Surgical downstaging and neo-adjuvant therapy in metastatic colorectal carcinoma with irinotecan drug-eluting beads: a multi-institutional study
Language English Country Great Britain, England Media print
Document type Journal Article, Multicenter Study
PubMed
20495642
PubMed Central
PMC2814401
DOI
10.1111/j.1477-2574.2009.00117.x
PII: S1365-182X(15)30245-8
Knihovny.cz E-resources
- MeSH
- Chemotherapy, Adjuvant MeSH
- Hepatic Artery MeSH
- Chemoembolization, Therapeutic * adverse effects MeSH
- Adult MeSH
- Antineoplastic Agents, Phytogenic administration & dosage adverse effects MeSH
- Hepatectomy * adverse effects MeSH
- Infusions, Intra-Arterial MeSH
- Irinotecan MeSH
- Camptothecin administration & dosage adverse effects analogs & derivatives MeSH
- Carcinoma diagnosis secondary surgery therapy MeSH
- Catheter Ablation * adverse effects MeSH
- Colorectal Neoplasms pathology therapy MeSH
- Middle Aged MeSH
- Humans MeSH
- Microspheres * MeSH
- Liver Neoplasms diagnosis secondary surgery therapy MeSH
- Neoadjuvant Therapy MeSH
- Tomography, X-Ray Computed MeSH
- Positron-Emission Tomography MeSH
- Proportional Hazards Models MeSH
- Prospective Studies MeSH
- Registries MeSH
- Chi-Square Distribution MeSH
- Aged MeSH
- Treatment Outcome MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Multicenter Study MeSH
- Geographicals
- Alabama MeSH
- Czech Republic MeSH
- Kentucky MeSH
- Names of Substances
- Antineoplastic Agents, Phytogenic MeSH
- Irinotecan MeSH
- Camptothecin MeSH
BACKGROUND: Neoadjuvant chemotherapy for potentially resectable metastatic colorectal cancer (MCC) is becoming a more common treatment algorithm. The aim of the present study was to evaluate the efficacy of precision hepatic arterial Irinotecan therapy in unresectable MCC. METHODS: An open-label, multi-centre, multi-national single arm study of MCC patients, who received hepatic arterial irinotecan. Primary endpoints were safety, tolerance and metastatic tumour resection. RESULTS: Fifty-five patients with metastatic colorectal to the liver underwent a total of 90 hepatic arterial irinotecan treatments. The extent of liver involvement was < 25% in 75% of the patients (n= 41), between 26 and 50% in 15% of the patients (n= 11) and >50% in 10% of the patients (n= 24). The median number of hepatic lesions was four (range 1-20), with a median total size of all target lesions of 9 cm (range 5.5-28 cm) with 50% of patients having bilobar tumour distribution. The median number of irinotecan treatments was two (range 1-5). The median treatment dose was 100 mg (range 100-200) with a median total hepatic treatment of 200 mg (range 200-650). The majority of treatments (86%) were performed as lobar infusion treatments, and 30% of patients were treated with concurrent simultaneous chemotherapy. Eleven (20%) patients demonstrated significant response and downstage of their disease or demonstrated stable disease without extra-hepatic disease progression allowing resection, ablation or resection and ablation. There were no post-operative deaths. Post-operative complications morbidity occurred in 18% of patients, with none of them hepatic related. Non-tumorous liver resected demonstrated no evidence of steatohepatitis from the irinotecan arterial infusion. CONCLUSIONS: Hepatic arterial infusion irinotecan drug-eluting beads is safe and effective in pre-surgical therapy and helpful in evaluating the biology of metastatic colorectal cancer to the liver prior to planned hepatic resection.
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