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A phase II study of capecitabine, oxaliplatin, bevacizumab and cetuximab in the treatment of metastatic colorectal cancer.

Publication ,  Journal Article
Wong, NS; Fernando, NH; Nixon, AB; Cushman, S; Aklilu, M; Bendell, JC; Morse, MA; Blobe, GC; Ashton, J; Pang, H; Hurwitz, HI
Published in: Anticancer Res
January 2011

AIM: This study was designed to determine the efficacy and tolerability of capecitabine, oxaliplatin and bevacizumab in combination with cetuximab as first-line therapy for advanced colorectal cancer. PATIENTS AND METHODS: Patients with previously untreated advanced colorectal cancer received oxaliplatin 130 mg/m² and bevacizumab 7.5 mg/kg every three weeks, capecitabine 850 mg/m² twice daily on days 1-14, and cetuximab at 400 mg/m² load and 250 mg/m² weekly. KRAS, BRAF and PI3K mutation status from paraffin-embedded tumor samples were assessed using real-time polymerase chain reaction. RESULTS: Thirty patients were evaluable for safety and efficacy. One patient had a complete response and 12 patients had a partial response, giving an overall response rate of 43% (95% confidence interval (CI) 25%-63%). Fifteen patients had stable disease. The median time to progression was 10.3 months (95% CI, 6.8-16.3 months). The median overall survival was 18.8 months (95% CI, 14.2-23.7 months). Common grade ≥ 3 non-hematological toxicities were skin rash (37%), sensory neuropathy (27%) and diarrhea (17%). Grade ≥ 3 hematological toxicities were uncommon. Mutations in KRAS, BRAF and PI3K occurred in 34.5%, 10.3% and 10.3% of patients respectively, but did not correlate with treatment outcome. CONCLUSION: The addition of cetuximab to capecitabine, oxaliplatin and bevacizumab did not improve the three-drug regimen activity compared to published data and was associated with significant toxicities requiring frequent dose modifications. KRAS, BRAF, and PI3K mutation status were consistent with published literature, but did not affect outcome in this small study.

Duke Scholars

Published In

Anticancer Res

EISSN

1791-7530

Publication Date

January 2011

Volume

31

Issue

1

Start / End Page

255 / 261

Location

Greece

Related Subject Headings

  • ras Proteins
  • Treatment Outcome
  • Survival Rate
  • Proto-Oncogene Proteins p21(ras)
  • Proto-Oncogene Proteins B-raf
  • Proto-Oncogene Proteins
  • Polymerase Chain Reaction
  • Phosphatidylinositol 3-Kinases
  • Oxaliplatin
  • Organoplatinum Compounds
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Wong, N. S., Fernando, N. H., Nixon, A. B., Cushman, S., Aklilu, M., Bendell, J. C., … Hurwitz, H. I. (2011). A phase II study of capecitabine, oxaliplatin, bevacizumab and cetuximab in the treatment of metastatic colorectal cancer. Anticancer Res, 31(1), 255–261.
Wong, Nan Soon, Nishan H. Fernando, Andrew B. Nixon, Stephanie Cushman, Mebea Aklilu, Johanna C. Bendell, Michael A. Morse, et al. “A phase II study of capecitabine, oxaliplatin, bevacizumab and cetuximab in the treatment of metastatic colorectal cancer.Anticancer Res 31, no. 1 (January 2011): 255–61.
Wong NS, Fernando NH, Nixon AB, Cushman S, Aklilu M, Bendell JC, et al. A phase II study of capecitabine, oxaliplatin, bevacizumab and cetuximab in the treatment of metastatic colorectal cancer. Anticancer Res. 2011 Jan;31(1):255–61.
Wong, Nan Soon, et al. “A phase II study of capecitabine, oxaliplatin, bevacizumab and cetuximab in the treatment of metastatic colorectal cancer.Anticancer Res, vol. 31, no. 1, Jan. 2011, pp. 255–61.
Wong NS, Fernando NH, Nixon AB, Cushman S, Aklilu M, Bendell JC, Morse MA, Blobe GC, Ashton J, Pang H, Hurwitz HI. A phase II study of capecitabine, oxaliplatin, bevacizumab and cetuximab in the treatment of metastatic colorectal cancer. Anticancer Res. 2011 Jan;31(1):255–261.

Published In

Anticancer Res

EISSN

1791-7530

Publication Date

January 2011

Volume

31

Issue

1

Start / End Page

255 / 261

Location

Greece

Related Subject Headings

  • ras Proteins
  • Treatment Outcome
  • Survival Rate
  • Proto-Oncogene Proteins p21(ras)
  • Proto-Oncogene Proteins B-raf
  • Proto-Oncogene Proteins
  • Polymerase Chain Reaction
  • Phosphatidylinositol 3-Kinases
  • Oxaliplatin
  • Organoplatinum Compounds