Status:
UNKNOWN
Efficacy of Palbociclib in Advanced Acral Melanoma With Cell Cycle Gene Aberrations
Lead Sponsor:
Peking University Cancer Hospital & Institute
Collaborating Sponsors:
Kiang Wu Hospital
Conditions:
Melanoma
Eligibility:
All Genders
18-75 years
Phase:
PHASE2
Brief Summary
It is a prospective, phase II, open-labeled, clinical trial aimed to determine the efficacy of palbociclib in advanced melanoma patients who bear gene aberrations in cell cycle pathways \[including CD...
Detailed Description
This study is to evaluate efficacy of palbociclib in advanced acral melanoma patients with gene aberrations in cell cycle pathways \[including CDK4 amplification and/or CCND1 amplification and/or P16 ...
Eligibility Criteria
Inclusion
- Age from 18 to 75 years;
- ECOG performance status 0 or 1 before treatment;
- Metastatic melanoma or unresectable acral melanoma;
- Histologically confirmed melanoma.
- Bearing gene aberrations in cell cycle pathways \[including CDK4 amplification and/or CCND1 amplification and/or P16 (CDKN2A) loss\].;
- Anticipated life expectancy ≥ 3 month;
- Adequate organ function, defined as following criteria:
- Platelets 75 x 109/L, Hemoglobin 9.0 g/dL, Absolute Neutrophils(ANC) ≥ 1.5x109/L;
- Serum bilirubin ≤ 1.5\*upper limit of normal (ULN) (could be ignored in the case of Gilbert's syndrome) ，Serum aspartate transaminase (AST) and serum alanine transaminase (ALT) ≤ 1.5 \* ULN;
- Blood urea nitrogen (BUN) ≤ 1.5 \* ULN, serum creatinine (Cr) ≤ 1.5 \* ULN.
- Left ventricular ejection fraction (LVEF) ≥ lower limit of normal (LLN) as assessed by multigated acquisition (MUGA) scan or echocardiography;
- QTc interval: male \< 450msec, female \< 470msec (via Fridericia method)
- Willingness and ability to comply with scheduled visits, treatment plans, laboratory tests, and other study procedures.
- Written informed consent signed.
Exclusion
- Previous or current administration of any kind of CDK4/6 inhibitors;
- Administration of any other anti-tumor therapy (including but not limited to radiotherapy, chemotherapy, endocrinal therapy, surgery, molecular targeted therapy, immunotherapy or biological therapy) 4 weeks before inclusion; administration of mitocycin or nitrosamines 8 weeks before inclusion;
- Non-treated brain metastasis (treatment controlled stable brain metastasis judged by investigators excluded);
- Presence of third space fluid that cannot be controlled by drainage or other means (i.e. pleural effusion or ascites);
- Long-term steroid therapy required;
- Uncorrectable hypokalemia or hypomagnesaemia before inclusion;
- Concurrent administration of drugs with potential of QT interval prolongation (such as antiarrhythmic drugs);
- Allergies or previous history of severe allergies;
- Active HBV or HCV infection (HBV viral copy number ≥ 104 copies/ml, HCV ≥ 103 copies/ml);
- NCICTCAE Grade 2 toxicity before inclusion;
- Diagnosed as any second primary malignant tumor in 5 years before inclusion;
- Following conditions occur in the 6 months before drug administration: severe/ unstable angina pectoris, myocardial infarction, congestive heart failure with symptoms, cerebrovascular accident, including transient ischemic attack, pulmonary embolism, ≥ grade II renal dysfunction, and other severe diseases that investigators judged to be unsuitable for this trial;
- Administration of potent CYP3A4 inhibitors in 7 days before inclusion , or administration of potent CYP3A4 inhibitors in 12 days before randomization ；
- NCICTCAE Grade ≥ 2 Active arrhythmias;
- Hypertension, defined as systolic blood pressure \>150mmHg and/or diastolic blood pressure \>100mmHg，and cannot be controlled by medication;
- No recommendation to receive \>2 mg Warfarin treatment in 2 weeks before study beginning. It is permitted to use low dose Warfarin(\<2 mg／3day) to prevent deep venous thrombosis. Low molecular weight heparin (fractionated) or aspirin are also allowed;
- Existence of any disease affecting drug absorption, including but not limited to: no ability to swallow oral medications, active inflammatory bowel disease, partial or complete obstruction, partial or total gastrectomy, extensive bowel resection or chronic diarrhea;
- Known infection of human immunodeficiency virus (HIV) or acquired immunodeficiency syndrome (AIDS)-related illness, or congenital immune deficiency diseases, organ transplantation history;
- Pregnancy, breastfeeding, childbearing age female who is reluctant to take effective contraceptive measures throughout trial period. All female patients with reproductive potential must have a negative pregnancy test (serum or urine) within 7 days before randomization and at first day of every cycle on visit.
- Other severe acute or chronic physiological or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or study drug administration, or may interfere with the interpretation of study results, and in the judgment of the investigator would make the patient inappropriate for entry into this study.
- Current treatment on another clinical trial. Supportive care or non-therapeutic clinical trials are allowed.
Key Trial Info
Start Date :
March 30 2018
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
June 30 2020
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT03454919
Start Date
March 30 2018
End Date
June 30 2020
Last Update
March 6 2018
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