Survival Comparison between Melanoma Patients Treated with Patient-Specific Dendritic Cell Vaccines and Other Immunotherapies Based on Extent of Disease at the Time of Treatment

Encouraging survival was observed in single arm and randomized phase 2 trials of patient-specific dendritic cell vaccines presenting autologous tumor antigens from autologous cancer cells that were derived from surgically resected metastases whose cells were self-renewing in vitro. Based on most adv...

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Main Authors: Robert Owen Dillman, Candace Hsieh
Format: Article
Language:English
Published: MDPI AG 2019-10-01
Series:Biomedicines
Subjects:
Online Access:https://www.mdpi.com/2227-9059/7/4/80
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spelling doaj-e50d2c18007e48a2b2b5f778646996302020-11-25T01:58:27ZengMDPI AGBiomedicines2227-90592019-10-01748010.3390/biomedicines7040080biomedicines7040080Survival Comparison between Melanoma Patients Treated with Patient-Specific Dendritic Cell Vaccines and Other Immunotherapies Based on Extent of Disease at the Time of TreatmentRobert Owen Dillman0Candace Hsieh1Oncology Department, AIVITA Biomedical Inc., Irvine, CA 92612, USAOncology Department, AIVITA Biomedical Inc., Irvine, CA 92612, USAEncouraging survival was observed in single arm and randomized phase 2 trials of patient-specific dendritic cell vaccines presenting autologous tumor antigens from autologous cancer cells that were derived from surgically resected metastases whose cells were self-renewing in vitro. Based on most advanced clinical stage and extent of tumor at the time of treatment, survival was best in patients classified as recurrent stage 3 without measurable disease. Next best was in stage 4 without measurable disease, and the worst survival was for measurable stage 4 disease. In this study, the survival of these patients was compared to the best contemporary controls that were gleaned from the clinical trial literature. The most comparable controls typically were from clinical trials testing other immunotherapy approaches. Even though contemporary controls typically had better prognostic features, median and/or long-term survival was consistently better in patients treated with this dendritic cell vaccine, except when compared to anti-programmed death molecule 1 (anti-PD-1). The clinical benefit of this patient-specific vaccine appears superior to a number of other immunotherapy approaches, but it is more complex to deliver than anti-PD-1 while equally effective. However, there is a strong rationale for combining such a product with anti-PD-1 in the treatment of patients with metastatic melanoma.https://www.mdpi.com/2227-9059/7/4/80melanomadendritic cellautologous tumor antigenstumor initiating cellsvaccineimmunotherapy
collection DOAJ
language English
format Article
sources DOAJ
author Robert Owen Dillman
Candace Hsieh
spellingShingle Robert Owen Dillman
Candace Hsieh
Survival Comparison between Melanoma Patients Treated with Patient-Specific Dendritic Cell Vaccines and Other Immunotherapies Based on Extent of Disease at the Time of Treatment
Biomedicines
melanoma
dendritic cell
autologous tumor antigens
tumor initiating cells
vaccine
immunotherapy
author_facet Robert Owen Dillman
Candace Hsieh
author_sort Robert Owen Dillman
title Survival Comparison between Melanoma Patients Treated with Patient-Specific Dendritic Cell Vaccines and Other Immunotherapies Based on Extent of Disease at the Time of Treatment
title_short Survival Comparison between Melanoma Patients Treated with Patient-Specific Dendritic Cell Vaccines and Other Immunotherapies Based on Extent of Disease at the Time of Treatment
title_full Survival Comparison between Melanoma Patients Treated with Patient-Specific Dendritic Cell Vaccines and Other Immunotherapies Based on Extent of Disease at the Time of Treatment
title_fullStr Survival Comparison between Melanoma Patients Treated with Patient-Specific Dendritic Cell Vaccines and Other Immunotherapies Based on Extent of Disease at the Time of Treatment
title_full_unstemmed Survival Comparison between Melanoma Patients Treated with Patient-Specific Dendritic Cell Vaccines and Other Immunotherapies Based on Extent of Disease at the Time of Treatment
title_sort survival comparison between melanoma patients treated with patient-specific dendritic cell vaccines and other immunotherapies based on extent of disease at the time of treatment
publisher MDPI AG
series Biomedicines
issn 2227-9059
publishDate 2019-10-01
description Encouraging survival was observed in single arm and randomized phase 2 trials of patient-specific dendritic cell vaccines presenting autologous tumor antigens from autologous cancer cells that were derived from surgically resected metastases whose cells were self-renewing in vitro. Based on most advanced clinical stage and extent of tumor at the time of treatment, survival was best in patients classified as recurrent stage 3 without measurable disease. Next best was in stage 4 without measurable disease, and the worst survival was for measurable stage 4 disease. In this study, the survival of these patients was compared to the best contemporary controls that were gleaned from the clinical trial literature. The most comparable controls typically were from clinical trials testing other immunotherapy approaches. Even though contemporary controls typically had better prognostic features, median and/or long-term survival was consistently better in patients treated with this dendritic cell vaccine, except when compared to anti-programmed death molecule 1 (anti-PD-1). The clinical benefit of this patient-specific vaccine appears superior to a number of other immunotherapy approaches, but it is more complex to deliver than anti-PD-1 while equally effective. However, there is a strong rationale for combining such a product with anti-PD-1 in the treatment of patients with metastatic melanoma.
topic melanoma
dendritic cell
autologous tumor antigens
tumor initiating cells
vaccine
immunotherapy
url https://www.mdpi.com/2227-9059/7/4/80
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AT candacehsieh survivalcomparisonbetweenmelanomapatientstreatedwithpatientspecificdendriticcellvaccinesandotherimmunotherapiesbasedonextentofdiseaseatthetimeoftreatment
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