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Conversion to resection of liver metastases from colorectal cancer with hepatic artery infusion of combined chemotherapy and systemic cetuximab in multicenter trial OPTILIV.
dc.contributor.author | Lévi, FA | |
dc.contributor.author | Boige, V | |
dc.contributor.author | Hebbar, M | |
dc.contributor.author | Smith, D | |
dc.contributor.author | Lepère, C | |
dc.contributor.author | Focan, C | |
dc.contributor.author | Karaboué, A | |
dc.contributor.author | Guimbaud, R | |
dc.contributor.author | Carvalho, C | |
dc.contributor.author | Tumolo, S | |
dc.contributor.author | Innominato, P | |
dc.contributor.author | Ajavon, Y | |
dc.contributor.author | Truant, S | |
dc.contributor.author | Castaing, D | |
dc.contributor.author | De Baere, T | |
dc.contributor.author | Kunstlinger, F | |
dc.contributor.author | Bouchahda, M | |
dc.contributor.author | Afshar, M | |
dc.contributor.author | Rougier, P | |
dc.contributor.author | Adam, R | |
dc.contributor.author | Ducreux, M | |
dc.contributor.author | Association Internationale pour Recherche sur Temps Biologique et Chronothérapie (ARTBC International) | |
dc.date.accessioned | 2017-06-26T10:12:29Z | |
dc.date.available | 2017-06-26T10:12:29Z | |
dc.date.issued | 2016 | |
dc.description.abstract | BACKGROUND: Systemic chemotherapy typically converts previously unresectable liver metastases (LM) from colorectal cancer to curative intent resection in ∼15% of patients. This European multicenter phase II trial tested whether hepatic artery infusion (HAI) with triplet chemotherapy and systemic cetuximab could increase this rate to 30% in previously treated patients. PATIENTS AND METHODS: Participants had unresectable LM from wt KRAS colorectal cancer. Main non-inclusion criteria were advanced extra hepatic disease, prior HAI and grade 3 neuropathy. Irinotecan (180 mg/m(2)), oxaliplatin (85 mg/m(2)) and 5-fluorouracil (2800 mg/m(2)) were delivered via an implanted HAI access port and combined with i.v. cetuximab (500 mg/m(2)) every 14 days. Multidisciplinary decisions to resect LM were taken after every three courses. The rate of macroscopic complete resections (R0 + R1) of LM, progression-free survival (PFS) and overall survival (OS) were computed according to intent to treat. RESULTS: The patient population consisted of 42 men and 22 women, aged 33-76 years, with a median of 10 LM involving a median of six segments. Up to 3 extrahepatic lesions of <1 cm were found in 41% of the patients. A median of six courses was delivered. The primary end point was met, with R0-R1 hepatectomy for 19 of the 64 previously treated patients, 29.7% (95% confidence interval 18.5-40.9). Grade 3-4 neutropenia (42.6%), abdominal pain (26.2%), fatigue (18%) and diarrhea (16.4%) were frequent. Objective response rate was 40.6% (28.6-52.3). Median PFS and OS reached 9.3 (7.8-10.9) and 25.5 months (18.8-32.1) respectively. Those with R0-R1 hepatectomy had a median OS of 35.2 months (32.6-37.8), with 37.4% (23.6-51.2) alive at 4 years. CONCLUSION: The coordination of liver-specific intensive chemotherapy and surgery had a high curative intent potential that deserves upfront randomized testing. | pt_PT |
dc.description.version | info:eu-repo/semantics/publishedVersion | pt_PT |
dc.identifier.citation | Ann Oncol. 2016 Feb;27(2):267-74 | pt_PT |
dc.identifier.doi | 10.1093/annonc/mdv548 | pt_PT |
dc.identifier.issn | 1569-8041 | |
dc.identifier.uri | http://hdl.handle.net/10400.10/1883 | |
dc.language.iso | eng | pt_PT |
dc.peerreviewed | yes | pt_PT |
dc.publisher | European Society for Medical Oncology | pt_PT |
dc.subject | Cetuximab | pt_PT |
dc.subject | Clinical trials | pt_PT |
dc.subject | Colorectal neoplasms | pt_PT |
dc.subject | Antineoplastic combined chemotherapy protocols | pt_PT |
dc.subject | Liver neoplasms | pt_PT |
dc.title | Conversion to resection of liver metastases from colorectal cancer with hepatic artery infusion of combined chemotherapy and systemic cetuximab in multicenter trial OPTILIV. | pt_PT |
dc.type | journal article | |
dspace.entity.type | Publication | |
oaire.citation.conferencePlace | London | pt_PT |
oaire.citation.endPage | 274 | pt_PT |
oaire.citation.startPage | 267 | pt_PT |
oaire.citation.title | Annals of Oncology | pt_PT |
oaire.citation.volume | 27 | pt_PT |
rcaap.rights | closedAccess | pt_PT |
rcaap.type | article | pt_PT |
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