Description:
This phase 2 clinical trial will evaluate the effectiveness and safety of fludarabine in
combination with CPX-351 in patients with untreated AML. Patients will receive fludarabine
and CPX-351 during Induction 1 and 2 as well as 2 cycles of consolidation therapy.
Title
- Brief Title: Fludarabine in Combination With Daunorubicin and Cytarabine Liposome in Newly-diagnosed Acute Myeloid Leukemia.
- Official Title: A Phase II Trial of Fludarabine in Combination With Daunorubicin and Cytarabine Liposome for Adults With Newly-diagnosed Acute Myeloid Leukemia: University of California Hematologic Malignancies Consortium Protocol 1914
Clinical Trial IDs
- ORG STUDY ID:
UCHMC1914
- NCT ID:
NCT04425655
Conditions
- Acute Myeloid Leukemia, Adult
- AML
- AML, Adult
Interventions
Drug | Synonyms | Arms |
---|
Fludarabine | Oforta, Fludara | Fludarabine and CPX351 |
Vyxeos | CPX-351 | Fludarabine and CPX351 |
Purpose
This phase 2 clinical trial will evaluate the effectiveness and safety of fludarabine in
combination with CPX-351 in patients with untreated AML. Patients will receive fludarabine
and CPX-351 during Induction 1 and 2 as well as 2 cycles of consolidation therapy.
Detailed Description
This is a phase 2, open label single arm study to look at the effectives and safety of
fludarabine in combination with CPX-351 in patients with untreated AML. The rationale for
this combination stems from data which indicated that pre-treatment of the THP-1 cell line
with fludarabine for 4 hours prior to CPX-351 administration (Flu-CPX) significantly
potentiated intracellular ara-CTP accumulation compared to CPX-351 alone. This suggests that
fludarabine combined with CPX-351 may have efficacy against leukemic clones that would be
resistant to CPX-351 or standard chemotherapy in first induction. It has been demonstrated
that treatment with CPX-351 produces superior clinical outcomes in secondary AML likely due
to its novel formulation, which results in sustained exposure of the cytotoxic agents
cytarabine and daunorubicin in a synergistic 5:1 ratio within the plasma and bone marrow.
Fludarabine can potentially improve upon the outcomes observed with CPX-351 monotherapy and
7+3 by enhancing intracellular ara-CTP accumulation from CPX-351. Patients will received
fludarabine and CPX-351 for up to 2 cycles of induction and 2 cycles of consolidation.
Trial Arms
Name | Type | Description | Interventions |
---|
Fludarabine and CPX351 | Experimental | Induction 1:
Fludarabine 30 mg/m2/day IV on days 1-5 for 5 doses Daunorubicin and cytarabine liposome (CPX-351) daunorubicin 44 mg/m2/day and cytarabine 100 mg/m2/day IV on days 1, 3, 5 (given 4 hours after fludarabine infusion) for 3 doses
Induction 2 (residual leukemia after Induction 1):
Fludarabine 30 mg/m2/day IV on days 1-3 for 3 doses
Daunorubicin and cytarabine liposome (CPX-351) daunorubicin 44 mg/m2/day and cytarabine 100 mg/m2/day IV on days 1, 3 (given 4 hours after fludarabine infusion) for 2 doses
Optional consolidation, up to 2 cycles:
Daunorubicin and cytarabine liposome (CPX-351) daunorubicin 29 mg/m2/day and cytarabine 65 mg/m2/day IV on days 1, 3 for 2 doses | |
Eligibility Criteria
Inclusion Criteria:
1. Histologically confirmed de novo or secondary AML as defined by WHO criteria
2. Intermediate- or poor-risk disease by ELN 2017 criteria
3. Adults 18 years of age or older
4. ECOG performance status of 0, 1, or 2
5. Able to give informed consent and follow study guidelines
6. Organ function requirements:
1. Adequate renal function defined as creatinine clearance greater than 60 ml/min
2. Adequate hepatic function defined by serum bilirubin less than or equal 2 mg/dL.
If serum bilirubin greater than 2 mg/dl and direct bilirubin is less than 30
percent of total bilirubin contact study chair for eligibility exception for
Gilbert's syndrome.
3. ALT/AST less than or equal to 3 times the upper limit of normal
4. LVEF 50 percent by echocardiogram or MUGA
7. Patients with history of second malignancies in complete remission and without history
of metastasis are eligible if there is clinical evidence of disease stability for a
period of greater than 6 months off cytotoxic chemotherapy, documented by imaging,
tumor marker studies, etc., at screening.
8. 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 120
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.
9. Women of child-bearing potential has negative pregnancy test prior to initiating study
drug dosing.
Exclusion Criteria:
1. Current or anticipated use of additional investigational agents.
2. Any prior treatment for AML with the exception of corticosteroids, hydroxyurea, and/or
leukapheresis to prevent or treat early complications prior to starting study therapy.
Permitted prior therapy must be stopped 24 hours prior to starting study therapy.
3. Prior use of hypomethylating agents is permitted for patients with history of
antecedent MDS. Last dose of hypomethylating therapy must have been 15 or more days
prior to starting study therapy. Toxicities associated with prior MDS therapy must
have recovered to grade 1 or less prior to start of treatment.
4. Favorable risk cytogenetics as defined by 2017 ELN risk stratification including acute
promyelocytic leukemia
5. Chronic myeloid leukemia in myeloid blast crisis
6. Except for CMML, patients with history of myeloproliferative neoplasms (MPN) (defined
as a history of essential thrombocytosis or polycythemia vera, or idiopathic
myelofibrosis prior to the diagnosis of AML) or combined MDS/MPN are not eligible
7. Clinical evidence of active CNS leukemia
8. Active or metastatic second malignancy
9. Any major surgery or radiation therapy within four weeks.
10. Patients with prior cumulative anthracycline exposure of greater than 368 mg/m2
daunorubicin (or equivalent).
11. Any serious medical condition, laboratory abnormality or psychiatric illness that
would prevent obtaining informed consent
12. Patients with myocardial impairment of any cause (e.g. cardiomyopathy, ischemic heart
disease, significant valvular dysfunction, hypertensive heart disease, and congestive
heart failure) resulting in heart failure by New York Heart Association Criteria
(Class III or IV staging)
13. Active or uncontrolled infection. Patients with an infection receiving treatment
(antibiotic, antifungal or antiviral treatment) may be entered into the study but must
be afebrile and hemodynamically stable for greater than or equal to 72 hrs.
14. Current evidence of invasive fungal infection (blood or tissue culture); patients with
recent fungal infection must have subsequent negative culture(s) to be eligible
15. Known HIV infection
16. Active hepatitis B or hepatitis C infection
17. Hypersensitivity to cytarabine, daunorubicin or liposomal products
18. History of Wilson's disease or copper-metabolism disorder
19. Pregnant or breastfeeding
20. Any condition which in the opinion of the investigator will interfere with the ability
of the subject to comply with the requirements of the study
Maximum Eligible Age: | N/A |
Minimum Eligible Age: | 18 Years |
Eligible Gender: | All |
Healthy Volunteers: | No |
Primary Outcome Measures
Measure: | Overall response rate after induction |
Time Frame: | 35 days |
Safety Issue: | |
Description: | Overall response rate after induction, defined as the sum of complete response (CR) rate and complete response with incomplete count recovery (CRi) rate after 1-2 cycles of induction therapy, in accordance with 2017 ELN criteria. |
Secondary Outcome Measures
Measure: | Safety and Tolerability |
Time Frame: | 6 months |
Safety Issue: | |
Description: | Safety and tolerability will be determined by rates of NCI CTCAE 5.0 Grade 3-5 toxicities and rate of discontinuation from study therapy due to intolerance |
Measure: | Incidence of Grade 3 Treatment Emergent Adverse Events [Safety and Tolerability] |
Time Frame: | 6 months |
Safety Issue: | |
Description: | Safety and tolerability will be determined by rates of NCI CTCAE 5.0 Grade 3 toxicities and rate of discontinuation from study therapy due to intolerance |
Measure: | Incidence of Grade 4 Treatment Emergent Adverse Events [Safety and Tolerability] |
Time Frame: | 6 months |
Safety Issue: | |
Description: | Safety and tolerability will be determined by rates of NCI CTCAE 5.0 Grade 4 toxicities and rate of discontinuation from study therapy due to intolerance |
Measure: | Incidence of Grade 5 Treatment Emergent Adverse Events [Safety and Tolerability] |
Time Frame: | 6 months |
Safety Issue: | |
Description: | Safety and tolerability will be determined by rates of NCI CTCAE 5.0 Grade 5 toxicities and rate of discontinuation from study therapy due to intolerance |
Measure: | CR Rate |
Time Frame: | 60 days |
Safety Issue: | |
Description: | CR rate defined as proportion of patients achieving a CR after 1-2 cycles of induction |
Measure: | Overall response rate |
Time Frame: | 35 days |
Safety Issue: | |
Description: | Overall response rate (CR +CRi) after 1 cycle of induction |
Measure: | Overall survival |
Time Frame: | 1 year |
Safety Issue: | |
Description: | Overall survival (OS) at 1 year, with OS defined as time from start of study therapy to death from any cause |
Measure: | Overall survival |
Time Frame: | 3 years |
Safety Issue: | |
Description: | Overall survival (OS) at 3 years, with OS defined as time from start of study therapy to death from any cause |
Measure: | Leukemia-free survival |
Time Frame: | 1 years |
Safety Issue: | |
Description: | Leukemia-free survival (LFS) at 1 year, with EFS defined as the time from start of study therapy until failure to attain CR, relapse, or death from any cause |
Measure: | Leukemia-free survival |
Time Frame: | 3 years |
Safety Issue: | |
Description: | Leukemia-free survival (LFS) at 3 years, with EFS defined as the time from start of study therapy until failure to attain CR, relapse, or death from any cause |
Measure: | Event free survival |
Time Frame: | 1 year |
Safety Issue: | |
Description: | Event Free Survival (EFS) at 1 year, with EFS defined as the time from start of study therapy until failure to attain CR, relapse, or death from any cause. |
Measure: | Event free survival |
Time Frame: | 3 years |
Safety Issue: | |
Description: | Event Free Survival (EFS) at 3 years, with EFS defined as the time from start of study therapy until failure to attain CR, relapse, or death from any cause. |
Measure: | Platelet Recovery |
Time Frame: | 60 days |
Safety Issue: | |
Description: | Platelet recovery, defined as the time from start of study therapy until absolute neutrophil count >1,000/mcl in patients achieving a CR |
Measure: | 30-day |
Time Frame: | 30 days from start of study therapy |
Safety Issue: | |
Description: | 30-day mortality defined as death from any cause within 30 days of starting study therapy |
Measure: | 60-day mortality |
Time Frame: | 60 days from start of study therapy |
Safety Issue: | |
Description: | 60-day mortality defined as death from any cause within 60 days of starting study therapy |
Details
Phase: | Phase 2 |
Primary Purpose: | Interventional |
Overall Status: | Recruiting |
Lead Sponsor: | University of California, San Diego |
Trial Keywords
- Vyxeos
- CPX-351
- Fludarabine
- Untreated AML
Last Updated
April 1, 2021