Subcutaneous administration of amifostine during fractionated radiotherapy: A randomized phase II study

被引:206
作者
Koukourakis, MI
Kyrias, G
Kakolyris, S
Kouroussis, C
Frangiadaki, C
Giatromanolaki, A
Retalis, G
Georgoulias, V
机构
[1] Tumour & Angiogenesis Res Grp, Iraklion 71306, Crete, Greece
[2] Univ Hosp Iraklion, Dept Radiotherapy Oncol & Med Oncol, Iraklion, Greece
[3] Schering Plough SA, Agiou Dimitriou, Alimos, Greece
关键词
D O I
10.1200/JCO.2000.18.11.2226
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Amifostine (WR-2721) is an impotant cytoprotective agent. Although intravenous administration is the standard route, pharmacokinetic studies have shown acceptable plasma levels of the active metabolite of amifostine (WR-1605) after subcutaneous administration, The subcutaneous route, due to ifs simplicity, presents multiple advantages over the intravenous route when amifostine is used during fractionated radiotherapy. Patients and Methods: Sixty patients with thoracic, 40 with head and neck, and 40 wish pelvic tumors who were undergoing radical radiotherapy were enrolled onto ct randomized phase II trial to assess the feasibility, tolerance, and cytoprotective efficacy of amifostine administered subcutaneously, A flat dose of amifostine 500 mg, diluted in 2.5 mL of normal saline, was injected subcutaneously 20 minutes before each radiotherapy fraction. Results: The subcutaneous amifostine regimen wets well tolerated by 85% of patients. In approximately 5% of patients, amifostine therapy was interrupted due to cumulative asthenia, and in 10%, due to a fever/rash reaction. Hypotension was never noted, whereas nausea was frequent. A significant reduction of pharyngeal, esophageal, and rectal mucositis was noted in the amifostine arm (P < .04). The delays in radiotherapy because of grade 3 mucositis were significantly longer in the group of patients treated with radiotherapy alone (P < .04). Amifostine significantly reduced the incidence of acute perineal skin and bladder toxicity (P < .0006). Conclusion: Subcutaneous administration of amifostine is well tolerated, effectively reduces radiotherapy's early toxicity, and prevents delays in radiotherapy. The subcutaneous route is much simpler and saves time compared with the intravenous route of administration and can be safely and effectively applied in the daily, busy radiotherapy practice. J Clin Oncol 18:2226-2233. (C) 2000 by American Society of Clinical Oncology.
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页码:2226 / 2233
页数:8
相关论文
共 35 条
  • [1] [Anonymous], 1979, HDB REP RES CANC TRE
  • [2] ANTONADOU D, 1999, RADIOPROTECTION NEW
  • [3] MECHANISM OF ACTION OF AMINOTHIOL RADIOPROTECTORS
    BROWN, PE
    [J]. NATURE, 1967, 213 (5074) : 363 - &
  • [4] Role of HIF-1α or in hypoxia-mediated apoptosis, cell proliferation and tumour angiogenesis
    Carmeliet, P
    Dor, Y
    Herbert, JM
    Fukumura, D
    Brusselmans, K
    Dewerchin, M
    Neeman, M
    Bono, F
    Abramovitch, R
    Maxwell, P
    Koch, CJ
    Ratcliffe, P
    Moons, L
    Jain, RK
    Collen, D
    Keshet, E
    [J]. NATURE, 1998, 394 (6692) : 485 - 490
  • [5] DOUAY L, 1995, BLOOD, V86, P2849
  • [6] Amifostine does not alter the antitumor activity of cisplatin in a pre-clinical model of testicular cancer
    Dunn, TA
    Schmoll, HJ
    Grunwald, V
    Bokemeyer, C
    Casper, J
    [J]. ANTI-CANCER DRUGS, 1996, 7 (07) : 795 - 799
  • [7] Effects of amifostine (WR-2721, ethyol) on tumor growth and pharmacology of cytotoxic drugs in human xenotransplanted neuroblastomas
    Fichtner, I
    Lemm, M
    Becker, M
    Berthold, F
    [J]. ANTI-CANCER DRUGS, 1997, 8 (02) : 174 - 181
  • [8] GIATROMANOLAKI A, IN PRESS J PATHOL
  • [9] ALTERATIONS IN OXYGEN-TRANSPORT FOLLOWING WR-2721
    GLOVER, D
    NEGENDANK, W
    DELIVORIAPAPADOPOULOS, M
    GLICK, JH
    [J]. INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1984, 10 (09): : 1565 - 1568
  • [10] THIOL AND DISULFIDE METABOLITES OF THE RADIATION PROTECTOR AND POTENTIAL CHEMOPREVENTIVE AGENT WR-2721 ARE LINKED TO BOTH ITS ANTI-CYTOTOXIC AND ANTIMUTAGENIC MECHANISMS OF ACTION
    GRDINA, DJ
    SHIGEMATSU, N
    DALE, P
    NEWTON, GL
    AGUILERA, JA
    FAHEY, RC
    [J]. CARCINOGENESIS, 1995, 16 (04) : 767 - 774