dc.contributor.author | Wilkins, A | |
dc.contributor.author | Shahidi, M | |
dc.contributor.author | Parker, C | |
dc.contributor.author | Gunapala, R | |
dc.contributor.author | Thomas, K | |
dc.contributor.author | Huddart, R | |
dc.contributor.author | Horwich, A | |
dc.contributor.author | Dearnaley, D | |
dc.date.accessioned | 2018-07-23T15:18:29Z | |
dc.date.issued | 2012-12 | |
dc.identifier.citation | BJU international, 2012, 110 (11 Pt B), pp. E727 - E735 | |
dc.identifier.issn | 1464-4096 | |
dc.identifier.uri | https://repository.icr.ac.uk/handle/internal/2122 | |
dc.identifier.eissn | 1464-410X | |
dc.identifier.doi | 10.1111/j.1464-410x.2012.11546.x | |
dc.description.abstract | Unlabelled What's known on the subject? and What does the study add? Diethylstilbestrol (DES) was the first hormone treatment used for prostate cancer and has also shown effectiveness in castration-resistant disease in small studies; however, concerns over thromboembolic toxicity have restricted its use in the past. Over 200 elderly men with castration-resistant prostate cancer were treated with 1-3 mg of DES, given with 75 mg aspirin and breast bud irradiation. Almost 30% of men showed a significant PSA response and the median time to PSA progression was 4.6 months. Almost 20% of patients with pain had a significant analgesic benefit. The most important toxicity was thromboembolism in 10% of men. Overall the drug has an acceptable toxicity profile and offers a palliative benefit in frail elderly men who may not be fit for chemotherapy.Objective • To assess the efficacy and toxicity of diethylstilbestrol (DES) in the management of castration-resistant prostate cancer (CRPC).Patients and methods • A total of 231 patients with CRPC received treatment with DES at the Royal Marsden Hospital between August 1992 and August 2000. • The median pre-treatment prostate-specific antigen (PSA) level was 221 ng/mL. • DES was used at a dose of 1-3 mg daily, with aspirin 75 mg. • The primary endpoint was PSA response rate.Results • The PSA response rate (using PSA Working Group criteria) was 28.9%. • The median time to PSA progression was 4.6 months. • Of patients with bone pain, 18% had an improvement in their European Organisation for the Research and Treatment of Cancer pain score. • Thromboembolic complications were seen in 9.9% of all patients.Conclusions • DES has significant activity in CRPC and can be of palliative benefit. • DES has an acceptable toxicity profile in the management of patients with symptomatic CRPC when used at a dose of 1-3 mg, combined with aspirin and prophylactic breast bud radiotherapy. | |
dc.format | Print-Electronic | |
dc.format.extent | E727 - E735 | |
dc.language | eng | |
dc.language.iso | eng | |
dc.subject | Humans | |
dc.subject | Prostatic Neoplasms | |
dc.subject | Disease Progression | |
dc.subject | Diethylstilbestrol | |
dc.subject | Prostate-Specific Antigen | |
dc.subject | Estrogens, Non-Steroidal | |
dc.subject | Treatment Outcome | |
dc.subject | Orchiectomy | |
dc.subject | Follow-Up Studies | |
dc.subject | Prospective Studies | |
dc.subject | Aged | |
dc.subject | Male | |
dc.title | Diethylstilbestrol in castration-resistant prostate cancer. | |
dc.type | Journal Article | |
rioxxterms.versionofrecord | 10.1111/j.1464-410x.2012.11546.x | |
rioxxterms.licenseref.startdate | 2012-12 | |
rioxxterms.type | Journal Article/Review | |
dc.relation.isPartOf | BJU international | |
pubs.issue | 11 Pt B | |
pubs.notes | Not known | |
pubs.organisational-group | /ICR | |
pubs.organisational-group | /ICR/Primary Group | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Cancer Biology | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Cancer Biology/Targeted Therapy | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Closed research teams | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Closed research teams/Clinical Academic Radiotherapy (Dearnaley) | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Clinical Academic Radiotherapy (Huddart) | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Targeted Therapy | |
pubs.organisational-group | /ICR/Primary Group/Royal Marsden Clinical Units | |
pubs.organisational-group | /ICR | |
pubs.organisational-group | /ICR/Primary Group | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Cancer Biology | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Cancer Biology/Targeted Therapy | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Closed research teams | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Closed research teams/Clinical Academic Radiotherapy (Dearnaley) | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Clinical Academic Radiotherapy (Huddart) | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Targeted Therapy | |
pubs.organisational-group | /ICR/Primary Group/Royal Marsden Clinical Units | |
pubs.publication-status | Published | |
pubs.volume | 110 | |
pubs.embargo.terms | Not known | |
icr.researchteam | Clinical Academic Radiotherapy (Dearnaley) | en_US |
icr.researchteam | Clinical Academic Radiotherapy (Huddart) | en_US |
icr.researchteam | Targeted Therapy | en_US |
dc.contributor.icrauthor | Horwich, Alan | en |
dc.contributor.icrauthor | Dearnaley, David | en |
dc.contributor.icrauthor | Huddart, Robert | en |
dc.contributor.icrauthor | Parker, Chris | en |
dc.contributor.icrauthor | Corbett, Anna | en |