» Articles » PMID: 6647187

Corticosteroids in Terminal Cancer--a Prospective Analysis of Current Practice

Overview
Journal Postgrad Med J
Specialty General Medicine
Date 1983 Nov 1
PMID 6647187
Citations 22
Authors
Affiliations
Soon will be listed here.
Abstract

Over half of a group of 373 inpatients with advanced malignant disease were treated with corticosteroids for a variety of reasons. They received either prednisolone or dexamethasone, or replacement therapy with cortisone acetate. Forty percent of those receiving corticosteroids benefited from them. A higher response rate was seen when corticosteroids were prescribed for nerve compression pain, for raised intracranial pressure, and when used in conjunction with chemotherapy. No significant difference in efficacy was noted between the 2 drugs. The results, however, suggest that with a larger sample, dexamethasone would have been shown to be significantly better than prednisolone in the management of nerve compression pain. The incidence of side effects was broadly similar with dexamethasone and prednisolone. The most common side effect was oral candidosis and there was a highly significant relationship between the use of corticosteroids and the prescription of nystatin suspension. Dexamethasone was more likely than prednisolone to cause oro-pharyngeal candidosis. Dexamethasone was also associated with significantly more cases of psychological disturbance and hyperactivity. On the other hand, dexamethasone seems less likely to cause oedema, weight gain and dyspepsia. Corticosteroids were withdrawn because of side effects in only 11 patients (5%)--6 were receiving dexamethasone and 5 prednisolone. Dexamethasone has been adopted as the standard corticosteroid for terminal cancer patients at Sir Michael Sobell House.

Citing Articles

Development of Care Pathway for Assessment and Treatment of Fatigue in Palliative Care.

Mochamat M, Przyborek M, Jaspers B, Cuhls H, Conrad R, Mucke M Indian J Palliat Care. 2023; 29(3):256-265.

PMID: 37700894 PMC: 10493685. DOI: 10.25259/IJPC_194_2022.


Effects of exercise in patients with connective tissue disease receiving high-dose glucocorticoids: A pilot prospective cohort study.

Nagashima M, Takahashi D, Mizushima T, Yamauchi K Eur J Appl Physiol. 2021; 121(8):2253-2263.

PMID: 33914153 DOI: 10.1007/s00421-021-04697-2.


Cancer-Associated Anorexia and Cachexia : Implications for Drug Therapy.

Loprinzi C, Goldberg R, Burnham N Drugs. 2017; 43(4):499-506.

PMID: 28421557 DOI: 10.2165/00003495-199243040-00006.


A Prospective Observational Study on Effect of Short-Term Periodic Steroid Premedication on Bone Metabolism in Gastrointestinal Cancer (ESPRESSO-01).

Nakamura M, Ishiguro A, Muranaka T, Fukushima H, Yuki S, Ono K Oncologist. 2017; 22(5):592-600.

PMID: 28341762 PMC: 5423502. DOI: 10.1634/theoncologist.2016-0308.


A little help from steroids in oncology.

Lossignol D J Transl Int Med. 2017; 4(1):52-54.

PMID: 28191519 PMC: 5290916. DOI: 10.1515/jtim-2016-0011.


References
1.
KING D, Moon W, Brown N . Corticosteroid drugs in the management of primary and secondary malignant cerebral tumours. Med J Aust. 1965; 2(21):878-81. View

2.
SCHELL H . The risk of adrenal corticosteroid therapy in far-advanced cancer. Am J Med Sci. 1966; 252(6):641-9. View

3.
SCHELL H . Adrenal corticosteroid therapy in far-advanced cancer. Geriatrics. 1972; 27(1):131-41. View

4.
MOERTEL C, SCHUTT A, Reitemeier R, Hahn R . Corticosteroid therapy of preterminal gastrointestinal cancer. Cancer. 1974; 33(6):1607-9. DOI: 10.1002/1097-0142(197406)33:6<1607::aid-cncr2820330620>3.0.co;2-v. View

5.
Boland E . 16a-Methyl corticosteroids; a new series of anti-inflammatory compounds; clinical appraisal of their antirheumatic potencies. Calif Med. 1958; 88(6):417-22. PMC: 1512303. View