients (27.1%). Wild-type KRAS was associated with a better response rate (p < 0.001), longer progression-free survival (p < 0.001) and longer overall survival (p < 0.001). FcγRIIa H/H, H/R and R/R polymorphisms were observed in 54, 49 and 4 patients, respectively, and FcγRIIIa V/V, V/F and F/F polymorphisms were observed in 6, 65, and 36 patients, respectively. Clinical outcomes were not significantly associated with either FcγRIIa or FcγRIIIa polymorphisms or with combinations of KRAS status and FcγR polymorphisms. CONCLUSION: The FcγRIIa and FcγRIIIa polymorphisms may not be useful molecular biomarkers for the activity of cetuximab in patients with mCRC.
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Authors | Seong Joon Park, Yong Sang Hong, Jae-Lyun Lee, Min-Hee Ryu, Heung Moon Chang, Kyu-pyo Kim, Yong Chel Ahn, Young-Soon Na, Dong-Hoon Jin, Chang Sik Yu, Jin Cheon Kim, Yoon-Koo Kang, Tae Won Kim |
Journal | Oncology
(Oncology)
Vol. 82
Issue 2
Pg. 83-9
( 2012)
ISSN: 1423-0232 [Electronic] Switzerland |
PMID | 22327884
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2012 S. Karger AG, Basel. |
Chemical References |
- Antibodies, Monoclonal
- Antibodies, Monoclonal, Humanized
- FCGR3A protein, human
- Fc gamma receptor IIA
- KRAS protein, human
- Proto-Oncogene Proteins
- Receptors, IgG
- Irinotecan
- Proto-Oncogene Proteins p21(ras)
- ras Proteins
- Cetuximab
- Camptothecin
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Topics |
- Adult
- Aged
- Antibodies, Monoclonal
(administration & dosage)
- Antibodies, Monoclonal, Humanized
- Antineoplastic Combined Chemotherapy Protocols
(therapeutic use)
- Camptothecin
(administration & dosage, analogs & derivatives)
- Cetuximab
- Colorectal Neoplasms
(drug therapy, genetics, pathology)
- Female
- Humans
- Irinotecan
- Male
- Middle Aged
- Mutation
- Neoplasm Metastasis
- Polymorphism, Genetic
- Proto-Oncogene Proteins
(genetics)
- Proto-Oncogene Proteins p21(ras)
- Receptors, IgG
(genetics)
- ras Proteins
(genetics)
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