Abstract
The optimal duration and intensity of first-line therapy in metastatic colorectal cancer patients once they have achieved an objective response is controversial. In a molecularly selected RAS and BRAF wild-type (wt) population, this concern is amplified. Once disease control has been achieved with a combination therapy including an anti-EGFR antibody, further exposure both to cytotoxic drugs and targeted therapy might result only in increased toxicity. In unresectable metastatic RAS and BRAF wt colorectal cancer patients, a deintensified therapy could represent a valuable option that might preserve quality of life. We designed a study to compare FOLFIRI/cetuximab to FOLFIRI/cetuximab for eight cycles followed by cetuximab alone in first-line treatment of RAS and BRAF (wt) metastatic colorectal cancer patients.
Keywords:
RAS and BRAF wild-type; cetuximab; colorectal cancer; de-escalation therapy.
Publication types
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Clinical Trial, Phase III
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Comparative Study
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Equivalence Trial
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Multicenter Study
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Randomized Controlled Trial
MeSH terms
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Adult
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Aged
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Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
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Camptothecin / analogs & derivatives*
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Camptothecin / therapeutic use
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Cetuximab / therapeutic use*
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Colorectal Neoplasms / drug therapy*
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Colorectal Neoplasms / genetics
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Colorectal Neoplasms / mortality
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Colorectal Neoplasms / pathology
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DNA Mutational Analysis
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Disease-Free Survival
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ErbB Receptors / antagonists & inhibitors
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Female
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Fluorouracil / therapeutic use
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Humans
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Leucovorin / therapeutic use
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Male
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Middle Aged
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Mutation
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Proto-Oncogene Proteins B-raf / genetics*
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Proto-Oncogene Proteins p21(ras) / genetics*
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Quality of Life
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Treatment Outcome
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Young Adult
Substances
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KRAS protein, human
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EGFR protein, human
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ErbB Receptors
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BRAF protein, human
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Proto-Oncogene Proteins B-raf
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Proto-Oncogene Proteins p21(ras)
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Cetuximab
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Leucovorin
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Fluorouracil
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Camptothecin