Lack of neuroprotection by an ACTH (4-9) analogue.: A randomized trial in patients treated with vincristine for Hodgkin's or non-Hodgkin's lymphoma

被引:27
作者
Koeppen, S
Verstappen, CCP
Körte, R
Scheulen, ME
Strumberg, D
Postma, TJ
Heimans, JJ
Huijgens, PC
Kiburg, B
Renzing-Köhler, K
Diener, HC
机构
[1] Univ Essen Gesamthsch, Dept Neurol, D-45122 Essen, Germany
[2] Univ Essen Gesamthsch, Dept Internal Med Canc Res, Essen, Germany
[3] Vrije Univ Amsterdam, Med Ctr, Dept Neurol, Amsterdam, Netherlands
[4] Vrije Univ Amsterdam, Med Ctr, Dept Haematol, Amsterdam, Netherlands
[5] Univ Essen Gesamthsch, Inst Med Informat Biometry & Epidemiol, Essen, Germany
关键词
neuroprotection; ACTH (4-9) analogue; vincristine-induced neuropathy;
D O I
10.1007/s00432-003-0524-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose. This randomized, double-blind, placebo-controlled study evaluates the effect of the corticotropin (4-9) analogue Org 2766 on the neuropathy-free interval in patients receiving vincristine (VCR) containing chemotherapy for Hodgkin's or non-Hodgkin's lymphoma.<LF>Patients and methods. In a longitudinal design, 150 patients were evaluated by interview, neurological examination, and neurophysiological techniques. Patients with an expected cumulative VCR dose of at least 8 mg received a single dose of Org 2766 or placebo before and after each intravenous VCR injection and 3-4 weeks after cessation of VCR. The final patient assessment was performed 1 month after discontinuation of study medication. The neuropathy-free interval as the major end point of this study was defined as the first occurrence of bilateral paresthesias and expressed as the administered cumulative VCR dose. This bi-center study represents the largest cohort of patients monitored for the effect of an ACTH-analogue on VCR neurotoxicity.<LF>Results. A total of 147 patients were included in the final analysis. No significant differences were observed between the placebo and actively treated group for the major and secondary endpoints. Conclusion. Contrary to a single previous pilot study in patients receiving VCR-based chemotherapy, in our study the ACTH (4-9) analogue Org 2766 did not provide protection from VCR-induced neuropathy.
引用
收藏
页码:153 / 160
页数:8
相关论文
共 48 条
  • [11] GANGLIOSIDE TREATMENT OF VINCRISTINE-INDUCED NEUROPATHY - AN ELECTROPHYSIOLOGIC STUDY
    FAVARO, G
    DIGREGORIO, F
    PANOZZO, C
    FIORI, MG
    [J]. TOXICOLOGY, 1988, 49 (2-3) : 325 - 329
  • [12] THE POTENTIAL OF MELANOTROPINS IN THE TREATMENT OF NERVOUS-SYSTEM DISEASES
    GISPEN, WH
    [J]. ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1993, 680 : 401 - 411
  • [13] Gispen WH, 1999, ANN NY ACAD SCI, V885, P342
  • [14] STANDARDIZED METHOD OF DETERMINING VIBRATORY PERCEPTION THRESHOLDS FOR DIAGNOSIS AND SCREENING IN NEUROLOGICAL INVESTIGATION
    GOLDBERG, JM
    LINDBLOM, U
    [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1979, 42 (09) : 793 - 803
  • [15] GOTTSCHALK PG, 1968, NEUROLOGY, V18, P875
  • [16] CISPLATIN-INDUCED NEUROPATHY IN MATURE RATS - EFFECTS OF THE MELANOCORTIN-DERIVED PEPTIDE ORG-2766
    HAMERS, FPT
    PETTE, C
    BRAVENBOER, B
    VECHT, CJ
    NEIJT, JP
    GISPEN, WH
    [J]. CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1993, 32 (02) : 162 - 166
  • [17] NGF prevention of neurotoxicity induced by cisplatin, vincristine and taxol depends on toxicity of each drug and NGF treatment schedule: In vitro study of adult rat sympathetic ganglion explants
    Hayakawa, K
    Itoh, T
    Niwa, H
    Mutoh, T
    Sobue, G
    [J]. BRAIN RESEARCH, 1998, 794 (02) : 313 - 319
  • [18] HOLLAND JF, 1973, CANCER RES, V33, P1258
  • [19] THE COURSE OF NEUROPATHY AFTER CESSATION OF CISPLATIN TREATMENT, COMBINED WITH ORG-2766 OR PLACEBO
    HOVESTADT, A
    VANDERBURG, MEL
    VERBIEST, HBC
    VANPUTTEN, WLJ
    VECHT, CJ
    [J]. JOURNAL OF NEUROLOGY, 1992, 239 (03) : 143 - 146
  • [20] EFFECTS OF THE ACTH(4-9) ANALOG, ORG-2766, ON VINCRISTINE CYTOTOXICITY IN 2 HUMAN LYMPHOMA CELL-LINES, U937 AND U715
    KIBURG, B
    VANDELOOSDRECHT, AA
    SCHWEITZER, KM
    OSSENKOPPELE, GJ
    MULLER, LJ
    HEIMANS, JJ
    HUIJGENS, PC
    [J]. BRITISH JOURNAL OF CANCER, 1994, 69 (03) : 497 - 501