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Precision Diagnosis Directing HDACi Chidamide Target Therapy for Adult ETP-ALL

Primary Purpose

Leukemia, Acute, Leukemia, T Cell, Leukemia, Lymphoblastic

Status
Unknown status
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Chidamide
Dexamethasone
vincristine
Cyclophosphamide
Idarubicin
Pegaspargase
Adriamycin
Methotrexate
6-Mercaptopurine
Etoposide
Cytarabine
Bone marrow aspiration
Intrathecal injection
Radiation therapy
NGS
allogeneic hematopoietic stem cell transplantation
Flow-MRD
FISH
Flow immunophenotyping
Karyotyping
Sponsored by
Nanfang Hospital, Southern Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Leukemia, Acute focused on measuring Early T-cell Precursor, Acute Lymphoblastic Leukemia, Histone Deacetylase Inhibitor, Chidamide

Eligibility Criteria

14 Years - 55 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 14-55 years old;
  • ETP-ALL newly diagnosed;
  • signed written informed consent

Exclusion Criteria:

  • Pregnant women;
  • History of pancreatitis;
  • History of diabetes;
  • History of active peptic ulcer disease in the past 6 months;
  • History of arteriovenous thrombosis in the past 6 months;
  • Severe active infection;
  • Allergic to any drugs in PDT-ETP-ALL.

Sites / Locations

  • Nanfang Hospital, Southern Medical UniversityRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

ETP-ALL

Arm Description

Chidamide at a dose of 10mg/day will be added to PDT-ETP-ALL protocol. The intervention of PDT-ETP-ALL consists of diagnostic test (bone marrow aspiration, flow immunophenotyping, Karyotyping ,FISH, NGS, Flow-MRD, PET-CT scan), induction regimen (chidamide, dexamethasone, vincristine, cyclophosphamide, idarubicin, pegaspargase), consolidation regimen (chidamide, prednisone, cytarabine, methotrexate, cyclophosphamide, etoposide, adriamycin, 6-mercaptopurine, pegaspargase), MRD assessment and maintenance regimen (chidamide, prednisone, vincristine, methotrexate, 6-mercaptopurine), intrathecal injection chemotherapy, radiation therapy (for mediastinum- and/or central nervous system-involved lymphoma/leukemia) and allogeneic hematopoietic stem cell transplantation for patients with donor.

Outcomes

Primary Outcome Measures

Event free survival

Secondary Outcome Measures

Minimum residual disease after induction
CR after Induction Therapy
Death in induction
Adverse events
Relapse
Relapse free survival
Overall survival

Full Information

First Posted
April 21, 2018
Last Updated
June 11, 2018
Sponsor
Nanfang Hospital, Southern Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT03553238
Brief Title
Precision Diagnosis Directing HDACi Chidamide Target Therapy for Adult ETP-ALL
Official Title
An Open-Label, One-Arm, Multi-Site Trial of Precision Diagnosis Directing Histone Deacetylase Inhibitor Chidamide Target Total Therapy for Adult Early T-cell Progenitor Acute Lymphoblastic Leukemia/Lymphoma
Study Type
Interventional

2. Study Status

Record Verification Date
June 2018
Overall Recruitment Status
Unknown status
Study Start Date
February 14, 2016 (Actual)
Primary Completion Date
May 30, 2020 (Anticipated)
Study Completion Date
August 30, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Nanfang Hospital, Southern Medical University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
ETP-ALL is a recently recognized high-risk subgroup and the optimal therapeutic approaches are poorly characterized. Based on the pediatric-inspired, PEG-L-asparaginase-intensified and MRD-directed PDT-ALL-2016 protocol, this open-label, one-arm, multi-site trial is aimed to evaluate the safety and effect of a novel oral histone deacetylase inhibitor chidamide for adult ETP-ALL/LBL in CHINA.
Detailed Description
Early T-cell precursor (ETP) lymphoblastic leukemia (ETP-ALL) is a neoplasm composed of cells committed to the T-cell lineage but with an unique immunophenotype indicating only limited early T differentiation. In the highly orchestrated development of T cell fate specification under physiological condition, the most immature early thymic progenitors (ETPs) retain multilineage potentials. ETP-ALL blasts have a characteristic immunophenotype, with reduced/absent expression of T-lymphoid markers CD1a, CD5, CD8; and positivity for at least one HSC and/or myeloid antigen CD34, CD117, HLA-DR, CD13, CD33, CD11b, CD65. Recent study shed light on the genetic landscape of adult ETP-ALL, which revealed that more than 40% adult ETP-ALL harbored histone modification mutations. Chidamide is a novel oral HDACi with promising activity in non-Hodgkin lymphoma (NHL). Based on the pediatric-inspired, PEG-L-asparaginase-intensified and MRD-directed PDT-ALL-2016 protocol, this open-label, one-arm, multi-site trial is aimed to evaluate the safety and effect of a novel oral histone deacetylase inhibitor chidamide for adult ETP-ALL/LBL. HDACi chidamide at a dose of 10mg/day will be added to ETP-ALL group from induction therapy to consolidation therapy (total courses of chidamide treatment: 5 courses for allo-HSCT after Consolidation Module-3; 12 courses for patients non-allo-HSCT after Consolidation Module 1-9). Primary study endpoint of PDT-ETP-ALL is event-free survival of ETP-ALL group and secondary study endpoints are complete remission and MRD after induction, adverse event and overall survival of ETP-ALL group. Pretreatment: Dexamethasone, -3 to 0d; Induction:VCR: 1, 8, 15, 22; IDA: 1, 8; CTX: 1g/m2, 1, 8; PEG-asp: 2000-2500IU/m2, 1, 15; Dex: 1-24, chidamide: 10mg/d, po, qd. MRD: d14, 24, 45, and pre-allo-HSCT. VLCAM (MRD1/d14>1%): CTX, d25; AraC 2g/m2, q12h, d25, 26; 6-MP: 25-31, PEG-asp: 26; chidamide: 10mg/d, po, qd. Consolidation Module: CM-1: AraC 3g/m2, q12h, 1-2, Dex: 10mg/m2, 1-2, PEG-asp: 2, 6-MP: 1-7. IT: d1, chidamide: 10mg/d, po, qd. CM-2: MTX 5g/m2, 1, Dex: 10mg/m2, 1-2, PEG-asp: 2; 6-MP: 1-7; IT: d1; chidamide: 10mg/d, po, qd. CM-3: CTX 0.5g/m2, 1-3, PEG-asp: 2, Doxorubicin: 40mg/m2, 4, 6-MP: 1-7, IT: d1;chidamide: 10mg/d, po, qd. Allo-HSCT: after CM-3 when donors available. Non-HSCT: finish CM 4-9 and POMP maintenance. CM 4-6: repeat CM 1-3. Re-Induction: after CM-6. CM 7-9: repeat CM1-3. Maintenance: CPOMP-chidamide 10mg/d, po, qd; Pred for 12 months; VCR for 12 months; MTX for 24 months; 6-MP for 24 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Leukemia, Acute, Leukemia, T Cell, Leukemia, Lymphoblastic
Keywords
Early T-cell Precursor, Acute Lymphoblastic Leukemia, Histone Deacetylase Inhibitor, Chidamide

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
70 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
ETP-ALL
Arm Type
Experimental
Arm Description
Chidamide at a dose of 10mg/day will be added to PDT-ETP-ALL protocol. The intervention of PDT-ETP-ALL consists of diagnostic test (bone marrow aspiration, flow immunophenotyping, Karyotyping ,FISH, NGS, Flow-MRD, PET-CT scan), induction regimen (chidamide, dexamethasone, vincristine, cyclophosphamide, idarubicin, pegaspargase), consolidation regimen (chidamide, prednisone, cytarabine, methotrexate, cyclophosphamide, etoposide, adriamycin, 6-mercaptopurine, pegaspargase), MRD assessment and maintenance regimen (chidamide, prednisone, vincristine, methotrexate, 6-mercaptopurine), intrathecal injection chemotherapy, radiation therapy (for mediastinum- and/or central nervous system-involved lymphoma/leukemia) and allogeneic hematopoietic stem cell transplantation for patients with donor.
Intervention Type
Drug
Intervention Name(s)
Chidamide
Other Intervention Name(s)
HDACi chidamide
Intervention Description
Chidamide will be administrated at a dose of 10mg/day in PDT-ETP-ALL protocol.
Intervention Type
Drug
Intervention Name(s)
Dexamethasone
Other Intervention Name(s)
DXM
Intervention Description
Dexamethasone will be added in Pre-phase Regimen, Induction-Regimen, Consolidation-Module of PDT-ETP-ALL protocol.
Intervention Type
Drug
Intervention Name(s)
vincristine
Other Intervention Name(s)
VCR
Intervention Description
Vincristine will be added to Induction-Regimen, Consolidation-Module and Maintenance-Module of PDT-ETP-ALL protocol.
Intervention Type
Drug
Intervention Name(s)
Cyclophosphamide
Other Intervention Name(s)
CTX
Intervention Description
CTX will be added to Induction-Regimen, Consolidation-Module and Maintenance-Module of PDT-ETP-ALL protocol.
Intervention Type
Drug
Intervention Name(s)
Idarubicin
Other Intervention Name(s)
IDA
Intervention Description
IDA will be added to Induction-Regimen and Consolidation-Module of PDT-ETP-ALL protocol.
Intervention Type
Drug
Intervention Name(s)
Pegaspargase
Other Intervention Name(s)
PEG-ASP
Intervention Description
PEG-ASP will be added to Induction-Regimen and Consolidation-Module of PDT-ETP-ALL protocol.
Intervention Type
Drug
Intervention Name(s)
Adriamycin
Other Intervention Name(s)
ADR
Intervention Description
Adriamycin will be added to Consolidation-Module of PDT-ETP-ALL protocol.
Intervention Type
Drug
Intervention Name(s)
Methotrexate
Other Intervention Name(s)
MTX
Intervention Description
Methotrexate will be added to consolidation module of PDT-ETP-ALL protocol.
Intervention Type
Drug
Intervention Name(s)
6-Mercaptopurine
Other Intervention Name(s)
6-MP
Intervention Description
Mercaptopurine will be added to Consolidation-Module and Maintenance-Module of PDT-ETP-ALL protocol.
Intervention Type
Drug
Intervention Name(s)
Etoposide
Other Intervention Name(s)
VP-16
Intervention Description
VP-16 will be added to Consolidation-Module of PDT-ETP-ALL protocol.
Intervention Type
Drug
Intervention Name(s)
Cytarabine
Other Intervention Name(s)
AraC
Intervention Description
AraC will be added to Consolidation-Module of PDT-ETP-ALL protocol.
Intervention Type
Procedure
Intervention Name(s)
Bone marrow aspiration
Other Intervention Name(s)
BM test
Intervention Description
Bone marrow aspiration and additional tests will be performed in all module of PDT-ETP-ALL protocol.
Intervention Type
Procedure
Intervention Name(s)
Intrathecal injection
Other Intervention Name(s)
IT
Intervention Description
Intrathecal injection chemotherapy will be performed in PDT-ETP-ALL protocol.
Intervention Type
Radiation
Intervention Name(s)
Radiation therapy
Other Intervention Name(s)
RT
Intervention Description
Radiation therapy will be performed for mediastinum and/or central nervous system leukemia in PDT-ETP-ALL protocol.
Intervention Type
Genetic
Intervention Name(s)
NGS
Intervention Description
Next-Generation-Sequencing (NGS) will be performed in PDT-ETP-ALL protocol.
Intervention Type
Procedure
Intervention Name(s)
allogeneic hematopoietic stem cell transplantation
Other Intervention Name(s)
allo-HSCT
Intervention Description
Allo-HSCT will be performed for patients with available donor in PDT-ETP-ALL protocol.
Intervention Type
Diagnostic Test
Intervention Name(s)
Flow-MRD
Intervention Description
Flow-MRD will be added to PDT-ETP-ALL for bone marrow and cerebrospinal fluid samples.
Intervention Type
Diagnostic Test
Intervention Name(s)
FISH
Intervention Description
FISH will be performed in PDT-ETP-ALL for bone marrow samples.
Intervention Type
Diagnostic Test
Intervention Name(s)
Flow immunophenotyping
Intervention Description
Flow immunophenotyping will be performed in PDT-ETP-ALL protocol.
Intervention Type
Diagnostic Test
Intervention Name(s)
Karyotyping
Intervention Description
Karyotyping will be performed in PDT-ETP-ALL protocol.
Primary Outcome Measure Information:
Title
Event free survival
Time Frame
3 years
Secondary Outcome Measure Information:
Title
Minimum residual disease after induction
Time Frame
3 months
Title
CR after Induction Therapy
Time Frame
3 years
Title
Death in induction
Time Frame
3 month
Title
Adverse events
Time Frame
3 years
Title
Relapse
Time Frame
3 years
Title
Relapse free survival
Time Frame
3 years
Title
Overall survival
Time Frame
3 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
14 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 14-55 years old; ETP-ALL newly diagnosed; signed written informed consent Exclusion Criteria: Pregnant women; History of pancreatitis; History of diabetes; History of active peptic ulcer disease in the past 6 months; History of arteriovenous thrombosis in the past 6 months; Severe active infection; Allergic to any drugs in PDT-ETP-ALL.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hongsheng Zhou, MD, Ph.D
Phone
+862062787349
Email
zhs1@i.smu.edu.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hongsheng Zhou, MD, PhD
Organizational Affiliation
Nanfang Hospital, Southern Medical University, CHINA
Official's Role
Study Director
Facility Information:
Facility Name
Nanfang Hospital, Southern Medical University
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510515
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hongsheng Zhou, MD, PhD
Phone
+862062787349
Email
zhs1@i.smu.edu.cn

12. IPD Sharing Statement

Citations:
PubMed Identifier
21740230
Citation
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Results Reference
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PubMed Identifier
27069254
Citation
Arber DA, Orazi A, Hasserjian R, Thiele J, Borowitz MJ, Le Beau MM, Bloomfield CD, Cazzola M, Vardiman JW. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia. Blood. 2016 May 19;127(20):2391-405. doi: 10.1182/blood-2016-03-643544. Epub 2016 Apr 11.
Results Reference
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PubMed Identifier
28605290
Citation
Bond J, Graux C, Lhermitte L, Lara D, Cluzeau T, Leguay T, Cieslak A, Trinquand A, Pastoret C, Belhocine M, Spicuglia S, Lheritier V, Lepretre S, Thomas X, Huguet F, Ifrah N, Dombret H, Macintyre E, Boissel N, Asnafi V. Early Response-Based Therapy Stratification Improves Survival in Adult Early Thymic Precursor Acute Lymphoblastic Leukemia: A Group for Research on Adult Acute Lymphoblastic Leukemia Study. J Clin Oncol. 2017 Aug 10;35(23):2683-2691. doi: 10.1200/JCO.2016.71.8585. Epub 2017 Jun 12.
Results Reference
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PubMed Identifier
23103132
Citation
Yu S, Zhou X, Steinke FC, Liu C, Chen SC, Zagorodna O, Jing X, Yokota Y, Meyerholz DK, Mullighan CG, Knudson CM, Zhao DM, Xue HH. The TCF-1 and LEF-1 transcription factors have cooperative and opposing roles in T cell development and malignancy. Immunity. 2012 Nov 16;37(5):813-26. doi: 10.1016/j.immuni.2012.08.009. Epub 2012 Oct 25. Erratum In: Immunity. 2014 Jan 16;40(1):166.
Results Reference
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Precision Diagnosis Directing HDACi Chidamide Target Therapy for Adult ETP-ALL

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