دورية أكاديمية

Hepatic arterial infusion of oxaliplatin plus systemic chemotherapy and targeted therapy for unresectable colorectal liver metastases.

التفاصيل البيبلوغرافية
العنوان: Hepatic arterial infusion of oxaliplatin plus systemic chemotherapy and targeted therapy for unresectable colorectal liver metastases.
المؤلفون: Boilève, Alice, De Cuyper, Astrid, Larive, Alicia, Mahjoubi, Linda, Najdawi, Milan, Tazdait, Mélodie, Gelli, Maximiliano, Tselikas, Lambros, Smolenschi, Cristina, Malka, David, Pignon, Jean-Pierre, Ducreux, Michel, Boige, Valérie
المساهمون: UCL - (SLuc) Unité d'oncologie médicale
المصدر: European journal of cancer, Vol. 138, p. 89-98 (2020)
بيانات النشر: Elsevier Science Ltd
سنة النشر: 2020
المجموعة: DIAL@UCL (Université catholique de Louvain)
مصطلحات موضوعية: Adult, Aged, Antineoplastic Combined Chemotherapy Protocols, Bevacizumab, Camptothecin, Colorectal Neoplasms, ErbB Receptors, Female, Fluorouracil, Hepatic Artery, Humans, Infusions, Intra-Arterial, Leucovorin, Liver Neoplasms, Male, Middle Aged, Oxaliplatin, Colorectal cancer, Hepatic arterial infusion, Liver metastases, Targeted therapy
الوصف: BACKGROUND: Hepatic arterial infusion (HAI) combined with systemic chemotherapy has shown promising results in patients with unresectable colorectal liver metastases (CRLM), even after failure to systemic therapy. Addition of systemic targeted therapies has been investigated with controversial results regarding tolerance, especially with HAI-floruxidine when combined with systemic bevacizumab. Our study aimed to analyse feasibility, safety and efficacy of HAI-oxaliplatin plus systemic chemotherapy and targeted therapies. METHODS: Between 2005 and 2016, single-centre consecutive patients with unresectable CRLM who received at least one cycle of HAI-oxaliplatin plus systemic chemotherapy and targeted therapies (cetuximab/panitumumab or bevacizumab) were analysed. RESULTS: A total of 89 patients (median age 55 years (range, 26-76 years) who previously received a median number of one systemic chemotherapy regimen (range, 0-5) including oxaliplatin in 78% of cases were included. Median number of HAI-oxaliplatin cycles was 9 (range, 1-28) combined with systemic chemotherapy and targeted therapies (LV5FU2 [63%], FOLFIRI [36%]) plus anti-EGFR (30%), or bevacizumab (70%). Grade 3/4 toxicities included neutropenia (40%), HAI-related abdominal pain (43%) and neurotoxicity (12%). The intent-to-treat objective response rate was 42%, and 45% had stable disease, allowing complete CRLM resection/ablation in 27% of patients. After a median follow-up of 72 months, median overall and progression-free survival was 20 and 9 months, respectively. CONCLUSION: Addition of targeted therapy to systemic chemotherapy combined with HAI-oxaliplatin is feasible, safe and shows promising activity, even after systemic chemotherapy failure.
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 0959-8049
1879-0852
العلاقة: boreal:250322; http://hdl.handle.net/2078.1/250322Test; info:pmid/32871526; urn:ISSN:0959-8049; urn:EISSN:1879-0852
DOI: 10.1016/j.ejca.2020.07.022
الإتاحة: https://doi.org/10.1016/j.ejca.2020.07.022Test
http://hdl.handle.net/2078.1/250322Test
حقوق: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.DDEED684
قاعدة البيانات: BASE
الوصف
تدمد:09598049
18790852
DOI:10.1016/j.ejca.2020.07.022