Ataxia-TelangiectasiaNCT00187057
Study for Treatment of Cancer in Children With Ataxia-telangiectasia
A study testing vinblastine, vincristine, prednisone, daunorubicin, doxorubicin, methotrexate, cyclophosphamide, L-asparaginase and etoposide, cytarabine, mercaptopurine in people with Ataxia-Telangiectasia, run by St. Jude Children's Research Hospital at 1 site in United States.
Trial summary
This is a pilot/feasibility study designed to investigate the feasibility of treating children with Ataxia-Telangiectasia (A-T) and cancer with regimens nearly as intense as non-A-T patients with cancer would receive. Read more about this study
- Who is it for?
- Ages Up to 10 years
- Conditions the study is for
- Ataxia-Telangiectasia
- What is being tested?
- vinblastine, vincristine, prednisone, daunorubicin, doxorubicin, methotrexate, cyclophosphamide, L-asparaginase and etoposide, cytarabine, mercaptopurine
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 6 participants
- Where
- 1 siteUnited States
- Study dates
- Sep 2002to Jun 2013
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Up to 10 years
- All sexes
- No healthy volunteers
- Child
Who may be able to join
- Patient must have a diagnosis of Ataxia-Telangiectasia (A-T).
- Patient must have a diagnosis of either acute lymphoblastic leukemia (ALL) or lymphoma (non-Hodgkin lymphoma or Hodgkin's disease).
- Patients with other malignancies (solid tumors, rare malignancies, or relapsed hematopoietic malignancies) will be eligible for the biologic studies of this protocol; they will receive best clinical management chemotherapy.
- Patients do not have to be previously untreated. If prior chemotherapy has already started (up through induction), therapy will be continued according to protocol at a clinically appropriate time point.
Who cannot join
- Patients who do not have a diagnosis of Ataxia Telangiectasia (A-T).
Trial locations and contacts
1 site in 1 country.
United States1 site
St. Jude Children's Research Hospital
Memphis, Tennessee, 38105
About this study
Official title: Pilot Study I for Treatment of Cancer in Children With Ataxia-Telangiectasia
This is a pilot/feasibility study designed to investigate the feasibility of treating children with Ataxia-Telangiectasia (A-T) and cancer with regimens nearly as intense as non-A-T patients with cancer would receive.
Read the detailed description
Approximately 10-30% of A-T patients will develop a malignancy during their lifetime. The vast majority of these cancers are of lymphoid origin. There is no consensus regarding the optimal strategy for treating children with A-T who develop hematopoietic malignancies. Historically, many of these children have been treated with therapy that is much less intensive than the conventional approach for non-A-T patients with similar malignancies during the corresponding treatment era. Although these less intensive approaches may have stemmed from perceptions that these children would not tolerate intensive therapy, there is in fact no data to suggest that these children cannot tolerate intensive therapy. However, it is clear that children with A-T require a modification in certain components of intensive therapy.
To provide children with A-T and either ALL or malignant lymphoma the best chance for a cure, we propose to use modern therapeutic strategies with minimal modifications which address the unique toxicity profile encountered in treating children with A-T.
Secondary objectives include:
- To clinically and biologically characterize the malignancies occurring in children with A-T (usually malignant lymphoma or ALL). This will include in vitro drug sensitivity screening.
- To study chemotherapy-induced DNA damage in children with A-T.
Detailed Description of Treatment Plan:
- Acute Lymphoblastic Leukemia (ALL) Low Risk:
Induction:
Prednisone 40 mg/m2/day PO days 1-28
Vinblastine 6 mg/m2/dose IV day 8
Vincristine 1.5 mg/m2/dose days 1, 15
Daunomycin 20 mg/m2/week IV days 1,15
Asparaginase 10,000 U/m2/dose IM days 2, 4, 6, 8, 10, 12
VP-16 225 mg/m2/dose Days 22, 25, 29
Ara-C 300 mg/m2/dose Days 22, 25, 29
All patients will receive CNS therapy with triple intrathecal therapy on days 1, 22 and 43 of induction treatment, dose age adjusted.
Consolidation:
Methotrexate 2 mg/m2 IV day 43 and 50 and mercaptopurine 75 mg/m2 days 43-56.
Continuation therapy (120 weeks):
Week:
- 6-MP + MTX
- 6-MP + MTX
- 6-MP + MTX
- Dex + VCR
- 6-MP + MTX
- 6-MP + MTX
- 6-MP + HDMTX
- Dex + VCR
- 6-MP + MTX
- 6-MP + MTX
- 6-MP + MTX
- Dex + VCR
- 6-MP + MTX
- 6-MP + MTX
- 6-MP + HDMTX
This sequence will be repeated through week 52 after which 6-MP + MTX will be given weekly to complete 120 weeks. IT MHA (MTX, hydrocortisone, Ara-C) on weeks 1, 2, 7, and 15 and then every 4-8 weeks depending on CNS status.
Dosages, Schedules and Routes:
6-MP 75 mg/m2 PO; daily x 7
MTX 40 mg/m2 IM or IV; q (every) week;
Dex 6 mg/m2 PO; in 3 divided doses daily x 7
VCR 1.5 mg/m2 IV (max. 2.0 mg)
HDMTX 2 g/m2 IV over 2 hours, every 8 weeks
Reinduction:
Reinduction therapy (weeks 16-21). Reinduction therapy (same as initial induction treatment minus dose 2 and 3 of VP16 +ara-C and minus day 22 intrathecal therapy) will be given after bone marrow examination on week 15 confirms complete remission.
- Acute Lymphoblastic Leukemia (ALL) - High Risk
Induction:
Prednisone 40 mg/m2/day PO) divided in 3 doses days 1-28
Vinblastine 6 mg/m2/dose IV day 8
Vincristine 1.5 mg/m2/dose days 1, 15
Daunomycin 20 mg/m2/week IV days 1, 15
Asparaginase 10,000 U/m2/dose IM days 2, 4, 6, 8, 10, 12, (15, 17, 19)
VP16 225 mg/m2/dose days 22, 25, 29
Ara-C 300 mg/m2/dose days 22,25,29
All patients will receive triple IT therapy on days 1, 22 and 43 of induction with additional IT therapy on days 8 and 15 if CNS leukemia (CNS 2 or CNS 3) is present at diagnosis. If required, for patients with CNS 2 and 3 at diagnosis, IT therapy will continue until 2 consecutive CSF studies are normal (i.e., days 29 and 36).
Consolidation:
HDMTX 2 mg/m2 IV day 43 and 50
6 MP 75 mg/m2 PO days 43-56
Continuation Therapy (120 weeks):
Week:
- Dex + VCR
- VP-16 + CTX
- 6-MP + MTX
- MTX + Ara-C
- Dex + VCR
- VP-16 + CTX
- 6-MP + HDMTX
- 6-MP + MTX
- Dex + VCR
- VP-16 + CTX
- 6-MP + MTX
- MTX + Ara-C
- Dex + VCR
- VP-16 + CTX
- 6-MP + HDMTX
These sequences will be repeated through week 52, after which 6MP/MTX will be given weekly to complete 120 weeks.
IT MHA (MTX, hydrocortisone, Ara-C) on weeks 1, 2, 7, and 15 and then every 4-8 weeks depending on CNS status and risk status.
Dosages, Schedules and Routes:
VP 16 225 mg/m2 IV once a week
Cyclophosphamide 300 mg/m2 IV (with MESNA) once a week in addition to the 6 hour IV hydration
6-MP 75 mg/m2 PO; daily x 7
MTX 40 mg/m2 IM or IV once a week
Ara-C 300 mg/m2 IV push; once a week
Dex 8 mg/m2/day PO; in 3 divided doses daily x 7
VCR 1.5 mg/m2 IV push (max. 2.0 mg)
HDMTX 2 g/m2 IV over 2 hours; every 8 weeks x 7
- B-Cell Non-Hodgkins Lymphoma
Overview - the chemotherapy regimen used varies with grouping based on extent of disease
Group A
Induction (COPAD x 2 cycles):
Cyclophosphamide 500 mg/m2/day (divided every 12 hour) IV (with MESNA) Day 1, 2, 3
Vincristine 2.0 mg/m2 IV Day 1
Vinblastine 6 mg/m2 IV Day 6
Prednisone 60 mg/m2/day (bid) PO Day 1-5
Adriamycin 50 mg/m2 (over 6 hrs) IV Day 1
G-CSF 5 mcg/kg/day until count recovery.
Group B
COP Induction:
Cyclophosphamide 300 mg/m2 IV (divided every 12 hours) IV (with MESNA) Day 1
Vincristine 1.0 mg/m2 IV Day 1
Prednisone 60 mg/m2/day (divided bid) PO days 1-7
CNS Therapy Intrathecal Day 1 - dose age adjusted
COPAD-M3 Induction x 2 cycles:
Vinblastine 6 mg/m2 IV Day 1
HD MTX 3 mg/m2 IV over 3 hours Day 1 with leucovorin rescue
CNS Therapy intrathecal each age adjusted Day 2, 6
Cyclophosphamide 500 mg/m2/day (second course 1 mg/m2/day) IV (with MESNA) Day 2, 3, 4
Adriamycin 50 mg/m2 IV Day 2
Prednisone 60 mg/m2 (divided bid) PO Day 1-5
G-CSF 5 mcg/kg/day until count recovery
CYM Consolidation x 2 cycles:
HD MTX 3 mg/m2 IV over 3 hours Day 1 with leucovorin rescue
Ara-C 100 mg/m2/day CI/IV (x 5 days) Day 2-6
CNS Therapy intrathecal each age adjusted Day 2 and 7
Maintenance:
Prednisone 60 mg/m2/day (divided bid) PO Day 1-5
HDMTX 3 mg/m2 IV over 3 hours Day 1 with leucovorin rescue
CNS Therapy intrathecal each age adjusted Day 2
Cyclophosphamide 500 mg/m2/day IV (with MESNA) Day 2, 3
Adriamycin 50 mg/m2 IV Day 3
Vincristine 2 mg/m2 IV Day 1
G-CSF 5 mcg/kg/day until count recovery
- Limited Stage Non-Hodgkins Lymphoma
Induction:
Vincristine 2 mg/m2 IV days 1, 22 (maximum dose 2 mg)
Vinblastine 6 mg/m2 IV, day 8
Prednisone 40 mg/m2/day in 3 divided doses x 28 days
Adriamycin 30 mg/m2/day IV over one hour days 1 and 22
Cyclophosphamide 750 mg/m2/day IV days 1 and 22
Triple IT chemotherapy for participants with head and neck primary tumors on days 1, 8, 22. Each dose age adjusted.
Consolidation - start day 43:
Adriamycin 30 mg/m2 by IV
Cyclophosphamide 750 mg/m2
Prednisone 40 mg/m2 in 3 divided doses x 5 days
Vincristine 2.0 mg/m2 (max. 2.0 mg) by IV
Triple IT chemotherapy for head and neck primaries on days 43 and 64.
Maintenance:
Maintenance chemotherapy will be administered only to patients with lymphoblastic lymphoma and will consist of 24 weeks of chemotherapy with oral daily 6-MP and weekly oral methotrexate (and TIT every 6 weeks for patients with head and neck primaries) after induction/consolidation.
- Hodgkins Disease
Participants with favorable disease will receive VAMP chemotherapy:
VAMP chemotherapy doses and schedule:
Vinblastine 6 mg/m2, IV day 1, 15 (maximum dosage: 10 mg)
Adriamycin 25 mg/m2, IV day 1, 15
Methotrexate 20 mg/m2, IV day 1, 15
Prednisone 40 mg/m2 PO day 1-14 divided into 3 daily doses
Repeat cycle every 28 days, total number of cycles = 6 (NO RADIATION THERAPY)
Participants with unfavorable disease will receive VAMP and COP:
VAMP chemotherapy doses (cycles 1, 3, 5, 7)
Vinblastine 6 mg/m2 IV day 1, 15
Adriamycin 25 mg/m2 IV day 1,15
Methotrexate 20 mg/m2 IV day 1, 15
Prednisone 40 mg/m2 (divided into 3 daily doses) PO day 1-14
COP chemotherapy doses (cycles 2, 4, 6, 8)
Cyclophosphamide 600 mg/m2 IV (with MESNA) day 1, 8
Vincristine 1.4 mg/m2 IV day 1,8 (max dose 2 mg)
Procarbazine 100 mg/m2 PO day 1-14
(NO RADIATION THERAPY)
- Conditions
- Ataxia-Telangiectasia
- Being tested
- vinblastine, vincristine, prednisone, daunorubicin, doxorubicin, methotrexate, cyclophosphamide, L-asparaginase, etoposide, cytarabine, mercaptopurine, dexamethasone, procarbazine, chemotherapy, intrathecal chemotherapy, steroid therapy
- Keywords
- Ataxia, alphafetoprotein
- Medical subject headings
- Ataxia Telangiectasia, Ataxia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
vinblastine, vincristine, prednisone, daunorubicinDrug
See Detailed Description section for details of treatment interventions.
doxorubicin, methotrexate, cyclophosphamide, L-asparaginaseDrug
See Detailed Description section for details of treatment interventions.
etoposide, cytarabine, mercaptopurineDrug
See Detailed Description section for details of treatment interventions.
dexamethasone, procarbazineDrug
See Detailed Description section for details of treatment interventions.
chemotherapy, intrathecal chemotherapy, steroid therapyProcedure or surgery
See Detailed Description section for details of treatment interventions.
| Study group | Role | What they receive |
|---|---|---|
| 1 | Other | Acute Lymphoblastic Leukemia (ALL) Low Risk Receives: Drug: vinblastine, vincristine, prednisone, daunorubicin; Drug: doxorubicin, methotrexate, cyclophosphamide, L-asparaginase; Drug: etoposide, cytarabine, mercaptopurine; Drug: dexamethasone, procarbazine; Procedure: chemotherapy, intrathecal chemotherapy, steroid therapy |
| 2 | Other | Acute Lymphoblastic Leukemia (ALL) - High Risk Receives: Drug: vinblastine, vincristine, prednisone, daunorubicin; Drug: doxorubicin, methotrexate, cyclophosphamide, L-asparaginase; Drug: etoposide, cytarabine, mercaptopurine; Drug: dexamethasone, procarbazine; Procedure: chemotherapy, intrathecal chemotherapy, steroid therapy |
| 3A | Other | B-Cell Non-Hodgkins Lymphoma (Group A) Receives: Drug: vinblastine, vincristine, prednisone, daunorubicin; Drug: doxorubicin, methotrexate, cyclophosphamide, L-asparaginase; Drug: etoposide, cytarabine, mercaptopurine; Drug: dexamethasone, procarbazine; Procedure: chemotherapy, intrathecal chemotherapy, steroid therapy |
| 3B | Other | B-Cell Non-Hodgkins Lymphoma (Group B) Receives: Drug: vinblastine, vincristine, prednisone, daunorubicin; Drug: doxorubicin, methotrexate, cyclophosphamide, L-asparaginase; Drug: etoposide, cytarabine, mercaptopurine; Drug: dexamethasone, procarbazine; Procedure: chemotherapy, intrathecal chemotherapy, steroid therapy |
| 4 | Other | Hodgkins Disease Receives: Drug: vinblastine, vincristine, prednisone, daunorubicin; Drug: doxorubicin, methotrexate, cyclophosphamide, L-asparaginase; Drug: etoposide, cytarabine, mercaptopurine; Drug: dexamethasone, procarbazine; Procedure: chemotherapy, intrathecal chemotherapy, steroid therapy |
What is being measured
The primary outcome is the main question the study is designed to answer.
To determine the feasibility of delivering modified intensive chemotherapy to children with A-T who present with cancer.
Measured: The completion of treatment
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted16 Sep 2005 (estimated)
- Study startSep 2002
- Primary completionAug 2006
- Study completionJun 2013
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Ataxia-TelangiectasiaStudies of the same condition, open and under way.
- More trials run by St. Jude Children's Research HospitalThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 6 participants (actual)
Sponsor and investigators
- Lead sponsor
- St. Jude Children's Research Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- John T. Sandlund, MD, Principal investigator, St. Jude Children's Research Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00187057
- Sponsor's protocol ID
- AT-1
- Status last verified
- Aug 2013
- First submitted
- 12 Sep 2005
- Last updated
- 27 Aug 2015
- Results posted
- No
- Data monitoring committee
- No
Publications
Sandlund JT, Kastan MB, Kennedy W, Behm F, Entrekin E, Pui CH, Kalwinsky DT, Raimondi SC. A subtle t(3;8) results in plausible juxtaposition of MYC and BCL6 in a child with Burkitt lymphoma/leukemia and ataxia-telangiectasia. Cancer Genet Cytogenet. 2006 Jul 1;168(1):69-72. doi: 10.1016/j.cancergencyto.2005.12.013.
PubMed 16772123
Study at a glance
From the registry record, last updated by the sponsor on 27 Aug 2015. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Pilot Study I for Treatment of Cancer in Children With Ataxia-Telangiectasia
- ClinicalTrials.gov ID
- NCT00187057
- Acronym / sponsor ID
- AT-1
- Conditions
- Ataxia-Telangiectasia
- Keywords
- Ataxia, alphafetoprotein
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 6 participants (actual)
- Lead sponsor
- St. Jude Children's Research HospitalUniversity, hospital or other
- Collaborators
- Children's Hospital of Philadelphia, National Cancer Institute (NCI)
- Study start
- Sep 2002
- Primary completion
- Aug 2006 (actual)
- Study completion
- Jun 2013 (actual)
- First posted
- 16 Sep 2005 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This is a pilot/feasibility study designed to investigate the feasibility of treating children with Ataxia-Telangiectasia (A-T) and cancer with regimens nearly as intense as non-A-T patients with cancer would receive.
Detailed description
Approximately 10-30% of A-T patients will develop a malignancy during their lifetime. The vast majority of these cancers are of lymphoid origin. There is no consensus regarding the optimal strategy for treating children with A-T who develop hematopoietic malignancies. Historically, many of these children have been treated with therapy that is much less intensive than the conventional approach for non-A-T patients with similar malignancies during the corresponding treatment era. Although these less intensive approaches may have stemmed from perceptions that these children would not tolerate intensive therapy, there is in fact no data to suggest that these children cannot tolerate intensive therapy. However, it is clear that children with A-T require a modification in certain components of intensive therapy.
To provide children with A-T and either ALL or malignant lymphoma the best chance for a cure, we propose to use modern therapeutic strategies with minimal modifications which address the unique toxicity profile encountered in treating children with A-T.
Secondary objectives include:
- To clinically and biologically characterize the malignancies occurring in children with A-T (usually malignant lymphoma or ALL). This will include in vitro drug sensitivity screening.
- To study chemotherapy-induced DNA damage in children with A-T.
Detailed Description of Treatment Plan:
- Acute Lymphoblastic Leukemia (ALL) Low Risk:
Induction:
Prednisone 40 mg/m2/day PO days 1-28
Vinblastine 6 mg/m2/dose IV day 8
Vincristine 1.5 mg/m2/dose days 1, 15
Daunomycin 20 mg/m2/week IV days 1,15
Asparaginase 10,000 U/m2/dose IM days 2, 4, 6, 8, 10, 12
VP-16 225 mg/m2/dose Days 22, 25, 29
Ara-C 300 mg/m2/dose Days 22, 25, 29
All patients will receive CNS therapy with triple intrathecal therapy on days 1, 22 and 43 of induction treatment, dose age adjusted.
Consolidation:
Methotrexate 2 mg/m2 IV day 43 and 50 and mercaptopurine 75 mg/m2 days 43-56.
Continuation therapy (120 weeks):
Week:
- 6-MP + MTX
- 6-MP + MTX
- 6-MP + MTX
- Dex + VCR
- 6-MP + MTX
- 6-MP + MTX
- 6-MP + HDMTX
- Dex + VCR
- 6-MP + MTX
- 6-MP + MTX
- 6-MP + MTX
- Dex + VCR
- 6-MP + MTX
- 6-MP + MTX
- 6-MP + HDMTX
This sequence will be repeated through week 52 after which 6-MP + MTX will be given weekly to complete 120 weeks. IT MHA (MTX, hydrocortisone, Ara-C) on weeks 1, 2, 7, and 15 and then every 4-8 weeks depending on CNS status.
Dosages, Schedules and Routes:
6-MP 75 mg/m2 PO; daily x 7
MTX 40 mg/m2 IM or IV; q (every) week;
Dex 6 mg/m2 PO; in 3 divided doses daily x 7
VCR 1.5 mg/m2 IV (max. 2.0 mg)
HDMTX 2 g/m2 IV over 2 hours, every 8 weeks
Reinduction:
Reinduction therapy (weeks 16-21). Reinduction therapy (same as initial induction treatment minus dose 2 and 3 of VP16 +ara-C and minus day 22 intrathecal therapy) will be given after bone marrow examination on week 15 confirms complete remission.
- Acute Lymphoblastic Leukemia (ALL) - High Risk
Induction:
Prednisone 40 mg/m2/day PO) divided in 3 doses days 1-28
Vinblastine 6 mg/m2/dose IV day 8
Vincristine 1.5 mg/m2/dose days 1, 15
Daunomycin 20 mg/m2/week IV days 1, 15
Asparaginase 10,000 U/m2/dose IM days 2, 4, 6, 8, 10, 12, (15, 17, 19)
VP16 225 mg/m2/dose days 22, 25, 29
Ara-C 300 mg/m2/dose days 22,25,29
All patients will receive triple IT therapy on days 1, 22 and 43 of induction with additional IT therapy on days 8 and 15 if CNS leukemia (CNS 2 or CNS 3) is present at diagnosis. If required, for patients with CNS 2 and 3 at diagnosis, IT therapy will continue until 2 consecutive CSF studies are normal (i.e., days 29 and 36).
Consolidation:
HDMTX 2 mg/m2 IV day 43 and 50
6 MP 75 mg/m2 PO days 43-56
Continuation Therapy (120 weeks):
Week:
- Dex + VCR
- VP-16 + CTX
- 6-MP + MTX
- MTX + Ara-C
- Dex + VCR
- VP-16 + CTX
- 6-MP + HDMTX
- 6-MP + MTX
- Dex + VCR
- VP-16 + CTX
- 6-MP + MTX
- MTX + Ara-C
- Dex + VCR
- VP-16 + CTX
- 6-MP + HDMTX
These sequences will be repeated through week 52, after which 6MP/MTX will be given weekly to complete 120 weeks.
IT MHA (MTX, hydrocortisone, Ara-C) on weeks 1, 2, 7, and 15 and then every 4-8 weeks depending on CNS status and risk status.
Dosages, Schedules and Routes:
VP 16 225 mg/m2 IV once a week
Cyclophosphamide 300 mg/m2 IV (with MESNA) once a week in addition to the 6 hour IV hydration
6-MP 75 mg/m2 PO; daily x 7
MTX 40 mg/m2 IM or IV once a week
Ara-C 300 mg/m2 IV push; once a week
Dex 8 mg/m2/day PO; in 3 divided doses daily x 7
VCR 1.5 mg/m2 IV push (max. 2.0 mg)
HDMTX 2 g/m2 IV over 2 hours; every 8 weeks x 7
- B-Cell Non-Hodgkins Lymphoma
Overview - the chemotherapy regimen used varies with grouping based on extent of disease
Group A
Induction (COPAD x 2 cycles):
Cyclophosphamide 500 mg/m2/day (divided every 12 hour) IV (with MESNA) Day 1, 2, 3
Vincristine 2.0 mg/m2 IV Day 1
Vinblastine 6 mg/m2 IV Day 6
Prednisone 60 mg/m2/day (bid) PO Day 1-5
Adriamycin 50 mg/m2 (over 6 hrs) IV Day 1
G-CSF 5 mcg/kg/day until count recovery.
Group B
COP Induction:
Cyclophosphamide 300 mg/m2 IV (divided every 12 hours) IV (with MESNA) Day 1
Vincristine 1.0 mg/m2 IV Day 1
Prednisone 60 mg/m2/day (divided bid) PO days 1-7
CNS Therapy Intrathecal Day 1 - dose age adjusted
COPAD-M3 Induction x 2 cycles:
Vinblastine 6 mg/m2 IV Day 1
HD MTX 3 mg/m2 IV over 3 hours Day 1 with leucovorin rescue
CNS Therapy intrathecal each age adjusted Day 2, 6
Cyclophosphamide 500 mg/m2/day (second course 1 mg/m2/day) IV (with MESNA) Day 2, 3, 4
Adriamycin 50 mg/m2 IV Day 2
Prednisone 60 mg/m2 (divided bid) PO Day 1-5
G-CSF 5 mcg/kg/day until count recovery
CYM Consolidation x 2 cycles:
HD MTX 3 mg/m2 IV over 3 hours Day 1 with leucovorin rescue
Ara-C 100 mg/m2/day CI/IV (x 5 days) Day 2-6
CNS Therapy intrathecal each age adjusted Day 2 and 7
Maintenance:
Prednisone 60 mg/m2/day (divided bid) PO Day 1-5
HDMTX 3 mg/m2 IV over 3 hours Day 1 with leucovorin rescue
CNS Therapy intrathecal each age adjusted Day 2
Cyclophosphamide 500 mg/m2/day IV (with MESNA) Day 2, 3
Adriamycin 50 mg/m2 IV Day 3
Vincristine 2 mg/m2 IV Day 1
G-CSF 5 mcg/kg/day until count recovery
- Limited Stage Non-Hodgkins Lymphoma
Induction:
Vincristine 2 mg/m2 IV days 1, 22 (maximum dose 2 mg)
Vinblastine 6 mg/m2 IV, day 8
Prednisone 40 mg/m2/day in 3 divided doses x 28 days
Adriamycin 30 mg/m2/day IV over one hour days 1 and 22
Cyclophosphamide 750 mg/m2/day IV days 1 and 22
Triple IT chemotherapy for participants with head and neck primary tumors on days 1, 8, 22. Each dose age adjusted.
Consolidation - start day 43:
Adriamycin 30 mg/m2 by IV
Cyclophosphamide 750 mg/m2
Prednisone 40 mg/m2 in 3 divided doses x 5 days
Vincristine 2.0 mg/m2 (max. 2.0 mg) by IV
Triple IT chemotherapy for head and neck primaries on days 43 and 64.
Maintenance:
Maintenance chemotherapy will be administered only to patients with lymphoblastic lymphoma and will consist of 24 weeks of chemotherapy with oral daily 6-MP and weekly oral methotrexate (and TIT every 6 weeks for patients with head and neck primaries) after induction/consolidation.
- Hodgkins Disease
Participants with favorable disease will receive VAMP chemotherapy:
VAMP chemotherapy doses and schedule:
Vinblastine 6 mg/m2, IV day 1, 15 (maximum dosage: 10 mg)
Adriamycin 25 mg/m2, IV day 1, 15
Methotrexate 20 mg/m2, IV day 1, 15
Prednisone 40 mg/m2 PO day 1-14 divided into 3 daily doses
Repeat cycle every 28 days, total number of cycles = 6 (NO RADIATION THERAPY)
Participants with unfavorable disease will receive VAMP and COP:
VAMP chemotherapy doses (cycles 1, 3, 5, 7)
Vinblastine 6 mg/m2 IV day 1, 15
Adriamycin 25 mg/m2 IV day 1,15
Methotrexate 20 mg/m2 IV day 1, 15
Prednisone 40 mg/m2 (divided into 3 daily doses) PO day 1-14
COP chemotherapy doses (cycles 2, 4, 6, 8)
Cyclophosphamide 600 mg/m2 IV (with MESNA) day 1, 8
Vincristine 1.4 mg/m2 IV day 1,8 (max dose 2 mg)
Procarbazine 100 mg/m2 PO day 1-14
(NO RADIATION THERAPY)
Study design
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 5
| Arm | Type | Receives |
|---|---|---|
| 1 | Other | Drug: vinblastine, vincristine, prednisone, daunorubicin, Drug: doxorubicin, methotrexate, cyclophosphamide, L-asparaginase, Drug: etoposide, cytarabine, mercaptopurine, Drug: dexamethasone, procarbazine, Procedure: chemotherapy, intrathecal chemotherapy, steroid therapyAcute Lymphoblastic Leukemia (ALL) Low Risk |
| 2 | Other | Drug: vinblastine, vincristine, prednisone, daunorubicin, Drug: doxorubicin, methotrexate, cyclophosphamide, L-asparaginase, Drug: etoposide, cytarabine, mercaptopurine, Drug: dexamethasone, procarbazine, Procedure: chemotherapy, intrathecal chemotherapy, steroid therapyAcute Lymphoblastic Leukemia (ALL) - High Risk |
| 3A | Other | Drug: vinblastine, vincristine, prednisone, daunorubicin, Drug: doxorubicin, methotrexate, cyclophosphamide, L-asparaginase, Drug: etoposide, cytarabine, mercaptopurine, Drug: dexamethasone, procarbazine, Procedure: chemotherapy, intrathecal chemotherapy, steroid therapyB-Cell Non-Hodgkins Lymphoma (Group A) |
| 3B | Other | Drug: vinblastine, vincristine, prednisone, daunorubicin, Drug: doxorubicin, methotrexate, cyclophosphamide, L-asparaginase, Drug: etoposide, cytarabine, mercaptopurine, Drug: dexamethasone, procarbazine, Procedure: chemotherapy, intrathecal chemotherapy, steroid therapyB-Cell Non-Hodgkins Lymphoma (Group B) |
| 4 | Other | Drug: vinblastine, vincristine, prednisone, daunorubicin, Drug: doxorubicin, methotrexate, cyclophosphamide, L-asparaginase, Drug: etoposide, cytarabine, mercaptopurine, Drug: dexamethasone, procarbazine, Procedure: chemotherapy, intrathecal chemotherapy, steroid therapyHodgkins Disease |
Who may qualify
- Ages
- Up to 10 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (4 listed)
- Patient must have a diagnosis of Ataxia-Telangiectasia (A-T).
- Patient must have a diagnosis of either acute lymphoblastic leukemia (ALL) or lymphoma (non-Hodgkin lymphoma or Hodgkin's disease).
- Patients with other malignancies (solid tumors, rare malignancies, or relapsed hematopoietic malignancies) will be eligible for the biologic studies of this protocol; they will receive best clinical management chemotherapy.
- Patients do not have to be previously untreated. If prior chemotherapy has already started (up through induction), therapy will be continued according to protocol at a clinically appropriate time point.
Key exclusion criteria (1 listed)
- Patients who do not have a diagnosis of Ataxia Telangiectasia (A-T).
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| vinblastine, vincristine, prednisone, daunorubicinSee Detailed Description section for details of treatment interventions. | Drug | 1, 2, 3A, 3B, 4 |
| doxorubicin, methotrexate, cyclophosphamide, L-asparaginaseSee Detailed Description section for details of treatment interventions. | Drug | 1, 2, 3A, 3B, 4 |
| etoposide, cytarabine, mercaptopurineSee Detailed Description section for details of treatment interventions. | Drug | 1, 2, 3A, 3B, 4 |
| dexamethasone, procarbazineSee Detailed Description section for details of treatment interventions. | Drug | 1, 2, 3A, 3B, 4 |
| chemotherapy, intrathecal chemotherapy, steroid therapySee Detailed Description section for details of treatment interventions. | Procedure or surgery | 1, 2, 3A, 3B, 4 |
Primary outcome
To determine the feasibility of delivering modified intensive chemotherapy to children with A-T who present with cancer.
Time frame: The completion of treatment
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 27 Aug 2015.
- Background: PubMed 16772123Sandlund JT, Kastan MB, Kennedy W, Behm F, Entrekin E, Pui CH, Kalwinsky DT, Raimondi SC. A subtle t(3;8) results in plausible juxtaposition of MYC and BCL6 in a child with Burkitt lymphoma/leukemia and ataxia-telangiectasia. Cancer Genet Cytogenet. 2006 Jul 1;168(1):69-72. doi: 10.1016/j.cancergencyto.2005.12.013.
- St. Jude Children's Research HospitalLink provided by the sponsor.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
John T. Sandlund, MD principal investigator
St. Jude Children's Research Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing vinblastine, vincristine, prednisone, daunorubicin, doxorubicin, methotrexate, cyclophosphamide, L-asparaginase and etoposide, cytarabine, mercaptopurine in people with Ataxia-Telangiectasia, run by St. Jude Children's Research Hospital at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 27 Aug 2015. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
To determine the feasibility of delivering modified intensive chemotherapy to children with A-T who present with cancer. (time frame: The completion of treatment). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT00187057, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Aug 2015.