决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Oral Toxicities of PSMA-Targeted Immunotherapies for The Management of Prostate Cancer.
Oral Toxicities of PSMA-Targeted Immunotherapies for The Management of Prostate Cancer.
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。
接受 PSMA 靶向免疫疗法治疗的前列腺癌患者可能出现各种短期和长期脱靶在靶口腔毒性,包括口干症和味觉障碍,这些可能影响生活质量。本研究为未来更大样本量的前瞻性研究奠定了基础,也有助于肿瘤科医生在管理接受靶向免疫治疗的前列腺癌患者时熟悉常见的口腔毒性。此外,我们强调口腔医学会诊对于全面口腔检查和口腔并发症管理的重要性。
前列腺特异性膜抗原(PSMA)靶向放射性核素治疗已被证明会导致口干,但PSMA靶向免疫治疗的口腔表现尚未得到广泛研究。本研究旨在描述和量化PSMA靶向免疫治疗(双特异性抗体或CAR-T 细胞疗法)在转移性去势抵抗性前列腺癌治疗中的口腔表现。
我们对2020年至2023年间在单一机构癌症中心就诊的患者接受PSMA靶向免疫治疗后的口腔毒性进行了回顾性分析。采用描述性统计对数据进行总结。
在2020年至2023年间共19例接受PSMA靶向免疫治疗的患者中,9例(47%)出现了以下口腔毒性:口干症(n = 6;32%)、黏膜炎(n = 2;10%)、味觉障碍、咽喉干燥和牙齿敏感各(n = 1;5%)。未在任何患者中观察到口腔感染,如念珠菌病和单纯疱疹。黏膜炎通过盐水漱口进行管理,并在发病后数月内消退。在数据收集时报告口干的患者中,口干症在所有患者中持续存在(中位时间:306天,范围:98-484天),尽管接受了唾液刺激剂治疗(n = 5;83%)。味觉障碍也持续存在,尽管未接受专门治疗。
We performed a retrospective analysis of the oral toxicities of PSMA-targeted immunotherapies of the patients seen at a single institution's cancer center between 2020 and 2023. Descriptive statistics were used to summarize the data.
In a total of 19 patients treated with PSMA-targeted immunotherapies between 2020 and 2023, 9 patients (47%) experienced the following oral toxicities: xerostomia (n = 6; 32%), mucositis (n = 2; 10%), dysgeusia, dry throat and teeth sensitivity in (n = 1 each; 5%), respectively. Oral infections, such as candidiasis and herpes simplex, were not observed in any patients. Mucositis was managed with salt rinses and resolved within few months from onset. Xerostomia persisted in all the patients (median: 306 days, range: 98-484 days) among those who reported dry mouth at the time of data collection, despite treatment with salivary stimulants (n = 5; 83%). Dysgeusia was also persistent, although it was not specifically treated.
Patients treated with PSMA-targeted immunotherapies for prostate cancer can present with various short-term and long-term off-tumor on-target oral toxicities including xerostomia and dysgeusia that may affect quality of life. This study serves as a foundation to future prospective studies with a larger sample size and also helps oncologists managing prostate cancer patients with targeted immunotherapies to familiarize common oral toxicities. Furthermore, we emphasize the importance of oral medicine consultation for a comprehensive oral examination and management of oral complications.
MEMBER ACCOUNT
登录成功会直接打开下一页。