Literature DB >> 10430077

Therapy of advanced prostate cancer with granulocyte macrophage colony-stimulating factor.

E J Small1, D M Reese, B Um, S Whisenant, S C Dixon, W D Figg.   

Abstract

Granulocyte macrophage colony-stimulating factor is a pleiotropic cytokine capable of inducing systemic immune responses against experimental and human tumors. To evaluate the efficacy of GM-CSF treatment in patients with hormone-refractory prostate cancer, we conducted sequential Phase II studies in 36 men with progressive disease after androgen deprivation and antiandrogen withdrawal. In a first cohort of patients (n = 23), GM-CSF was administered s.c. at a dose of 250 microg/m2 daily for 14 days of a 28-day treatment period. After we observed oscillating prostate-specific antigen (PSA) responses in several patients in this first cohort, a second trial was performed in which patients (n = 13) received maintenance GM-CSF (250 microg/m2 three times weekly) after the first 14 days of daily GM-CSF. All patients were treated until disease progression. Response was assessed by evaluation of serial changes in serum PSA and sequential imaging studies. In cohort I, 10 of 22 patients (45%) had a PSA versus time plot with a sawtooth pattern, with PSA declining during GM-CSF therapy and climbing during the off-therapy period; 5 patients had at least two consecutive declines in PSA, with a median response duration of 3.5 months. All but one patient in cohort II experienced a decline in PSA (median decline, 32%), but a PSA decline greater than 50% and sustained for more than 6 weeks was seen in only one patient, who had a >99% decline in PSA and an improvement in bone scan lasting for 14+ months. Changes in PSA levels could not be attributed to direct or indirect effects of GM-CSF on the PSA assay or down-regulation of PSA expression by GM-CSF. Toxicity was very mild, consisting primarily of transient constitutional symptoms and injection site reactions. These data suggest that GM-CSF may have antitumor activity in advanced prostate cancer, and the use of GM-CSF may be a confounding variable when PSA responses are used as an end point in clinical trials evaluating new regimens for the treatment of advanced prostate cancer.

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Year:  1999        PMID: 10430077

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  43 in total

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Review 4.  Beyond sipuleucel-T: immune approaches to treating prostate cancer.

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Review 5.  Immunotherapy for prostate cancer: biology and therapeutic approaches.

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Journal:  J Clin Oncol       Date:  2011-08-08       Impact factor: 44.544

Review 6.  Immune Therapy for Prostate Cancer.

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Journal:  Proc Natl Acad Sci U S A       Date:  2001-12-04       Impact factor: 11.205

8.  Single Institution Experience of Ipilimumab 3 mg/kg with Sargramostim (GM-CSF) in Metastatic Melanoma.

Authors:  Jason J Luke; Hilary Donahue; Mizuki Nishino; Anita Giobbie-Hurder; Meredith Davis; Nancy Bailey; Patrick A Ott; F Stephen Hodi
Journal:  Cancer Immunol Res       Date:  2015-05-05       Impact factor: 11.151

9.  Recombinant human granulocyte macrophage colony stimulating factor (hGM-CSF): Possibility of nanoparticle-mediated delivery in cancer immunotherapy.

Authors:  Selvarajan Vanitha; Nidhi Chaubey; Siddhartha S Ghosh; Pallab Sanpui
Journal:  Bioengineered       Date:  2016-07-26       Impact factor: 3.269

10.  Complete biochemical (prostate-specific antigen) response to sipuleucel-T with enzalutamide in castration-resistant prostate cancer: a case report with implications for future research.

Authors:  Julie N Graff; Charles G Drake; Tomasz M Beer
Journal:  Urology       Date:  2013-02       Impact factor: 2.649

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