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Samarium-153-EDTMP (Quadramet(®)) with or without vaccine in metastatic castration-resistant prostate cancer: A randomized Phase 2 trial
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 causin...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5340090/ https://www.ncbi.nlm.nih.gov/pubmed/27486817 http://dx.doi.org/10.18632/oncotarget.10883 |
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author | Heery, Christopher R. Madan, Ravi A. Stein, Mark N. Stadler, Walter M. Di Paola, Robert S. Rauckhorst, Myrna Steinberg, Seth M. Marté, Jennifer L. Chen, Clara C. Grenga, Italia Donahue, Renee N. Jochems, Caroline Dahut, William L. Schlom, Jeffrey Gulley, James L. |
author_facet | Heery, Christopher R. Madan, Ravi A. Stein, Mark N. Stadler, Walter M. Di Paola, Robert S. Rauckhorst, Myrna Steinberg, Seth M. Marté, Jennifer L. Chen, Clara C. Grenga, Italia Donahue, Renee N. Jochems, Caroline Dahut, William L. Schlom, Jeffrey Gulley, James L. |
author_sort | Heery, Christopher R. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5340090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53400902017-03-08 Samarium-153-EDTMP (Quadramet(®)) with or without vaccine in metastatic castration-resistant prostate cancer: A randomized Phase 2 trial Heery, Christopher R. Madan, Ravi A. Stein, Mark N. Stadler, Walter M. Di Paola, Robert S. Rauckhorst, Myrna Steinberg, Seth M. Marté, Jennifer L. Chen, Clara C. Grenga, Italia Donahue, Renee N. Jochems, Caroline Dahut, William L. Schlom, Jeffrey Gulley, James L. Oncotarget Clinical Research Paper 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. Impact Journals LLC 2016-07-28 /pmc/articles/PMC5340090/ /pubmed/27486817 http://dx.doi.org/10.18632/oncotarget.10883 Text en Copyright: © 2016 Heery et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Clinical Research Paper Heery, Christopher R. Madan, Ravi A. Stein, Mark N. Stadler, Walter M. Di Paola, Robert S. Rauckhorst, Myrna Steinberg, Seth M. Marté, Jennifer L. Chen, Clara C. Grenga, Italia Donahue, Renee N. Jochems, Caroline Dahut, William L. Schlom, Jeffrey Gulley, James L. Samarium-153-EDTMP (Quadramet(®)) with or without vaccine in metastatic castration-resistant prostate cancer: A randomized Phase 2 trial |
title | Samarium-153-EDTMP (Quadramet(®)) with or without vaccine in metastatic castration-resistant prostate cancer: A randomized Phase 2 trial |
title_full | Samarium-153-EDTMP (Quadramet(®)) with or without vaccine in metastatic castration-resistant prostate cancer: A randomized Phase 2 trial |
title_fullStr | Samarium-153-EDTMP (Quadramet(®)) with or without vaccine in metastatic castration-resistant prostate cancer: A randomized Phase 2 trial |
title_full_unstemmed | Samarium-153-EDTMP (Quadramet(®)) with or without vaccine in metastatic castration-resistant prostate cancer: A randomized Phase 2 trial |
title_short | Samarium-153-EDTMP (Quadramet(®)) with or without vaccine in metastatic castration-resistant prostate cancer: A randomized Phase 2 trial |
title_sort | samarium-153-edtmp (quadramet(®)) with or without vaccine in metastatic castration-resistant prostate cancer: a randomized phase 2 trial |
topic | Clinical Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5340090/ https://www.ncbi.nlm.nih.gov/pubmed/27486817 http://dx.doi.org/10.18632/oncotarget.10883 |
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