IMR Press / FBL / Volume 11 / Issue 1 / 10.2741/1836

Frontiers in Bioscience-Landmark (FBL) is published by IMR Press from Volume 26 Issue 5 (2021). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on imrpress.com as a courtesy and upon agreement with Frontiers in Bioscience.

Article
Second-line intra-arterial chemotherapy in advanced pancreatic adenocarcinoma
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1 G. Rummo” Hospital, Department of Oncology, via Dell’Angelo 1, 82100, Benevento, Italy
2 National Cancer Institute, G. Pascale” foundation, Division of Diagnostic and Interventional Radiology, via M. Semmola, 80131, Naples, Italy
3 National Cancer Institute , G Pascale foundation , Division of Immunology , via M. Semmola, 80131 , Naples, Italy
4 National Cancer Institute, G. Pascale” foundation, Division of Medical Oncology B, via M. Semmola, 80131, Naples, Italy
5 S. Maria delle Grazie Hospital, Department of Oncoematology, Pozzuoli, Naples, Italy
6 A.R.C.O., Medical Oncology, Agnano, Naples, Italy
Front. Biosci. (Landmark Ed) 2006, 11(1), 782–787;
Published: 1 January 2006
Abstract

The present study was conducted to evaluate activity and toxicity of the FLEC (folinic acid 100 mg/m2; 5-fluorouracil 1000 mg/m2; carboplatin 300 mg/m2; epirubicin 60 mg/m2) schedule as second-line treatment for progressive locally advanced or metastatic pancreatic cancer (LAMPC). FLEC was administered every 3 weeks with an angiographic catheter introduced into the tumor vascular bed. Thirty-two patients were enrolled. Twenty patients had a PS of 2. Twenty-five patients had metastatic disease to liver. Seven (21.9%) partial responses were observed (WHO criteria). Fifteen patients (46.9%) had stable disease and ten patients (31.2%) had progressive disease. The median OS from the diagnosis was 11.8 months. PS (p=0.0308) and pain (WHO scale, p=0.0222; analogic scale, p=0.0446) significantly improved after therapy. No patient discontinued treatment because of toxicity (NCI-CTC criteria). The current study shows that intraarterial chemotherapy is a good therapeutic option in second-line treatment of LAMPC.

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