FIND DRUGS:

BRAND NAME GENERIC NAME INDICATION MANUFACTURERS COMPARE DRUGS

Galeterone Safe, Active in Men with Castration-Resistant Prostate Cancer

Share this article:

(ChemotherapyAdvisor) – The oral small-molecule galeterone (TOK-001) was safe and led to a decline in prostate-specific antigen (PSA) expression in chemotherapy-naïve patients with castration-resistant prostate cancer (CRPC), results of a Phase I trial presented during the AACR Annual Meeting 2012 in Chicago, IL, have found.

Galeterone, a semi-synthetic steroid analog, is known to inhibit CYP17 lyase activation, bind and inhibit the androgen receptor, and degrade androgen receptor protein. The dose-escalation ARMOR1 study enrolled 49 men ages 48 to 93 years with metastatic and nonmetastatic CRPC that had progressed during androgen ablation therapy. Patients were randomized to one of eight dose-escalation cohorts in which galeterone capsules were administered in daily single or split oral doses of 650mg, 975mg, 1,300mg, 1,950mg, or 2,600mg for 12 weeks.

At 12 weeks, the maximum tolerated dose was not reached. Overall, 58% of patients had grade 1 adverse events (AEs) and 30%, grade 2. The most commonly reported AEs were fatigue (36.7%), increase in aspartate aminotransferase (32.7%), increase in alanine aminotransferase (30.6%), nausea (28.6%), diarrhea (26.5%), and pruritus (24.5%). In 15 patients, grade 2 and 3 transient elevations of liver function tests (LFT) were observed, the majority asymptomatic. Of these, 11 patients underwent drug interruptions; 6 of 7 were successfully rechallenged and returned to treatment with no recurring ≥grade 3 LFT elevations.

Nine serious AEs were reported, eight unrelated to galeterone. One patient had grade 4 rhabdomyolysis in the setting of simvastatin 40mg qd and underlying renal insufficiency. No events of adrenal mineralocorticoid excess were observed.

Of the 49 patients, 24 (49%) had >30% maximal PSA reductions, including 11 (22%) with >50% maximal PSA reductions. In addition, CT scans revealed reduction in tumor size for some patients.

The manufacturer, Tokai Pharmaceuticals (Cambridge, MA), has planned a Phase 2 study later this year to explore the long-term safety and efficacy of galeterone.

Abstract

Share this article:

Related Resources

You must be a registered member of Cancer Therapy Advisor to post a comment.
close

Next Article in Male Reproductive Cancers

Sign Up for Free e-newsletters

CTA Community Poll

Regimen and Drug Listings

GET FULL LISTINGS OF TREATMENT Regimens and Drug INFORMATION

Bone Cancer Regimens Drugs
Brain Cancer Regimens Drugs
Breast Cancer Regimens Drugs
Endocrine Cancer Regimens Drugs
Gastrointestinal Cancer Regimens Drugs
Genitourinary Cancer Regimens Drugs
Gynecologic Cancer Regimens Drugs
Head and Neck Cancer Regimens Drugs
Hematologic Cancer Regimens Drugs
Lung Cancer Regimens Drugs
Other Cancers Regimens
Rare Cancers Regimens
Skin Cancer Regimens Drugs

More in Male Reproductive Cancers

Sexual Function Retained in Prostate Cancer Combination Therapy

Sexual Function Retained in Prostate Cancer Combination Therapy

High rates of preserved sexual function with combination beam plus brachytherapy.

New Gene Mutations Identified that Promote Prostate Cancer

New Gene Mutations Identified that Promote Prostate Cancer

Researchers have identified 23 genes that are associated with an increased risk for developing prostate cancer.

Primary Androgen-Deprivation Therapy (ADT) for Localized Prostate Cancer: Potential for Harm May Outweigh Benefit in Low-Risk Disease

Primary Androgen-Deprivation Therapy (ADT) for Localized Prostate Cancer: ...

Although ADT remains an important treatment, its use as primary therapy in low-risk prostate cancer seems increasingly ill advised.