Neoadjuvant hormonal manipulation: A strategy for chemoprevention trials Conference Paper


Authors: Fair, W. R.; Aprikian, A.; Reuter, V.
Title: Neoadjuvant hormonal manipulation: A strategy for chemoprevention trials
Conference Title: Premalignant and Early Malignant Lesions of the Prostate
Abstract: Androgen ablation using hormonal manipulation is used extensively in metastatic prostate cancer; however, its use in localized disease combined with surgical extirpation of the gland has not been thoroughly and systematically investigated. The rationale for neoadjuvant therapy stems from the demonstrated effectiveness of androgen ablative therapy in metastatic disease and the high rate of “positive” surgical margins, especially in patients with Stage B2 disease. In addition, the essentially anecdotal clinical report of Scott and Boyd [1], using endocrine therapy plus radical prostatectomy in patients with Stage C disease, gives 15 years survival results comparable to those obtained by Jewett [2] in Stage 1 patients treated by radical prostatectomy. Finally, experimental observations in the androgen‐sensitive mammary tumor (Shionogi) lend support to the concept of neoadjuvant hormonal manipulation. A pilot study of neoadjuvant endocrine therapy in 55 patients treated at Memorial Sloan‐Kettering Cancer Center with 3 months of diethylstilbestrol (DES) (3 mg/day) prior to radical prostatectomy indicates marked reductions in the prostate‐specific antigen (PSA), although persistent evidence of adverse local tumor features was common. Some patients, however, exhibited evidence of significant downstaging. Whether or not any alternation in disease progression will accrue from demonstrated local downstaging is, of course, uncertain. However, clinical and laboratory effects of such treatment may provide a means for correlation with subsequent tumor behavior, and may prove useful in treatment decisions. Additionally, a decrease in the number of foci of grade 3 prostatic intraepithelial neoplasia (PIN‐3) was noted in a small number of patients. The effects of hormonal and chemical agents on microfocal “early” prostatic cancer and PIN can be readily evaluated by comparing biopsies obtained before the initiation of such therapy with the effects noted in the radical prostatectomy specimen. Thus, potentially useful agents can be readily evaluated in such a neoadjuvant trial and serve as a means of developing potential chemopreventive strategies. © 1992 Wiley‐Liss, Inc. Copyright © 1992 Wiley‐Liss, Inc.
Keywords: major clinical study; androgen; clinical trial; review; multimodality cancer therapy; conference paper; chemotherapy, adjuvant; combined modality therapy; neoadjuvant therapy; prostate specific antigen; chemoprophylaxis; physiology; prostate cancer; prostatic neoplasms; goserelin; prostate; prostatectomy; adjuvant chemotherapy; prostate tumor; androgen ablation; diethylstilbestrol; antiandrogen; flutamide; gonadorelin derivative; androgens; adjuvant; chemoprevention; pin; humans; human; male; priority journal; des
Journal Title Journal of Cellular Biochemistry
Volume: 50
Issue: Suppl. 16H
Conference Dates: 1992 Mar 27-29
Conference Location: Scottsdale, AZ
ISBN: 0730-2312
Publisher: John Wiley & Sons  
Date Published: 1992-01-01
Start Page: 118
End Page: 121
Language: English
DOI: 10.1002/jcb.240501227
PUBMED: 1289666
PROVIDER: scopus
DOI/URL:
Notes: Article -- Source: Scopus
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  1. Victor Reuter
    1228 Reuter
  2. William R Fair
    342 Fair