HRA004715
Title:
A Pilot Study of Lymphodepletion Intensity for Peripheral Blood Mononuclear Cell-Derived Neoantigen-Specific CD8+ T cell Therapy in Patients with Advanced Solid Tumors
Release date:
2023-06-03
Description:
We report a phase 1 study (NCT02959905) of Neo-T therapy with lymphodepletion at various dose intensity in patients with locally advanced or metastatic melanoma and colon cancers that are refractory to standard therapies. The primary end point is safety and the secondary end point is objective response rate (ORR). Results show that the treatment is well tolerated with lymphopenia being the most common adverse event in the highest-intensity lymphodepletion groups. Neo-T infusion-related adverse events are only grade 1-2 in the no lymphodepletion group. The median progression-free survival is 7.1 months (95% CI:3.7-9.8), the median overall survival is 16.8 months (95% CI: 11.9-31.7), and the ORR is 33.3% (3/9) among all groups.
Data Accessibility:   
Controlled access Request Data
BioProject:
Study type:
Disease Study
Disease name:
cancer
Data Access Committee

For each controlled access study, there is a corresponding Data Access Committee(DAC) to determine the access permissions. Access to actual data files is not managed by NGDC.


DAC NO.:
DAC name:
BGI
Contact person:
Li Bo
Email:
libo@genomics.cn
Description:
Data manager
Individuals & samples
Submitter:   Li Bo / libo@genomics.cn
Organization:   BGI-Shenzhen
Submission date:   2023-05-24
Requests:   -