Samarium-153-EDTMP (Quadramet®) with or without vaccine in metastatic castration-resistant prostate cancer: A randomized Phase 2 trial

Christopher R. Heery, Ravi A. Madan, Mark N. Stein, Walter M. Stadler, Robert S. Di Paola, Myrna Rauckhorst, Seth M. Steinberg, Jennifer L. Marté, Clara C. Chen, Italia Grenga, Renee N. Donahue, Caroline Jochems, William L. Dahut, Jeffrey Schlom, James L. Gulley

Research output: Contribution to journalArticlepeer-review

46 Scopus citations

Abstract

PSA-TRICOM is a therapeutic vaccine in late stage clinical testing in metastatic castration-resistant prostate cancer (mCRPC). Samarium-153-ethylene diamine tetramethylene phosphonate (Sm-153-EDTMP; Quadramet®), a radiopharmaceutical, binds osteoblastic bone lesions and emits beta particles causing local tumor cell destruction. Preclinically, Sm-153-EDTMP alters tumor cell phenotype facilitating immune-mediated killing. This phase 2 multi-center trial randomized patients to Sm-153-EDTMP alone or with PSA-TRICOM vaccine. Eligibility required mCRPC, bone metastases, prior docetaxel and no visceral disease. The primary endpoint was the proportion of patients without radiographic disease progression at 4 months. Secondary endpoints included progression-free survival (PFS), overall survival (OS), and immune responses. Forty-four patients enrolled. Eighteen and 21 patients were evaluable for the primary endpoint in Sm-153-EDTMP alone and combination arms, respectively. There was no statistical difference in the primary endpoint, with two of 18 (11.1%) and five of 21 (23.8%) in Sm-153-EDTMP alone and combination arms, respectively, having stable disease at approximately the 4-month evaluation time point (P = 0.27). Median PFS was 1.7 vs. 3.7 months in the Sm-153-EDTMP alone and combination arms (P = 0.041, HR = 0.51, P = 0.046). No patient in the Sm-153-EDTMP alone arm achieved prostate-specific antigen (PSA) decline > 30% compared with four patients (of 21) in the combination arm, including three with PSA decline > 50%. Toxicities were similar between arms and related to number of Sm-153-EDTMP doses administered. These results provide the rationale for clinical evaluation of new radiopharmaceuticals, such as Ra-223, in combination with PSA-TRICOM.

Original languageEnglish
Pages (from-to)69014-69023
Number of pages10
JournalOncotarget
Volume7
Issue number42
DOIs
StatePublished - 2016

Bibliographical note

Publisher Copyright:
© 2015. Oncotarget.

Funding

The authors thank Jorge Carrasquillo, MD, previously affiliated with the National Cancer Institute, currently at Memorial Sloan Kettering Cancer Center, New York, NY, for his role in the development of this clinical trial. The authors also thank EUSA Pharma for providing Sm153-EDTMP at no cost to the patients enrolled on this clinical trial. The authors thank Debra Weingarten for her editorial assistance in the preparation of the manuscript Funding for this study was provided through the Intramural Research Program of the Center for Cancer Research, National Cancer Institute, National Institutes of Health, and the Cancer Therapy Evaluation Program (CTEP), National Cancer Institute, National Institutes of Health.

FundersFunder number
Cancer Therapy Evaluation Program
Center for Cancer Research
National Institutes of Health (NIH)
National Childhood Cancer Registry – National Cancer InstituteP50CA180995
National Childhood Cancer Registry – National Cancer Institute

    Keywords

    • Cancer immunotherapy
    • Prostate cancer
    • Quadramet®
    • Radionuclide
    • Therapeutic vaccine

    ASJC Scopus subject areas

    • Oncology

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