This study will evaluate the safety and efficacy of glofitamab as a single agent in Chinese patients with relapsed or refractory (R/R) diffuse large B-cell lymphoma (DLBCL) who have failed two or more lines of systemic therapy.
Study Type
OBSERVATIONAL
Enrollment
20
Glofitamab given in standard dosage
Peking Union Medical College Hospital
Beijing, Beijing Municipality, China
RECRUITINGPFS
Progression-free survival
Time frame: 1 year
OS
overall survival
Time frame: 2 year
CR rate
complete response
Time frame: 6 weeks, 18 weeks, 36 weeks
ORR
overall response rate
Time frame: 6 weeks, 18 weeks, 36 weeks
DOR
duration of response
Time frame: 2 year
AE
Rate and type of adverse events (AEs) and serious adverse events (SAEs)
Time frame: 2 year
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