A prospective study investigating the efficacy and toxicity of definitive ChemoRadiation and ImmunOtherapy (CRIO) in locally and/or regionally advanced unresectable cutaneous squamous cell carcinoma
Abstract Background Patients with unresectable advanced cutaneous squamous cell carcinoma (cSCC) are generally treated with palliative intent. Immune checkpoint blockade has significant activity in the palliative setting in patients with recurrent or metastatic cSCC. This single arm phase 2 prospect...
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doaj-724133bc3d914f09a780fd4e48db3a692021-04-11T11:44:41ZengBMCRadiation Oncology1748-717X2021-04-0116111310.1186/s13014-021-01795-5A prospective study investigating the efficacy and toxicity of definitive ChemoRadiation and ImmunOtherapy (CRIO) in locally and/or regionally advanced unresectable cutaneous squamous cell carcinomaCharles Lin0Trishna Ballah1Michelle Nottage2Karen Hay3Benjamin Chua4Lizbeth Kenny5Paul Thomas6Michele Teng7Jacqui Keller8Trang Le9Jennifer Edmunds10Brett Hughes11Department of Radiation Oncology, Royal Brisbane and Women’s HospitalDepartment of Radiation Oncology, Royal Brisbane and Women’s HospitalDepartment of Medical Oncology, Royal Brisbane and Women’s HospitalQueensland Institute of Medical Research, Berghofer Medical Research InstituteDepartment of Radiation Oncology, Royal Brisbane and Women’s HospitalDepartment of Radiation Oncology, Royal Brisbane and Women’s HospitalDepartment of Nuclear Medicine, Royal Brisbane and Women’s HospitalQueensland Institute of Medical Research, Berghofer Medical Research InstituteDepartment of Radiation Oncology, Royal Brisbane and Women’s HospitalDepartment of Radiation Oncology, Royal Brisbane and Women’s HospitalDepartment of Radiation Oncology, Royal Brisbane and Women’s HospitalDepartment of Medical Oncology, Royal Brisbane and Women’s HospitalAbstract Background Patients with unresectable advanced cutaneous squamous cell carcinoma (cSCC) are generally treated with palliative intent. Immune checkpoint blockade has significant activity in the palliative setting in patients with recurrent or metastatic cSCC. This single arm phase 2 prospective study aims to investigate the combination of curative intent chemoradiation and durvalumab (anti-PD-L1 checkpoint inhibitor) for this patient cohort. Methods Patients with unresectable locally and or regionally advanced pathologically confirmed cSCC (stage III-IVa) deemed fit for CRIO by consensus of the Multidisciplinary meeting will be eligible. In the first stage of a two-stage minimax design, we aim to recruit a total of 15 patients. If fewer than 7 patients achieved a complete response in the first stage, we will conclude the treatment is not more effective than standard treatment. The co-primary endpoints of CRIO are the safety of treatment (acute and late toxicities) and the rate of complete response. Secondary endpoints would include overall survival, progression free survival, and locoregional control. Translational research endpoints including biomarkers (CD73, CD39, PD-1, PD-L1) will also be explored utilising multiplex immunohistochemistry on tumour biopsy samples obtained prior to commencing treatment and during treatment (week 2). In addition, the utility of CXCR-4 PET/CT scan will be explored. Discussion CRIO is a novel trial evaluating the combination of curative intent chemoradiotherapy with concurrent and adjuvant durvalumab for patients with unresectable stage III-IVa cSCC. Trial registration: Trial registered with the Australian New Zealand Clinical Trial Registry (ACTRN12618001573246)https://doi.org/10.1186/s13014-021-01795-5Skin cancerSCCCurativeRadiotherapyImmunotherapy |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Charles Lin Trishna Ballah Michelle Nottage Karen Hay Benjamin Chua Lizbeth Kenny Paul Thomas Michele Teng Jacqui Keller Trang Le Jennifer Edmunds Brett Hughes |
spellingShingle |
Charles Lin Trishna Ballah Michelle Nottage Karen Hay Benjamin Chua Lizbeth Kenny Paul Thomas Michele Teng Jacqui Keller Trang Le Jennifer Edmunds Brett Hughes A prospective study investigating the efficacy and toxicity of definitive ChemoRadiation and ImmunOtherapy (CRIO) in locally and/or regionally advanced unresectable cutaneous squamous cell carcinoma Radiation Oncology Skin cancer SCC Curative Radiotherapy Immunotherapy |
author_facet |
Charles Lin Trishna Ballah Michelle Nottage Karen Hay Benjamin Chua Lizbeth Kenny Paul Thomas Michele Teng Jacqui Keller Trang Le Jennifer Edmunds Brett Hughes |
author_sort |
Charles Lin |
title |
A prospective study investigating the efficacy and toxicity of definitive ChemoRadiation and ImmunOtherapy (CRIO) in locally and/or regionally advanced unresectable cutaneous squamous cell carcinoma |
title_short |
A prospective study investigating the efficacy and toxicity of definitive ChemoRadiation and ImmunOtherapy (CRIO) in locally and/or regionally advanced unresectable cutaneous squamous cell carcinoma |
title_full |
A prospective study investigating the efficacy and toxicity of definitive ChemoRadiation and ImmunOtherapy (CRIO) in locally and/or regionally advanced unresectable cutaneous squamous cell carcinoma |
title_fullStr |
A prospective study investigating the efficacy and toxicity of definitive ChemoRadiation and ImmunOtherapy (CRIO) in locally and/or regionally advanced unresectable cutaneous squamous cell carcinoma |
title_full_unstemmed |
A prospective study investigating the efficacy and toxicity of definitive ChemoRadiation and ImmunOtherapy (CRIO) in locally and/or regionally advanced unresectable cutaneous squamous cell carcinoma |
title_sort |
prospective study investigating the efficacy and toxicity of definitive chemoradiation and immunotherapy (crio) in locally and/or regionally advanced unresectable cutaneous squamous cell carcinoma |
publisher |
BMC |
series |
Radiation Oncology |
issn |
1748-717X |
publishDate |
2021-04-01 |
description |
Abstract Background Patients with unresectable advanced cutaneous squamous cell carcinoma (cSCC) are generally treated with palliative intent. Immune checkpoint blockade has significant activity in the palliative setting in patients with recurrent or metastatic cSCC. This single arm phase 2 prospective study aims to investigate the combination of curative intent chemoradiation and durvalumab (anti-PD-L1 checkpoint inhibitor) for this patient cohort. Methods Patients with unresectable locally and or regionally advanced pathologically confirmed cSCC (stage III-IVa) deemed fit for CRIO by consensus of the Multidisciplinary meeting will be eligible. In the first stage of a two-stage minimax design, we aim to recruit a total of 15 patients. If fewer than 7 patients achieved a complete response in the first stage, we will conclude the treatment is not more effective than standard treatment. The co-primary endpoints of CRIO are the safety of treatment (acute and late toxicities) and the rate of complete response. Secondary endpoints would include overall survival, progression free survival, and locoregional control. Translational research endpoints including biomarkers (CD73, CD39, PD-1, PD-L1) will also be explored utilising multiplex immunohistochemistry on tumour biopsy samples obtained prior to commencing treatment and during treatment (week 2). In addition, the utility of CXCR-4 PET/CT scan will be explored. Discussion CRIO is a novel trial evaluating the combination of curative intent chemoradiotherapy with concurrent and adjuvant durvalumab for patients with unresectable stage III-IVa cSCC. Trial registration: Trial registered with the Australian New Zealand Clinical Trial Registry (ACTRN12618001573246) |
topic |
Skin cancer SCC Curative Radiotherapy Immunotherapy |
url |
https://doi.org/10.1186/s13014-021-01795-5 |
work_keys_str_mv |
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