A Prospective Phase I / II Study: Combination Chemotherapy with Docetaxel and Pemetrexed as Second-Line Treatment in Patients with Stage IIIB / IV Non-Small Cell Lung Cancer
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作者:
Kroeber, Vinzenz
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Krankenhaus Martha Maria Halle Doelau, Dept Internal Med 2, Roentgenstr 1, DE-06120 Halle, Saale, GermanyKrankenhaus Martha Maria Halle Doelau, Dept Internal Med 2, Roentgenstr 1, DE-06120 Halle, Saale, Germany
Kroeber, Vinzenz
[1
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Nagel, Sylke
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Krankenhaus Martha Maria Halle Doelau, Dept Internal Med 2, Roentgenstr 1, DE-06120 Halle, Saale, GermanyKrankenhaus Martha Maria Halle Doelau, Dept Internal Med 2, Roentgenstr 1, DE-06120 Halle, Saale, Germany
Nagel, Sylke
[1
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Schuette, Wolfgang
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Krankenhaus Martha Maria Halle Doelau, Dept Internal Med 2, Roentgenstr 1, DE-06120 Halle, Saale, GermanyKrankenhaus Martha Maria Halle Doelau, Dept Internal Med 2, Roentgenstr 1, DE-06120 Halle, Saale, Germany
Schuette, Wolfgang
[1
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Blankenburg, Thomas
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Krankenhaus Martha Maria Halle Doelau, Dept Internal Med 2, Roentgenstr 1, DE-06120 Halle, Saale, GermanyKrankenhaus Martha Maria Halle Doelau, Dept Internal Med 2, Roentgenstr 1, DE-06120 Halle, Saale, Germany
Blankenburg, Thomas
[1
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机构:
[1] Krankenhaus Martha Maria Halle Doelau, Dept Internal Med 2, Roentgenstr 1, DE-06120 Halle, Saale, Germany
Introduction: Two standard single-agent chemotherapy treatments (docetaxel and pemetrexed) were combined in this trial and administered as second-line treatment in patients with non-small cell lung cancer (NSCLC). The aim of this study was to evaluate the safety and feasibility of combining docetaxel with pemetrexed. Methods: Six patients were enrolled between August 2007 and March 2009 with stage IIIB/IV NSCLC. The doseescalation model included a pemetrexed infusion on day 1 of 200-300 mg/m(2) followed by infusion of docetaxel on days 1, 8 and 15 at doses from 20 to 30 mg/m(2). Primary study endpoints included efficacy and safety variables, also progression-free, overall and 1-year survival and time to progression. Results: The study was abandoned due to adverse effects defined in the protocol. The major toxicities were all of grade 3 and included fatigue, stomatitis/mucositis, diarrhea and in one case, an episode of febrile neutropenia. Two patients died during the study, but not as a direct result of the treatment. Conclusions: We recommend that docetaxel or pemetrexed monotherapies should continue to be considered the standard second-line chemotherapy treatment against NSCLC. The results of this study warrant no further investigation into this particular combination treatment due to the severe toxicity effects encountered. (C) 2014 S. Karger AG, Basel