Literature DB >> 2244016

The effects of single dose oral hydralazine on blood flow through human lung tumours.

N P Rowell1, M A Flower, V R McCready, B Cronin, A Horwich.   

Abstract

Hydralazine has been shown to reduce tumour blood flow and to potentiate the cytotoxicity of melphalan and bioreductive agents in mice. In order to determine whether such a strategy might have clinical potential, a study was undertaken to investigate the effects of hydralazine on blood flow through human tumours. Twenty-two patients with carcinoma of the bronchus received a single oral dose of hydralazine in the range 25 to 150 mg (0.37-2.86 mg/kg) according to age and acetylator status. Tumour blood flow was assessed by single photon emission computed tomography (SPECT) performed 10 min following intravenous 99Tcm-HMPAO on two occasions 2-8 days apart, the second being performed 60 min after hydralazine administration. In 20 evaluable patients, hydralazine caused a 38% increase in blood flow through the whole tumour (p = 0.007) and a 28% increase in flow through the tumour centre (p = 0.03) with greater increases occurring in patients sustaining greater falls in peripheral resistance. Tumour vascular resistance fell indicating active vasodilation in arterioles supplying tumours. Side-effects due to hydralazine were reported by eight patients.

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Year:  1990        PMID: 2244016     DOI: 10.1016/0167-8140(90)90108-9

Source DB:  PubMed          Journal:  Radiother Oncol        ISSN: 0167-8140            Impact factor:   6.280


  12 in total

1.  Anatomically derived attenuation coefficients for use in quantitative single photon emission tomography studies of the thorax.

Authors:  N P Rowell; J Glaholm; M A Flower; B Cronin; V R McCready
Journal:  Eur J Nucl Med       Date:  1992

2.  A different approach to the use of unsealed radionuclides for cancer therapy.

Authors:  V R McCready
Journal:  Eur J Nucl Med       Date:  1995-01

3.  Quantitative single-photon emission tomography for tumour blood flow measurement in bronchial carcinoma.

Authors:  N P Rowell; M A Flower; B Cronin; V R McCready
Journal:  Eur J Nucl Med       Date:  1993-07

Review 4.  Assessing the bioreductive effectiveness of the nitroimidazole RSU1069 and its prodrug RB6145: with particular reference to in vivo methods of evaluation.

Authors:  J C Bremner
Journal:  Cancer Metastasis Rev       Date:  1993-06       Impact factor: 9.264

Review 5.  Bioreducible mustards: a paradigm for hypoxia-selective prodrugs of diffusible cytotoxins (HPDCs).

Authors:  W A Denny; W R Wilson
Journal:  Cancer Metastasis Rev       Date:  1993-06       Impact factor: 9.264

6.  In vivo 31P nuclear magnetic resonance spectroscopy of experimental murine tumours and human tumour xenografts: effects of blood flow modification.

Authors:  J C Bremner; C J Counsell; G E Adams; I J Stratford; P J Wood; J F Dunn; G K Radda
Journal:  Br J Cancer       Date:  1991-11       Impact factor: 7.640

7.  The potential for prazosin and calcitonin gene-related peptide (CGRP) in causing hypoxia in tumours.

Authors:  I A Burney; R J Maxwell; J R Griffiths; S B Field
Journal:  Br J Cancer       Date:  1991-10       Impact factor: 7.640

8.  The influence of hydralazine on the vasculature, blood perfusion and chemosensitivity of MAC tumours.

Authors:  P K Quinn; M C Bibby; J A Cox; S M Crawford
Journal:  Br J Cancer       Date:  1992-08       Impact factor: 7.640

9.  Radiation effects on uptake of 99Tcm-hexamethylpropylen amine oxime (HMPAO) in head and neck tumours.

Authors:  H Minn; A Ahonen; R Paul
Journal:  Br J Cancer       Date:  1991-10       Impact factor: 7.640

10.  31P-magnetic resonance spectroscopy and 2H-magnetic resonance imaging studies of a panel of early-generation transplanted murine tumour models.

Authors:  S P Robinson; A van den Boogaart; R J Maxwell; J R Griffiths; E Hamilton; J C Waterton
Journal:  Br J Cancer       Date:  1998-06       Impact factor: 7.640

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