免疫检查点阻断通过扩增效应 CD8⁺ T 细胞克隆增强淋巴细胞清除性化疗诱导的抗肿瘤免疫
Immune Checkpoint Blockade Augments Lymphodepleting Chemotherapy-Induced Antitumor Immunity by Expanding Effector CD8+ T-cell Clones.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Vitamin D supplementation increases objective response rate and prolongs progression-free time in patients with advanced melanoma undergoing anti-PD-1 therapy.
Vitamin D supplementation increases objective response rate and prolongs progression-free time in patients with advanced melanoma undergoing anti-PD-1 therapy.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
我们认为,在晚期黑色素瘤患者接受抗 PD-1 免疫治疗期间,将维生素 D 水平维持在正常范围内应作为标准操作,从而有助于改善治疗结局。
维生素D3是一种具有多效性作用的前激素,包括调节免疫系统功能,并可能影响癌症患者抗PD-1治疗的有效性。根据文献,维生素D影响治疗有效性的潜在机制最可能与TIL(肿瘤浸润淋巴细胞)的数量和活性有关。有数据显示维生素D对调节CD8淋巴细胞活性的细胞有影响。
共纳入200例晚期黑色素瘤患者。所有患者均接受抗PD-1免疫治疗(nivolumab或pembrolizumab)作为一线治疗。在治疗前及治疗期间每12周测量患者血清维生素D水平。部分患者的维生素D是从保存的血清中回顾性检测的。补充组的另一部分则是前瞻性检测的。
维生素D水平低且未补充组的缓解率为36.2%,而基线水平正常或通过补充达到正常水平的组为56.0%(p = .01)。此外,这两组的无进展生存期分别为5.75个月和11.25个月(p = .03)。在总生存期方面,维生素D水平正常组也更有优势(分别为27个月和31.5个月;p = .39)。
Vitamin D3 is a prohormone with pleiotropic effects, including modulating the functions of the immune system and may affect the effectiveness of anti-PD-1 treatment in patients with cancer. According to the literature, the potential mechanism of vitamin D's influence on the effectiveness of therapy is most likely related to the amount and activity of tumor-infiltrating lymphocytes. There are data showing the effect of vitamin D on cells regulating the activity of CD8 lymphocytes.
A total of 200 patients with advanced melanoma were included in the study. All patients received anti-PD-1 immunotherapy (nivolumab or pembrolizumab) as first-line treatment. Serum vitamin D levels were measured in patients both before and every 12 weeks during treatment. Part of the group had vitamin D measured retrospectively from the preserved serum. The other part of the supplementation group was tested prospectively.
The response rate in the group with low vitamin D levels and not supplemented was 36.2%, whereas in the group with normal baseline levels or a normal level obtained with supplementation was 56.0% (p = .01). Moreover, progression-free survival in these groups was 5.75 and 11.25 months, respectively (p = .03). In terms of overall survival, there was also a difference in favor of the group with normal vitamin D levels (27 vs. 31.5 months, respectively; p = .39).
In our opinion, maintaining the vitamin D level within the normal range during anti-PD-1 immunotherapy in advanced melanoma patients should be a standard procedure allowing the improvement of treatment outcomes.
MEMBER ACCOUNT
登录成功会直接打开下一页。