Antoniotti C, Carullo M, Rossini D, Pietrantonio F, Salvatore L, Lonardi S, Tamberi S, Sciortino C, Conca V, Calegari M A, Ciracì P, Tamburini E, Bergamo F, Boccaccio C, Passardi A, Ritorto G, Ugolini C, Aprile G, Galon J, Cremolini C
Unit of Medical Oncology 2, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy; Department of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, Pisa, Italy.
Department of Experimental and Clinical Medicine, University of Florence and Oncology Unit, Careggi University Hospital, Florence, Italy.
ESMO Open. 2025 Feb;10(2):104135. doi: 10.1016/j.esmoop.2025.104135. Epub 2025 Feb 4.
Liver metastases (LMs) are related to poor efficacy of immune checkpoint inhibitor (ICI)-containing therapies. In the AtezoTRIBE trial, Immunoscore-Immune-Checkpoint (immunoscore-IC) was a predictor of benefit from atezolizumab in mismatch repair-proficient (pMMR) metastatic colorectal cancer (mCRC).
In pMMR patients enrolled in the AtezoTRIBE study, we investigated the association of LMs with immune-related biomarkers and treatment outcomes, and the predictive role of immunoscore-IC in the LMs group.
Out of 202 pMMR patients, 151 (75%) had LMs. No differences in immune-related features were observed according to the presence or not of LMs, except for a lower prevalence of tumour-infiltrating lymphocytes-high tumours in the LMs group (33% versus 52%, P = 0.03). Worse outcomes were observed among patients with LMs [progression-free survival (PFS), P = 0.002; overall survival (OS), P = 0.011], also in multivariable models. The effect of adding atezolizumab to FOLFOXIRI/bevacizumab was independent from LMs in terms of PFS (P = 0.990) and OS (P = 0.800). Among patients with pMMR mCRC and LMs, those with immunoscore-IC-high but not those with immunoscore-IC-low tumours achieved benefit from atezolizumab, though in the absence of a statistically significant interaction effect (P for PFS and OS = 0.166 and 0.473, respectively).
LMs are associated with poor prognosis in pMMR mCRC and do not predict resistance to the addition of atezolizumab to FOLFOXIRI/bevacizumab. Immunoscore-IC seems to retain its predictive impact also among patients with LMs.
肝转移(LMs)与含免疫检查点抑制剂(ICI)治疗的疗效不佳相关。在AtezoTRIBE试验中,免疫评分-免疫检查点(immunoscore-IC)是错配修复功能正常(pMMR)转移性结直肠癌(mCRC)患者从阿替利珠单抗治疗中获益的预测指标。
在参与AtezoTRIBE研究的pMMR患者中,我们研究了肝转移与免疫相关生物标志物及治疗结局的关联,以及免疫评分-IC在肝转移组中的预测作用。
在202例pMMR患者中,151例(75%)有肝转移。根据有无肝转移,未观察到免疫相关特征的差异,但肝转移组肿瘤浸润淋巴细胞高的肿瘤发生率较低(33%对52%,P = 0.03)。肝转移患者的预后较差[无进展生存期(PFS),P = 0.002;总生存期(OS),P = 0.011],多变量模型中也是如此。在PFS(P = 0.990)和OS(P = 0.800)方面,FOLFOXIRI/贝伐单抗加用阿替利珠单抗的疗效与肝转移无关。在pMMR mCRC和肝转移患者中,免疫评分-IC高的患者而非免疫评分-IC低的患者从阿替利珠单抗治疗中获益,尽管不存在统计学上显著的交互作用(PFS和OS的P值分别为0.166和0.473)。
肝转移与pMMR mCRC的预后不良相关,且不能预测FOLFOXIRI/贝伐单抗加用阿替利珠单抗的耐药性。免疫评分-IC似乎在肝转移患者中也保留了其预测作用。