A Phase 2 Study of Amrubicin in Relapsed or Refractory Thymic Malignancies
Trial ID or NCT#
NCT01364727
Status
NOT RECRUITING
Purpose
A research study of the drug amrubicin in patients with cancer of the thymus (thymoma or thymic carcinoma). We hope to learn whether this drug is an effective and safe treatment for thymic cancers.
Official Title
A Phase II Study of Amrubicin in Relapsed or Refractory Thymic Malignancies
Eligibility Criteria
Ages Eligible for Study: Older than 18 Years
Sexes Eligible for Study: All
Accepts Healthy Volunteers: No
Inclusion Criteria:
- - Histologically or cytologically confirmed invasive or metastatic thymoma or thymic carcinoma. Locally invasive disease is acceptable, provided it is not resectable. - Previous treatment with at least one prior chemotherapy regimen. - Documented progressive disease after the most recent chemotherapy regimen. - Presence of measurable disease on imaging within 4 weeks prior to first dose - Completion of prior systemic therapy at least 4 weeks prior to first dose. - Any prior immunotherapy therapy completed at least 8 weeks prior to first dose. - Any prior surgery completed at least 4 weeks prior to first dose, with adequate recovered from surgery. - Any prior radiation therapy must have no residual toxic effects of therapy. Chest radiotherapy with curative intent to the primary disease complex must have been completed ≥ 28 days prior to first dose. Cranial radiation must have been completed ≥ 21 days prior to first dose. Radiotherapy to all other areas must have been completed ≥ 7 days prior to first dose. - Age ≥ 18 years. - Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1. - Leukocytes ≥ 3000/mm³ - Absolute neutrophil count ≥ 1500/mm³ - Platelets ≥ 100,000/mm³ - Hemoglobin ≥ 9 g/d - Serum bilirubin < 1.5 x institutional upper limit of normal (ULN) - Aspartate transaminase (AST) and alanine transaminase (ALT) ratio < 3 x ULN - Serum creatinine < 1.5 times institutional upper limit of normal if serum creatinine above institutional upper limit of normal, calculated serum creatinine clearance by the Cockcroft Gault method > 60 mL/min - Left ventricular ejection fraction (LVEF) ≥ 50% by transthoracic echocardiogram (TTE) or multiple gated acquisition scan (MUGA) - For females of childbearing potential, negative serum pregnancy test within 4 weeks of first dose. - For males and females of childbearing potential, use of effective contraceptive methods during the study. - Ability to understand and willingness to sign a written informed consent document.
Exclusion Criteria:
- - Current use, or use within 4 weeks prior to first dose, of any other investigational agents. - Known history of allergic reactions attributed to compounds of similar chemical or biologic composition to amrubicin. - Active malignancy requiring treatment other than thymic malignancy. - Pregnant or nursing females due to unknown toxic effects of amrubicin on the developing fetus or in breast milk. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately. - Symptomatic central nervous system metastatic disease. Patients with asymptomatic brain metastases allowed. If treated with surgical resection or radiation therapy, the patient must be stable for >= 2 weeks after completion of therapy. If the patient is on corticosteroids, the dose of corticosteroids, the dose of corticosteroids must have been stable for >= 2 weeks prior to first dose of study treatment, or be in the process of being tapered. - Concurrent severe or uncontrolled medical disease (including but not limited to active systemic infection, diabetes, hypertension, coronary artery disease, congestive hear failure and mental illness) that in the opinion of the investigator would compromise the safety of the patient or compromise the ability of the patient to complete the study. - Known history of seropositive human immunodeficiency virus (HIV) or use of immunosuppressive medications for other conditions that would, in the opinion of the investigator, increase the risk of serious neutropenic complications.
Investigator(s)
Joel Neal, MD, PhD
Medical oncologist,
Thoracic specialist
Associate Professor of Medicine (Oncology)
A. Dimitrios Colevas, MD
Medical oncologist,
Head and neck specialist,
Cutaneous oncology specialist
Professor of Medicine (Oncology) and, by courtesy, of Otolaryngology - Head & Neck Surgery (OHNS) and of Radiation Oncology (Radiation Therapy)
Contact us to find out if this trial is right for you.
Contact
ccto-office@stanford.edu
650-498-7061
View on ClinicalTrials.gov