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Olaparib & Radiation Therapy for Patients Triple Negative Breast Cancer (TNBC) (RadioPARP)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03109080
Recruitment Status : Active, not recruiting
First Posted : April 12, 2017
Last Update Posted : October 27, 2020
Sponsor:
Collaborator:
AstraZeneca
Information provided by (Responsible Party):
Institut Curie

Brief Summary:
A Phase I of Olaparib with Radiation Therapy in Patients With Inflammatory, Loco-regionally Advanced or Metastatic TNBC (triple negative breast cancer) or Patient With Operated TNBC with Residual Disease.

Condition or disease Intervention/treatment Phase
Breast Neoplasms, Triple-Negative Breast Neoplasm Malignant Female Radiotherapy Side Effect Drug: Olaparib Radiation: Radiation therapy Phase 1

Detailed Description:
Open label phase I, dose escalation trial for patients with triple negative inflammatory, loco-regional advanced or metastatic breast cancer either inoperable after neoadjuvant chemotherapy or operated with residual disease (after neoadjuvant chemotherapy).

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 24 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Phase I of Olaparib With Radiation Therapy in Patients With Inflammatory, Loco-regionally Advanced or Metastatic TNBC (Triple Negative Breast Cancer) or Patient With Operated TNBC With Residual Disease
Actual Study Start Date : July 24, 2017
Actual Primary Completion Date : February 17, 2020
Estimated Study Completion Date : April 2022

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Breast Cancer
Drug Information available for: Olaparib

Arm Intervention/treatment
Experimental: Olaparib + radiation therapy
One week of Olaparib alone followed by 5 weeks of Olaparib and concurrent loco-regional radiotherapy. Five levels of dose of Olaparib are expected.
Drug: Olaparib
five levels of dose, per os administration, twice daily each day
Other Name: PARP (Poly (Adenosine diphosphate [ADP]-Ribose) Polymerase) inhibitor, Lynparza, AZD-2281

Radiation: Radiation therapy
3D conformal radiotherapy or intensity-modulated radiotherapy (IMRT), Simultaneous Integrated Boost (SIB), postoperative radiotherapy
Other Name: Radiotherapy




Primary Outcome Measures :
  1. Determination of the Maximal Tolerated Dose of Olaparib administered with concurrent loco regional radiotherapy [ Time Frame: 2 years ]
    Incidence of early Dose Limited Toxicity (DLTs: early adverse effects related to Olaparib administered with concurrent radiotherapy) to determinate the Maximal Tolerated Dose (MTD) of Olaparib administered with concurrent loco regional radiotherapy in patients who have triple negative inflammatory, loco-regional advanced or metastatic breast cancer either inoperable after neoadjuvant chemotherapy or operated patient with residual disease (after neoadjuvant chemotherapy).


Secondary Outcome Measures :
  1. Incidence of Serious Adverse Events (SAEs), graded according to NCI-CTCAE version 4.03 criteria to assess the safety profile of Olaparib administered with concurrent loco-regional radiotherapy. [ Time Frame: 2 years ]
    Incidence of Serious Adverse Events (SAEs), graded according to NCI-CTCAE version 4.03 criteria

  2. Incidence and severity of Adverse Events (AEs), graded according to NCI-CTCAE version 4.03 criteria to assess the safety profile of Olaparib administered with concurrent loco-regional radiotherapy. [ Time Frame: 2 years ]
    Incidence and severity of Adverse Events (AEs), graded according to NCI-CTCAE version 4.03 criteria

  3. Incidence and severity of laboratory abnormalities, graded according to NCI-CTCAE version 4.03 criteria to assess the safety profile of Olaparib administered with concurrent loco-regional radiotherapy. [ Time Frame: 2 years ]
    Incidence and severity of laboratory abnormalities, graded according to NCI-CTCAE version 4.03 criteria

  4. Incidence of acute toxicity 2 weeks and 6 weeks after the end of radiotherapy to assess the safety profile of Olaparib administered with concurrent loco-regional radiotherapy. [ Time Frame: 2 years ]
    Incidence of acute toxicity 2 weeks and 6 weeks after the end of radiotherapy

  5. Incidence of late toxicity at 1 year and at 2 years as of initiation of radiation therapy to assess the safety profile of Olaparib administered with concurrent loco-regional radiotherapy. [ Time Frame: 2 years ]
    Incidence of late toxicity at 1 year and at 2 years as of initiation of radiation therapy

  6. Incidence of treatment discontinuations and treatment modifications due to AEs to assess the safety profile of Olaparib administered with concurrent loco-regional radiotherapy. [ Time Frame: 2 years ]
    Incidence of treatment discontinuations and treatment modifications due to AEs

  7. Evaluation of the Objective Response Rate (ORR) to evaluate Olaparib administered with concurrent loco regional radiotherapy efficacy profile [ Time Frame: 2 years ]
    Evaluation of the Objective Response Rate (ORR) to treatment

  8. Evaluation of the Complete Response Rate to evaluate Olaparib administered with concurrent loco regional radiotherapy efficacy profile [ Time Frame: 2 years ]
    Evaluation of the Complete Response Rate to treatment

  9. Evaluation of Pathological Response Rate (pRR) after salvage surgery to evaluate Olaparib administered with concurrent loco regional radiotherapy efficacy profile [ Time Frame: 2 years ]
    Evaluation of Pathological Response Rate (pRR) after salvage surgery

  10. Evaluation of the loco-regional Progression Free Survival (l-PFS) to evaluate Olaparib administered with concurrent loco regional radiotherapy efficacy profile [ Time Frame: 2 years ]
    Evaluation of the loco-regional Progression Free Survival (l-PFS)

  11. Evaluation of the Progression Free Survival (PFS) or Disease Free survival (DFS) according to stage of disease to evaluate patient outcome [ Time Frame: 2 years ]
    Evaluation of the Progression Free Survival (PFS) or Disease Free survival (DFS)

  12. Evaluation of the distant relapse rate to evaluate patient outcome [ Time Frame: 2 years ]
    Evaluation of the distant relapse rate

  13. Evaluation of patient outcome by evaluation of the Overall Survival (OS). [ Time Frame: 2 years ]
    Evaluation Overall Survival (OS).

  14. Evaluation of patient outcome by evaluate disease specific survival rate. [ Time Frame: 2 years ]
    Evaluation of the disease specific survival rate.

  15. Explore biomarkers of Olaparib activity in combination with concurrent radiotherapy. [ Time Frame: 2 years ]
    Exploration of biomarkers of Olaparib associated with radiotherapy on biopsies.



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Woman aged >18 years.
  2. Histologically confirmed triple negative breast cancer with loco-regional radiotherapy indication :

    1. Non-operated with either:

      1. Inflammatory breast cancer in progression during neoadjuvant chemotherapy or inoperable after neoadjuvant chemotherapy.
      2. Loco-regional advanced breast cancer in progression during neoadjuvant chemotherapy or inoperable after neoadjuvant chemotherapy (T ≥ 3 and/or N ≥ 1; with evaluable disease according to RECIST 1.1 criteria).
      3. Non operable metastatic breast cancer (all T, all N, M1; with evaluable disease according to RECIST 1.1 criteria) needing local and regional treatment in case of good metastatic control after chemotherapy.
    2. Or patient operated after neoadjuvant treatment and surgery with residual disease (non-pCR and/or pN+ disease).
  3. Neoadjuvant chemotherapy (containing anthracyclines or taxanes or the combination of both or containing platinum-based chemotherapy) willingness to discontinue any cytotoxic chemotherapeutic agents, immunotherapy, and targeted therapies at least two weeks prior to start of Olaparib.
  4. ECOG performance status < 2.
  5. Life expectancy greater than 6 months.
  6. Adequate hematologic, renal and hepatic function (assessed within the two weeks prior to registration and within the month prior to the commencement of protocol treatment). For patients who have stopped chemotherapy two weeks prior to protocol treatment, hematologic function must be re-assessment 1 or 2 days before the first Olaparib intake:

    1. Haemoglobin ≥ 10.0 g/dL.
    2. Absolute Neutrophil Count (ANC) ≥ 1.5 x 109/L.
    3. White Blood Cells (WBC) > 3 x 109/L.
    4. Platelet count ≥ 100 x 109/L.
    5. Total bilirubin ≤ 1.5 x institutional upper limit of normal (ULN) (except in case of Gilbert syndrome).
    6. AST (SGOT)/ALT (SGPT) ≤ 2.5 x institutional upper limit of normal unless liver metastases are present in which case it must be ≤ 5 x ULN.
    7. Patients must have Creatinine Clearance estimated using the Cockcroft-Gault equation of ≥ 51 mL/min
  7. Urine or serum negative pregnancy test within two weeks prior to registration for non-postmenopausal patients. Negative pregnancy test confirmed within 1 or 2 days prior to first Olaparib intake.
  8. For woman with child-bearing potential, an efficacious contraception following sponsor recommendations must be used during the whole treatment period and up to three months after the last Olaparib administration.
  9. Ability to swallow and retain oral medications without gastrointestinal disorders likely to interfere with absorption of the study medication.
  10. Affiliation to the French Social Security System.
  11. Ability to understand and the willingness to sign a written informed consent document.

Exclusion Criteria:

  1. Radiation therapy: prior history of radiation therapy to the ipsilateral breast and/or regional nodes (except prior radiation therapy to other sites).
  2. Patient with unresolved or unstable, NCI-CTCAE v4.03 (National Cancer Institute Common Toxicity Criteria for Adverse Events) Grade 3 or greater toxicity from prior administration of prior anti-cancer treatment.
  3. Patient with clinically and uncontrolled significant comorbidity: major cardiac, respiratory, renal, hepatic, gastrointestinal, hematologic or neurological/psychiatric disease or disorder, including but not limited to: active uncontrolled infection; symptomatic congestive heart failure, unstable angina pectoris, or cardiac arrhythmia; any other illness condition(s) that could exacerbate potential toxicities, require excluded therapy for management, or limit compliance with study requirements.
  4. Patient with second primary cancer, except : adequately treated non-melanoma skin cancer, curatively treated in-situ cancer of the cervix, or other solid tumors curatively treated with no evidence of disease for ≥ 5 years.
  5. Concomitant anti-cancer treatment during protocol treatment and/or not completed at least 2 weeks prior to Olaparib initiation, except bisphosphonates and RANK inhibitors without restriction even during protocol treatment as long as these where started at least 4 weeks prior to study treatment initiation.
  6. Any previous treatment with a PARP (Poly (Adenosine diphosphate [ADP]-Ribose) Polymerase) inhibitor, including Olaparib.
  7. History of allergic reactions attributed to compounds of similar chemical or biologic composition to Olaparib.
  8. Patient being treated with drugs recognized as being strong inhibitors or inducers of the isoenzyme CYP3A (Rifabutin, Rifampicin, Clarithromycin, Ketoconazole, Itraconazole, Voriconazole, Ritonavir, Telithromycin) within the last 7 days before first Olaparib intake.
  9. Resting ECG with QTc > 470 msec on 2 or more time points within a 24 hour period or family history of long QT syndrome.
  10. Blood transfusions within 14 days prior to treatment start.
  11. Patient with myelodysplastic syndrome / acute myeloid leukaemia.
  12. Pregnant or breastfeeding woman.
  13. Patient already included in another clinical trial with an investigational drug.
  14. Patient individually deprived of liberty or placed under the authority of a tutor.
  15. Patient with any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03109080


Locations
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France
Institut Curie
Paris, France, 75005
Sponsors and Collaborators
Institut Curie
AstraZeneca
Investigators
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Study Director: Youlia KIROVA, MD Institut Curie
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: Institut Curie
ClinicalTrials.gov Identifier: NCT03109080    
Other Study ID Numbers: IC 2016-01 RadioPARP
2016-001837-28 ( EudraCT Number )
First Posted: April 12, 2017    Key Record Dates
Last Update Posted: October 27, 2020
Last Verified: September 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Neoplasms
Triple Negative Breast Neoplasms
Breast Neoplasms
Neoplasms by Site
Breast Diseases
Skin Diseases
Olaparib
Adenosine
Poly(ADP-ribose) Polymerase Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action
Antineoplastic Agents
Analgesics
Sensory System Agents
Peripheral Nervous System Agents
Physiological Effects of Drugs
Anti-Arrhythmia Agents
Vasodilator Agents
Purinergic P1 Receptor Agonists
Purinergic Agonists
Purinergic Agents
Neurotransmitter Agents