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Completed

NCT Number: NCT03618238

Anlotinib for Advanced and Refractory Natural Killer /T-cell Lymphoma

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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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Xinhua Hospital

Shanghai, China

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Pathological diagnosis of extranodal natural killer/T-cell lymphoma, nasal type.
  • stage IV disease and resistant to L-asparaginase-based combined chemotherapy.(Definition of L-asparaginase resistance: Progression during treatment or no response to treatment).
  • Eastern Cooperative Oncology Group (ECOG ) performance status 0~3.
  • Preserved organ functions for: absolute neutrophil counter (ANC)>1.0×109/L, Platelet>50×109/L, hemoglobin>80g/L, total bilirubin (TBIL)<2×ULN, alanine transaminase (ALT)<2×ULN, normal serum creatinine,fibrinogen≥1.0g/L, LVEF≥50%.
  • Signed Informed consented.

Exclusion criteria

  • patients with a disease resistant to L-asparaginase but may benefit from a radiotherapy.
  • HIV, hepatitis virus C (HCV), or active hepatitis virus B (HBV) infection with HBV DNA≥105 copies/ml.
  • Significant complications: autoimmune disease, severe infection, or liver cirrhosis, hemophagocytic lymphohistiocytosis, disseminated intravascular coagulation, uncontrolled hypertension or diabetes, hemorrhagic or thrombotic events within 6 months.
  • Mental disorders.
  • Pregnant or lactation
  • Peptic ulcer
  • Enrolled in other trial treatment

Treatment and study plan

Anlotinib

Drug

12 mg daily for continus 14 days every 21 days

Other names: Anlotinib Hydrochloride

Primary outcomes

  1. Overall response rate

    Time frame: 12 weeks after the initiation of anlotinib treatment

    The treatment response will be assessed every 12 weeks.

Secondary outcomes

  1. Treatment-Related Adverse Events as Assessed by CTCAE v4.0

    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.

Sponsors and collaborators

Lead sponsor

Xinhua Hospital, Shanghai Jiao Tong University School of Medicine

Other

Registry information

Official study title

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

Important dates

Study start
2018
Primary completion
2021
Study completion
2021
First posted
Aug 7, 2018
Registry last updated
Sep 14, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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