INTRAARTERIAL INFUSION CHEMOTHERAPY WITH [SAR1, ILE8]ANGIOTENSIN-II FOR BLADDER-CANCER

被引:4
|
作者
MORITA, T [1 ]
KIKUCHI, T [1 ]
HARA, Y [1 ]
ISHIKAWA, S [1 ]
KOBAYASHI, Y [1 ]
ISHIYAMA, S [1 ]
TOZUKA, K [1 ]
GOTO, K [1 ]
TAKAHASHI, K [1 ]
YOSHIKAWA, H [1 ]
TANAKA, O [1 ]
TOKUE, A [1 ]
机构
[1] JICHI MED SCH,DEPT RADIOL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
关键词
BLADDER CANCER; INTRAARTERIAL INFUSION CHEMOTHERAPY; SAR1; ILE8]ANGIOTENSIN-II;
D O I
10.1097/00000421-199206000-00002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Thirty-three Patients with primary bladder cancer (nine stage T1 with multifocal tumors and 24 stage T2-4) were treated with intraarterial infusion chemotherapy including cisplatin, doxorubicin, and [Sar1,Ile8]Angiotensin II(AT II). Of the 32 evaluable patients, 12 had pathologically proven complete response (CR), 19 showed partial response (PR), and one showed no change (NC); the overall response rate (CR + PR) was 97%. The blood pressure increased in response to the administration of [Sar1,Ile8]AT II in all the patients; the mean increase in the systolic blood pressure was 36 mmHg. Most of the side effects were mild to moderate in severity, transient in nature, and included nausea/vomiting (100%), alopecia (84%), leukopenia (66%), headache (9%), nephrotoxicity (6%), diarrhea (3%), skin pigmentation (3%), and neurotoxicity (3%). One patient who dropped out of the study developed hemiplegia as a result of cerebral infarction. The findings indicate that it is necessary to exercise caution in selecting the patients to be subjected to this therapy. We conclude that intraarterial infusion chemotherapy combined with a vasoconstrictor has a significant effect not only against multifocal superficial bladder cancer but also against invasive bladder cancer.
引用
收藏
页码:188 / 193
页数:6
相关论文
共 50 条
  • [31] The β-Arrestin Pathway-selective Type 1A Angiotensin Receptor (AT1A) Agonist [Sar1, Ile4, Ile8] Angiotensin II Regulates a Robust G Protein-independent Signaling Network
    Kendall, Ryan T.
    Strungs, Erik G.
    Rachidi, Saleh M.
    Lee, Mi-Hye
    El-Shewy, Hesham M.
    Luttrell, Deirdre K.
    Janech, Michael G.
    Luttrell, Louis M.
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (22) : 19880 - 19891
  • [32] LOCALIZATION OF CENTRAL ANGIOTENSIN-II RECEPTORS WITH [I-125] SAR1, ILE8-ANGIOTENSIN-II - PERIVENTRICULAR SITES OF THE ANTERIOR 3RD VENTRICLE
    HEALY, DP
    MACIEJEWSKI, AR
    PRINTZ, MP
    NEUROENDOCRINOLOGY, 1986, 44 (01) : 15 - 21
  • [33] LOCAL-CONTROL OF PROSTATE-CANCER BY INTRAARTERIAL INFUSION CHEMOTHERAPY FACILITATED BY THE USE OF ANGIOTENSIN-II
    MUTOH, S
    AIKOU, I
    SOEJIMA, K
    UEDA, S
    FUKUSHIMA, S
    KISHIMOTO, S
    TAKAGI, Y
    UROLOGIA INTERNATIONALIS, 1992, 48 (02) : 175 - 180
  • [34] SYNTHESIS AND BIOLOGICAL-ACTIVITY OF N-TERMINUS MODIFIED [ILE8] ANGIOTENSIN-II ANALOGS
    BOVY, PR
    ONEAL, JM
    MCMAHON, E
    PALOMO, M
    SMITS, GJ
    TRAPANI, AJ
    MCGRAW, D
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 1990, 25 (07) : 589 - 594
  • [35] AUGMENTATION OF ANTICANCER EFFECT WITH ANGIOTENSIN-II IN INTRAARTERIAL INFUSION CHEMOTHERAPY FOR BREAST-CARCINOMA
    NOGUCHI, S
    MIYAUCHI, K
    NISHIZAWA, Y
    SASAKI, Y
    IMAOKA, S
    IWANAGA, T
    KOYAMA, H
    TERASAWA, T
    CANCER, 1988, 62 (03) : 467 - 473
  • [36] 2 ANGIOTENSIN-II BINDING-SITES IN RAT-BRAIN REVEALED USING [I-125] SAR1, ILE8-ANGIOTENSIN-II AND SELECTIVE NONPEPTIDE ANTAGONISTS
    CHANG, RSL
    LOTTI, VJ
    CHEN, TB
    FAUST, KA
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 171 (02) : 813 - 817
  • [37] INFLUENCE OF SAR1 ALA8 ANGIOTENSIN-II (SARALASIN) ON PLASMA-ALDOSTERONE IN HYPERTENSIVE PATIENTS
    DONKER, AJM
    VANHOOGDALEM, P
    PRATT, JJ
    LEENEN, FHH
    ACTA MEDICA SCANDINAVICA, 1979, 205 (03): : 207 - 212
  • [38] CLASSIFICATION OF ANGIOTENSIN RECEPTORS IN RAT ISOLATED UTERUS, PORTAL-VEIN, AND AORTA USING A SLOWLY DISSOCIATING ANTAGONIST [SAR1,ILE8]ANG-II FOR RECEPTOR BLOCKADE
    SCANLON, MN
    MOORE, GJ
    JOURNAL OF PHARMACOLOGICAL METHODS, 1988, 20 (03): : 207 - 224
  • [39] PARTIAL ATTENUATION OF ADRENAL CATECHOLAMINE (CA) OUTPUT BY SAR1-ILE8 ANGIOTENSIN-II (SAR-ILE AII) DURING HEMORRHAGE
    ROBINSON, RL
    FEDERATION PROCEEDINGS, 1978, 37 (03) : 509 - 509
  • [40] PROCESSING OF ANGIOTENSIN-II (A-II) AND (SAR1,ALA8)A-II BY CULTURED BOVINE ADRENOCORTICAL-CELLS
    CROZAT, A
    PENHOAT, A
    SAEZ, JM
    ENDOCRINOLOGY, 1986, 118 (06) : 2312 - 2318