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dc.contributor.authorJiménez-Labaig, P
dc.contributor.authorRullan, A
dc.contributor.authorBraña, I
dc.contributor.authorHernando-Calvo, A
dc.contributor.authorMoreno, V
dc.contributor.authorDoger, B
dc.contributor.authorBitar, G
dc.contributor.authorAp Dafydd, D
dc.contributor.authorMelcher, A
dc.contributor.authorHarrington, KJ
dc.coverage.spatialNetherlands
dc.date.accessioned2024-06-07T08:26:55Z
dc.date.available2024-06-07T08:26:55Z
dc.date.issued2024-06-01
dc.identifier102746
dc.identifierS0305-7372(24)00074-4
dc.identifier.citationCancer Treatment Reviews, 2024, 127 pp. 102746 -
dc.identifier.issn0305-7372
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/6264
dc.identifier.eissn1532-1967
dc.identifier.eissn1532-1967
dc.identifier.doi10.1016/j.ctrv.2024.102746
dc.identifier.doi10.1016/j.ctrv.2024.102746
dc.description.abstractBACKGROUND: Head and neck squamous cell carcinoma (HNSCC) presents an ideal scenario for intratumoral therapies (IT), due to its local recurrence pattern and frequent superficial extension. IT therapies aim to effect tumor regression by directly injecting antineoplastic agents into lesions. However, there is a lack of updated evidence regarding IT therapies in HNSCC. PATIENTS AND METHODS: A systematic literature search (CRD42023462291) was conducted using WebOfScience, ClinicalTrials.gov, and conference abstracts from ESMO and ASCO, identifying for IT clinical trials in patients with HNSCC, from database creation to September 12th, 2023. Efficacy as well as safety (grade ≥ 3 treatment-related adverse events[trAEs]) were reported. RESULTS: After evaluation of 1180 articles identified by the systematic search, 31 studies treating 948 patients were included. IT injectables were categorized as chemotherapies with or without electroporation (k = 4, N = 268), oncolytic viruses, plasmids, and bacteria-based (k = 16, N = 446), immunotherapies and EGFR-based therapies (k = 5, N = 160), radioenhancer particles (k = 2, N = 68), and calcium electroporation (k = 1, n = 6). EGFR-antisense plasmids, NBTXR3 radioenhancer and immune innate agonists show best overall response rates, at 83 %, 81 % and 44 % respectively. Eleven (35 %) studies added systemic therapy or radiotherapy to the IT injections. No study used predictive biomarkers to guide patient selection. 97 % studies were phase I-II. Safety-wise, electroporation and epinephrine-based injectable trials had significant local symptoms such as necrosis, fistula formation and post-injection dysphagia. Treatment-related tumor haemorrhages of various grades were described in several trials. Grade ≥ 3 trAEs attributable to the other therapies mainly comprised general symptoms such as fatigue. There were 3 injectable-related deaths across the systematic review. CONCLUSION: This is the first review to summarize all available evidence of IT in HNSCC. As of today, IT therapies lack sufficient evidence to recommend their use in clinical practice. Continuing research on potential molecules, patient selection, safe administration of injections and controlled randomized trials are needed to assess their added benefit.
dc.formatPrint-Electronic
dc.format.extent102746 -
dc.languageeng
dc.language.isoeng
dc.publisherELSEVIER SCI LTD
dc.relation.ispartofCancer Treatment Reviews
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectHNSCC
dc.subjectHead and neck cancer
dc.subjectIntralesional therapy
dc.subjectIntratumoral therapy
dc.subjectSquamous cell carcinoma
dc.subjectHumans
dc.subjectSquamous Cell Carcinoma of Head and Neck
dc.subjectHead and Neck Neoplasms
dc.subjectAntineoplastic Agents
dc.subjectInjections, Intralesional
dc.subjectImmunotherapy
dc.titleIntratumoral therapies in head and neck squamous cell carcinoma: A systematic review and future perspectives.
dc.typeJournal Article
dcterms.dateAccepted2024-04-25
dc.date.updated2024-06-07T08:22:09Z
rioxxterms.versionAM
rioxxterms.versionofrecord10.1016/j.ctrv.2024.102746
rioxxterms.licenseref.startdate2024-06-01
rioxxterms.typeJournal Article/Review
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/38696902
pubs.organisational-groupICR
pubs.organisational-groupICR/Primary Group
pubs.organisational-groupICR/Primary Group/ICR Divisions
pubs.organisational-groupICR/Primary Group/ICR Divisions/Cancer Biology
pubs.organisational-groupICR/Primary Group/ICR Divisions/Cancer Biology/Targeted Therapy
pubs.organisational-groupICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-groupICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Targeted Therapy
pubs.organisational-groupICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Translational Immunotherapy
pubs.organisational-groupICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Translational Immunotherapy/Translational Immunotherapy (TL)
pubs.organisational-groupICR/ImmNet
pubs.publication-statusPublished
pubs.publisher-urlhttp://dx.doi.org/10.1016/j.ctrv.2024.102746
pubs.volume127
icr.researchteamTrans Immunotherapy
icr.researchteamTargeted Therapy
dc.contributor.icrauthorMelcher, Alan
dc.contributor.icrauthorHarrington, Kevin
icr.provenanceDeposited by Mr Arek Surman (impersonating Pablo Jimenez) on 2024-06-07. Deposit type is initial. No. of files: 1. Files: IntratumouralTherapiesHNSCC Clean 20April2024.pdf


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