Cryosurgery in Treating Patients With Unresectable Liver Metastases From Colorectal Cancer



Status:Completed
Conditions:Colorectal Cancer, Cancer, Cancer, Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - 120
Updated:1/3/2019
Start Date:August 1997
End Date:March 2, 2004

Use our guide to learn which trials are right for you!

Phase II Trial of Cryoablation for Treatment of Unresectable Colorectal Hepatic Metastases

RATIONALE: Cryosurgery for liver metastases may have fewer side effects and improve recovery.

PURPOSE: Phase II trial to study the effectiveness of cryosurgery for patients with
unresectable liver metastases from colorectal cancer.

OBJECTIVES: I. Evaluate the feasibility of conducting a multi-institutional clinical study of
cryosurgery for liver metastases. II. Evaluate the morbidity and mortality of cryosurgery for
liver metastases when applied in a multi-institutional setting. III. Evaluate the efficacy of
cryosurgery for liver metastases as measured by total liver control, local lesion control,
and overall survival.

OUTLINE: This is a multi-institutional study. Patients are first confirmed by exploratory
laparotomy to have no extrahepatic metastases. They then undergo biopsy of the portal lymph
node, after which, full mobilization of liver is recommended. Cholecystectomy is optional but
recommended for treatment of tumors adjacent to the gallbladder. After mapping out the
location and size of the metastatic tumor by ultrasound, cryoablation of the metastases is
carried out. Cryoablation involves the delivery of nitrogen through metallic probes placed
surgically into the center of the liver metastases. There are two freeze and thaw cycles for
each lesion with synchronous intraoperative ultrasound monitoring of the cryoablation. One
centimeter margin of cryoablation is determined by this ultrasound image. Treatment of the
liver with regional chemotherapy is not allowed until radiographic and pathologic
confirmation of disease progression in the liver. Follow-up is at 3 weeks after surgery and
then every 3 months.

PROJECTED ACCRUAL: There will be a maximum of 45 patients accrued in approximately 3 years
for this study. This is a two stage accrual design in which 17 patients are first accrued of
which 15 should be eligible. If fewer than 11 of the initial 15 eligible patients show no
evidence of disease at 3 months, the study stops and treatment is abandoned. If at least 11
patients show no evidence of disease, then 28 additional patients are accrued.

DISEASE CHARACTERISTICS: Histologically confirmed primary colorectal adenocarcinoma with
synchronous and metachronous metastases to liver 1 to 5 liver metastases demonstrated by
rapid sequence CT scan or Feridex-enhanced MRI within 2 weeks of registration CT
portography not required No single metastasis greater than 6 cm Maximum liver involvement
must not be more than 40% by volume No extrahepatic metastases

PATIENT CHARACTERISTICS: Age: 18 and over Performance status: ECOG 0-2 Hematopoietic:
Platelet count greater than 80,000/mm3 Prothrombin time less than 15.0 seconds Hepatic:
Bilirubin less than 2.0 mg/dL Renal: Not specified Other: Must be disease free for at least
5 years except for treated basal cell or squamous cell skin cancer

PRIOR CONCURRENT THERAPY: Biologic therapy: Not specified Chemotherapy: Prior chemotherapy
allowed No concurrent regional chemotherapy allowed Endocrine therapy: Not specified
Radiotherapy: Not specified Surgery: Not specified
We found this trial at
3
sites
Rochester, New York 14642
?
mi
from
Rochester, NY
Click here to add this to my saved trials
30 Prospect Ave
Hackensack, New Jersey 07601
(201) 996-2000
Hackensack University Medical Center Hackensack University Medical Center, part of the Hackensack University Health Network,...
?
mi
from
Hackensack, NJ
Click here to add this to my saved trials
Philadelphia, Pennsylvania 19102
?
mi
from
Philadelphia, PA
Click here to add this to my saved trials