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This is a Phase I/II study to determine the safety, tolerability and to identify the MTD and DLT of Plitidepsin in combination with a fixed dose of Cytarabine in patients with relapsed/refractory leukemia and to determine the response rate of the combination of Plitidepsin with Cytarabine in patients with relapsed/refractory AML treated at the MTD.
Full description
This is a Phase I/II study to determine:
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Inclusion criteria
Patients must have cytologically (or by flow cytometry) documented relapsed/refractory Acute Myeloid leukemia or Acute Lymphoid leukemia for which no standard therapy is anticipated to result in a durable remission. Chronic Myeloid leukemia in blast crisis who progress through Gleevec® or is intolerant to Gleevec® or other FDA approved BCR-ABL Tyrosine Kinase Inhibitors. Patients with untreated AML or ALL who are electing not to receive standard therapy are also eligible. Relapsed/refractory leukemia patients may combination after 1 course of chemotherapy. In addition,leukemia secondary to pre-existing hematologic disorders high-grade myelodysplastic syndromes are also eligible.
≥18 years of age.
Patients must be informed of the investigational nature of this study and must give written informed consent in accordance with institutional and federal guidelines.
Patients who cannot provide informed consent will not be eligible for the study.
Prior radiotherapy, chemotherapy or biologic therapies are allowed. Previous line(s) of systemic chemotherapy should have been completed at least 2 weeks prior to starting protocol treatment. Concurrent hydroxyurea administration will be allowed to control WBC count, platelet count, or symptoms and will be discontinued 24 hours prior to the first APLIDIN® dose. For patients with CML in blast crisis, Gleevec® or other BCR-ABL Tyrosine Kinase Inhibitors must be stopped at least 7 days prior to the first APLIDIN® dose. t.
Patients must have an ECOG performance status ≤2 (Appendix C).
Laboratory data:
Negative pregnancy test for women of childbearing potential.
Bone Marrow Assessment within two weeks before the first Aplidin® administration.
Estimated life expectancy of > 1 month.
Left ventricular ejection fraction within normal limits.
Exclusion criteria
Previous treatment with Plitidepsin.
Prior autologous and/or allogeneic hematopoietic stem cell transplantation (HSCT) patients are not eligible due to higher risk of toxicity related to treatment after such procedure.
Active or metastatic secondary primary malignancy.
Patients with known Central Nervous System involvement will be excluded from this clinical trial because of their poor prognosis and because they often develop progressive neurologic dysfunction that would confound the evaluation of neurologic and other adverse events.
Serious concomitant systemic disorders that would compromise the safety of the patient or compromise the patient's ability to complete the study, including the following specific conditions:
Other relevant cardiac conditions:
History of hypersensitivity reaction to cremophor, Cytarabine, Mannitol, or Plitidepsin (Aplidin®).
Myopathy or any clinical situation that causes significant and persistent elevation of CK (> 2.5 ULN in two different determinations performed with one week apart).
History of significant Cytarabine related neurotoxicity.
Grade >2 motor or sensory neuropathy of any cause.
Men and women of reproductive potential who are not using effective contraceptive methods. The effects of Plitidepsin on the developing human fetus at the recommended therapeutic dose are unknown. For this reason, women of child-bearing potential and men 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 6 months after. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately. Also, if the wife or female partner of a male patient becomes pregnant during the study, the investigator must be notified promptly and the pregnant woman will be referred for appropriate follow-up with a High-risk Obstetrician.
Pregnant and/or lactating women.
Patients with immune deficiency are at increased risk of lethal infections when treated with marrow-suppressive therapy, therefore, known HIV-positive patients with active HIV infection and/or receiving combination anti-retroviral therapy are excluded from the study because of possible pharmacokinetic interactions with Plitidepsin or other agents administered during the study. HIV testing is not required unless infection is clinically suspected.
Known active HBV or HCV infection. Patients with any serological evidence of current or past hepatitis B exposure are excluded unless the serological findings are clearly due to vaccination. HBV or HCV testing are not required unless infection is clinically suspected.
Concomitant therapy with therapeutic dose of coumadin is not permitted. A suboptimal dose for permeability venous access devices is allowed.
Treatment with any investigational product in the 30 days period before inclusion in the study. Wash-out periods since the end of the precedent therapy less than:
Limitation of the patient´s ability to comply with the treatment or follow-up protocol.
Primary purpose
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Interventional model
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3 participants in 1 patient group
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Data sourced from clinicaltrials.gov
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