2006
DOI: 10.1016/j.ygyno.2005.10.027
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Pegylated liposomal doxorubicin (Lipo-Dox®) for platinum-resistant or refractory epithelial ovarian carcinoma: A Taiwanese gynecologic oncology group study with long-term follow-up

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Cited by 74 publications
(45 citation statements)
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“…Although recently, there is a multi-institutional phase II trial regarding combination of PLD to another agent such as panitumumab, the first fully human monoclonal antibody specific to EGF receptor in platinum resistant/ refractory ovarian cancer patients, the progression free and overall survival are still not apparently superior comparing the combination of PLD with carboplatin (Steffensen et al, 2013). According to our study, we found the overall response rate was 23.07% which was similar to previous Taiwanese study (Chou et al, 2006). With a median follow-up of 27.4 months, the median progression-free and median overall survivals in the 36 patients was 4.46 months and 8.76 months respectively which were rather shorter than previous study.…”
Section: Discussionsupporting
confidence: 83%
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“…Although recently, there is a multi-institutional phase II trial regarding combination of PLD to another agent such as panitumumab, the first fully human monoclonal antibody specific to EGF receptor in platinum resistant/ refractory ovarian cancer patients, the progression free and overall survival are still not apparently superior comparing the combination of PLD with carboplatin (Steffensen et al, 2013). According to our study, we found the overall response rate was 23.07% which was similar to previous Taiwanese study (Chou et al, 2006). With a median follow-up of 27.4 months, the median progression-free and median overall survivals in the 36 patients was 4.46 months and 8.76 months respectively which were rather shorter than previous study.…”
Section: Discussionsupporting
confidence: 83%
“…Chou et al studied second-generation PLD drug, Lipo-Dox ® with a dose of 45 mg/m 2 at a 4-week interval in 26 heavily pretreated resistant or refractory ovarian cancers patients and found the response rate of 23.1% with median progression-free interval and median overall survival time of 5.4 months and 13.8 months, respectively. They found that Lipo-Dox ® provided a response rate comparable with that of Doxil on similar patients (Chou et al, 2006). In our study ,we prescribed Lipo-Dox ® , combined with carboplatin which was reported in a number of studies to have synergistic combination and found superior with regard to progression free survival and also safety profile (du Bois et al, 2007;Ferrero 2007;Alberts et al, 2008;Power et al, 2009;Strother and Matei, 2009;Grenader et al, 2012).…”
Section: Discussionsupporting
confidence: 50%
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“…Portanto, são pequenos o suficiente para extravasar do sangue para o espaço intersticial do tumor passando através desses poros (Lasic, 1998;Sapra, Allen, 2003). Chou et al (2006) avaliaram a atividade da doxorrubicina encapsulada em lipossomas furtivos (LipoDox ® ) em pacientes com carcinoma ovariano epitelial resistente à platina na dose de 45 mg/m 2 a cada quatro semanas. A eficácia do Lipo-Dox foi constatada em câncer recorrente e platina-resistente.…”
Section: Lipossomas No Tratamento Do Câncerunclassified