Literature DB >> 7579781

Estramustine phosphate sodium. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic efficacy in prostate cancer.

C M Perry1, D McTavish.   

Abstract

Estramustine phosphate sodium (estramustine phosphate), a unique antitumour agent, is selectively taken up by prostate cells and exerts antineoplastic effects by interfering with microtubule of dynamics and by reducing plasma levels of testosterone. In noncomparative studies of estramustine phosphate in patients with hormone-refractory disease, objective response rates ranging from 19 to 69% have been reported. Preliminary clinical investigations indicate that combining estramustine phosphate with vinblastine, etoposide or paclitaxel improves objective response rates over single-agent treatment, although no survival benefit over single-agent treatment has been demonstrated to date. In comparative studies, estramustine phosphate produces similar objective response rates to conventional antineoplastic agents in patients with hormone-refractory prostate cancer. In previously untreated patients with advanced metastatic hormone-responsive prostate cancer, objective responses are achieved in approximately 80% of patients. Estramustine phosphate appears to be at least as effective as estrogen or flutamide therapy in these patients. Nausea and vomiting are the most frequently observed adverse effects of treatment with estramustine phosphate. While these symptoms are usually mild to moderate in nature, they may occasionally be more troublesome to the patient and necessitate withdrawal of treatment. Cardiovascular complications are a more serious, though less frequently encountered, adverse effect of the drug. However, these complications may be avoided by careful patient selection and prophylactic treatment measures. Unlike some other antineoplastic agents, estramustine phosphate is rarely associated with myelosuppression. In addition to producing similar objective response rates to other established agents, estramustine phosphate improves the subjective status of many patients and has been shown to reduce the intensity of pain and improve the performance status of patients.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1995        PMID: 7579781     DOI: 10.2165/00002512-199507010-00006

Source DB:  PubMed          Journal:  Drugs Aging        ISSN: 1170-229X            Impact factor:   3.923


  111 in total

1.  A comparison of estramustine phosphate and streptozotocin in patients with advanced prostatic carcinoma who have had extensive irradiation.

Authors:  G P Murphy; R P Gibbons; D E Johnson; S A Loening; G R Prout; J D Schmidt; D S Bross; T M Chu; J F Gaeta; J Saroff; W W Scott
Journal:  J Urol       Date:  1977-08       Impact factor: 7.450

Review 2.  Estracyt--mode of action and clinical experience.

Authors:  P O Hedlund
Journal:  Prog Clin Biol Res       Date:  1987

3.  Nuclear protein matrix as a target for estramustine-induced cell death.

Authors:  B Hartley-Asp; E Kruse
Journal:  Prostate       Date:  1986       Impact factor: 4.104

Review 4.  The present role of estramustine phosphate in advanced prostate cancer.

Authors:  H Van Poppel; L Baert
Journal:  Prog Clin Biol Res       Date:  1991

5.  Pharmacokinetics of estramustine phosphate (Estracyt) in prostatic cancer patients.

Authors:  P O Gunnarsson; S B Andersson; S A Johansson; T Nilsson; G Plym-Forshell
Journal:  Eur J Clin Pharmacol       Date:  1984       Impact factor: 2.953

6.  Clinical relevance of plasma testosterone and prolactin changes in advanced cancer of prostate treated with diethylstilbestrol or estramustine phosphate.

Authors:  A Morales; J C Nickel
Journal:  Urology       Date:  1985-11       Impact factor: 2.649

7.  Estramustine-induced mitotic arrest in two human prostatic carcinoma cell lines DU 145 and PC-3.

Authors:  B Hartley-Asp
Journal:  Prostate       Date:  1984       Impact factor: 4.104

8.  Distribution and metabolism of estramustine in HeLa cells and the human prostatic tumour cell line 1013L.

Authors:  E Kruse; S A Johansson; B Hartley-Asp; P O Gunnarsson
Journal:  Biochem Pharmacol       Date:  1988-08-15       Impact factor: 5.858

9.  P-glycoprotein binding and modulation of the multidrug-resistant phenotype by estramustine.

Authors:  L A Speicher; L R Barone; A E Chapman; G R Hudes; N Laing; C D Smith; K D Tew
Journal:  J Natl Cancer Inst       Date:  1994-05-04       Impact factor: 13.506

10.  Inhibition of prostate cancer growth by estramustine and etoposide: evidence for interaction at the nuclear matrix.

Authors:  K J Pienta; J E Lehr
Journal:  J Urol       Date:  1993-06       Impact factor: 7.450

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  21 in total

1.  Rationale for the Radiation Therapy Oncology Group Study RTOG P-0014.

Authors:  Howard M Sandler; Kenneth J Pienta
Journal:  Rev Urol       Date:  2003

2.  Androgen deprivation and other treatments for advanced prostate cancer.

Authors:  M K Brawer; E D Crawford; F Labrie; A Mendoza-Valdes; P D Miller; D P Petrylak
Journal:  Rev Urol       Date:  2001

3.  Rationale for the Radiation Therapy Oncology Group Study RTOG P-0014.

Authors:  Howard M Sandler; Kenneth J Pienta
Journal:  Rev Urol       Date:  2003

4.  Phase 2 Study of Weekly Paclitaxel Plus Estramustine in Metastatic Hormone-Refractory Prostate Carcinoma: ECOG-ACRIN Cancer Research Group (E1898) Trial.

Authors:  Yu-Ning Wong; Judith Manola; Gary R Hudes; Bruce J Roth; Judd W Moul; Andrea M Barsevick; Richard M Scher; Michael J Volk; David J Vaughn; Stephen D Williams; Michael J Fisch; David Cella; Michael A Carducci; George Wilding
Journal:  Clin Genitourin Cancer       Date:  2017-10-16       Impact factor: 2.872

5.  Novel hybrids of natural oridonin-bearing nitrogen mustards as potential anticancer drug candidates.

Authors:  Shengtao Xu; Lingling Pei; Chengqian Wang; Yun-Kai Zhang; Dahong Li; Hequan Yao; Xiaoming Wu; Zhe-Sheng Chen; Yijun Sun; Jinyi Xu
Journal:  ACS Med Chem Lett       Date:  2014-05-28       Impact factor: 4.345

6.  Docetaxel-based therapy with or without estramustine as first-line chemotherapy for castration-resistant prostate cancer: a meta-analysis of four randomized controlled trials.

Authors:  Wei-Xiang Qi; Zan Shen; Yang Yao
Journal:  J Cancer Res Clin Oncol       Date:  2011-09-14       Impact factor: 4.553

7.  Docetaxel for the treatment of hormone-refractory prostate cancer.

Authors:  Daniel P Petrylak
Journal:  Rev Urol       Date:  2003

8.  Weekly, low-dose docetaxel combined with estramustine for Japanese castration-resistant prostate cancer: its efficacy and safety profile compared with tri-weekly standard-dose treatment.

Authors:  Yasutomo Nakai; Kazuo Nishimura; Masashi Nakayama; Motohide Uemura; Hitoshi Takayama; Norio Nonomura; Akira Tsujimura
Journal:  Int J Clin Oncol       Date:  2013-03-01       Impact factor: 3.402

9.  Intermittent docetaxel therapy with estramustine for hormone-refractory prostate cancer in Japanese patients.

Authors:  Norihito Soga; Manabu Kato; Kouhei Nishikawa; Yoshihiro Hasegawa; Yasushi Yamada; Hideaki Kise; Kiminobu Arima; Yoshiki Sugimura
Journal:  Int J Clin Oncol       Date:  2009-04-24       Impact factor: 3.402

Review 10.  Targeting prostate cancer based on signal transduction and cell cycle pathways.

Authors:  John T Lee; Brian D Lehmann; David M Terrian; William H Chappell; Franca Stivala; Massimo Libra; Alberto M Martelli; Linda S Steelman; James A McCubrey
Journal:  Cell Cycle       Date:  2008-06-16       Impact factor: 4.534

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