Żak Klaudia, Satora Małgorzata, Skrabalak Ilona, Tarkowski Rafał, Ostrowska-Leśko Marta, Bobiński Marcin
Department of Medical Chemistry, Medical University of Lublin, 20-059 Lublin, Poland.
I Chair and Department of Oncological Gynaecology and Gynaecology, Student Scientific Association, Medical University of Lublin, 20-059 Lublin, Poland.
Cancers (Basel). 2024 Mar 5;16(5):1063. doi: 10.3390/cancers16051063.
There were high hopes for the new antiangiogenic medicament, bevacizumab, which could inhibit the creation of new blood vessels through binding to isoform A of vascular endothelial growth factor (VEGF). However, it is not only blood vessels that are responsible for tumor cell spread. During the process of tumor growth, lymphangiogenesis is mediated by other members of the VEGF family, specifically VEGF-C and VEGF-D, which act independent to bevacizumab. Therefore, based on the mechanism of bevacizumab action and the processes of angio- and lymphangiogenesis, we formed three hypotheses: (1) if the lymph nodes in primary ovarian cancers are metastatic, the outcome of bevacizumab treatment is worsened; (2) concerning the second-line treatment, bevacizumab will act in a weakened manner if recurrence occurs in lymph nodes as opposed to a local recurrence; (3) patients treated by bevacizumab are more likely to have recurrences in lymph nodes. These hypotheses raise the issue of the existing knowledge gap, which concerns the effect of bevacizumab on metastatic lymph nodes.
人们对新型抗血管生成药物贝伐单抗寄予厚望,它可以通过与血管内皮生长因子(VEGF)的A亚型结合来抑制新血管的生成。然而,负责肿瘤细胞扩散的不仅仅是血管。在肿瘤生长过程中,淋巴管生成是由VEGF家族的其他成员介导的,特别是VEGF-C和VEGF-D,它们的作用独立于贝伐单抗。因此,基于贝伐单抗的作用机制以及血管生成和淋巴管生成过程,我们形成了三个假设:(1)如果原发性卵巢癌的淋巴结发生转移,贝伐单抗治疗的结果会恶化;(2)关于二线治疗,如果复发发生在淋巴结而不是局部复发,贝伐单抗的作用会减弱;(3)接受贝伐单抗治疗的患者更有可能在淋巴结复发。这些假设引发了现有知识差距的问题,即贝伐单抗对转移性淋巴结的影响。