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Vinorelbine for Recurrent ALCL-2017

Primary Purpose

Anaplastic Large Cell Lymphoma, Vinorelbine

Status
Recruiting
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Vinorelbine
Sponsored by
Children's Cancer Group, China
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anaplastic Large Cell Lymphoma focused on measuring Anaplastic Large Cell Lymphoma, Recurrent, Childhood, Adolescent, Treatment

Eligibility Criteria

undefined - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Children and adolescents with a clear diagnosis of recurrent / progressive ALCL at Shanghai Children's Medical Center or other centers since September 2017 include:

Diagnosed as ALCL, already received first-line treatment, but get disease progression; After receiving ALCL treatment has got CR then diagnosed relapse, need for pathological diagnosis.

Exclusion Criteria:

Patients with other systemic diseases, severe infections or critically illness.

Sites / Locations

  • Shanghai Children's Medical CenterRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Vinorelbine monotherapy treatment

Arm Description

Patients will be treated with Vinorelbine. Four weeks as a course. There are 20 courses in total.

Outcomes

Primary Outcome Measures

Progression Rate
The progression rate will be obtained from the results of simple assessment after one course.
CR/CRu Rate
The CR/CRu rate will be obtained from the results of simple assessment, CT and FDG-PET after two courses.

Secondary Outcome Measures

Progression-free Survival
Overall Survival
Compared with historical data.

Full Information

First Posted
February 17, 2018
Last Updated
September 10, 2022
Sponsor
Children's Cancer Group, China
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1. Study Identification

Unique Protocol Identification Number
NCT03443128
Brief Title
Vinorelbine for Recurrent ALCL-2017
Official Title
Phase II Study of Vinorelbine for Children With Recurrent Anaplastic Large Cell Lymphoma
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Recruiting
Study Start Date
November 2016 (Actual)
Primary Completion Date
December 2024 (Anticipated)
Study Completion Date
September 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Children's Cancer Group, China

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
The purpose of this study is to assess the efficiency and safety of vinorelbine in the treatment of relapsed / advanced ALCL in children and adolescents.
Detailed Description
Anaplastic large cell lymphoma (ALCL) is a rare non-Hodgkin's lymphoma, around 30% patients would get relapse. Vinorelbine(Navelbine) is a third-line treatment option for Hodgkin's disease(HD) after transplantation failed, while both HD and ALCL express CD30. When ALCL recurred, vinblastine monotherapy was used and the 5-year EFS up to 30%, 5-year OS up to 60%. In China vinblastine is unavailable. Vinorelbine is very similar to vinblastine in molecular formula, and is available in China. From November 2016 to March 2017, two patients with recurrent ALCL were recruited in the Department of Hematology and Oncology, Shanghai Children's Medical Center. They received vinorelbine monotherapy and achieved clinical remission (PET CR) at 8 weeks. One patient with bone marrow recurrence showed negative ALK / NPM by PCR . Based on this, the investigators will expand the sample to further investigate the therapeutic efficiency and safety of vinorelbine in children and adolescents with ALCL.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anaplastic Large Cell Lymphoma, Vinorelbine
Keywords
Anaplastic Large Cell Lymphoma, Recurrent, Childhood, Adolescent, Treatment

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Vinorelbine monotherapy treatment
Arm Type
Experimental
Arm Description
Patients will be treated with Vinorelbine. Four weeks as a course. There are 20 courses in total.
Intervention Type
Drug
Intervention Name(s)
Vinorelbine
Intervention Description
During each course, patients will be treated with vinorelbine (25mg/m2/week on weeks 1-3). After 1 course(4 weeks) of vinorelbine, response will be evaluated by simple assessment: clinical symptoms, signs, B ultrasound, chest X-ray, peripheral blood test and bone marrow smear(if needed). After 2 courses, response will be evaluatedy by simple assessment, CT and FDG-PET. The CR/CRu was defined by anatomic tumour shrinkage more than 75% after 2 courses based on CT with negative PET assessment, with negative bone marrow PCR(if needed) and without CNS involvement. Patients who achieved a CR/CRu after two courses either will proceed to stem cell transplantation (SCT) or will receive additional courses of therapy while awaiting SCT. Response was re-evaluated at the end of every 2 courses. Patients with progressive disease at any time during treatment will be removed from protocol therapy.
Primary Outcome Measure Information:
Title
Progression Rate
Description
The progression rate will be obtained from the results of simple assessment after one course.
Time Frame
4 weeks
Title
CR/CRu Rate
Description
The CR/CRu rate will be obtained from the results of simple assessment, CT and FDG-PET after two courses.
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Progression-free Survival
Time Frame
2 years
Title
Overall Survival
Description
Compared with historical data.
Time Frame
2 years
Other Pre-specified Outcome Measures:
Title
Safety statistics: adverse reactions during the trial through NCI CTCAE version 4.0.
Description
The investigators will record the adverse reactions during the trial through NCI CTCAE version 4.0.
Time Frame
2 years

10. Eligibility

Sex
All
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Children and adolescents with a clear diagnosis of recurrent / progressive ALCL at Shanghai Children's Medical Center or other centers since September 2017 include: Diagnosed as ALCL, already received first-line treatment, but get disease progression; After receiving ALCL treatment has got CR then diagnosed relapse, need for pathological diagnosis. Exclusion Criteria: Patients with other systemic diseases, severe infections or critically illness.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yijin Gao, MD
Phone
86-21-38626161
Ext
82064
Email
gaoyijin@scmc.com.cn
First Name & Middle Initial & Last Name or Official Title & Degree
Xingwei Wang, MD
Phone
86-21-38626161
Email
wangxingwei@scmc.com.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yijin Gao, MD
Organizational Affiliation
Shanghai Children's Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Shanghai Children's Medical Center
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200127
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yi-Jin Gao, MD
Phone
0086-21-38626161
Email
gaoyijin@scmc.com.cn
First Name & Middle Initial & Last Name & Degree
Xing-Wei Wang, MD
Phone
0086-21-38626161
Email
wangxingwei@scmc.com.cn

12. IPD Sharing Statement

Learn more about this trial

Vinorelbine for Recurrent ALCL-2017

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