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The Combination of Olaratumab with Doxorubicin and Cisplatinum Regresses a Chemotherapy-Resistant Osteosarcoma in a Patient-Derived Orthotopic Xenograft Mouse Model.

Authors :
Higuchi, Takashi
Higuchi, Takashi
Sugisawa, Norihiko
Miyake, Kentaro
Oshiro, Hiromichi
Yamamoto, Norio
Hayashi, Katsuhiro
Kimura, Hiroaki
Miwa, Shinji
Igarashi, Kentaro
Bouvet, Michael
Singh, Shree Ram
Tsuchiya, Hiroyuki
Hoffman, Robert M
Higuchi, Takashi
Higuchi, Takashi
Sugisawa, Norihiko
Miyake, Kentaro
Oshiro, Hiromichi
Yamamoto, Norio
Hayashi, Katsuhiro
Kimura, Hiroaki
Miwa, Shinji
Igarashi, Kentaro
Bouvet, Michael
Singh, Shree Ram
Tsuchiya, Hiroyuki
Hoffman, Robert M
Source :
Translational oncology; vol 12, iss 9, 1257-1263; 1936-5233
Publication Year :
2019

Abstract

Chemotherapy-resistant osteosarcoma is a recalcitrant disease. It is a frequent cause of death to the patients who are usually adolescent or young adults. The goal of the present study was to determine the efficacy of the combination of olaratumab (OLA), doxorubicin (DOX), and cisplatinum (CDDP) on osteosarcoma, which is resistant to first-line therapy, in a patient-derived orthotopic xenograft (PDOX) model. The osteosarcoma PDOX model was randomized into six treatment groups of six mice: control; CDDP alone; DOX and CDDP; OLA + DOX; OLA + CDDP; and OLA + DOX and CDDP. Tumor size and body weight were measured during 14 days of treatment. Tumor growth was regressed only by the treatment with a combination of OLA + DOX and CDDP. Tumors treated with this three-drug combination had the most tumor necrosis and the lowest Ki-67 index. The present study demonstrates the power of the PDOX model to identify novel effective treatment strategy for chemotherapy-resistant osteosarcoma.

Details

Database :
OAIster
Journal :
Translational oncology; vol 12, iss 9, 1257-1263; 1936-5233
Notes :
application/pdf, Translational oncology vol 12, iss 9, 1257-1263 1936-5233
Publication Type :
Electronic Resource
Accession number :
edsoai.on1341877965
Document Type :
Electronic Resource