Method and device for treating microscopic tumors remaining in tissues following surgical resection
This invention concerns treating apparently normal tissue surrounding sites of cancerous tumors so as to reduce both the probability of a recurrence of cancer at and near the site of a cancerous tissue, and to reduce the amount of apparently healthy tissue that is usually excised along with the tumor, thereby providing a substantial benefit to the cancer patient by eliminating or delaying tumor recurrence and sparing normal tissue for its functionality and for avoiding unnecessary disfigurement.
1. A method of reducing recurrence of tumor cell growth in a mammalian tissue, the method comprising:
(a) providing a source for applying an electroporative electric pulse to a tumor and marginal tissue around the tumor;
(b) providing an agent capable of reducing tumor growth to the tumor and marginal tissue around the tumor;
(c) administering said agent to the tumor and marginal tissue around the tumor;
(d) applying the electroporative electric pulse by said source to the tumor and marginal tissue around the tumor, thereby delivering said agent into said cells;
(e) excising the entire tumor, resulting in reducing or eliminating tumor cell growth, wherein excision occurs about 15 minutes after application of the electroporative electric pulse in step (d); and
(f) closing a wound associated with tumor excision,
wherein a second electroporative electric pulse is not applied after steps (e) and (f).
2. The method of claim 1 wherein said agent is selected from the group consisting of Bleomycin, cisplatin, a polypeptide, an antibody, RNAi, an antisense nucleic acid, an expressible gene encoding a therapeutically active polypeptide, a chemokine, and a cytokine.
3. The method of claim 2 wherein said agent is delivered into said mammalian tissue either intravenously or intratumorally.
4. The method of claim 2 wherein said RNAi, anti sense nucleic acid, and expressible gene are formulated in poly-L-glutamate solution.
5. The method of claim 1 wherein said tumor is selected from the group consisting of a cancer cell in cutaneous tissue, a cancer cell located on the head or neck of a mammal, and a melanoma cell.
6. The method of claim 1 wherein said electroporative electric pulse comprises a pulse having a nominal field strength selected from the group consisting of 1500 V/cm, 1200 V/cm, between 800 and 1500 V/cm, between 200 and 800 V/cm.