Ros Javier, Baraibar Iosune, Saoudi Nadia, Rodriguez Marta, Salvà Francesc, Tabernero Josep, Élez Elena
Medical Oncology Department, Vall d'Hebron University Hospital, 08035 Barcelona, Spain.
Vall d'Hebron Institute of Oncology, 08035 Barcelona, Spain.
Cancers (Basel). 2023 Aug 24;15(17):4245. doi: 10.3390/cancers15174245.
Microsatellite instability (MSI) is a biological condition associated with inflamed tumors, high tumor mutational burden (TMB), and responses to immune checkpoint inhibitors. In colorectal cancer (CRC), MSI tumors are found in 5% of patients in the metastatic setting and 15% in early-stage disease. Following the impressive clinical activity of immune checkpoint inhibitors in the metastatic setting, associated with deep and long-lasting responses, the development of immune checkpoint inhibitors has expanded to early-stage disease. Several phase II trials have demonstrated a high rate of pathological complete responses, with some patients even spared from surgery. However, in both settings, not all patients respond and some responses are short, emphasizing the importance of the ongoing search for accurate biomarkers. While various biomarkers of response have been evaluated in the context of MSI CRC, including and /2 mutations, TMB, pathway mutations, and Lynch syndrome, with mixed results, liver metastases have been associated with a lack of activity in such strategies. To improve patient selection and treatment outcomes, further research is required to identify additional biomarkers and refine existing ones. This will allow for the development of personalized treatment approaches and the integration of novel therapeutic strategies for MSI CRC patients with liver metastases.
微卫星不稳定性(MSI)是一种与炎症性肿瘤、高肿瘤突变负荷(TMB)以及对免疫检查点抑制剂的反应相关的生物学状态。在结直肠癌(CRC)中,转移性疾病患者中有5%的肿瘤存在MSI,早期疾病患者中这一比例为15%。在转移性疾病中免疫检查点抑制剂展现出令人瞩目的临床活性,伴随着深度且持久的反应,免疫检查点抑制剂的应用已扩展至早期疾病。多项II期试验已证明病理完全缓解率很高,有些患者甚至无需手术。然而,在这两种情况下,并非所有患者都有反应,且有些反应持续时间较短,这凸显了持续寻找准确生物标志物的重要性。虽然在MSI CRC背景下已对多种反应生物标志物进行了评估,包括 和 /2突变、TMB、 通路突变以及林奇综合征,结果不一,但肝转移与此类策略中活性的缺乏有关。为了改善患者选择和治疗结果,需要进一步研究以识别其他生物标志物并优化现有生物标志物。这将有助于开发个性化治疗方法,并为伴有肝转移的MSI CRC患者整合新型治疗策略。