Cargando…
A phase II study of talimogene laherparepvec for patients with inoperable locoregional recurrence of breast cancer
Talimogene laherparepvec (T-VEC) is an immunotherapy that generates local tumor lysis and systemic antitumor immune response. We studied the efficacy of intratumoral administration of T-VEC as monotherapy for inoperable locoregional recurrence of breast cancer. T-VEC was injected intratumorally at 1...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8593093/ https://www.ncbi.nlm.nih.gov/pubmed/34782633 http://dx.doi.org/10.1038/s41598-021-01473-2 |
_version_ | 1784599638926426112 |
---|---|
author | Kai, Megumi Marx, Angela N. Liu, Diane D. Shen, Yu Gao, Hui Reuben, James M. Whitman, Gary Krishnamurthy, Savitri Ross, Merrick I. Litton, Jennifer K. Lim, Bora Ibrahim, Nuhad Kogawa, Takahiro Ueno, Naoto T. |
author_facet | Kai, Megumi Marx, Angela N. Liu, Diane D. Shen, Yu Gao, Hui Reuben, James M. Whitman, Gary Krishnamurthy, Savitri Ross, Merrick I. Litton, Jennifer K. Lim, Bora Ibrahim, Nuhad Kogawa, Takahiro Ueno, Naoto T. |
author_sort | Kai, Megumi |
collection | PubMed |
description | Talimogene laherparepvec (T-VEC) is an immunotherapy that generates local tumor lysis and systemic antitumor immune response. We studied the efficacy of intratumoral administration of T-VEC as monotherapy for inoperable locoregional recurrence of breast cancer. T-VEC was injected intratumorally at 10(6) PFU/mL on day 1 (cycle 1), 10(8) PFU/mL on day 22 (cycle 2), and 10(8) PFU/mL every 2 weeks thereafter (cycles ≥ 3). Nine patients were enrolled, 6 with only locoregional disease and 3 with both locoregional and distant disease. No patient completed the planned 10 cycles or achieved complete or partial response. The median number of cycles administered was 4 (range, 3–8). Seven patients withdrew prematurely because of uncontrolled disease progression, 1 withdrew after cycle 3 because of fatigue, and 1 withdrew after cycle 4 for reasons unrelated to study treatment. Median progression-free survival and overall survival were 77 days (95% CI, 63–NA) and 361 days (95% CI, 240–NA). Two patients received 8 cycles with clinically stable disease as the best response. The most common grade 2 or higher adverse event was injection site reaction (n = 7, 78%). Future studies could examine whether combining intratumoral T-VEC with concurrent systemic therapy produces better outcomes. |
format | Online Article Text |
id | pubmed-8593093 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85930932021-11-17 A phase II study of talimogene laherparepvec for patients with inoperable locoregional recurrence of breast cancer Kai, Megumi Marx, Angela N. Liu, Diane D. Shen, Yu Gao, Hui Reuben, James M. Whitman, Gary Krishnamurthy, Savitri Ross, Merrick I. Litton, Jennifer K. Lim, Bora Ibrahim, Nuhad Kogawa, Takahiro Ueno, Naoto T. Sci Rep Article Talimogene laherparepvec (T-VEC) is an immunotherapy that generates local tumor lysis and systemic antitumor immune response. We studied the efficacy of intratumoral administration of T-VEC as monotherapy for inoperable locoregional recurrence of breast cancer. T-VEC was injected intratumorally at 10(6) PFU/mL on day 1 (cycle 1), 10(8) PFU/mL on day 22 (cycle 2), and 10(8) PFU/mL every 2 weeks thereafter (cycles ≥ 3). Nine patients were enrolled, 6 with only locoregional disease and 3 with both locoregional and distant disease. No patient completed the planned 10 cycles or achieved complete or partial response. The median number of cycles administered was 4 (range, 3–8). Seven patients withdrew prematurely because of uncontrolled disease progression, 1 withdrew after cycle 3 because of fatigue, and 1 withdrew after cycle 4 for reasons unrelated to study treatment. Median progression-free survival and overall survival were 77 days (95% CI, 63–NA) and 361 days (95% CI, 240–NA). Two patients received 8 cycles with clinically stable disease as the best response. The most common grade 2 or higher adverse event was injection site reaction (n = 7, 78%). Future studies could examine whether combining intratumoral T-VEC with concurrent systemic therapy produces better outcomes. Nature Publishing Group UK 2021-11-15 /pmc/articles/PMC8593093/ /pubmed/34782633 http://dx.doi.org/10.1038/s41598-021-01473-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Kai, Megumi Marx, Angela N. Liu, Diane D. Shen, Yu Gao, Hui Reuben, James M. Whitman, Gary Krishnamurthy, Savitri Ross, Merrick I. Litton, Jennifer K. Lim, Bora Ibrahim, Nuhad Kogawa, Takahiro Ueno, Naoto T. A phase II study of talimogene laherparepvec for patients with inoperable locoregional recurrence of breast cancer |
title | A phase II study of talimogene laherparepvec for patients with inoperable locoregional recurrence of breast cancer |
title_full | A phase II study of talimogene laherparepvec for patients with inoperable locoregional recurrence of breast cancer |
title_fullStr | A phase II study of talimogene laherparepvec for patients with inoperable locoregional recurrence of breast cancer |
title_full_unstemmed | A phase II study of talimogene laherparepvec for patients with inoperable locoregional recurrence of breast cancer |
title_short | A phase II study of talimogene laherparepvec for patients with inoperable locoregional recurrence of breast cancer |
title_sort | phase ii study of talimogene laherparepvec for patients with inoperable locoregional recurrence of breast cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8593093/ https://www.ncbi.nlm.nih.gov/pubmed/34782633 http://dx.doi.org/10.1038/s41598-021-01473-2 |
work_keys_str_mv | AT kaimegumi aphaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer AT marxangelan aphaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer AT liudianed aphaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer AT shenyu aphaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer AT gaohui aphaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer AT reubenjamesm aphaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer AT whitmangary aphaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer AT krishnamurthysavitri aphaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer AT rossmerricki aphaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer AT littonjenniferk aphaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer AT limbora aphaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer AT ibrahimnuhad aphaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer AT kogawatakahiro aphaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer AT uenonaotot aphaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer AT kaimegumi phaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer AT marxangelan phaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer AT liudianed phaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer AT shenyu phaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer AT gaohui phaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer AT reubenjamesm phaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer AT whitmangary phaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer AT krishnamurthysavitri phaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer AT rossmerricki phaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer AT littonjenniferk phaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer AT limbora phaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer AT ibrahimnuhad phaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer AT kogawatakahiro phaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer AT uenonaotot phaseiistudyoftalimogenelaherparepvecforpatientswithinoperablelocoregionalrecurrenceofbreastcancer |