A pilot trial of doxorubicin containing phosphatidyldiglycerol based thermosensitive liposomes in spontaneous feline soft tissue sarcoma

被引:21
作者
Zimmermann, Katja [1 ]
Hossann, Martin [2 ,7 ]
Hirschberger, Johannes [1 ]
Troedson, Karin [1 ]
Peller, Michael [3 ]
Schneider, Moritz [3 ]
Bruehschwein, Andreas [4 ]
Meyer-Lindenberg, Andrea [4 ]
Wess, Gerhard [1 ]
Wergin, Melanie [1 ]
Doerfelt, Rene [1 ]
Knoesel, Thomas [5 ]
Schwaiger, Markus [6 ]
Baumgartner, Christine [6 ]
Brandl, Johanna [6 ]
Schwamberger, Sabine [6 ]
Lindner, Lars H. [2 ]
机构
[1] Ludwig Maximilians Univ Munchen, Ctr Clin Vet Med, Clin Small Anim Med, Vet Str 13, D-80539 Munich, Germany
[2] Ludwig Maximilians Univ Munchen, Univ Hosp Munich, Dept Internal Med 3, Munich, Germany
[3] Ludwig Maximilians Univ Munchen, Univ Hosp Munich, Inst Clin Radiol, Munich, Germany
[4] Ludwig Maximilians Univ Munchen, Ctr Clin Vet Med, Clin Small Anim Surg & Reprod, Munich, Germany
[5] Ludwig Maximilians Univ Munchen, Dept Pathol, Munich, Germany
[6] Tech Univ Munich, Dept Nucl Med, Clin Rechts Isar, Munich, Germany
[7] Thermosome GmbH, Klopferspitz 19, D-82152 Planegg Martinsried, Germany
关键词
Hyperthermia; thermosensitive liposomes; phosphatidyldiglycerol; drug delivery; doxorubicin; feline soft tissue sarcoma; TEMPERATURE-SENSITIVE LIPOSOMES; INJECTION-SITE SARCOMAS; PHASE-I; NEOADJUVANT CHEMOTHERAPY; RADIOFREQUENCY ABLATION; RADIATION-THERAPY; CONTENT RELEASE; HYPERTHERMIA; CATS; RECURRENT;
D O I
10.1080/02656736.2016.1230233
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Doxorubicin (DOX)-loaded phosphatidyldiglycerol-based thermosensitive liposomes (DPPG(2)-TSL-DOX) combined with local hyperthermia (HT) was evaluated in cats with locally advanced spontaneous fibrosarcomas (soft tissue sarcoma [STS]). The study was designed to evaluate the safety and pharmacokinetic profile of the drug. Results from four dose-levels are reported.Methods: Eleven client-owned cats with advanced STS were enrolled. Five cats received escalating doses of 0.1-0.4mg/kg DOX (group I), three received 0.4mg/kg constantly (group II) and three 0.6mg/kg (group III) IV over 15min. HT with a target temperature of 41.5 degrees C was started 15min before drug application and continued for a total of 60min. Six HT treatments were applied every other week using a radiofrequency applicator. Tumour growth was monitored by magnetic resonance imaging (MRI) and for dose level III also with F-18-FDG PET.Results: Treatment was generally well tolerated and reasons for premature study termination in four cats were not associated with drug-induced toxicity. No DPPG(2)-TSL-DOX based hypersensitivity reaction was observed. One cat showed simultaneous partial response (PR) in MRI and positron emission tomography (PET) whereas one cat showed stable disease in MRI and PR in PET (both cats in dose level III). Pharmacokinetic measurements demonstrated DOX release triggered by HT.Conclusion: DPPG(2)-TSL-DOX+HT is a promising treatment option for advanced feline STS by means of targeted drug delivery. As MTD was not reached further investigation is warranted to determine if higher doses would result in even better tumour responses.
引用
收藏
页码:178 / 190
页数:13
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