医学
环磷酰胺
细胞因子释放综合征
氟达拉滨
队列
肉瘤
内科学
免疫学
化疗
免疫疗法
嵌合抗原受体
免疫系统
病理
作者
Meenakshi Hegde,Shoba A. Navai,Christopher DeRenzo,Sujith K. Joseph,Khaled Sanber,Meng‐Fen Wu,A. Gad,Katherine A. Janeway,Matthew Campbell,Dolores Mullikin,Zeid Nawas,Catherine Robertson,Pretty Mathew,Huimin Zhang,Birju Mehta,Raksha Bhat,Angela Major,Ankita Shree,Claudia Gerken,Mamta Kalra
出处
期刊:Nature cancer
[Nature Portfolio]
日期:2024-04-24
卷期号:5 (6): 880-894
被引量:16
标识
DOI:10.1038/s43018-024-00749-6
摘要
In this prospective, interventional phase 1 study for individuals with advanced sarcoma, we infused autologous HER2-specific chimeric antigen receptor T cells (HER2 CAR T cells) after lymphodepletion with fludarabine (Flu) ± cyclophosphamide (Cy): 1 × 108 T cells per m2 after Flu (cohort A) or Flu/Cy (cohort B) and 1 × 108 CAR+ T cells per m2 after Flu/Cy (cohort C). The primary outcome was assessment of safety of one dose of HER2 CAR T cells after lymphodepletion. Determination of antitumor responses was the secondary outcome. Thirteen individuals were treated in 14 enrollments, and seven received multiple infusions. HER2 CAR T cells expanded after 19 of 21 infusions. Nine of 12 individuals in cohorts A and B developed grade 1–2 cytokine release syndrome. Two individuals in cohort C experienced dose-limiting toxicity with grade 3–4 cytokine release syndrome. Antitumor activity was observed with clinical benefit in 50% of individuals treated. The tumor samples analyzed showed spatial heterogeneity of immune cells and clustering by sarcoma type and by treatment response. Our results affirm HER2 as a CAR T cell target and demonstrate the safety of this therapeutic approach in sarcoma. ClinicalTrials.gov registration: NCT00902044 . In this phase 1 trial, Hegde et al. treat 13 individuals with advanced sarcoma with lymphodepletion followed by HER2-specific CAR T cells, which were found to be safe and showed antitumor activity.
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