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成熟的三级淋巴结构可独立于PD-L1表达预测实体瘤中免疫检查点抑制剂的疗效。

Mature tertiary lymphoid structures predict immune checkpoint inhibitor efficacy in solid tumors independently of PD-L1 expression.

作者信息

Vanhersecke Lucile, Brunet Maxime, Guégan Jean-Philippe, Rey Christophe, Bougouin Antoine, Cousin Sophie, Moulec Sylvestre Le, Besse Benjamin, Loriot Yohann, Larroquette Mathieu, Soubeyran Isabelle, Toulmonde Maud, Roubaud Guilhem, Pernot Simon, Cabart Mathilde, Chomy François, Lefevre Corentin, Bourcier Kevin, Kind Michèle, Giglioli Ilenia, Sautès-Fridman Catherine, Velasco Valérie, Courgeon Félicie, Oflazoglu Ezoglin, Savina Ariel, Marabelle Aurélien, Soria Jean-Charles, Bellera Carine, Sofeu Casimir, Bessede Alban, Fridman Wolf H, Loarer François Le, Italiano Antoine

机构信息

Department of Pathology, Institut Bergonié, Bordeaux, France.

Faculty of Medicine, University of Bordeaux, Bordeaux, France.

出版信息

Nat Cancer. 2021 Aug;2(8):794-802. doi: 10.1038/s43018-021-00232-6. Epub 2021 Aug 12.

Abstract

Only a minority of patients derive long-term clinical benefit from anti-PD1/PD-L1 monoclonal antibodies. The presence of tertiary lymphoid structures (TLS) has been associated with improved survival in several tumor types. Here, using a large-scale retrospective analysis of three independent cohorts of cancer patients treated with anti-PD1/PD-L1 antibodies, we showed that the presence of mature TLS was associated with improved objective response rate, progression-free survival, and overall survival independently of PD-L1 expression status and CD8+ T-cell density. These results pave the way for using TLS detection to select patients who are more likely to benefit from immune checkpoint blockade.

摘要

只有少数患者能从抗PD1/PD-L1单克隆抗体中获得长期临床益处。三级淋巴结构(TLS)的存在与多种肿瘤类型患者生存率的提高相关。在此,我们通过对接受抗PD1/PD-L1抗体治疗的三个独立癌症患者队列进行大规模回顾性分析,发现成熟TLS的存在与客观缓解率、无进展生存期和总生存期的改善相关,且与PD-L1表达状态和CD8+T细胞密度无关。这些结果为利用TLS检测来选择更有可能从免疫检查点阻断治疗中获益的患者铺平了道路。

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Complement Signals Determine Opposite Effects of B Cells in Chemotherapy-Induced Immunity.
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4
New predictors for immunotherapy responses sharpen our view of the tumour microenvironment.
Nature. 2020 Jan;577(7791):474-476. doi: 10.1038/d41586-019-03943-0.
5
B cells are associated with survival and immunotherapy response in sarcoma.
Nature. 2020 Jan;577(7791):556-560. doi: 10.1038/s41586-019-1906-8. Epub 2020 Jan 15.
6
B cells and tertiary lymphoid structures promote immunotherapy response.
Nature. 2020 Jan;577(7791):549-555. doi: 10.1038/s41586-019-1922-8. Epub 2020 Jan 15.
7
Tertiary lymphoid structures improve immunotherapy and survival in melanoma.
Nature. 2020 Jan;577(7791):561-565. doi: 10.1038/s41586-019-1914-8. Epub 2020 Jan 15.
9
Tertiary lymphoid structures in the era of cancer immunotherapy.
Nat Rev Cancer. 2019 Jun;19(6):307-325. doi: 10.1038/s41568-019-0144-6.

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