A Study of Yttrium-90 Radioactive Resin Microspheres to Treat Colorectal Adenocarcinoma Metastatic to the Liver

Not Applicable

Terminated

Conditions: Colorectal Neoplasms
Liver Neoplasms

Interventions: Device: Yttrium-90 Radioactive Resin Microspheres

Registration Number: NCT01098422

Lead Sponsor: Tony Reid, M.D., Ph.D.

Brief Summary: The purpose of this study is to determine the effectiveness of radioactive microsphere infusion as a treatment for liver metastases from colon or rectal cancer. The investigators hypothesis is that the administration of microspheres between first and second line chemotherapy will increase progression-free survival time by about 2.5 months and may also improve tumor response rates to subsequent second line chemotherapy.

Detailed Description: This is a phase II, single-arm study of Yttrium-90 (Y-90) radioactive resin microspheres in the treatment of colorectal adenocarcinoma metastatic to the liver in patients who have had progressive disease through first line combination chemotherapy or have otherwise failed first line chemotherapy due to toxicity. Expected enrollment at University of California, San Diego (UCSD) is approximately 34 subjects.

The dose of Yttrium-90 radioactive resin microspheres is calculated based on body surface area (to estimate normal liver volume), percentage of total liver represented by the targeted lobe, and percentage of the lobe that is occupied by tumor, corrected for percentage lung shunt. The prescribed dose, calculated by the nuclear medicine physician, will be delivered by the interventional radiologist using the standard delivery system with frequent fluoroscopic monitoring to assure ante grade blood flow immediately after treatment. Additional current standard practice includes obtaining a nuclear medicine scan of the patient immediately after each therapeutic Yttrium-90 microspheres administration to prove delivery of the agent to the targeted portion of the liver and absence of either extra-hepatic Yttrium-90 delivery or free Yttrium-90.

Blood samples will be obtained one week after the first treatment with microspheres. If the patient has bi-lobar disease and the results of lab tests meet protocol specified criteria, the dose will be repeated in the initially-untreated lobe. If the lab tests do not meet protocol specified criteria (i.e. study inclusion/exclusion criteria), the treatment will be deferred for fourteen days and labs repeated. If they are then within parameters, the patient will receive the second dose. If they are not within parameters, the patient will proceed to chemotherapy.

Patients will remain off chemotherapy after their final microspheres treatment for a minimum of three weeks. Second line treatment options include FDA approved anti-neoplastic agents used in colorectal cancer metastatic to the liver with the exception of bevacizumab and capecitabine, which has been less rigorously studied with relation to Yttrium-90 radioactive microspheres and therefore will not be used. When patients are found to have progressive disease while receiving second line chemotherapy, they will then undergo a comprehensive clinical, laboratory, and imaging assessment and enter the follow-up phase in which they are assessed every five to seven months until death or withdrawal of consent.

A contrast enhanced ultrasound (CEUS) will be performed pre microsphere treatment (within 14 days), post microsphere treatment (2 weeks, 4 weeks, 8 weeks and 12 weeks post the microsphere treatment). If patients require two treatments with microspheres, they will be evaluated 2, 4, 8 and 12 weeks post the second treatment.

Recruitment & Eligibility

Status: TERMINATED

Sex: All

Target Recruitment: 10

Inclusion Criteria

Histologically confirmed colorectal carcinoma. Liver metastasis will be confirmed by either PET scan or biopsy.
Ability to understand and willingness to sign written informed consent
Minimum of 18 years of age
Liver dominant metastases measurable by CT or MRI and therefore amenable to serial assessment using RECIST criteria
Progressive disease of metastatic colorectal carcinoma on first line combination chemotherapy with a 5-fluorouracil/leucovorin with oxaliplatin (FOLFOX) based regimen (Folinic Acid, Oxaliplatin and Fluorouracil)or failure of first line chemotherapy due to toxicity
Candidate for second line chemotherapy with a fluorouracil, leucovorin, and irinotecan (FOLFIRI) regimen. Per standard of care, second line chemotherapy will not include Bevacizumab.
Karnofsky Performance Score (KPS) of 70% or greater
Life expectancy of greater than or equal to four months by investigator estimation
Females with negative urine or serum pregnancy test
Effective double barrier contraception for a minimum of two months following the final infusion of microspheres
Patients who are not candidates for transarterial chemoembolization (TACE), thermal ablation or surgical resection

Exclusion Criteria

Dominant extra-hepatic disease including cerebral metastases or other extra-hepatic metastases that are symptomatic
Large volume ascites assessed by cross sectional CT imaging
Any chemotherapy < 4 weeks prior to the first microsphere treatment
Anticipated to need Avastin chemotherapy within eight weeks of day M1
Absolute neutrophil count (ANC) < 1.5 x 109/L
Platelets (PLT) < 60,000/mm3
Hemoglobin (Hgb) < 9.0 gm/dL
Prothrombin time (PT) or Partial Prothrombin time (PTT) > upper limit of normal (ULN)
Serum Creatinine > 2.0 mg/dL
Forced expiratory volume (FEV1) < 1L by baseline pulmonary function tests (ordered if investigator judges it to be clinically indicated)
Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) > 5 times upper limits of normal (ULN) or total bilirubin > 2.0 mg/dL
History of incompetent sphincter of oddi (e.g.: sphincterotomy, biliary-enteric anastamosis, or percutaneous biliary drain)
Severe hypoalbuminemia (albumin < 2.0 g/dL)
Alkaline phosphatase > 2.5 times ULN
Greater than 20% lung shunting (determined by the MAA - Tc 99 nuclear medicine lung shunt scan)
Pre assessment angiogram and MAA scan demonstrating any uncorrectable activity in the stomach, bowel or pancreas
Major surgery < 4 weeks prior to the first microsphere treatment
Female who is pregnant or nursing
Men and women of childbearing potential wishing to conceive < 2 months following the completion of the microsphere portion of the study.
Any investigational agent administered < 4 weeks prior to microsphere treatment
A known history of hepatitis B or hepatitis C
Known hypersensitivity to any component of microsphere infusion
History of, or current coagulation or bleeding disorder
History of significant hepatic cirrhosis, fibrosis or hemochromatosis
History of malignancy, other than colorectal cancer, within five years of the start of study participation, except in situ cervical or skin cancer
Active severe infection or any other concurrent disease or medical conditions that are likely to interfere with the study as judged by the investigator
Prior treatment with radioactive microspheres or external beam radiation therapy to the liver
Prophylactic anticoagulation and nonsteroidal antiplatelet drugs are only a contraindication, if the PT/PTT are above the ULN. Plavix (clopidogrel) will need to be stopped 5 days prior to the hepatic-angiogram and the microsphere procedures, then started the next day.
History of right to left, bi-directional or transient right to left cardiac shunts, worsening or clinically unstable congestive heart failure, acute myocardial infarction or acute coronary syndromes serious ventricular arrhythmias or high risk for arrhythmias due to prolongation of the QT interval, respiratory failure as manifested by signs or symptoms of carbon dioxide retention or hypoxemia or severe emphysema, pulmonary emboli or other conditions that causes pulmonary hypertension due to compromised pulmonary arterial vasculature

Study & Design

Study Type: INTERVENTIONAL

Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Yttrium-90 Radioactive Resin Microspheres	Yttrium-90 Radioactive Resin Microspheres	Yttrium-90 Radioactive Resin Microspheres

Primary Outcome Measures

Name	Time	Method
PFS	2 years	Progression-free survival assessed by Response Evaluation Criteria in Solid Tumors (RECIST) criteria using Computerized Tomography (CT) assessment of tumor(s)

Secondary Outcome Measures

Name	Time	Method
Number of Participants With Responses as Determined by RECIST Criteria Using CT or Magnetic Resonance Imaging (MRI) Assessment	2 years	Tumor response rate as determined by RECIST criteria using CT or Magnetic Resonance Imaging (MRI) assessment of tumor size every 3 months
60 Day All-cause Mortality Rate	60 days	Number of Participants with 60 Day All-cause Mortality
Adverse Events	1 years	Number of adverse events by grade
Percentage of Participants Achieving Overall Survival at 6 Months	6 Months	Overall survival assessed at 6 months since diagnosis of progression on first-line therapy

Trial Locations

Locations (2): The Rebecca and John Moores UCSD Cancer Center
🇺🇸
La Jolla, California, United States
UCSD Medical Center
🇺🇸
San Diego, California, United States