Department of Medical Oncology, Infanta Sofía University Hospital, Infanta Sofía and Henares Hospitals Foundation for Biomedical Research and Innovation (FIIB HUIS HHEN), Madrid, Spain; Molecular Oncology and Nutritional Genomics of Cancer, IMDEA-Food Institute, CEI UAM+CSIC, Madrid, 28049, Spain.
Department of Medical Oncology, Infanta Sofía University Hospital, Infanta Sofía and Henares Hospitals Foundation for Biomedical Research and Innovation (FIIB HUIS HHEN), Madrid, Spain.
Crit Rev Oncol Hematol. 2021 May;161:103306. doi: 10.1016/j.critrevonc.2021.103306. Epub 2021 Apr 8.
The incidence of endometrial cancer (EC) is increasing worldwide. The prognosis for patients diagnosed with early-stage remains good, whereas for patients with recurrent or metastatic disease, the prognosis is poor and treatment options, until recently, were limited. In 2017, pembrolizumab was approved by the US Food and Drug Administration (FDA) for those patients with mistmach repair deficiency (MMRd) or high microsatellite instability (MSI-H) tumors. However, only 20-30 % of EC have MSI, and just over half of these patients benefit from treatment. In 2019, the FDA granted breakthrough therapy designation to lenvatinib in combination with pembrolizumab for the potential treatment of patients with advanced microsatellite stable EC that has progressed after treatment with at least one previous systemic therapy. It appears clear that immune check-point inhibitors will have a definite place in the management of EC, both as single agent or in combination with other targeted agents. In this review, we summarize the current evidence of immune check point blockade and the identification of potential biomarkers, beyond MSI-H or MMRd, that could help to predict response to this agents in correlation with the genomic EC subtypes.
子宫内膜癌(EC)的发病率在全球范围内呈上升趋势。对于诊断为早期的患者,预后仍然良好,而对于复发性或转移性疾病的患者,预后较差,且治疗选择有限。直到最近,2017 年,派姆单抗被美国食品和药物管理局(FDA)批准用于错配修复缺陷(MMRd)或高微卫星不稳定性(MSI-H)肿瘤的患者。然而,只有 20-30%的 EC 具有 MSI,而这些患者中只有超过一半的患者从中受益。2019 年,FDA 授予仑伐替尼联合派姆单抗突破性治疗药物认定,用于治疗至少接受过一次先前全身治疗后进展的晚期微卫星稳定 EC 患者。很明显,免疫检查点抑制剂将在 EC 的治疗中占据明确的地位,无论是作为单一药物还是与其他靶向药物联合使用。在这篇综述中,我们总结了目前免疫检查点阻断的证据,并确定了除 MSI-H 或 MMRd 之外的潜在生物标志物,这些标志物可能有助于预测这些药物与基因组 EC 亚型相关的反应。