Radiofrequency Ablation of Painful Soft Tissue Neoplasms

Inclusion Criteria

INCLUSION CRITERIA

All patients must have pain poorly controlled by conventional methods, defined as ongoing
pain despite maximum pharmacologic interventions, or severe side effects like mental
status alteration from medication, as determined by the patient along with the palliative
care/ pain consult service and/or the patient's physician.

Persistent or recalcitrant pain will be localized to a specific neoplastic lesion
determined by consensus review by the P.I. with the pain/palliative care service, the
patient's physician, and the diagnostic radiologist reviewing the case. Only patients
with a limited number of lesions causing pain will be enrolled, and only if there is a
target lesion which can be the focus of ablation.

All patients must have had a diagnostic CT scan which conclusively reveal a soft tissue
metastasis, which is the source of pain as determined by the Palliative care oncologist.
One independent radiologist who is not a co-investigator in this study must confirm this.
Tumor does not have to be completely destroyable by RFA, as patients may benefit from
simple debulking, denervation, or decrease in intratumoral pressure.

Age greater than or equal to 18 years.

Biopsy of lesion in question for histologic or cytologic confirmation of cancer will be
obtained when safe and clinically indicated, or if there is reasonable doubt as to
diagnosis. Reasonable doubt will be determined by the PI, the surgeon, and the palliative
care oncologist by consensus.

Performance Status ECOG 0-2.

Life expectancy of 3 months or greater.

Platelet count greater than 50,000/mL, absolute granulocyte count (AGC) greater than
1,000/mL, serum creatine less than 1.5 mg/dl (or if greater than 1.5, measured creatine
clearance greater than 50mL/min). Any patient with elevated PTT or PT that is
uncorrectable will be evaluated by NIH hematology for safety of procedure. This will
allow patients with "falsely-elevated" values to undergo the same evaluation that they
would have for surgery or other invasive procedure. Dr. Horne is the hematologist and
coinvestigator on this protocol.

No serious concurrent medical illness.

Bi-dimensionally measurable disease by radiographic means or physical examination.

The ability to understand and willingness to sign a written informed consent form, and to
comply with the protocol. If in question will be reviewed by the ethics committee.

Consult with an NCI surgeon and Palliative care oncologist who will determine if the
patient's pain medications and other options (surgical) have been optimized prior to entry
in this protocol. Surgical options must be either not possible, or rejected by the
patient. Surgery will be either offered or ruled out as an alternative by the NCI surgeon
prior to treatment.

Chemotherapy, radiation therapy, and classification of drug therapy must be stable without
changes for 2 weeks prior to tumor ablation.

EXCLUSION CRITERIA

Patients with a coagulopathy which cannot be corrected, or a bleeding diathesis, will be
excluded from this study. Patients taking anti-inflammatory agents or aspirin, heparin,
heparinoids, or coumadin will be excluded until the prothrombin time and partial
thromboplastin time have normalized.

Patients with an altered mental status that precludes understanding or consenting for a
procedure will be excluded from this study.

Pregnant or nursing women and women of childbearing potential unless using effective
contraception as determined by the patient's physician.

Patients who are poor medical risk because of other non malignant systemic disease or
active, uncontrolled infection.

Patients should not change the class of pain medication for two weeks prior to treatment
and are ineligible if class is changed within two weeks prior. If the class of pain
medication is switched within two weeks after treatment, the patient becomes inevaluable.