Treatment of Patients With Advanced Renal Cancer With a Radiolabeled Antibody, Yttrium-90 Conjugated Chimeric G250

Patients were enrolled sequentially into cohorts of 3 to 6 patients until determination of
the maximum tolerated dose (MTD) of ^90Y-DOTA-cG250, defined as the dose level below the dose
at which ≥ 2 patients experienced dose-limiting toxicity (DLT). In an attempt to mitigate
liver uptake and toxicity, patients initially received a nontherapeutic injection with
^111In-DOTA-cG250 at an imaging dose of 5 mCi of ^111In + 10 mg of cG250 on Day 1. Whole body
and blood measurements of radioactivity were obtained on at least 3 occasions for 1 week to
determine targeting and dosimetry. Provided that protocol-specified criteria were met,
including targeting to lesions > 2 cm detected on computed tomography (CT) scan, a single
dose of therapeutic ^90Y-DOTA-cG250 was administered on Day 8, 9, or 10. The starting dose of
^90Y-DOTA-cG250 was 0.2 mCi/kg of ^90Y + 10 mg of cG250 administered as an intravenous (IV)
infusion, with escalation of the ^90Y dose in subsequent cohorts in 0.05 to 0.1 mCi/kg
increments.

Patients were treated in an outpatient setting and were observed for at least 2 hours
following each infusion, at which point vital signs and blood samples were obtained. Patients
were followed for 6 to 8 weeks post-treatment (or after recovery from toxicity) with imaging,
biochemical, serological, and hematologic tests to determine the safety of ^90Y-DOTA-cG250
and to inform dose-escalation decisions. Extent of disease evaluations, preferably by
positron emission tomography (PET)/CT or standard CT, were performed at baseline and 6 to 8
weeks post-treatment (or after recovery from toxicity). Long-term follow-up was performed,
when possible, every 12 weeks thereafter for up to 2 years.

Inclusion Criteria:

1. All patients must have had histologically proven clear cell renal carcinoma.

2. Age ≥ 18 years. Children were not enrolled because clear cell renal cancer is rarely
seen in children.

3. All patients must have had a clinical presentation consistent with metastatic renal
carcinoma.

4. Patients must have had bidimensionally measurable disease by conventional imaging
methods including radiography, ultrasound, CT, or other anatomic imaging modalities.
Lesions seen on skeletal scintigraphy alone were not considered measurable.

5. Female patients of childbearing age were required to have a negative pregnancy test
carried out the day of and prior to receiving therapy, and were asked to use effective
contraception during the study.

6. All patients must have been ambulatory with a Karnofsky Performance Status of at least
70.

7. The following laboratory results within the last 2 weeks prior to study Day 1:

- serum creatinine ≤ 2.0 mg/dL

- serum bilirubin (total) ≤ 2.0 mg/dL

- aspartate aminotransferase (AST) ≤ 2.5 × the upper limit of normal (ULN)

- alanine aminotransferase (ALT) ≤ 2.5 × ULN

- white blood cell (WBC) count ≥ 3500/mm^3

- platelet count ≥ 100,000/mm^3

- prothrombin time ≤ 1.3 × control

8. Able and willing to give valid written informed consent.

Exclusion Criteria:

1. Significant prior radiotherapy (> 30 Gy) to the entire pelvis and/or lumbosacral
spine.

2. Clinically significant cardiac disease (New York Heart Association Class [III/IV]).

3. Serious infection requiring treatment with antibiotics, or other serious illness.

4. Chemotherapy, radiation therapy, or immunotherapy within 4 weeks prior to study agent
administration.

5. Survival expectancy of less than 12 weeks.

6. Patients with central nervous system (CNS) involvement were excluded under the
following criteria:

- Brain metastasis, except for stable disease over 3 months.

- Untreated brain metastasis.

- Evidence of progression of neurologic CNS involvement within 3 months prior to
entering the protocol.

7. Hypercalcemia > 12.5 mg/100 mL or symptomatic.

8. Mental impairment that may have compromised the ability to give informed consent and
comply with the requirements of the study.

9. Lack of availability of the patient for clinical and laboratory follow-up assessment.

10. Patients known to have hepatobiliary disease and/or human immunodeficiency
virus/acquired immune deficiency syndrome.

11. Participation in any other clinical trial involving another investigational agent
within 4 weeks prior to enrollment.

12. Pregnancy or breastfeeding.

13. Refusal or inability to use effective means of contraception in men or women of
childbearing potential.