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Cetuximab plus irinotecan after irinotecan failure in elderly metastatic colorectal cancer patients: Clinical outcome according to KRAS and BRAF mutational status

Lorenzo Fornaroa, Giacomo Giulio Baldia, Gianluca MasiaCorresponding Author Informationemail address, Giacomo Allegrinib, Fotios Loupakisa, Enrico Vasilea, Samanta Cupinic, Irene Stasia, Lisa Salvatorea, Chiara Cremolinia, Bruno Vincenzid, Daniele Santinid, Giuseppe Toninid, Francesco Grazianoe, Annamaria Ruzzof, Emanuele Canestrarif, Mauro Magnanif, Alfredo Falconea

Accepted 10 June 2010. published online 09 July 2010.
Corrected Proof

Abstract 

Background

Scarce data are available about safety and efficacy of cetuximab in elderly metastatic colorectal cancer (mCRC) patients.

Patients and methods

We retrospectively analysed 54 irinotecan-refractory mCRC patients aged70 years treated with cetuximab plus irinotecan and evaluated clinical outcome according to KRAS and BRAF mutational status.

Results

Median age was 73 years (70–82). Main grade 3–4 toxicities were skin rash (15%), diarrhea (19%) and neutropenia (13%). Irinotecan dose reduction was necessary in 39% of patients. Fifty-two (96%) patients were analysed for KRAS and BRAF status. The 29 KRAS wild-type patients achieved better RR (31% vs 4%; p=0.030) and median PFS (4.21 months vs 3.95 months; p=0.034; HR: 0.50, 95% CI: 0.27–0.95) when compared with KRAS mutated ones. RR (41% vs 3%; p=0.001) and mPFS (4.57 months vs 3.78 months, p=0.001; HR: 0.35, 95% CI: 0.19–0.66) were significantly higher among the 22 KRAS and BRAF wild-type patients compared to the 30 KRAS or BRAF mutated ones.

Conclusion

Cetuximab plus irinotecan has a favourable safety profile in elderly mCRC patients, but a reduced dose of irinotecan should be considered. Such a combination can be a useful option for elderly KRAS and BRAF wild-type patients.

a U.O. Oncologia Medica 2 Universitaria, Azienda Ospedaliero-Universitaria Pisana, Via Roma, 67 - 56126 Pisa, Italy

b U.O. Oncologia Medica, Ospedale F. Lotti, Pontedera, Italy

c U.O. Oncologia Medica, Azienda USL6 di Livorno, Livorno, Italy

d U.O. Oncologia Medica, Università Campus Bio-Medico, Roma, Italy

e U.O. Oncologia Medica, Ospedale di Pesaro, Pesaro, Italy

f Dipartimento di Scienze Biomolecolari, Università di Urbino, Urbino, Italy

Corresponding Author InformationCorresponding author. Tel.: +39 050 992451; fax: +39 050 992069.

PII: S1040-8428(10)00143-5

doi:10.1016/j.critrevonc.2010.06.003