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首页> 外文期刊>Oncology reports >Sustained effect of continuous treatment with bevacizumab following bevacizumab in combination with chemotherapy in a human ovarian clear cell carcinoma xenograft model
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Sustained effect of continuous treatment with bevacizumab following bevacizumab in combination with chemotherapy in a human ovarian clear cell carcinoma xenograft model

机译:贝伐单抗连续治疗与贝伐单抗组合在人卵巢透明细胞癌异种移植模型中的化疗组合持续治疗

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摘要

Although bevacizumab maintenance following bevacizumab in combination with chemotherapy has demonstrated significant prolongation of progression-free survival in clinical studies in patients with ovarian cancer, the majority of the cancer cases in the study were of the serous histotype; therefore, data regarding clear cell carcinoma is limited. Furthermore, the efficacy of bevacizumab beyond progression has not yet been demonstrated in ovarian cancer. A xenograft model using the human ovarian clear cell carcinoma cell line RMG-I was used to investigate the antitumor effects and the mechanisms of bevacizumab in maintenance treatment and bevacizumab when administered beyond disease progression. In the RMG-I model, bevacizumab maintenance following bevacizumab in combination with paclitaxel exhibited increased tumor suppression, compared with its absence, and inhibited the increase of microvessel density (MVD) in tumors. Following disease progression during bevacizumab maintenance, continued bevacizumab treatment in combination with PEGylated liposomal doxorubicin as a secondary chemotherapeutic agent had increased efficacy, compared with PEGylated liposomal doxorubicin alone, and resulted in lower MVD accompanied with lower levels of insulin-like growth factor binding protein-3, which is reported to have angiogenic activity. Continuous suppression of angiogenesis by bevacizumab may contribute to the superior efficacy of bevacizumab maintenance and bevacizumab beyond progression in ovarian cancer.
机译:虽然Bevacizumab与化疗组合后的Bevacizumab维持表现出卵巢癌患者临床研究中的无进展生存率的显着延长,但研究中的大多数癌症病例是浆液组织型;因此,关于透明细胞癌的数据有限。此外,在卵巢癌中尚未证明Bevacizumab超越进展的疗效。使用人卵巢透明细胞癌细胞系RMG-i的异种移植模型研究了在超出疾病进展之外时抗肿瘤效应和贝伐单抗在维持治疗中的机制和贝伐单抗。在RMG-I模型中,与紫杉醇组合的Bevacizumab维持表现出增加的肿瘤抑制,与其不存在相比,并抑制肿瘤中微血管密度(MVD)的增加。在Bevacizumab维护期间疾病进展后,与单独的聚乙二醇化脂质体DOXORUBININ相比,继续与聚乙二醇化脂质体DOXORUBININ与聚乙二醇化脂质体DOXORUBININ相结合的培养基治疗,并导致下部MVD伴随着较低水平的胰岛素样生长因子结合蛋白 - 3,据报道,据报道具有血管生成活性。 Bevacizumab的抗血管生成的连续抑制可能导致贝伐单抗维持和贝伐单抗超越卵巢癌的进展的优越疗效。

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