Chemotherapy With Liposomal Cytarabine CNS Prophylaxis for Adult Acute Lymphoblastic Leukemia & Lymphoblastic Lymphoma
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| ClinicalTrials.gov Identifier: NCT02043587 |
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Recruitment Status :
Active, not recruiting
First Posted : January 23, 2014
Last Update Posted : March 4, 2020
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Acute Lymphocytic Leukemia Adult Lymphoblastic Lymphoma | Drug: DNR Drug: VCR Drug: PEG-asp Drug: CTX Drug: Prednisone Drug: Liposomal AraC Drug: MTX Drug: LCV Drug: AraC Drug: Etoposide Drug: Dasatinib Drug: Rituximab Drug: Hydrocortisone | Phase 2 |
This treatment regimen builds on the "Linker" regimen/UCSF Protocol 8707 ALL regimen backbone with the goal of improved efficacy and acceptable toxicity by substituting pegylated asparaginase for native L-asparaginase, the addition of rituximab for pre-B-cell ALL, and the addition of dasatinib for Philadelphia chromosome/BCR-ABL positive ALL, and the addition of cyclophosphamide for younger adults. In addition, the study regimen aims to reduce CNS relapse through the use of intrathecal liposomal cytarabine in place of intrathecal methotrexate for CNS relapse prophylaxis and
The regimen uses 3 modules of therapy with non-cross-resistant chemotherapy agents. Rituximab is added for a total of 8 doses for patients with pre-B-cell ALL. Dasatinib is added for patients with Ph+ ALL.
Course 1A (Induction): Daunorubicin, vincristine, PEG-asparaginase, and prednisone for all patients with the addition of cyclophosphamide for patients 18-39 years of age. Treatment is intensified for patients with disease present on a day 14 bone marrow biopsies during Induction Course 1A. In addition to standard analyses, minimal residual disease will be assessed on day 14 and remission bone marrow aspirates and correlated with outcomes.
Course 1B: High-dose methotrexate, oral 6-mercaptopurine, and PEG-asparaginase.
Course 1C: High-dose cytarabine and etoposide.
The 3 courses then repeat (2A (Intensification), 2B, 2C) followed by a final "B" cycle (3B) of high-dose methotrexate, 6-mercaptopurine, and PEG-asparaginase.
After completion of Course 3B, patients proceed to maintenance chemotherapy with monthly methotrexate, vincristine, 6-mercaptopurine, and prednisone cycles for 24 months with a single dose PEG-asparaginase given in month 1 of Maintenance.
CNS prophylaxis: Intrathecal liposomal cytarabine replaces intrathecal methotrexate CNS prophylaxis and is given every 2 weeks during the "A" Induction and Intensification courses then every 3 months during Maintenance for a total of 8 doses. Given the presence of CNS penetrating chemotherapy in the "B" and "C" cycles, intrathecal liposomal cytarabine is not given due to risk of excessive CNS toxicity.
There is a randomization to hydrocortisone or placebo premedication prior to PEG-asparaginase.
| Study Type : | Interventional (Clinical Trial) |
| Estimated Enrollment : | 100 participants |
| Allocation: | N/A |
| Intervention Model: | Single Group Assignment |
| Masking: | None (Open Label) |
| Primary Purpose: | Treatment |
| Official Title: | A Phase II Study of Punctual, Cyclic, and Intensive Chemotherapy With Liposomal Cytarabine (Depocyt®) CNS Prophylaxis for Adults With Acute Lymphoblastic Leukemia and Lymphoblastic Lymphoma |
| Study Start Date : | January 2014 |
| Estimated Primary Completion Date : | January 2024 |
| Estimated Study Completion Date : | January 2026 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Chemotherapy for ALL
Course 1A: DNR 60 mg/m2 IV d1,2,3; VCR 1.4 mg/m2 d1,8,15,22 (cap 2 mg age >50); PEG-asp 2000 IU/m2 IV d16, age >50 1000 IU/m2, cap 3750 IU/m2; CTX 750 mg/m2 d1,15 age < 40; Prednisone 60 mg/m2 PO d1-28; Liposomal AraC 25 mg IT d1, 15 1B: MTX 220 mg/m2 IV then 60 mg/m2/h for 36h d2-3,d16-17; LCV 50 mg/m2 IV q6h x3 then 10 mg/m2 PO/IV q6h til MTX <0.1 uM; 6-MP 60 mg/m2 PO d2-8, d16-22; PEG-asp 2000 IU/m2 IV d18, age >50 1000 IU/m2, cap 3750 IU/m2 1C: AraC 2 g/m2 IV d1-4; Etoposide 500 mg/m2 IV d1-4 1A-C repeat x1(2A-C) then 3rd Course B (3B) Maintenance (monthly, 24 mo): Prednisone 60 mg/m2 PO d1-5; VCR 1.4 mg/m2 IV d1 (cap 2 mg age >50); MTX 20 mg/m2 PO wkly; 6-MP 60 mg/m2 PO qd PEG-asp 2000 IU/m2 IV d16, age >50 1000 IU/m2, cap 3,750 IU/m2 (Mo. 1) Maintenance mo. 1-4: Liposomal AraC 50 mg IT d1 Dasatinib 140 mg PO qd if Ph/BCR-ABL+; Rituximab 375 mg/m2 IV d1,15 of 1A-C, 2A (Pre-B) 1:1 randomization: hydrocortisone v. placebo before PEG-asp 1B, 2B, & Maint. |
Drug: DNR
Daunorubicin 60 mg/m2 IV (in the vein) daily 1,2,3 Courses 1A, 2A
Other Names:
Drug: VCR 1.4 mg/m2 IV, days 1, 8, 15, 22 (cap at 2mg for ages >50) during Courses 1A, 2A; Maintenance: Day 1 during months 2-12
Other Names:
Drug: PEG-asp 2,000 IU/m2 IV for ages </= 50, age > 50, 1000 IU/m2 IV Day 16, Courses 1A & 2A; Day 18, Course 1B; Day 17, Course 2B; Day 16, Maintenance, Month 1
Other Names:
Drug: CTX 750 mg/m2 IV, days 1 &15 for subjects <40 year of age, substitute cyclophosphamide 500 mg/m2 IV over 60 minutes every 12 hours for 4 doses on days 15 & 16 for subjects < 40 years of age if day 14 bone marrow M2 or M3; Courses 1A & 2A
Other Names:
Drug: Prednisone 60 mg/m2 orally once daily on days 1-28 during Courses 1A & 2A; Maintenance: Monthly, days 1-5
Other Name: Deltasone Drug: Liposomal AraC 25 mg intrathecal (IT), on days 1 & 15 during Courses 1A & 2A; 50 mg intrathecal on day 1 during Maintenance Months 1 through 4
Other Names:
Drug: MTX 220 mg/m2 IV bolus over 15 minutes then 60 mg/m2/hour for 36 hours once on days 2-3 and 16-17 during Courses 1B & 2B; 20 mg/m2 orally one day per week every 7 days during Maintenance Months
Other Names:
Drug: LCV 50 mg/m2 IV over 15-30 minutes every 6 hours for 3 doses to begin immediately after completion of methotrexate infusion, then 10 mg/m2 orally or IV over 15-30 minutes every 6 hours until methotrexate level less than 0.1 micromolar during Courses 1B & 2B
Other Name: Leucovorin Drug: AraC 2,000 mg/m2 IV, days 1-4 during Courses 1C & 2C
Other Names:
Drug: Etoposide 500 mg/m2 IV over 3 hours once daily on days 1-4 during Courses 1C & 2C
Other Names:
Drug: Dasatinib 140 mg orally daily if BCR/ABL positive and/or Ph+
Other Name: Sprycel Drug: Rituximab 375 mg/m2 IV once daily on days 1 & 15 (precursor B-cell ALL only, administer per institutional protocol) during Courses 1A, 1B, 1C & 2A
Other Name: Rituxan Drug: Hydrocortisone Randomize patients proceeding to Course 1B to hydrocortisone versus placebo prior to PEG-asparaginase treatments in Courses 1B, 2B, 3B, and Maintenance month 1
Other Names:
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- Event-free survival [ Time Frame: 3-year ]
- Liposomal cytarabine toxicity [ Time Frame: 3 years ]
- CNS relapse rate [ Time Frame: 3-year ]
- Overall survival [ Time Frame: 3-year ]
- Leukemia-free survival [ Time Frame: 3-year ]
- Efficacy of hydrocortisone premedication for reduced PEG-asparaginase allergic reactions [ Time Frame: 3 years ]
- PEG-asparaginase toxicities [ Time Frame: 3 years ]
- Complete and overall response rates [ Time Frame: 3 years ]
- Non-relapse mortality [ Time Frame: 3-year ]
- Minimal residual disease and outcomes [ Time Frame: 3 years ]
- Asparaginase antibodies and asparaginase activity [ Time Frame: 3 years ]
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| Ages Eligible for Study: | 18 Years to 60 Years (Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Ability to understand and the willingness to sign a written informed consent.
- Diagnosis of acute lymphoblastic leukemia or lymphoblastic lymphoma as defined by the World Health Organization [94]
- Untreated disease EXCEPT for corticosteroids, hydroxyurea, leukapheresis, and/or tyrosine kinase inhibitors for up to 2 weeks prior to initiation of study therapy.
- Age 18 through 60 years
- ECOG performance status 0,1, or 2 (see Appendix A)
- Adequate organ function defined as:
- Total bilirubin < 2 mg/dL (unless due to ALL)
- AST(SGOT)/ALT(SGPT) < 3 times institutional upper limit of normal (unless due to ALL)
- Serum creatinine < 2 mg/dL (unless elevated creatinine felt by investigator to be acute and reversible) OR creatinine clearance >60 mL/min/1.73 m2 for patients with creatinine levels above institutional normal
- Left ventricular ejection fraction ≥50%
- Women of child-bearing potential and men with partners of child- bearing potential must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry, for the duration of study participation, and for 90 days following completion of therapy. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately.
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A woman of child-bearing potential is any female (regardless of sexual orientation, having undergone a tubal ligation, or remaining celibate by choice) who meets the following criteria:
- Has not undergone a hysterectomy or bilateral oophorectomy; or
- Has not been naturally postmenopausal for at least 12 consecutive months (i.e., has had menses at any time in the preceding 12 consecutive months)
Exclusion Criteria:
- Current or anticipated use of other investigational agents during the study
- Known central nervous system mass lesion
- History of allergic reactions attributed to compounds of similar chemical or biologic composition to liposomal cytarabine or other agents used in study inclusive of known allergy to polyethylene glycol.
- History of unprovoked venous thrombosis/thromboembolism
- Recurrent or chronic pancreatitis
- Uncontrolled diabetes mellitus
- Uncontrolled intercurrent illness that would limit compliance with study requirements including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
- Pregnant or nursing.
- Any condition, in the opinion of the investigator, that compromises compliance with study requirements
- Known HIV positivity
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02043587
| United States, California | |
| UCSD, Division of Blood and Marrow Transplantation, Moores Cancer Center | |
| La Jolla, California, United States, 92093 | |
| Hematological Malignancies/Stem Cell Transplantation Unit, David Geffen School of Medicine at UCLA | |
| Los Angeles, California, United States, 90095 | |
| University of California Davis Comprehensive Cancer Center | |
| Sacramento, California, United States, 95817 | |
| UCSF Comprehensive Cancer Center | |
| San Francisco, California, United States, 94143-0324 | |
| Principal Investigator: | Matthew J Wieduwilt, MD, PhD | UC San Diego, Division of Blood and Marrow Transplantation |
| Responsible Party: | Matthew Wieduwilt, M.D., Ph.D., Assistant Clinical Professor, University of California, San Diego |
| ClinicalTrials.gov Identifier: | NCT02043587 |
| Other Study ID Numbers: |
130934 |
| First Posted: | January 23, 2014 Key Record Dates |
| Last Update Posted: | March 4, 2020 |
| Last Verified: | March 2020 |
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Acute lymphoblastic leukemia Lymphoblastic leukemia Lymphoblastic lymphoma |
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Lymphoma Leukemia Leukemia, Lymphoid Precursor Cell Lymphoblastic Leukemia-Lymphoma Lymphoma, Non-Hodgkin Neoplasms by Histologic Type Neoplasms Lymphoproliferative Disorders Lymphatic Diseases Immunoproliferative Disorders Immune System Diseases Leucovorin Cytarabine Prednisone Hydrocortisone |
Hydrocortisone 17-butyrate 21-propionate Hydrocortisone acetate Hydrocortisone hemisuccinate Cyclophosphamide Rituximab Methotrexate Etoposide Vincristine Daunorubicin Asparaginase Dasatinib Pegaspargase Immunosuppressive Agents Immunologic Factors Physiological Effects of Drugs |