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Cationic liposomal paclitaxel plus gemcitabine or gemcitabine alone in patients with advanced pancreatic cancer: a randomized controlled phase II trial.
Löhr, J M; Haas, S L; Bechstein, W-O; Bodoky, G; Cwiertka, K; Fischbach, W; Fölsch, U R; Jäger, D; Osinsky, D; Prausova, J; Schmidt, W E; Lutz, M P.
Afiliação
  • Löhr JM; Department of Medicine II, University Hospital Mannheim, Mannheim, Germany; Department of Surgical Gastroenterology, Karolinska Institutet, Stockholm, Sweden. Electronic address: matthias.lohr@ki.se.
  • Haas SL; Department of Medicine II, University Hospital Mannheim, Mannheim, Germany; Department of Surgical Gastroenterology, Karolinska Institutet, Stockholm, Sweden.
  • Bechstein WO; Department of General and Visceral Surgery, University Hospital Frankfurt, Frankfurt/Main, Germany.
  • Bodoky G; Department of Oncology, Szent Laszlo Hospital, Budapest, Hungary.
  • Cwiertka K; Department of Oncology, University Hospital Olomouc, Olomouc, Czech Republic.
  • Fischbach W; Department of Medicine II, Klinikum Aschaffenburg, Aschaffenburg.
  • Fölsch UR; Department of General Internal Medicine, University Hospital Schleswig-Holstein, Kiel.
  • Jäger D; Department of Medical Oncology, National Center for Tumor Diseases, University Hospital Heidelberg, Heidelberg, Germany.
  • Osinsky D; Institute of Oncology AMS of Ukraine, Kiev, Ukraine.
  • Prausova J; Department of Oncological Radiotherapy, University Hospital Prague, Prague, Czech Republic.
  • Schmidt WE; Department of Medicine I, St. Josef-Hospital, Ruhr-University, Bochum.
  • Lutz MP; Department of Medicine, Caritasklinik St. Theresia, Saarbrücken, Germany.
Ann Oncol ; 23(5): 1214-1222, 2012 May.
Article em En | MEDLINE | ID: mdl-21896540
ABSTRACT

BACKGROUND:

Paclitaxel embedded in cationic liposomes (EndoTAG™-1; ET) is an innovative agent targeting tumor endothelial cells. This randomized controlled phase II trial evaluated the safety and efficacy of ET in combination with gemcitabine (GEM) in advanced pancreatic cancer (PDAC). PATIENTS AND

METHODS:

Chemotherapy-naive patients with locally advanced or metastatic disease were randomly assigned to receive weekly GEM 1000 mg/m(2) or GEM plus twice-weekly ET 11, 22 or 44 mg/m(2) for 7 weeks. After a safety run-in of 100 patients, a second cohort continued treatment. End points included overall survival (OS), progression-free survival (PFS), tumor response and safety.

RESULTS:

Two hundred and twelve patients were randomly allocated to the study and 200 were treated (80% metastatic, 20% locally advanced). Adverse events were manageable and reversible. Transient thrombocytopenia and infusion reactions with chills and pyrexia mostly grade 1 or 2 occurred in the ET groups. Disease control rate after the first treatment cycle was 43% with GEM and 60%, 65% and 52% in the GEM + ET cohorts. Median PFS reached 2.7 compared with 4.1, 4.6 and 4.4 months, respectively. Median OS was 6.8 compared with 8.1, 8.7 and 9.3 months, respectively.

CONCLUSIONS:

Treatment of advanced PDAC with GEM + ET was generally well tolerated. GEM + ET showed beneficial survival and efficacy. A randomized phase III trial should confirm this positive trend.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / Carcinoma / Protocolos de Quimioterapia Combinada Antineoplásica / Paclitaxel / Desoxicitidina Tipo de estudo: Clinical_trials Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2012 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / Carcinoma / Protocolos de Quimioterapia Combinada Antineoplásica / Paclitaxel / Desoxicitidina Tipo de estudo: Clinical_trials Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2012 Tipo de documento: Article