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Long-Term Clinical Responses of Neoadjuvant Dendritic Cell Infusions and Radiation in Soft Tissue Sarcoma
Purpose. Patients with large >5 cm, high-grade resectable soft tissue sarcomas (STS) have the highest risk of distant metastases. Previously we have shown that dendritic cell (DC) based vaccines show consistent immune responses. Methods. This was a Phase I single institution study of neoadjuvant...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4735941/ https://www.ncbi.nlm.nih.gov/pubmed/26880867 http://dx.doi.org/10.1155/2015/614736 |
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author | Raj, Shailaja Bui, Marilyn M. Springett, Gregory Conley, Anthony Lavilla-Alonso, Sergio Zhao, Xiuhua Chen, Dungsa Haysek, Randy Gonzalez, Ricardo Letson, G. Douglas Finkelstein, Steven Eric Chiappori, Alberto A. Gabrilovitch, Dmitry I. Antonia, Scott J. |
author_facet | Raj, Shailaja Bui, Marilyn M. Springett, Gregory Conley, Anthony Lavilla-Alonso, Sergio Zhao, Xiuhua Chen, Dungsa Haysek, Randy Gonzalez, Ricardo Letson, G. Douglas Finkelstein, Steven Eric Chiappori, Alberto A. Gabrilovitch, Dmitry I. Antonia, Scott J. |
author_sort | Raj, Shailaja |
collection | PubMed |
description | Purpose. Patients with large >5 cm, high-grade resectable soft tissue sarcomas (STS) have the highest risk of distant metastases. Previously we have shown that dendritic cell (DC) based vaccines show consistent immune responses. Methods. This was a Phase I single institution study of neoadjuvant radiation with DC injections on 18 newly diagnosed high-risk STS patients. Neoadjuvant treatment consisted of 50 Gy of external beam radiation (EBRT), given in 25 fractions delivered five days/week, combined with four intratumoral injections of DCs followed by complete resection. The primary endpoint was to establish the immunological response to neoadjuvant therapy and obtain data on its clinical safety and outcomes. Results. There were no unexpected toxicities or serious adverse events. Twelve out of 18 (67%) patients were alive, of which an encouraging 11/18 (61%) were alive with no systemic recurrence over a period of 2–8 years. Favorable immunological responses correlated with clinical responses in some cases. Conclusions. This study provides clinical support to using dendritic cell injections along with radiation in sarcomas, which when used optimally in combination can help clinical outcomes in soft tissue sarcoma. Study registration number is NCT00365872. |
format | Online Article Text |
id | pubmed-4735941 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-47359412016-02-15 Long-Term Clinical Responses of Neoadjuvant Dendritic Cell Infusions and Radiation in Soft Tissue Sarcoma Raj, Shailaja Bui, Marilyn M. Springett, Gregory Conley, Anthony Lavilla-Alonso, Sergio Zhao, Xiuhua Chen, Dungsa Haysek, Randy Gonzalez, Ricardo Letson, G. Douglas Finkelstein, Steven Eric Chiappori, Alberto A. Gabrilovitch, Dmitry I. Antonia, Scott J. Sarcoma Clinical Study Purpose. Patients with large >5 cm, high-grade resectable soft tissue sarcomas (STS) have the highest risk of distant metastases. Previously we have shown that dendritic cell (DC) based vaccines show consistent immune responses. Methods. This was a Phase I single institution study of neoadjuvant radiation with DC injections on 18 newly diagnosed high-risk STS patients. Neoadjuvant treatment consisted of 50 Gy of external beam radiation (EBRT), given in 25 fractions delivered five days/week, combined with four intratumoral injections of DCs followed by complete resection. The primary endpoint was to establish the immunological response to neoadjuvant therapy and obtain data on its clinical safety and outcomes. Results. There were no unexpected toxicities or serious adverse events. Twelve out of 18 (67%) patients were alive, of which an encouraging 11/18 (61%) were alive with no systemic recurrence over a period of 2–8 years. Favorable immunological responses correlated with clinical responses in some cases. Conclusions. This study provides clinical support to using dendritic cell injections along with radiation in sarcomas, which when used optimally in combination can help clinical outcomes in soft tissue sarcoma. Study registration number is NCT00365872. Hindawi Publishing Corporation 2015 2015-12-31 /pmc/articles/PMC4735941/ /pubmed/26880867 http://dx.doi.org/10.1155/2015/614736 Text en Copyright © 2015 Shailaja Raj et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Study Raj, Shailaja Bui, Marilyn M. Springett, Gregory Conley, Anthony Lavilla-Alonso, Sergio Zhao, Xiuhua Chen, Dungsa Haysek, Randy Gonzalez, Ricardo Letson, G. Douglas Finkelstein, Steven Eric Chiappori, Alberto A. Gabrilovitch, Dmitry I. Antonia, Scott J. Long-Term Clinical Responses of Neoadjuvant Dendritic Cell Infusions and Radiation in Soft Tissue Sarcoma |
title | Long-Term Clinical Responses of Neoadjuvant Dendritic Cell Infusions and Radiation in Soft Tissue Sarcoma |
title_full | Long-Term Clinical Responses of Neoadjuvant Dendritic Cell Infusions and Radiation in Soft Tissue Sarcoma |
title_fullStr | Long-Term Clinical Responses of Neoadjuvant Dendritic Cell Infusions and Radiation in Soft Tissue Sarcoma |
title_full_unstemmed | Long-Term Clinical Responses of Neoadjuvant Dendritic Cell Infusions and Radiation in Soft Tissue Sarcoma |
title_short | Long-Term Clinical Responses of Neoadjuvant Dendritic Cell Infusions and Radiation in Soft Tissue Sarcoma |
title_sort | long-term clinical responses of neoadjuvant dendritic cell infusions and radiation in soft tissue sarcoma |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4735941/ https://www.ncbi.nlm.nih.gov/pubmed/26880867 http://dx.doi.org/10.1155/2015/614736 |
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