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Tumour growth rate improves tumour assessment and first-line systemic treatment decision-making for immunotherapy in patients with liver metastatic uveal melanoma

黑色素瘤 医学 免疫疗法 肿瘤科 内科学 全身疗法 临床决策 病理 癌症 癌症研究 重症监护医学 乳腺癌
作者
Toulsie Ramtohul,Axel Cohen,Manuel Rodrigues,Sophie Piperno‐Neumann,Luc Cabel,Nathalie Cassoux,Livia Lumbroso‐Le Rouic,Maxime Denis,Sophie Gardrat,Gaëlle Pierron,Pascale Mariani,Vincent Servois
出处
期刊:British Journal of Cancer [Springer Nature]
卷期号:127 (2): 258-267 被引量:4
标识
DOI:10.1038/s41416-022-01793-8
摘要

The RECIST-based response variably matches the clinical benefit of systemic therapies for liver metastatic uveal melanoma (LMUM). The aims were to determine whether the tumour growth rate (TGR) can help predict the survival in patients with LMUM and to provide information for the management of first-line systemic treatment.This retrospective study included 147 (training: n = 110, validation: n = 37) patients with LMUM treated with first-line systemic treatment between 2010 and 2021. Two TGR-derived parameters were calculated, TGR0 and TGR3m. Multivariate Cox analyses identified independent predictors of progression-free survival (PFS) and overall survival (OS).TGR3m was a strong independent prognostic factor of PFS and OS (p < 0.001). The RECIST-based response was no longer significant in the OS analyses. Only immunotherapy regimens correlated with higher OS (HR = 0.2; 95% CI, 0.1-0.5; p < 0.001) in the low-TGR3m (≤50%/m) subgroup. These findings were confirmed in the validation cohort. TGR0, disease-free interval (DFI), and the sum of target lesions at baseline were predictive factors of low TGR3m.The use of TGR3m would improve tumour assessment by identifying patients who would benefit from first-line immunotherapy regimens despite PD. TGR0, DFI and the sum of target lesions were correlated with TGR3m, which can support first-line treatment decision-making for immunotherapy.

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