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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
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.
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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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