A Phase II study of Adjuvant PALbociclib as an Alternative to CHemotherapy in Elderly patientS with high-risk ER+/HER2- early breast cance (APPALACHES)

European Organisation for research and treatment of Cancer0 个研究点目标入组 366 人开始时间: 2019年5月22日最近更新: 2019年12月16日

试验速览

阶段: 1 期
状态: 进行中（未招募）
发起方
入组人数: 366

研究概览入排标准研究者记录与标识符相似试验

研究概览

简要总结

暂无简介。

研究设计

研究类型: Interventional clinical trial of medicinal product

入排标准

性别: All

入选标准

•- Women or men with stage II or stage III, early invasive breast cancer according to the UICC 8th edition for TNM classification
•- Histologically confirmed ER+ , HER-2 negative, early invasive breast cancer based on results of local pathology. Testing may be performed on
•diagnostic core biopsy or resection specimen.
•- In patients with multicentric, multifocal and/or bilateral breast cancer, all histopathologically examined invasive tumors must meet pathologic
•criteria regarding ER and HER2-status described above.
•- Adjuvant chemotherapy indicated and feasible according to treating physician and patient, based on standard clinicopathological parameters
•(tumor size, lymph node involvement, general health status, proliferation marker, patient wish) and gene expression profile if available.
•- Adjuvant chemotherapy with both anthracycline and taxanes (in combination or in sequence) considered not indicated or not feasible according to treating physician.
•- Age =70 years
•- WHO Performance status 0-2
•- Completed G8 geriatric assessment within 3 weeks of randomization.
•- Participation in translational research is mandatory and therefore patient must consent for it. Patient should allow sequential sampling of blood during the course of the trial
•- Patient must have undergone breast +/- axillary surgery with curative intent for the current malignancy =8 weeks before randomization. The
•final primary tumor surgical specimen must have R0 margins free from tumor.
•- Patients must have sufficient resolution of any surgical side effects from the last surgery per physician assessment, with no active wound
•healing complications at the time of randomization.
•- Incentive to undergo adjuvant radiation therapy when indicated per local institutional guidelines.
•Note: For patients in the palbociclib arm, radiation therapy when indicated has to start =9 weeks after last surgery. The endocrine therapy can be initiated during or after the radiation therapy but not later than 3 weeks after the last radiotherapy. Palbociclib has to start =3 weeks after the last radiotherapy. When radiation therapy is not indicated, endocrine
•therapy and palbociclib have to be initiated =9 weeks after last surgery.
•Note: For patients in the chemotherapy arm, chemotherapy has to be the first adjuvant treatment and has to start =9 weeks after the last surgery.
•When radiation therapy is indicated, this treatment has to start =6 weeks after the last chemotherapy administration. Adjuvant endocrine therapy can be initiated during or after the radiation therapy but not
•later than 3 weeks after the last radiotherapy. When radiation therapy is not indicated, endocrine therapy has to be initiated =6 weeks after last
•chemotherapy administration.
•- Adequate baseline organ function, evidenced by the following laboratory results within 3 weeks of randomization:
•- Hemoglobin = 9 g/dL
•- Absolute neutrophil count (ANC) = 1500/mm3
•- Platelet count = 100,000/mm3
•- Total bilirubin = 1.5 upper limit of normal (ULN), or total bilirubin = 3.0 × ULN in patients with documented Gilbert's Syndrome.
•- Glomerular Filtration Rate (GFR) = 30 ml/min according to MDRD formula or CKD-EPI formula or Cockcroft and Gault formula
•- SGOT (AST), SGPT (ALT) and alkaline phosphatase = 2.5 × ULN
•- Patients must be able and willing to swallow and retain oral medication without a condition that would interfere with enteric absorption.
•- For men participating in the trial:
•As fertility may b

排除标准

•- Evidence of macroscopic distant metastases, investigated according to local institutional guidelines.
•- Previous history of invasive breast cancer
•- Patients who received treatment with live vaccines within 30 days prior the first dose of study medication.
•- Systemic anticancer therapy prior to the breast cancer surgery
•- Prior therapy with any CDK4/6 inhibitor
•- Concurrent investigational agent within 28 days of randomization
•- Concomitant anticancer treatment with the exception of bone
•antiresorptive agents or LHRH agonists in male patients treated with an aromatase-inhibitor
•- History of allergic reactions attributed to compounds of chemical or biological composition similar to palbociclib or to chemotherapy components
•- Patients with rare hereditary problems of galactose intolerance, the Lapp lactase deficiency, or glucose-galactose malabsorption
•- Medications or substances that are potent inhibitors or inducers of CYP3A isoenzymes within 7 days of randomization
•- Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection (including known HIV, active hepatitis B and/or hepatitis C infection), symptomatic congestive heart failure, unstable angina pectoris, uncontrolled cardiac arrhythmia, or uncontrolled diabetes.
•Note: For patients for whom doxorubicin or epirubicin is planned, an adequate baseline cardiac function (left ventricular ejection fraction =
•50%) should have been proven no more than 1 year before treatment start.
•- Any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up
•schedule; those conditions should be discussed with the patient before registration in the trial
•- Other malignancy within the last 5 years except: adequately treated non-metastatic non-melanoma skin cancer, curatively treated in situ cancer of the cervix, ductal carcinoma in situ of the breast.

研究者

发起方

European Organisation for research and treatment of Cancer

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