SWOG clinical trial number
S1014

Abiraterone Acetate Treatment for Prostate Cancer Patients with a PSA of More Than Four Following Initial Androgen Deprivation Therapy, Phase II.

Closed
Phase
Accrual
98%
Published
Abbreviated Title
Metastatic PCa Suboptimal Response ADT, Abiraterone Acetate, Ph II
Activated
08/09/2011
Closed
08/01/2013
Participants
NCORP, Members, UCOP, Medical Oncologists, Surgeons, Affiliates

Research committees

Genitourinary Cancer

Treatment

Prednisone Abiraterone Acetate

Eligibility Criteria Expand/Collapse

Pts must have adeno ca of the prostate (small cell or neuroendocrine not allowed) which is metastatic as evidenced by soft tissue and/or bony mets at time of initiation of androgen deprivation (AD). Zubrod PS 0-2. Pt must be rec'g AD prior to reg (bilateral surgical orchiectomy is acceptable). Pt must have suboptimal response to AD as defined in Sect 5.4. Meas dis assessed by abd/pelv CT w/in 28 d prior reg. Non-meas dx assessed by bone scan w/in 42 d prior to reg. Hx of prior neoadj or adj GNRH agonist/antagonist therapy ok provided > 2 yrs prior reg. Prior finasteride or dutasteride ok if d/c'd > 6 wks prior reg. Prior enrollment to S0925 is not exclusionary. No prior chemo, radiopharmaceutical, ketoconazole for PCa. Pt must not require > 10 mg prednisone for other indications. Pt must not have received any prior Provenge. Prior RT or surgery ok provided > 28 days since completion and recovered from side effects. No plans to receive concurrent chemo, surgery or RT. No hormonal-acting agents. Pt must d/c antiandrogen therapy prior to reg. See Sect 5.4 for wash-out requirements. No hx or current brain mets. Pts w/clinical evidence of brain mets must have negative brain CT or MRI w/in 56 d prior to reg. Testosterone < 50, ANC >/= 1,500, PLT >/= 100,000, Hg >/= 10, creat < 1.5 x ULN or calc CrCl >/= 60, bili <1.5 ULN, SGOT & SGPT <1.5 ULN, potassium >/= 3.5 w/in 28 days prior to reg. Pts must be able to take oral meds. Pts must not have hx of GI disorders that may interfere w/ absorption of abiraterone acetate. Pt w/active or symptomatic viral hep, chronic liver dx or Child-Pugh B or C hepatic impairment are not eligible. Pt must have well controlled BP. No history of NY Heart Assoc Class III and IV heart failure. No other prior malignancy except as defined in Sect 5.22. Pt must be willing to use BC w/adequate barrier protection during and for 1 wk after last study drug administration.

Publication Information Expand/Collapse

2017

Abiraterone acetate for metastatic prostate cancer in patients with suboptimal biochemical response to hormone induction

T Flaig;M Plets;M Hussain;N Agarwal;N Mitsiades;H Deshpande;U Vaishampayan;IM Thompson JAMA Oncology Nov 9;3(11):e170231; Epub 2017 Nov 9.2017 Mar 30 [Epub ahead of print]

PMid: PMID28358937 | PMC number: PMC5824213

2015

Phase II trial of abiraterone acetate (AA) treatment for metastatic prostate cancer (PC) patients with a PSA of more than four following initial androgen deprivation therapy: SWOG S1014

T Flaig;C Tangen;M Hussain;N Agarwal;N Mitsiades;H Despande;U Vaishampayan;IM Thompson Journal of Clinical Oncology 33 (suppl 7; abstr 152);ASCO GU Cancers Sympos (February 26-28, 2015, Orlando, FL), poster;

Other Clinical Trials

SWOG Clinical Trial Number
S2210

S2210, "Targeted Neoadjuvant Treatment for Patients with Localized Prostate Cancer and Germline DNA Repair Deficiency"

Research Committee(s)
Genitourinary Cancer
Activated
08/14/2023
Accrual
2%
Open
Phase
SWOG Clinical Trial Number
S2200
SWOG Clinical Trial Number
CTSU/A031901