Trial of ICM With or Without AZD2281 (Olaparib) in Patients With Advanced Pancreatic Cancer

Completed · Phase 1

Conditions studied: Pancreatic Cancer

In brief

Patients whose pancreatic cancers have defects in the BRCA/Fanconi DNA repair pathway or other defects in homologous repair will have cancers that respond to olaparib when given in combination with the DNA damaging agents, irinotecan, cisplatin, mitomycin C (ICM).

Key facts

Study ID

NCT01296763

Run by

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

People needed

18

Starts

2011-01-01

Expected to finish

2016-02-01

Last updated by the study team

2016-03-22

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Provision of fully informed consent prior to any study specific procedures.
• Histologic or cytologic confirmation of exocrine pancreatic adenocarcinoma.
• Locally advanced, inoperable (due to venous or arterial encasement ≥ 180° of the vessel), and/or metastatic disease by imaging (CT, MRI, or EUS). Acquisition of tissue rather than cytology is encouraged if the patient gives informed consent.
• Measurable disease according to RECIST 1.1 criteria
• Prior neoadjuvant or adjuvant therapy is acceptable, as long as no more than one drug of the ICM regimen was used.
• No prior chemotherapy for advanced pancreatic cancer with Olaparib is permitted. Gemzar, Tarceva, and 5-FU or Xeloda, Oxaliplatin Taxotere, and FOLFIRINOX are permitted.
• Three weeks since last surgery or chemotherapy mentioned in #5 above or investigational therapies. Four weeks since radiation.
• No prior PARP inhibitors of any type
• ECOG status < 3
• Life expectancy > 3 months
• Patients must have normal organ and bone marrow function
• Age >=18.
• Patient is willing and able to comply with the protocol for the duration of the study including treatment, scheduled visits, and examinations.
• Evidence of non-childbearing status for women of childbearing potential, or postmenopausal status: negative urine or serum pregnancy test within 28 days of study treatment, confirmed prior to treatment on day 1
• For inclusion in genetic research, patients must fulfill the following criterion:
• Provision of informed consent for genetic research. If a patient declines to participate in the genetic research, there will be no penalty or loss of benefit to the patient. The patient will not be excluded from other aspects of the study.

You may not qualify if…

• Patients with second primary cancer, except: adequately treated non-melanoma skin cancer or curatively treated in-situ solid tumors with no evidence of disease for ≥ 5 years.
• Patients receiving any systemic chemotherapy, radiotherapy (except for palliative reasons), less than 3 weeks from the last dose prior to study treatment (or a longer period depending on the defined characteristics of the agents used). The patient can receive a stable dose of bisphosphonates for bone metastases before and during the study as long as these were started at least 4 weeks prior to treatment.
• For patients who have locally advanced pancreatic cancer only, if they have received therapeutic doses of radiation therapy to their pancreatic bed (\~50 Gy) for treatment of their locally advanced pancreatic cancer
• Patients having already had prior chemotherapy for more than 12 months for their advanced pancreatic cancer (not including adjuvant/neoadjuvant)
• Patients receiving the following classes of inhibitors of CYP3A4 (see Section for guidelines and wash out periods).
• Current use of azole antifungals, macrolide antibiotics, or protease inhibitors
• Unresolved toxicities (>CTCAE 4.0 grade 2) caused by previous cancer therapy.
• Patients with known brain metastases. A scan to confirm the absence of brain metastases is not required unless the initial examination reveals CNS signs of disease.
• Major surgery less than 3 weeks prior to starting study treatment and patients must have recovered from any effects of any major surgery.
• Patients considered a poor medical risk due to serious, uncontrolled medical disorders, non-malignant systemic disease, or active, uncontrolled infection. Examples include, but are not limited to, uncontrolled ventricular arrhythmia, recent (within 3 months) myocardial infarction, uncontrolled major seizure disorder, unstable spinal cord compression, superior vena cava syndrome, or any psychiatric disorder that prohibits obtaining informed consent.
• Patients unable to swallow oral medication and patients with gastrointestinal disorders likely to interfere with absorption of the study medication.
• Breast feeding and/or pregnant women.
• Immunocompromised patients, e.g., patients who are known to be serologically positive for human immunodeficiency virus (HIV).
• Patients with known active hepatic disease (i.e., Hepatitis B or C). Patients with a known hypersensitivity to Olaparib or any of the excipients of the product or history of severe allergic reactions to platinums or chemotherapy.
• Grade 2 neuropathy at entry from any etiology, including diabetes (in view of Cisplatin).
• Prior episodes of recurrent deep vein thrombosis or Trousseau's Syndrome unless the patient is successfully anticoagulated. If a patient has had a history of clotting or is suspected to have Trousseau's syndrome and is not anticoagulated, a D-Dimer level will be checked. If it is > 3 x ULN, patients will be expected to be anticoagulated with low molecular weight heparinoids (i.e. Lovonox).

Where it is running

• The Johns Hopkins University School of Medicine — Baltimore, Maryland, United States
• Columbia University Medical Center — New York, New York, United States

Full record on ClinicalTrials.gov

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