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Dokumenttyp:
Clinical Trial, Phase II; Journal Article; Multicenter Study; Article
Autor(en):
Sehouli, J; Oskay-Ozcelik, G; Kühne, J; Stengel, D; Hindenburg, HJ; Klare, P; Heinrich, G; Schmalfeldt, B; Mertens, H; Camara, O; Lichtenegger, W
Titel:
Biweekly pegylated liposomal doxorubicin in patients with relapsed ovarian cancer: results of a multicenter phase-II trial.
Abstract:
BACKGROUND: The obvious benefit of pegylated liposomal doxorubicin (PLD) for tumour control in recurrent ovarian cancer is frequently offset by severe palmar-plantar erythrodysesthesia (PPE). There is evidence that dose reduction from 50 to 40 mg/m(2) reduces the incidence of PPE without compromising cytotoxic activity. We set out to investigate whether biweekly application further improves the therapeutic index of PLD. PATIENTS AND METHODS: Patients with recurrent ovarian cancer after surgery and adjuvant chemotherapy with platinum and taxane compounds were eligible to participate in this multi-institutional phase II study. PLD was administered at a dose of 20 mg/m(2) every two weeks. Eligible patients had ECOG performance status of < or =2, and sufficient organ function. We employed an optimized two-stage design to test the hypothesis that biweekly application of PLD reduces the frequency of grade III and IV PPE from 25% to 10%. Response and survival were addressed descriptively. RESULTS: Between October 2001 and February 2004, 64 patients with median age of 59 (range 38-81) years were recruited onto this trial. We evaluated 553 (median 7, range 1-25) courses of PLD treatment. Most patients were in their third or fourth line of chemotherapy. PPE was noted in 30 patients (47.6%), but only three participants progressed to grade 3 severity (4.7%, 95% confidence interval 1.0-13.1%). Partial response, stable disease, and tumour progression were observed in 5, 13, and 24 patients, respectively. Median overall and progression-free survival were 18.2 (range, 1.4-34.0) and 4.3 (range 0.5-22.3) months. CONCLUSIONS: Biweekly PLD may reduce the incidence of PPE while retaining efficacy in relapsed ovarian cancer. Our data support the need for a randomized trial to strengthen these assumptions.
Zeitschriftentitel:
Ann Oncol
Jahr:
2006
Band / Volume:
17
Heft / Issue:
6
Seitenangaben Beitrag:
957-61
Sprache:
eng
Volltext / DOI:
doi:10.1093/annonc/mdl079
PubMed:
http://view.ncbi.nlm.nih.gov/pubmed/16600975
Print-ISSN:
0923-7534
TUM Einrichtung:
Frauenklinik und Poliklinik
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