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NCT Number: NCT02764281

MEDA Chemotherapy and Autologous Hematopoietic Stem Cell Transplantation for Stage IV Natural Killer/T-cell Lymphoma

The purpose of this study is to evaluate the efficacy and safety of methotrexate, etoposide, pegaspargase and dexamethasone (MEDA) chemotherapy and autologous hematopoietic stem cell transplantation (Auto-HSCT) 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

Not applicable

Primary location

Shanghai Dong Fang hospital, Shanghai, Shanghai Municipality, China

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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 optimal treatment schedule has not been established. This study is designed with four cycles MEDA chemotherapy, followed by Auto-HSCT for stage IV patients with newly onset, relapsed or refractory diseases. The efficacy and safety of this protocol in the treatment of will be measured.

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 based on WHO 2008 classification of tumors of haematopoietic and lymphoid tissue.

Eastern Cooperative Oncology Group (ECOG ) performance status 0~3.

Stage IV disease with at least one measurable lesion.

Preserved organ functions for: Platelet>50×10*9/L, hemoglobin>80g/L, total bilirubin (TBIL)<3×ULN, alanine transaminase (ALT)<5×ULN, serum creatinine (Cr)<1.5×ULN, fibrinogen≥0.5g/L, LVEF≥50%.

Signed Informed consented.

Exclusion criteria

Relapsed or progressive disease to prior L-asparaginase-based chemotherapy.

Concurrent cancers need surgery or chemotherapy within 6 months.

History of chemotherapy or radiotherapy for other solid cancers within 3 years.

Recent history of radiotherapy of upper-aero-digestive tract within last 3 months.

Significant complications: LVEF≤50%, coagulopathy, autoimmune disease, severe infection, or liver cirrhosis, severe hemophagocytic lymphohistiocytosis.

Mental disorders.

Pregnant or lactation.

HIV, hepatitis virus C (HCV), or active hepatitis virus B (HBV) infection with HBV DNA≥10*5 copies/ml.

History of pancreatitis.

Known history for grade 3/4 allergy to the drugs in chemotherapy regimen.

Enrolled in other trial treatment.

Treatment and study plan

MEDA

Drug

Methotrexate, 3.0g/m2/d iv, day 1

Etoposide, 100mg/m2 iv, day 2 to day 4

Dexamethasone, 40mg/d iv, day 1 to day 4

Pegaspargase, 2500IU/m2/d im, day 4

The MEDA chemotherapy will be repeated every 3 weeks.

Other names: Methotrexate, Etoposide,Dexamethasone,Pegaspargase

Auto-HSCT

Procedure

Auto-HSCT will be performed with patients who responded to the initial MEDA chemotherapy with standard BEAM conditioning regimen.

Primary outcomes

  1. Complete response rate

    Time frame: Day 28 of the 4th course of MEDA chemotherapy

    The complete response rate will be assessed on day 28 of the 4th course of MEDA chemotherapy.

Secondary outcomes

  1. Progression free survival

    Time frame: 2-year

    Progression free survival is the time from entry onto the treatment until lymphoma progression or death of any reason.

  2. Overall response rate

    Time frame: Day 28 of the 4th course of MEDA chemotherapy

    The overall response rate will be assessed on day 28 of the 4th course of MEDA chemotherapy.

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

    Time frame: Day 1 of each course of chemotherapy and then every 3 months for 2 years

    Treatment-Related Adverse Events will be assessed and graded by NCI CTCAE v4.0.

  4. Overall survival

    Time frame: 2-year

    Overall survival is defiend as the time from entry onto the treatment until death of any reason

Sponsors and collaborators

Lead sponsor

Xinhua Hospital, Shanghai Jiao Tong University School of Medicine

Other

Registry information

Official study title

The Efficacy and Safety of Methotrexate, Etoposide, Dexamethasone and Pegaspargase Chemotherapy (MEDA) With Autologous HSCT in the Treatment of Stage IV Natural Killer/T-Cell Lymphoma: A Multicenter, Prospective Study

Important dates

Study start
2015
Primary completion
2020
Study completion
2020
First posted
May 6, 2016
Registry last updated
Apr 27, 2020

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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