Radium-223 chloride (Ra-223) impact on skeletal-related events (SREs) and ECOG performance status (PS) in patients with castration-resistant prostate cancer (CRPC) with bone metastases: Interim results of a phase III trial (ALSYMPCA).

Authors

A. Sartor

A. Oliver Sartor

Tulane Cancer Center, New Orleans, LA

A. Oliver Sartor , Daniel Heinrich , Joe M. O'Sullivan , Sophie D. Fossa , Ales Chodacki , Pawel J. Wiechno , John P. Logue , Mihalj Seke , Anders Widmark , Dag Clement Johannessen , Sten Nilsson , Peter Hoskin , David Bottomley , Robert Edward Coleman , Nicholas J. Vogelzang , C. Gillies O'Bryan-Tear , Jose E. Garcia-Vargas , Minghua Shan , Chris Parker

Organizations

Tulane Cancer Center, New Orleans, LA, Akershus University Hospital, Lørenskog, Norway, Centre for Cancer Research and Cell Biology, Queen's University, Belfast, Ireland, Radiumhospitalet, Oslo, Norway, Hospital Kochova, Chomutov, Czech Republic, Centrum Onkologii – Instytut im Sklodowskiej-Curie, Warsaw, Poland, Christie Hospital, Manchester, United Kingdom, Centrallasarettet Växjö, Växjö, Sweden, Norrlands University Hospital, Umeå, Sweden, Ullevål University Hospital, Oslo, Norway, Karolinska Universitettsjukhuset, Stockholm, Sweden, Mount Vernon Hospital Cancer Centre, Middlesex, United Kingdom, St. James's Hospital, Leeds, United Kingdom, Weston Park Hospital, Sheffield, United Kingdom, Comprehensive Cancer Centers of Nevada, Las Vegas, NV, Algeta ASA, Oslo, Norway, Bayer HealthCare Pharmaceuticals, Montville, NJ, The Royal Marsden NHS Foundation Trust, Sutton, United Kingdom

Research Funding

Pharmaceutical/Biotech Company
Background: Ra-223, a 1st-in-class alpha-pharmaceutical, targets bone metastases (mets) with high-energy alpha-particles of short range (<100 μm). ALSYMPCA, a phase III, double-blind, randomized, multinational study, compared Ra-223 plus best standard of care (BSC) v placebo (pbo) plus BSC in patients (pts) with bone mets in CRPC. The primary endpoint was OS; secondary endpoints included SREs and ECOG PS. Methods: Eligible pts had progressive, symptomatic CRPC with ≥ 2 bone mets on scintigraphy and no known visceral mets; were receiving BSC; and either previously received docetaxel, were docetaxel ineligible, or refused docetaxel. Pts were randomized 2:1 to 6 injections of Ra‑223 (50 kBq/kg IV) q4 wks or matching pbo and stratified by prior docetaxel use, baseline ALP level, and current bisphosphonate use. Results: 921 pts were randomized from 6/2008-2/2011. In a planned interim analysis (n = 809), Ra-223 significantly improved OS v pbo (median OS 14.0 v 11.2 mo, respectively; two-sided P = .00185; HR = .695; 95% CI, .552-.875).SREs were lower in the Ra-223 v pbo group, and time to 1st SRE was significantly delayed (median time to SRE 13.6 mo v 8.4 mo, respectively; P = .00046; HR = .610; 95% CI, .461-.807). The proportion of pts with ECOG PS deterioration (≥ 2 points) was less in Ra-223 v pbo group at Wk 12 and Wk 24 (4%, 15/389 v 9%, 16/180 and 7%, 16/236 v 12%, 10/83, respectively). Time to ECOG PS deterioration (≥ 2 points) was significantly delayed by Ra-223 v pbo (P = .003; HR = .62; 95% CI, .46-.85). Conclusions: Ra-233 significantly delayed time to 1st SRE and SRE components, notably SCC. Fewer pts in the Ra-223 group had ECOG PS deterioration. Ra-223 improves OS with excellent safety and may provide a new standard of care for CRPC pts with bone mets.
SRE component No. (%) of patients
Time to 1st event
(Ra-223 vs Pbo)
Ra-223
n = 541
Pbo
n = 268
p value* HR
(95%CI)
External beam radiotherapy 122 (23) 72 (27) .0038 .65
(.48-.87)
Spinal cord compression 17 (3) 16 (6) .016 .44
(.22-.88)
Pathologic bone fracture 20 (4) 18 (7) .013 .45
(.24-.86)
Surgical intervention 9 (2) 5 (2) .69 .80
(.27-2.4)

*Not adjusted for multiplicity.

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Abstract Details

Meeting

2012 ASCO Annual Meeting

Session Type

Poster Discussion Session

Session Title

Genitourinary (Prostate) Cancer

Track

Genitourinary Cancer

Sub Track

Prostate Cancer

Clinical Trial Registration Number

NCT00699751

Citation

J Clin Oncol 30, 2012 (suppl; abstr 4551)

DOI

10.1200/jco.2012.30.15_suppl.4551

Abstract #

4551

Poster Bd #

5

Abstract Disclosures