Literature DB >> 3066853

Effect of HECNU in malignant supratentorial gliomas--a phase II study.

P Georges1, S Przedborski, J Brotchi, M Chatel, D Gédouin, J Hildebrand.   

Abstract

Forty adults with recurring brain gliomas were treated with HECNU 130 mg/m2, given i.v. every 5 to 6 weeks (mean 5.4) and corticosteroids. According to the response to treatment, patients were divided in 3 groups: 1. Group 1 included 8 pts (20%) with objective remission, defined as a clear-cut clinical improvement persisting at least 4 weeks after the complete discontinuation of corticosteroids. 2. Group 2 included 14 patients (35%) who improved or remained stable yet stayed corticosteroid-dependent. 3. The 18 patients (45%) of group 3 failed to respond. There was a fair correlation between clinical and radiological response. Thus sequential CT-scans showed a 50 to 100% tumour reduction in all patients of group 1, and in 5 of group 2. CT-scans remained unchanged in 8 patients of group 2 and in one of group 3, and showed tumour progression in 10 patients of group 3. Drug toxicity appeared mild, reversible and was not cumulative. The better tolerance of HECNU could represent a real advantage of this drug over the commonly used nitrosourea derivatives such as BCNU and CCNU.

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Year:  1988        PMID: 3066853     DOI: 10.1007/bf00163703

Source DB:  PubMed          Journal:  J Neurooncol        ISSN: 0167-594X            Impact factor:   4.130


  6 in total

1.  Effect of CCNU on survival, rate of objective remission and duration of free interval in patients with malignant brain glioma--first evaluation.

Authors: 
Journal:  Eur J Cancer       Date:  1976-01       Impact factor: 9.162

Review 2.  Chemotherapy of primary brain tumors.

Authors:  V A Levin
Journal:  Neurol Clin       Date:  1985-11       Impact factor: 3.806

3.  Evaluation of BCNU and/or radiotherapy in the treatment of anaplastic gliomas. A cooperative clinical trial.

Authors:  M D Walker; E Alexander; W E Hunt; C S MacCarty; M S Mahaley; J Mealey; H A Norrell; G Owens; J Ransohoff; C B Wilson; E A Gehan; T A Strike
Journal:  J Neurosurg       Date:  1978-09       Impact factor: 5.115

4.  Randomized comparisons of radiotherapy and nitrosoureas for the treatment of malignant glioma after surgery.

Authors:  M D Walker; S B Green; D P Byar; E Alexander; U Batzdorf; W H Brooks; W E Hunt; C S MacCarty; M S Mahaley; J Mealey; G Owens; J Ransohoff; J T Robertson; W R Shapiro; K R Smith; C B Wilson; T A Strike
Journal:  N Engl J Med       Date:  1980-12-04       Impact factor: 91.245

5.  Single-agent chemotherapy of brain tumors. A five-year review.

Authors:  C B Wilson; P Gutin; E B Boldrey; D Drafts; V A Levin; K J Enot
Journal:  Arch Neurol       Date:  1976-11

6.  Evaluation of CCNU, VM-26 plus CCNU, and procarbazine in supratentorial brain gliomas. Final evaluation of a randomized study. European Organization for Research on Treatment of Cancer (EORTC) Brain Tumor Group.

Authors: 
Journal:  J Neurosurg       Date:  1981-07       Impact factor: 5.115

  6 in total
  2 in total

1.  Response of recurrent glioblastoma and anaplastic astrocytoma to dibromodulcitol, BCNU and procarbazine--a phase-II study.

Authors:  J Hildebrand; O De Witte; T Sahmoud
Journal:  J Neurooncol       Date:  1998-04       Impact factor: 4.130

2.  Phase I study of temozolamide (TMZ) combined with procarbazine (PCB) in patients with gliomas.

Authors:  E S Newlands; T Foster; S Zaknoen
Journal:  Br J Cancer       Date:  2003-07-21       Impact factor: 7.640

  2 in total

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