Literature DB >> 8126497

Total lymphoid irradiation in multiple sclerosis.

C M Wiles1, L Omar, A V Swan, G Sawle, J Frankel, R Grunewald, T Joannides, P Jones, H Laing, P H Richardson.   

Abstract

Following a report of the efficacy of total lymphoid irradiation (TLI) in the treatment of chronic progressive multiple sclerosis a further randomised double-blind placebo-controlled study was undertaken with the intention of entering 56 patients. In the event it was possible to recruit only 27 patients in a 2.5 year period. Three patients received active treatment openly and 24 were randomised to either active (14) or sham (10) treatment. Treatment was 1980 cGy to the lymphoid system and spleen or sham treatment after full simulation. The primary outcome measure was a comparison of the mean rates of change between treatment groups on the expanded Kurtzke disability scale (EDSS) over the two year follow up period. Patients were also assessed on other clinical outcome measures, psychometry, and serial MRI of the brain. Active treatment resulted in a profound and prolonged fall in T lymphocytes especially those with the CD4 marker and a reversal in CD4:CD8 ratio. No significant benefit was demonstrated on the rate of clinical disease progression (EDSS). A small but significant benefit was found on a score of bladder function. No significant benefit was demonstrated on other clinical or psychometric indices or on subjective visual analogue scales. There was a small but significant difference in the rate of accumulation of lesions on brain MRI favouring the treatment group. The treated group had a higher incidence of clinically relevant side effects, notably amenorrhoea and infections: three deaths (one in the TLI group, two in the sham treated group) occurred. A post hoc calculation indicates that the study had a possible 35% risk of a false negative result using the principal outcome measure. The study fails to confirm the previously reported clinical benefit of TLI although there may be a minor benefit on disease progression as indicated by MRI lesion counts. It is concluded that TLI cannot be recommended for the routine treatment of chronic progressive multiple sclerosis but the beneficial effect on MRI lesions, though modest, suggests that further research into immune modulation of this condition may be worthwhile.

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Year:  1994        PMID: 8126497      PMCID: PMC1072441          DOI: 10.1136/jnnp.57.2.154

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  27 in total

1.  Risk of second primary cancers after Hodgkin's disease by type of treatment: analysis of 2846 patients in the British National Lymphoma Investigation.

Authors:  A J Swerdlow; A J Douglas; G V Hudson; B V Hudson; M H Bennett; K A MacLennan
Journal:  BMJ       Date:  1992-05-02

2.  A placebo-controlled, double-blind, randomized, two-center, pilot trial of Cop 1 in chronic progressive multiple sclerosis.

Authors:  M B Bornstein; A Miller; S Slagle; M Weitzman; E Drexler; M Keilson; V Spada; W Weiss; S Appel; L Rolak
Journal:  Neurology       Date:  1991-04       Impact factor: 9.910

3.  Overview of azathioprine treatment in multiple sclerosis.

Authors:  P L Yudkin; G W Ellison; A Ghezzi; D E Goodkin; R A Hughes; K McPherson; J Mertin; C Milanese
Journal:  Lancet       Date:  1991-10-26       Impact factor: 79.321

4.  Magnetic resonance imaging in monitoring the treatment of multiple sclerosis: concerted action guidelines.

Authors:  D H Miller; F Barkhof; I Berry; L Kappos; G Scotti; A J Thompson
Journal:  J Neurol Neurosurg Psychiatry       Date:  1991-08       Impact factor: 10.154

5.  Intensive immunosuppression in progressive multiple sclerosis. A randomized, three-arm study of high-dose intravenous cyclophosphamide, plasma exchange, and ACTH.

Authors:  S L Hauser; D M Dawson; J R Lehrich; M F Beal; S V Kevy; R D Propper; J A Mills; H L Weiner
Journal:  N Engl J Med       Date:  1983-01-27       Impact factor: 91.245

6.  Clinical and immunologic effects of fractionated total lymphoid irradiation in refractory rheumatoid arthritis.

Authors:  D E Trentham; J A Belli; R J Anderson; J A Buckley; E J Goetzl; J R David; K F Austen
Journal:  N Engl J Med       Date:  1981-10-22       Impact factor: 91.245

7.  A modified card sorting test sensitive to frontal lobe defects.

Authors:  H E Nelson
Journal:  Cortex       Date:  1976-12       Impact factor: 4.027

8.  Using gadolinium-enhanced magnetic resonance imaging lesions to monitor disease activity in multiple sclerosis.

Authors:  H F McFarland; J A Frank; P S Albert; M E Smith; R Martin; J O Harris; N Patronas; H Maloni; D E McFarlin
Journal:  Ann Neurol       Date:  1992-12       Impact factor: 10.422

Review 9.  Multiple sclerosis: a pivotal role for the T cell in lesion development.

Authors:  C S Raine
Journal:  Neuropathol Appl Neurobiol       Date:  1991-08       Impact factor: 8.090

10.  Fractionated total lymphoid irradiation as preparative immunosuppression in high risk renal transplantation: clinical and immunological studies.

Authors:  J S Najarian; R M Ferguson; D E Sutherland; S Slavin; T Kim; J Kersey; R S Simmons
Journal:  Ann Surg       Date:  1982-10       Impact factor: 12.969

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  3 in total

Review 1.  Neurology.

Authors:  R S Howard
Journal:  BMJ       Date:  1994-08-06

2.  Multiple Sclerosis: Immunotherapy.

Authors: 
Journal:  Curr Treat Options Neurol       Date:  1999-07       Impact factor: 3.972

Review 3.  Evaluation of Study and Patient Characteristics of Clinical Studies in Primary Progressive Multiple Sclerosis: A Systematic Review.

Authors:  T Ziemssen; S Rauer; C Stadelmann; T Henze; J Koehler; I-K Penner; M Lang; D Poehlau; M Baier-Ebert; H Schieb; S Meuth
Journal:  PLoS One       Date:  2015-09-22       Impact factor: 3.240

  3 in total

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