CLINICAL TOXICITY OF PERIPHERAL-NERVE TO INTRAOPERATIVE RADIOTHERAPY IN A CANINE MODEL

被引:15
|
作者
JOHNSTONE, PAS
DELUCA, AM
BACHER, JD
HAMPSHIRE, VA
TERRILL, RE
ANDERSON, WJ
KINSELLA, TJ
SINDELAR, WF
机构
[1] NCI,RADIAT ONCOL BRANCH,BETHESDA,MD 20892
[2] NCI,SURG BRANCH,BETHESDA,MD 20892
[3] NCI,OFF LAB ANIM SCI,BETHESDA,MD 20892
[4] NIH,NATL CTR RES RESOURCES,VET RESOURCES PROGRAM,BETHESDA,MD 20892
[5] INDIANA UNIV,SCH MED,TERRE HAUTE,IN 47809
[6] UNIV WISCONSIN,CTR CLIN SCI,DEPT HUMAN ONCOL,MADISON,WI 53792
[7] NCI,RADIAT BIOL BRANCH,BETHESDA,MD 20892
基金
美国国家卫生研究院;
关键词
ANIMAL MODELS; CANINE; INTRAOPERATIVE RADIOTHERAPY; NORMAL TISSUE TOLERANCE; PERIPHERAL NERVE;
D O I
10.1016/0360-3016(95)00028-W
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: The clinical late effects of intraoperative radiotherapy (IORT) on peripheral nerve were investigated in a foxhound model. Methods and Materials: Between 1982 and 1987, 40 animals underwent laparotomy with intraoperative radiotherapy of doses from 0-75 Gy administered to the right lumbosacral plexus, Subsequently, all animals were monitored closely and sacrificed to assess clinical effects to peripheral nerve, This analysis reports final clinical results of all animals, with follow-up to 5 years. Results: All animals treated with greater than or equal to 25 Gy developed ipsilateral neuropathy, An inverse relationship was noted between intraoperative radiotherapy dose and time to neuropathy, with an effective dose for 50% paralysis (ED(50)) of 17.2 Gy. One of the animals treated with 15 Gy IORT developed paralysis, after a much longer latency than the other animals. Conclusions: Doses of 15 Gy delivered intraoperatively may be accompanied by peripheral neuropathy with long-term follow-up, This threshold is less than that reported with shorter follow-up, The value of EDS, determined here is in keeping with data from other animal trials, and from clinical trials in humans.
引用
收藏
页码:1031 / 1034
页数:4
相关论文
共 50 条
  • [1] TOLERANCE OF PERIPHERAL-NERVE TO INTRAOPERATIVE RADIOTHERAPY (IORT) - CLINICAL AND EXPERIMENTAL STUDIES
    KINSELLA, TJ
    SINDELAR, WF
    DELUCA, AM
    PEZESHKPOUR, G
    SMITH, R
    MAHER, M
    TERRILL, R
    MILLER, R
    MIXON, A
    HARWELL, JF
    ROSENBERG, SA
    GLATSTEIN, E
    [J]. INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1985, 11 (09): : 1579 - 1585
  • [2] INTRAOPERATIVE PERIPHERAL-NERVE ACTION-POTENTIALS - TECHNIQUE
    NELSON, KR
    [J]. MUSCLE & NERVE, 1988, 11 (09) : 963 - 964
  • [3] CLINICAL USE OF PERIPHERAL-NERVE STIMULATORS
    KEMPEN, PM
    [J]. CANADIAN JOURNAL OF ANAESTHESIA-JOURNAL CANADIEN D ANESTHESIE, 1988, 35 (05): : 542 - 542
  • [4] CLINICAL ELECTROPHYSIOLOGIC PERIPHERAL-NERVE RECORDINGS
    TERZIS, JK
    PUBLICOVER, N
    [J]. CLINICS IN PLASTIC SURGERY, 1984, 11 (01) : 47 - 52
  • [5] USE OF PERIPHERAL-NERVE ACTION-POTENTIALS FOR INTRAOPERATIVE MONITORING
    NELSON, KR
    [J]. NEUROLOGIC CLINICS, 1988, 6 (04) : 917 - 933
  • [6] CLINICAL USE OF PERIPHERAL-NERVE STIMULATORS IN ANESTHESIA
    HUDES, E
    LEE, KC
    [J]. CANADIAN JOURNAL OF ANAESTHESIA-JOURNAL CANADIEN D ANESTHESIE, 1987, 34 (05): : 525 - 534
  • [7] CLINICAL-APPLICATION OF PERIPHERAL-NERVE TRANSPLANTATION
    MACKINNON, SE
    HUDSON, AR
    [J]. PLASTIC AND RECONSTRUCTIVE SURGERY, 1992, 90 (04): : 695 - 699
  • [8] PERIPHERAL-NERVE REGENERATION - ROLES OF CENTRAL AND PERIPHERAL-NERVE GLIA
    JENQ, CB
    JENQ, LL
    BUNGE, RP
    [J]. ANATOMICAL RECORD, 1988, 220 (04): : A48 - A49
  • [9] PERIPHERAL-NERVE HEMANGIOMA - POTENTIAL FOR CLINICAL AGGRESSIVENESS
    VIGNA, PA
    KUSIOR, MF
    COLLINS, MB
    ROSS, JS
    [J]. ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE, 1994, 118 (10) : 1038 - 1041
  • [10] COMPARISON OF 3 CLINICAL PERIPHERAL-NERVE STIMULATORS
    ROSS, WT
    [J]. ANESTHESIOLOGY, 1970, 32 (02) : 155 - &