Cargando…
Biweekly cetuximab in combination with capecitabine and oxaliplatin (XELOX) or irinotecan (XELIRI) in the first-line and second-line treatment of patients with RAS wild-type metastatic colorectal cancer
BACKGROUND: Oral capecitabine in combination with intravenous oxaliplatin (XELOX) or irinotecan (XELIRI) are acceptable substitutions to fully intravenous regimens. Biweekly (as opposed to weekly) cetuximab is more convenient when combined with biweekly chemotherapy. Here, we report the tolerability...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cancer Intelligence
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9934971/ https://www.ncbi.nlm.nih.gov/pubmed/36819803 http://dx.doi.org/10.3332/ecancer.2022.1490 |
_version_ | 1784889982232559616 |
---|---|
author | Zekri, Jamal Baghdadi, Mohammed Abbas Ibrahim, Refaei Belal Meliti, Abdelrazak Sobahy, Turki M |
author_facet | Zekri, Jamal Baghdadi, Mohammed Abbas Ibrahim, Refaei Belal Meliti, Abdelrazak Sobahy, Turki M |
author_sort | Zekri, Jamal |
collection | PubMed |
description | BACKGROUND: Oral capecitabine in combination with intravenous oxaliplatin (XELOX) or irinotecan (XELIRI) are acceptable substitutions to fully intravenous regimens. Biweekly (as opposed to weekly) cetuximab is more convenient when combined with biweekly chemotherapy. Here, we report the tolerability and efficacy of biweekly cetuximab in combination with biweekly XELOX or XELIRI in patients with RAS wild-type metastatic colorectal cancer (RAS-WT mCRC). METHODS: Clinical data of consecutive patients with mCRC who received biweekly cetuximab (500 mg/m(2)) in combination with XELOX or XELIRI between January 2009 and May 2019 in the first- or second-line settings was extracted. Dosage of XEL (Capecitabine/XELODA) was 1,000 mg/m(2) twice daily for 9 days, plus on day 1 oxaliplatin 85 mg/m(2) or irinotecan 180 mg/m(2). Treatment dose reduction and delay for ≥7 days was analysed as surrogates for toxicity. Extended RAS testing was performed in the context of this study for patients who received treatment based on limited KRAS-WT genotype. RESULTS: Sixty one patients with RAS-WT mCRC fulfilled the eligibility criteria. XELOX was administered to 26 (42.6%) and XELIRI to 35 (57.4%) of patients. For all patients in the first-line setting, the objective response rate (ORR), median progression free survival (PFS) and median overall survival (OS) were 54%, 8 months and 25 months, respectively. The corresponding outcomes for the subgroup of patients who received first-line XELOX were 68%, 10 months and not reached, respectively. For all patients in the second-line setting, the ORR, PFS and OS were 50%, 7 months and 20 months, respectively. Chemotherapy components dose reduction and delays were observed in 18 (29.5%) and 25 (41%) patients, respectively. The corresponding frequencies for cetuximab were 3 (5%) and 31 (50.8%). CONCLUSION: Biweekly cetuximab in combination with XELOX or XELIRI is tolerable and effective. The addition of cetuximab to capecitabine and oxaliplatin is associated with favourable outcome. |
format | Online Article Text |
id | pubmed-9934971 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cancer Intelligence |
record_format | MEDLINE/PubMed |
spelling | pubmed-99349712023-02-17 Biweekly cetuximab in combination with capecitabine and oxaliplatin (XELOX) or irinotecan (XELIRI) in the first-line and second-line treatment of patients with RAS wild-type metastatic colorectal cancer Zekri, Jamal Baghdadi, Mohammed Abbas Ibrahim, Refaei Belal Meliti, Abdelrazak Sobahy, Turki M Ecancermedicalscience Research BACKGROUND: Oral capecitabine in combination with intravenous oxaliplatin (XELOX) or irinotecan (XELIRI) are acceptable substitutions to fully intravenous regimens. Biweekly (as opposed to weekly) cetuximab is more convenient when combined with biweekly chemotherapy. Here, we report the tolerability and efficacy of biweekly cetuximab in combination with biweekly XELOX or XELIRI in patients with RAS wild-type metastatic colorectal cancer (RAS-WT mCRC). METHODS: Clinical data of consecutive patients with mCRC who received biweekly cetuximab (500 mg/m(2)) in combination with XELOX or XELIRI between January 2009 and May 2019 in the first- or second-line settings was extracted. Dosage of XEL (Capecitabine/XELODA) was 1,000 mg/m(2) twice daily for 9 days, plus on day 1 oxaliplatin 85 mg/m(2) or irinotecan 180 mg/m(2). Treatment dose reduction and delay for ≥7 days was analysed as surrogates for toxicity. Extended RAS testing was performed in the context of this study for patients who received treatment based on limited KRAS-WT genotype. RESULTS: Sixty one patients with RAS-WT mCRC fulfilled the eligibility criteria. XELOX was administered to 26 (42.6%) and XELIRI to 35 (57.4%) of patients. For all patients in the first-line setting, the objective response rate (ORR), median progression free survival (PFS) and median overall survival (OS) were 54%, 8 months and 25 months, respectively. The corresponding outcomes for the subgroup of patients who received first-line XELOX were 68%, 10 months and not reached, respectively. For all patients in the second-line setting, the ORR, PFS and OS were 50%, 7 months and 20 months, respectively. Chemotherapy components dose reduction and delays were observed in 18 (29.5%) and 25 (41%) patients, respectively. The corresponding frequencies for cetuximab were 3 (5%) and 31 (50.8%). CONCLUSION: Biweekly cetuximab in combination with XELOX or XELIRI is tolerable and effective. The addition of cetuximab to capecitabine and oxaliplatin is associated with favourable outcome. Cancer Intelligence 2022-12-15 /pmc/articles/PMC9934971/ /pubmed/36819803 http://dx.doi.org/10.3332/ecancer.2022.1490 Text en © the authors; licensee ecancermedicalscience. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Zekri, Jamal Baghdadi, Mohammed Abbas Ibrahim, Refaei Belal Meliti, Abdelrazak Sobahy, Turki M Biweekly cetuximab in combination with capecitabine and oxaliplatin (XELOX) or irinotecan (XELIRI) in the first-line and second-line treatment of patients with RAS wild-type metastatic colorectal cancer |
title | Biweekly cetuximab in combination with capecitabine and oxaliplatin (XELOX) or irinotecan (XELIRI) in the first-line and second-line treatment of patients with RAS wild-type metastatic colorectal cancer |
title_full | Biweekly cetuximab in combination with capecitabine and oxaliplatin (XELOX) or irinotecan (XELIRI) in the first-line and second-line treatment of patients with RAS wild-type metastatic colorectal cancer |
title_fullStr | Biweekly cetuximab in combination with capecitabine and oxaliplatin (XELOX) or irinotecan (XELIRI) in the first-line and second-line treatment of patients with RAS wild-type metastatic colorectal cancer |
title_full_unstemmed | Biweekly cetuximab in combination with capecitabine and oxaliplatin (XELOX) or irinotecan (XELIRI) in the first-line and second-line treatment of patients with RAS wild-type metastatic colorectal cancer |
title_short | Biweekly cetuximab in combination with capecitabine and oxaliplatin (XELOX) or irinotecan (XELIRI) in the first-line and second-line treatment of patients with RAS wild-type metastatic colorectal cancer |
title_sort | biweekly cetuximab in combination with capecitabine and oxaliplatin (xelox) or irinotecan (xeliri) in the first-line and second-line treatment of patients with ras wild-type metastatic colorectal cancer |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9934971/ https://www.ncbi.nlm.nih.gov/pubmed/36819803 http://dx.doi.org/10.3332/ecancer.2022.1490 |
work_keys_str_mv | AT zekrijamal biweeklycetuximabincombinationwithcapecitabineandoxaliplatinxeloxoririnotecanxeliriinthefirstlineandsecondlinetreatmentofpatientswithraswildtypemetastaticcolorectalcancer AT baghdadimohammedabbas biweeklycetuximabincombinationwithcapecitabineandoxaliplatinxeloxoririnotecanxeliriinthefirstlineandsecondlinetreatmentofpatientswithraswildtypemetastaticcolorectalcancer AT ibrahimrefaeibelal biweeklycetuximabincombinationwithcapecitabineandoxaliplatinxeloxoririnotecanxeliriinthefirstlineandsecondlinetreatmentofpatientswithraswildtypemetastaticcolorectalcancer AT melitiabdelrazak biweeklycetuximabincombinationwithcapecitabineandoxaliplatinxeloxoririnotecanxeliriinthefirstlineandsecondlinetreatmentofpatientswithraswildtypemetastaticcolorectalcancer AT sobahyturkim biweeklycetuximabincombinationwithcapecitabineandoxaliplatinxeloxoririnotecanxeliriinthefirstlineandsecondlinetreatmentofpatientswithraswildtypemetastaticcolorectalcancer |