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About
This is a multicenter randomized phase ll clinical trial to evaluate the pathological complete response (pCR) in the tumour burden (primary and lymph nodes) with olaparib alone or in the olaparib and durvalumab arm in TNBC patients candidate for neoadjuvant strategy showing a t/gBRCAmut or BRCAness/HRD profile.
Full description
Eligible patients will be registered for central testing of BRCA mutatinal status and HRD/BRCAness profile with central review of ER, PgR, TILs and PD-L1.
Eligible patients will be randomly assigned to either olparib or olaparib and durvalumab (=neoadjuvant treatment) in a 1:1 ratio. The treatment duration in both arms will last 16 weeks and both treatments are considered as experimental treatments in this study.
After completion of neoadjuvant systemic treatment, patients will undergo surgery and followed-up for 2 years after investigational drug discontinuation. After surgery, adjuvant treatment will be left at the investigator's decision.
Sex
Ages
Volunteers
Inclusion and exclusion criteria
Inclusion Criteria at registration:
Histologically confirmed, invasive TNBC, defined as:
Early-stage disease, defined as cT1c-T2, N0-N1, M0
Medically fit for a neoadjuvant strategy and for radical surgery as by the investigator's decision
No prior systemic therapy nor definitive surgery for BC
Age ≥18 years
Women and men can be included
ECOG performance status (PS) 0-1
Exclusion Criteria at registration:
Inclusion criteria at randomization:
Deleterious germline or somatic mutation in BRCA 1 and/or BRCA 2 or homologue repair deficiency (HRD) status as determined by central testing.
Tumour tissue available from primary tumour (fine needle aspiration cytology or lymph node metastasis tissue are not acceptable).
Normal organ and bone marrow function measured within 28 days prior to administration of study treatment as defined below:
Body weight >30 kg
Participation in translational research is mandatory
Women of childbearing potential (WOCBP) must have a negative serum pregnancy test in the screening period and confirmed prior to treatment on day 1.
Female patients of childbearing/reproductive potential must use adequate birth control measures, as defined by the investigator, during the study treatment period and for at least 3 months after the last dose of treatment. A highly effective method of birth control is defined as a method which results in a low failure rate (i.e., less than 1% per year) when used consistently and correctly. Such methods include:
Male patients must use a condom during treatment and for 3 months after the last dose of study treatment when having sexual intercourse with a pregnant woman or with a woman of childbearing potential. Female partners of male patients should also use a highly effective form of contraception (see above) if they are of childbearing potential.
Female subjects who are breast feeding must discontinue nursing prior to the first dose of study treatment and until 3 months after the last study treatment.
Registration to a National Health Care System
Exclusion criteria at randomization:
Inability to swallow and/or retain oral tablets
Blood transfusion within 28 days
History of human immunodeficiency virus (HIV) (positive HIV 1/2-antibodies)
Active Hepatitis B or Hepatitis C
Active bacterial, viral, or fungal infection requiring systemic therapy
History of active tuberculosis (TB, Bacillus Tuberculosis)
History of idiopathic pulmonary fibrosis, drug-induced pneumonitis, organizing pneumonia, interstitial lung disease or evidence of active pneumonitis on screening (TAP-CT-scan)
History of aortic disease (aneurysm or dissection)
History of myasthenia gravis
Mean QT interval corrected for heart rate (QTc) ≥ 500ms using Fridericia's Correction
Uncontrolled intercurrent illness
Psychiatric illness/social situations or addiction (chronic alcoholism or drug addiction) that would limit compliance with study requirement, substantially increase risk of incurring AEs or compromise the ability of the patient to give written informed consent.
Any other serious or uncontrolled illness or abnormality that, in the judgment of the investigator, limits compliance with study requirement, substantially increases risk of incurring AEs or compromises the ability to give written informed consent.
Current or prior use of immunosuppressive medication within 14 days before the first dose of durvalumab.
Receipt of live attenuated vaccine within 30 days prior to the first dose of study treatment.
Any concurrent systemic chemotherapy, immunotherapy, biologic or hormonal therapy for cancer treatment.
Any unresolved toxicity (Common Terminology Criteria for Adverse Event (CTCAE) grade ≥ 2) caused by previous cancer therapy, excluding alopecia, vitiligo.
Concomitant use of strong CYP3A inhibitors.The required washout period prior to starting study treatment (olaparib) is 2 weeks.
Concomitant use of strong CYP3A inducers. The required washout period prior to starting study treatment (olaparib) is 5 weeks for phenobarbital and 3 weeks for other agents.
Major surgery within 4 weeks prior to the first dose of study treatment. Patients must have recovered from the surgical procedure. Implanted port placement is not considered as a major surgery.
Known allergy or hypersensitivity to olaparib or durvalumab, or to any excipient.
Contraindication to MRI or to the contrast medium used for MRI (gadolinium).
Participation in another clinical study, unless it is an observational (non-interventional) clinical study or during the follow-up period of an interventional study
Female patients who are pregnant or male or female patients of reproductive potential who are not willing to employ effective birth control from screening to 3 months after the last dose of study treatment.
Primary purpose
Allocation
Interventional model
Masking
0 participants in 2 patient groups
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Central trial contact
EORTC HQ
Data sourced from clinicaltrials.gov
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