Jain Rakesh K
Edwin L. Steele Laboratory for Tumor Biology, Department of Radiation Oncology, Harvard Medical School and Massachusetts General Hospital, 100 Blossom Street, Cox 7, Boston, MA 02114, USA.
Cancer Cell. 2014 Nov 10;26(5):605-22. doi: 10.1016/j.ccell.2014.10.006.
Ten antiangiogenic drugs targeting VEGF or its receptors are approved for cancer treatment. However, these agents, intended to block tumors' blood supply, may cause hypoxia, which may fuel tumor progression and treatment resistance. Emerging clinical data suggest that patients whose tumor perfusion or oxygenation increases in response to these agents may actually survive longer. Hence, strategies aimed at alleviating tumor hypoxia while improving perfusion may enhance the outcome of radiotherapy, chemotherapy, and immunotherapy. Here I summarize lessons learned from preclinical and clinical studies over the past decade and propose strategies for improving antiangiogenic therapy outcomes for malignant and nonmalignant diseases.
十种靶向血管内皮生长因子(VEGF)或其受体的抗血管生成药物已获批用于癌症治疗。然而,这些旨在阻断肿瘤血液供应的药物可能会导致缺氧,而缺氧可能会加速肿瘤进展并产生治疗耐药性。新出现的临床数据表明,肿瘤灌注或氧合因这些药物而增加的患者实际上可能存活更长时间。因此,旨在缓解肿瘤缺氧同时改善灌注的策略可能会提高放疗、化疗和免疫治疗的效果。在此,我总结了过去十年临床前和临床研究的经验教训,并提出了改善恶性和非恶性疾病抗血管生成治疗效果的策略。