Literature DB >> 21532336

Combination therapy of recurrent prostate cancer with the proteasome inhibitor bortezomib plus hormone blockade.

Andrew S Kraft1, Elizabeth Garrett-Mayer, Amy E Wahlquist, Ali Golshayan, Chien-Shing Chen, William Butler, James Bearden, Michael Lilly.   

Abstract

A single arm phase II trial of single-agent bortezomib (BZM) alone or combined with hormone blockade was conducted in patients with early PSA recurrence after definitive local therapy. The primary endpoint of this study was to determine the time to PSA relapse after BZM therapy alone or when BZM was combined with hormone blockade. The secondary endpoint was to determine the safety of combination therapy. Part A of the treatment schedule consisted of three cycles of BZM 1.3 mg/m2 IV given on days 1,4,8,11. If patients progressed on Part A, they were entered on Part B which consisted of a single dose of LH-RH antagonist, daily oral antiandrogen, and weekly BZM 1.3 mg/m2 for three out of four weeks for a total of three months. BZM treatment significantly decreased the slope of the log PSA (p=0.024) demonstrating that this agent alone was capable of slowing the rise of the PSA. Of eight patients treated with BZM alone five had stable disease, two progressed and 1 went off study secondary to toxicity. The major toxicity was neurotoxicity requiring discontinuation of therapy in three patients and treatment interruption in nine patients. Of those receiving Parts A and B or B only, there were 11 of 15 CRs with the average time to progression of 5.5 months. BZM treatment can change the slope of PSA rise and can be combined with hormone deprivation therapy without significant additional side effects; these agents are associated with a median time to CR of 42 days.

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Year:  2011        PMID: 21532336     DOI: 10.4161/cbt.12.2.15723

Source DB:  PubMed          Journal:  Cancer Biol Ther        ISSN: 1538-4047            Impact factor:   4.742


  11 in total

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Journal:  Mol Cell Proteomics       Date:  2018-02-20       Impact factor: 5.911

4.  Restoration of tumor suppression in prostate cancer by targeting the E3 ligase E6AP.

Authors:  P J Paul; D Raghu; A-L Chan; T Gulati; L Lambeth; E Takano; M J Herold; J Hagekyriakou; R L Vessella; C Fedele; M Shackleton; E D Williams; S Fox; S Williams; S Haupt; C Gamell; Y Haupt
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5.  Proteasome inhibition by bortezomib increases IL-8 expression in androgen-independent prostate cancer cells: the role of IKKα.

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6.  High-throughput transcriptomic analysis nominates proteasomal genes as age-specific biomarkers and therapeutic targets in prostate cancer.

Authors:  S G Zhao; W C Jackson; V Kothari; M J Schipper; N Erho; J R Evans; C Speers; D A Hamstra; Y S Niknafs; P L Nguyen; E M Schaeffer; A E Ross; R B Den; E A Klein; R B Jenkins; E Davicioni; F Y Feng
Journal:  Prostate Cancer Prostatic Dis       Date:  2015-05-19       Impact factor: 5.554

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8.  Targeting NF-kappa B Signaling by Artesunate Restores Sensitivity of Castrate-Resistant Prostate Cancer Cells to Antiandrogens.

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9.  Inhibition of NF-kappa B signaling restores responsiveness of castrate-resistant prostate cancer cells to anti-androgen treatment by decreasing androgen receptor-variant expression.

Authors:  R Jin; H Yamashita; X Yu; J Wang; O E Franco; Y Wang; S W Hayward; R J Matusik
Journal:  Oncogene       Date:  2014-09-15       Impact factor: 9.867

10.  miR-30e* is overexpressed in prostate cancer and promotes NF-κB-mediated proliferation and tumor growth.

Authors:  Shawn M Egan; Ellen Karasik; Leigh Ellis; Sandra O Gollnick
Journal:  Oncotarget       Date:  2017-06-28
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