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dc.contributor.authorHaddad, R
dc.contributor.authorConcha-Benavente, F
dc.contributor.authorBlumenschein, G
dc.contributor.authorFayette, J
dc.contributor.authorGuigay, J
dc.contributor.authorColevas, AD
dc.contributor.authorLicitra, L
dc.contributor.authorKasper, S
dc.contributor.authorVokes, EE
dc.contributor.authorWorden, F
dc.contributor.authorSaba, NF
dc.contributor.authorTahara, M
dc.contributor.authorJayaprakash, V
dc.contributor.authorLynch, M
dc.contributor.authorLi, L
dc.contributor.authorGillison, ML
dc.contributor.authorHarrington, KJ
dc.contributor.authorFerris, RL
dc.date.accessioned2020-05-28T12:59:27Z
dc.date.issued2019-09-15
dc.identifier.citationCancer, 2019, 125 (18), pp. 3208 - 3218
dc.identifier.issn0008-543X
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/3662
dc.identifier.eissn1097-0142
dc.identifier.doi10.1002/cncr.32190
dc.description.abstractBACKGROUND: Response patterns with immune checkpoint inhibitors may be different from those with chemotherapy. Therefore, assessment of response to immunotherapy with the Response Evaluation Criteria in Solid Tumors (RECIST), version 1.1, could result in premature treatment termination. The randomized, open-label, phase 3 CheckMate 141 trial (NCT02105636), which evaluated nivolumab in recurrent/metastatic squamous cell carcinoma of the head and neck after platinum therapy, allowed treatment beyond first RECIST-defined progression (TBP) according to protocol-specified criteria. METHODS: In CheckMate 141, patients with RECIST-defined progression who had a stable performance status and demonstrated clinical benefit without rapid disease progression were permitted to receive TBP with nivolumab at 3 mg/kg every 2 weeks until further progression, which was defined as an additional ≥10% increase in tumor volume. This post hoc analysis evaluated outcomes for patients who received TBP with nivolumab. RESULTS: Of 240 patients randomized to nivolumab, 146 experienced RECIST-defined progression. Sixty-two of these patients received TBP, and 84 discontinued treatment (no TBP). Among the 60 TBP patients evaluable for response, 15 (25%) had no change in their tumor burden, and 15 (25%) had reductions in target lesion size; 3 patients (5%) had reductions >30%. The median overall survival among TBP patients was 12.7 months (95% confidence interval, 9.7-14.6 months). No new safety signals were observed with TBP. Exploratory analyses of immune cell biomarkers suggested a potential relationship with initial and TBP responses. CONCLUSIONS: Tumor burden reduction was noted in a proportion of patients who received TBP with nivolumab in CheckMate 141. Additional research is warranted to identify factors predictive of a TBP benefit in this population.
dc.formatPrint-Electronic
dc.format.extent3208 - 3218
dc.languageeng
dc.language.isoeng
dc.publisherWILEY
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectLymph Nodes
dc.subjectHumans
dc.subjectHead and Neck Neoplasms
dc.subjectLung Neoplasms
dc.subjectNeoplasm Recurrence, Local
dc.subjectDisease Progression
dc.subjectTreatment Outcome
dc.subjectAdult
dc.subjectAged
dc.subjectAged, 80 and over
dc.subjectMiddle Aged
dc.subjectFemale
dc.subjectMale
dc.subjectAntineoplastic Agents, Immunological
dc.subjectSquamous Cell Carcinoma of Head and Neck
dc.subjectNivolumab
dc.titleNivolumab treatment beyond RECIST-defined progression in recurrent or metastatic squamous cell carcinoma of the head and neck in CheckMate 141: A subgroup analysis of a randomized phase 3 clinical trial.
dc.typeJournal Article
dcterms.dateAccepted2019-04-18
rioxxterms.versionofrecord10.1002/cncr.32190
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by-nc-nd/4.0
rioxxterms.licenseref.startdate2019-09
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfCancer
pubs.issue18
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Biology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Biology/Targeted Therapy
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Targeted Therapy
pubs.publication-statusPublished
pubs.volume125
pubs.embargo.termsNot known
icr.researchteamTargeted Therapy
dc.contributor.icrauthorHarrington, Kevin


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