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[Intraarterial chemoembolization therapy for unresectable liver cancer using plachitin particles]
H Tabara1, H Matsuura, H Kohno
12nd Dept. of Surgery, Shimane Medical University.
Gan to Kagaku Ryoho. Cancer & Chemotherapy
|September 1, 1994
Summary
Plachitin, a novel arterial chemoembolization agent combining chitin and cis-diamminedichloroplatinum (CDDP), shows promise for unresectable liver cancer. This therapy demonstrated significant tumor regression and biomarker reduction in three patients with primary and secondary liver cancers.
Area of Science:
- Oncology
- Interventional Radiology
- Materials Science
Background:
- Unresectable liver cancer presents significant treatment challenges.
- Arterial chemoembolization offers a localized drug delivery approach.
- Plachitin, a composite of chitin and cis-diamminedichloroplatinum (CDDP), was developed for this purpose.
Observation:
- Three patients with unresectable liver cancer (hepatocellular carcinoma, bile duct cystadenocarcinoma, and liver metastases) received Plachitin arterial chemoembolization.
- Tumor regression rates varied from 39% to 84.4% after one to three courses.
- Tumor markers such as alpha-fetoprotein (AFP), carbohydrate antigen 19-9 (CA19-9), and carcinoembryonic antigen (CEA) showed significant decreases.
Findings:
- Plachitin chemoembolization achieved objective tumor responses in 66.7% of the treated patients.
- Pharmacokinetic studies indicated low systemic platinum (Pt) levels, with transient elevations in urine Pt.
- Adverse effects were generally transient and manageable, including nausea, fever, and elevated liver enzymes, with no observed renal hypofunction.
Implications:
- Plachitin demonstrates potential as an effective and tolerable intra-arterial therapy for primary and secondary liver cancers.
- The localized delivery minimizes systemic toxicity, offering a potential advantage over conventional chemotherapy.
- Further investigation is warranted to establish Plachitin's role in liver cancer treatment protocols.