Literature DB >> 6409491

Improved regional selectivity of hepatic arterial mitomycin by starch microspheres.

J W Gyves, W D Ensminger, D VanHarken, J Niederhuber, P Stetson, S Walker.   

Abstract

Biodegradable starch microspheres, 40 microns in diameter, were administered through hepatic arterial catheters in 16 subjects with primary and metastatic liver tumors. These microspheres temporarily obstruct blood flow at the precapillary arteriole (microcirculation) level. Our study was undertaken to determine whether such occlusion would enhance hepatic deposition of, and thereby decrease systemic exposure to, simultaneously administered hepatic arterial mitomycin C (mito). When mito (10 mg/m2 over 1 min) was given with 90 X 10(6) microspheres (10 subjects), there was a 17% to 70% reduction in systemic mito exposure. When mito (10 mg/m2 over 1 min) was given with 36 X 10(6) microspheres (six subjects), there was a 15% to 60% reduction in systemic exposure, which may correlate with dose-dependent shunting (8% to 29%) through the liver to the lung (and hence to the systemic circulation), attributed to the starch microspheres. No life-threatening myelosuppression was noted; hepatic toxicity consisted of transient pain and elevation of liver enzymes.

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Year:  1983        PMID: 6409491     DOI: 10.1038/clpt.1983.163

Source DB:  PubMed          Journal:  Clin Pharmacol Ther        ISSN: 0009-9236            Impact factor:   6.875


  11 in total

Review 1.  Pharmacokinetic rationale for chemotherapeutic drugs combined with intra-arterial degradable starch microspheres (Spherex).

Authors:  C J Johansson
Journal:  Clin Pharmacokinet       Date:  1996-09       Impact factor: 6.447

2.  Effect of microspheres in intra-arterial chemotherapy. A study of arterio-venous shunting and passage of a labelled marker.

Authors:  H Starkhammar; L Håkansson; O Morales; J Svedberg
Journal:  Med Oncol Tumor Pharmacother       Date:  1987

3.  A gamma camera method to monitor the use of degradable starch microspheres in hepatic arterial chemotherapy.

Authors:  A Britten; A Flowerdew; T Hunt; I Taylor; D Ackery; J Fleming
Journal:  Eur J Nucl Med       Date:  1989

Review 4.  Global approach to hepatic metastases from colorectal cancer: indication and outcome of intra-arterial chemotherapy and other hepatic-directed treatments.

Authors:  G Fiorentini; D B Poddie; U De Giorgi; D Guglielminetti; P Giovanis; M Leoni; W Latino; C Dazzi; A Cariello; D Turci; M Marangolo
Journal:  Med Oncol       Date:  2000-08       Impact factor: 3.064

5.  Temporary blood flow stasis with degradable starch microspheres (DSM) for liver metastases in a rat model.

Authors:  A D Flowerdew; H K Richards; I Taylor
Journal:  Gut       Date:  1987-10       Impact factor: 23.059

Review 6.  Chemo-occlusion for the treatment of liver cancer. A new technique using degradable starch microspheres.

Authors:  T Taguchi
Journal:  Clin Pharmacokinet       Date:  1994-04       Impact factor: 6.447

Review 7.  Clinical pharmacokinetic advantages of new drug delivery methods for the treatment of liver tumours.

Authors:  J H Anderson; H W Warren; C S McArdle
Journal:  Clin Pharmacokinet       Date:  1994-09       Impact factor: 6.447

8.  Systemic blood levels after intra-arterial administration of microencapsulated mitomycin C in cancer patients.

Authors:  G Milano; J L Boublil; J N Bruneton; J Bourry; N Renee; A Thyss; P Roux; M Namer
Journal:  Eur J Drug Metab Pharmacokinet       Date:  1985 Jul-Sep       Impact factor: 2.441

9.  Is liver to lung shunting in colorectal liver metastasis the cause of toxicity following treatment with cytotoxic microsphere aggregates?

Authors:  T W Hennigan; S Earlam; T G Allen-Mersh
Journal:  Br J Cancer       Date:  1992-12       Impact factor: 7.640

Review 10.  Hepatic arterial chemotherapy for metastatic colorectal carcinoma.

Authors:  P G de Takats; D J Kerr; C J Poole; H W Warren; C S McArdle
Journal:  Br J Cancer       Date:  1994-02       Impact factor: 7.640

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