Xinhua Hospital
Shanghai, China
NCT Number: NCT03618238
The purpose of this study is to evaluate the efficacy and safety of anlotinib in patients with stage IV extranodal natural killer/T-cell lymphoma, nasal type.
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Notify Me18 year–70 year
All sexes
Interventional
Phase 2
Shanghai, China
Extranodal natural killer/T-cell lymphoma (ENKTCL), nasal type, is a rare subtype of non-Hodgkin lymphoma (NHL) with relatively high incidence in China. L-asparaginase based chemotherapy improved overall response and prolonged the long-term survival for patients with stage IV. But the treatment for the patients with advanced disease and resistant to L-asparaginase based chemotherapy has not been established. The overall survival for these patients are very poor. This study is designed to evaluate the efficacy and safety of anlotinib in patients with stage IV ENKTCL and refractory to L-asparaginase based chemotherapy.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
12 mg daily for continus 14 days every 21 days
Other names: Anlotinib Hydrochloride
Time frame: 12 weeks after the initiation of anlotinib treatment
The treatment response will be assessed every 12 weeks.
Time frame: Day 1 of each course and then every 3 months for 2 years
Treatment-Related Adverse Events will be assessed and graded by NCI CTCAE v4.0.
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
Other
A Pilot Study of Anlotinib for the Evaluation of Safety and Efficacy in Patients With Stage IV Natural Killer/T-cell Lymphoma and Refractory to L-asparaginase Based Chemotherapy
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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