Efficacy and Safety of Low-Dose Cytarabine Combined With Thalidomide in Adult Patients With Untreated LCH

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-70
SponsorCancer Institute and Hospital, Chinese Academy of Medical Sciences

About this trial

Treatment of Adult Patients with Newly Diagnosed Langerhans Cell Histiocytosis (LCH) Using a Low-Dose Cytarabine Combined with Thalidomide Regimen.

Eligibility criteria

Qualifiers

Clearly diagnose and treat adult patients with multisystem or single-system multifocal LCH;

Aged between 18 and 70 years;

Multisystem involvement or single-system multifocal disease;

No prior systemic treatment (patients who have only received local radiotherapy or surgery may be enrolled);

Disqualifiers

Patients with LCH involving the central nervous system;

Single-system single-lesion LCH;

Subjects who have undergone major surgery within 4 weeks prior to the first dose in the study;

Subjects who have received radiotherapy within 4 weeks prior to the first dose in the study; subjects with a history of myocardial infarction within the past year;

Trial design

Treatments tested in this trial

  • Cytarabine (Ara-C)
  • Thalidomide (100mg)

Treatment groups

50 Participants
are divided into 1 treatment group