Cutaneous T-cell lymphoma
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) Cases in which UV therapy is being performed and the combined use of bexarotene and UV therapy is started during the registration period. However, if bexarotene has been used, cases that have not been administered for more than 4 weeks since the last administration (2) Cases registered for the first time in this survey (3) Patients who have been treated with UV therapy at a standard frequency (at least once a week) for about one month before the start of concomitant use with bexarotene, and the status of the treatment can be confirmed. (4) Cases in which the consent of the patient was obtained
Exclusion criteria
Exclusion criteria: adult T-cell leukemia/lymphoma
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of photosensitivity and similar skin adverse events and their 95% confidence intervals | — |
Secondary
| Measure | Time frame |
|---|---|
| The incidence of adverse events by System Organ Class(SOC) and Preferred Term(PT) using MedDRA / J and its 95% confidence interval Response rate (CR + PR) and its confidence interval based on the best overall effect of mSWAT. | — |
Contacts
Minophagen Pharmaceutical Co., Ltd.