Study of Hydroxychloroquine and Aldesleukin in Renal Cell Carcinoma Patients (RCC)
Phase: Phase 1/Phase 2
Diagnosis: Kidney Cancer
NCT ID: NCT01550367
(View complete trial on ClinicalTrials.gov)
DFCI Protocol ID:
The main goal of the research study is to determine whether treating renal cell cancer patients with the study drug, hydroxychloroquine, along with IL-2, a standard treatment of kidney cancer that has spread to other parts of the body, can make the cancer easier to kill and eliminate. Another goal is to see how the study drug affects the body's immune cells which fight cancer cells.
Beth-Israel Deaconess Medical Center, Dana-Farber Cancer Institute
David McDermott, MD,
Beth Israel Deaconess Medical Center
Beth-Israel Deaconess Medical Center:
Cancer Trials Call Center, 617-667-3060
- Histologically confirmed metastatic renal cell carcinoma with predominantly clear
- Have measurable disease by RECIST 1.1 criteria. For example, this would include tumor
in the lung, liver, and retroperitoneum. Bone disease is difficult to follow and
quantify and as a sole site would not be acceptable.
- Patients must be at least 4 weeks from radiation or surgery and recovered from all
- Age ≥18 years.
- Karnofsky Performance Status ≥80%.
- Adequate end organ function:
1. Hematologic: ANC ≥ 1000cells/uL, platelets ≥ 100,000/uL, hemoglobin ≥ 9g/dl
(pre transfusion values used for prognostic factor, can be transfused or use
recombinant erythropoietin growth factors but must not have active bleeding).
2. Liver: AST ≤ 2 x ULN (upper limit of normal), serum total bilirubin ≤ 2 x ULN
(except for patients with Gilbert's Syndrome).
3. Renal: serum creatinine ≤ 1.5 mg/dL or estimated creatinine clearance ≥
60ml/min using Cockcroft-Gault estimation using the formula per protocol.
4. Pulmonary: FEV1 ≥ 2.0 liters or ≥ 75% of predicted for height and age. (PFTs
are required for patients over 50 or with significant pulmonary or smoking
history defined as >20 pack years or history of COPD/emphysema).
5. Cardiac: No evidence of congestive heart failure, symptoms of coronary artery
disease, myocardial infarction less than one year prior to entry, serious
cardiac arrhythmias, or unstable angina. Patients who are over 40 or have had
previous cardiac disease will be required to have a negative or low probability
cardiac stress test for cardiac ischemia.
- Women should not be lactating and, if of childbearing age, have a negative pregnancy
test within two weeks of entry to the study.
- Appropriate contraception in both genders.
- The patient must be competent and have signed informed consent.
- CNS: No history of cerebrovascular accident, transient ischemic attacks, central
nervous system or brain metastases.
- Patients who have received prior systemic therapy for metastatic RCC or have
previously received IL-2 are not eligible. Patients on HCQ in neoadjuvant protocols
or in the past for clinical indications ARE eligible.
- Concomitant second malignancy except for non-melanoma skin cancer, and non-invasive
cancer such as cervical CIS, superficial bladder cancer without local recurrence or
- In patients with a prior history of invasive malignancy, less than five years in
- Positive serology for HIV, hepatitis B or hepatitis C.
- Significant co-morbid illness such as uncontrolled diabetes or active infection that
would preclude treatment on this regimen.
- Use of corticosteroids or other immunosuppression (if patient had been taking
steroids, at least 2 weeks must have passed since the last dose).
- History of inflammatory bowel disease or other serious autoimmune disease. (Not
including thyroiditis and rheumatoid arthritis). Patients already on
hydroxychloroquine for such disorders are not eligible.
- Patients with organ allografts.
- Uncontrolled hypertension (BP >150/100 mmHg).
- Proteinuria dipstick > 3+ or ≥ 2gm/24 hours.
- Urine protein:creatinine ratio ≥ 1.0 at screening.
- Major surgery, open biopsy, significant traumatic injury within 28 days of starting
treatment or anticipation of need for major surgical procedure during the course of
- Minor surgical procedures, fine needle aspirations or core biopsies within 7 days
prior to starting treatment. Central venous catheter placements are permitted.
- History of abdominal fistula, gastrointestinal perforation, or intra-abdominal
abscess within 6 months prior to starting treatment.
- Serious, non-healing wound, ulcer, or bone fracture.
- History of tumor-related or other serious hemorrhage, bleeding diathesis, or
- History of deep venous thrombosis, clinically significant peripheral vascular
disease, or other thrombotic event.
- Inability to comply with study and/or follow-up procedures.
- Individuals with known history of glucose 6 phosphate deficiency are excluded from
the trial (possible issue with HCQ tolerance).
- Patients with previously documented macular degeneration or diabetic retinopathy are
excluded from the trial.
- Baseline EKG with QTc > 470 msec (including subjects on medication). Subjects with
ventricular pacemaker for whom QT interval is not measurable will be eligible on a