About this trial

Single arm, single site, open-label Phase II study of the effects of oral olaparib in participants with metastatic renal cell carcinoma that harbor an inactivating mutation in BAP-1, ATM, BRCA1, BRCA2, PALB2, CHEK2, BRIP1, RAD51C, BARD1, CDK12, CHEK1, FANCL, PP2R2A, RAD51B, RAD51D, or RAD54L who have had prior treatment with at least one immune checkpoint inhibitor or anti-VEGF therapy. Must have measurable disease on CT imaging per RECIST 1.1 criteria.

Eligibility criteria

Qualifiers

Willing and able to provide written informed consent. Provision of informed consent is required prior to any study procedures.

Patients aged 18 years of age or older.

Histological proof of renal cell carcinoma (both clear cell and non-clear cell allowed).

Metastatic (AJCC Stage IV) renal cell carcinoma.

Disqualifiers

Other malignancy unless curatively treated with no evidence of disease for ≥ 5 years except: adequately treated non-melanoma skin cancer, curatively treated in situ cancer of the cervix, ductal carcinoma in situ (DCIS), Stage 1, grade 1 endometrial carcinoma. Patients with a history of localized triple negative breast cancer may be eligible, provided they completed their adjuvant chemotherapy > 3 years prior to registration, and that the patient remains free of recurrent or metastatic disease.

Patients with symptomatic uncontrolled brain metastases. A scan to confirm the absence of brain metastases is not required. The patient can receive a stable dose of corticosteroids before and during the study as long as these were started at least 4 weeks prior to treatment. Patients with spinal cord compression unless considered to have received definitive treatment for this and evidence of clinically stable disease for 28 days.

Previous allogenic bone marrow transplant or double umbilical cord blood transplantation (dUCBT).

Judgment by the investigator that the patient should not participate in the study if the patient is unlikely to comply with study procedures, restrictions and requirements.

Trial design

Treatments tested in this trial

  • Olaparib

Treatment groups

20 Participants
are divided into 1 treatment group

Locations

1
Johns Hopkins Sidney Kimmel Comprehensive Cancer Center21228, BaltimoreMaryland, United States

Sponsors and collaborators

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

Lead sponsor

AstraZeneca

Collaborator