Östrojen Reseptörü Pozitif/HER2 Negatif Meme Kanserinde Palbociclib ve Endokrin Tedavinin Birlikte Kullanıldığı Neoadjuvan Biyobelirteç Araştırma Çalışması (NeoRHEA)

Sade dilde özet

Bu çalışma, östrojen reseptörü pozitif ve HER2 negatif meme kanseri (breast cancer) olan hastalarda ameliyat öncesi (neoadjuvan) dönemde Palbociclib ilacının endokrin (hormon) tedavisiyle birlikte kullanımını ve tedaviye yanıtı gösteren biyobelirteçleri incelemektedir. Çalışmaya, 2 cm'den büyük, östrojen reseptörü pozitif ve HER2 negatif meme tümörü olan 18 yaş ve üzeri kadınlar katılabilmiştir. Çalışma Faz 2 aşamasında yürütülmüş ve tamamlanmıştır.

Yukarıdaki özet, resmî kaydın sade dile aktarılmış halidir. Orijinal İngilizce başlık referans için gösterilir.

Deney bilgileri

Faz

Faz 2 (Phase 2)

Durum

Tamamlandı

Sponsor

Jules Bordet Institute

Müdahale

Palbociclib

Başlangıç

05.07.2017

Tahmini bitiş

01.02.2023

Ülkeler

Belgium

İlgili genler

Merkezler

• Anderlecht, Belgium
• Brussels, Belgium
• Brussels, Belgium
• Leuven, Belgium
• Namur, Belgium

Uygunluk kriterleri

Kriterler ClinicalTrials.gov kaydından orijinal İngilizce haliyle alınmıştır. Uygunluk kararını yalnızca deneyi yürüten ekip verebilir.

Inclusion Criteria:

1. Female
2. Age ≥ 18 years
3. Histological diagnosis of breast adenocarcinoma that is estrogen receptor-positive, and HER2- negative as per the updated American Society of Clinical Oncology (ASCO) - College of American Pathologists (CAP) guidelines according to local testing.
4. Multifocal unilateral or bilateral breast adenocarcinoma tumours are allowed provided that all tested foci are ER-positive and HER2-negative.

   * ER-positive (ER+ is defined as having a IHC of 1% or more and/or and Allred of 2 or more and HER2-negative.
   * HER2 negative (HER2 negative is defined as having an IHC of 1+ without ISH OR IHC 2+ and ISH non-amplified with ratio less than 2.0 and if reported, average HER2 copy number \< 4 signals/cells OR ISH non-amplified with ratio less than 2.0 and if reported, average HER2 copy number \< 4 signals/cells (without IHC)
5. A primary non metastatic or locally advanced tumour of more than 2 cm (T2 or T3), N0 or N1 without prior treatment candidate for preoperative treatment
6. ECOG Performance Status (PS) 0 or 1.
7. Adequate Bone Marrow Function including:

   1. Absolute Neutrophil Count (ANC) ≥1500/μL or ≥1.5 x109/L;
   2. Platelets ≥100000/μL or ≥100 x 109/L;
   3. Hemoglobin ≥ 9 g/dL.
8. Adequate Renal Function including: Serum creatinine ≤ 1.5 x upper limit of normal (ULN) or estimated creatinine clearance ≥ 60 ml/min as calculated using the method standard for the institution.
9. Adequate Liver Function, including all of the following parameters:

   1. Total serum bilirubin ≤ 1.0 x ULN unless the subject has documented Gilbert syndrome (in which case up to 3 x ULN is acceptable) ;
   2. Aspartate and Alanine Aminotransferase (AST and ALT) ≤ 1.5 x ULN;
   3. Alkaline phosphatase ≤ 2.5 x ULN.
10. Signed consent form
11. Willingness and ability to comply with the study scheduled visits, treatment plans, laboratory tests, radiological exams, tumour and blood specimen collection and other procedures.
12. Women who are not postmenopausal or have not undergone hysterectomy must have documented negative pregnancy test (serum) prior to inclusion.
13. Female subjects of child bearing potential and their partners, who are sexually active, must agree to the use of two highly effective forms of contraception in combination throughout the period of taking study treatment and for at least 90 days after last dose of study drug, or they must totally/truly abstain from any form of sexual intercourse. Use of oral hormonal contraceptive agents in this study is not permitted.

Exclusion Criteria:

1. Clinical T4 disease including inflammatory breast cancer.
2. Prior history of invasive cancer including breast cancer except basal or squamous cell carcinoma of skin that has been definitively treated.
3. Known hypersensitivity to the study drugs or excipients.
4. Any illness or medical condition that is unstable or could jeopardize the safety of the subject or her compliance with study requirements.
5. Subjects unable to swallow oral medications.
6. Prior intake of letrozole, or any CDK inhibitor or anti-cancer therapy.
7. Concurrent treatment with any of the drugs not permitted, i.e. strong CYP3A inhibitors/inducers and drugs known to cause QTc interval prolongation (see section 5.7 for specific instructions).
8. QTc exceeding 480 msec, family or personal history of long or short QT syndrome, Brugada syndrome or known history of QTc prolongation, or Torsade de Pointes (TdP).
9. Uncontrolled diabetes, according to investigator's clinical judgment.
10. Pregnant or lactating women.