Durable radiologic and molecular complete response following nivolumab in an HNSCC patient with UV signature and HIV

•Cancer patients living with HIV (CPLWH) may experience increased mortality risk.•Our patient did not have HIV at diagnosis but experienced accidental HIV exposure later.•Genomic profiling revealed CDKN2A/B, PBRM1, TP53, and TERT alterations corresponding to UV signature, and high tumor mutational b...

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Veröffentlicht in:Oral oncology 2024-07, Vol.154, p.106859, Article 106859
Hauptverfasser: Adibi, Ashkan, Tokat, Ünal Metin, Özgü, Eylül, Mamyrov, Nurseit, Aydın, Esranur, Bilgiç, Şevval Nur, Tutar, Onur, Demiray, Mutlu
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container_end_page
container_issue
container_start_page 106859
container_title Oral oncology
container_volume 154
creator Adibi, Ashkan
Tokat, Ünal Metin
Özgü, Eylül
Mamyrov, Nurseit
Aydın, Esranur
Bilgiç, Şevval Nur
Tutar, Onur
Demiray, Mutlu
description •Cancer patients living with HIV (CPLWH) may experience increased mortality risk.•Our patient did not have HIV at diagnosis but experienced accidental HIV exposure later.•Genomic profiling revealed CDKN2A/B, PBRM1, TP53, and TERT alterations corresponding to UV signature, and high tumor mutational burden with positive PD-L1.•We report a durable radiologic and molecular complete response upon nivolumab plus IVC and antiretroviral therapy (ART).•We demonstrate the safety and efficacy of ICIs, and feasibility of managing adverse events caused by antitumor, antiviral, and integrative therapies. Cancer patients living with HIV (CPLWH) may experience increased mortality risk. Furthermore, they have been historically excluded from clinical trials due to safety concerns. Our patient with squamous cell carcinoma of the lower lip received radiotherapy and platinum-based chemotherapy but declined by multiple centers due to his accidental HIV status. Genomic profiling revealed CDKN2A/B, PBRM1, TP53, and TERT alterations corresponding to UV signature, and high tumor mutational burden with positive PD-L1 staining. Accordingly, we report a durable radiologic and molecular complete response upon nivolumab plus IVC and antiretroviral therapy (ART). We demonstrated the safety and efficacy of ICIs, and feasibility of managing adverse events caused by antitumor, antiviral, and integrative therapies.
doi_str_mv 10.1016/j.oraloncology.2024.106859
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Cancer patients living with HIV (CPLWH) may experience increased mortality risk. Furthermore, they have been historically excluded from clinical trials due to safety concerns. Our patient with squamous cell carcinoma of the lower lip received radiotherapy and platinum-based chemotherapy but declined by multiple centers due to his accidental HIV status. Genomic profiling revealed CDKN2A/B, PBRM1, TP53, and TERT alterations corresponding to UV signature, and high tumor mutational burden with positive PD-L1 staining. Accordingly, we report a durable radiologic and molecular complete response upon nivolumab plus IVC and antiretroviral therapy (ART). 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Cancer patients living with HIV (CPLWH) may experience increased mortality risk. Furthermore, they have been historically excluded from clinical trials due to safety concerns. Our patient with squamous cell carcinoma of the lower lip received radiotherapy and platinum-based chemotherapy but declined by multiple centers due to his accidental HIV status. Genomic profiling revealed CDKN2A/B, PBRM1, TP53, and TERT alterations corresponding to UV signature, and high tumor mutational burden with positive PD-L1 staining. Accordingly, we report a durable radiologic and molecular complete response upon nivolumab plus IVC and antiretroviral therapy (ART). 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Cancer patients living with HIV (CPLWH) may experience increased mortality risk. Furthermore, they have been historically excluded from clinical trials due to safety concerns. Our patient with squamous cell carcinoma of the lower lip received radiotherapy and platinum-based chemotherapy but declined by multiple centers due to his accidental HIV status. Genomic profiling revealed CDKN2A/B, PBRM1, TP53, and TERT alterations corresponding to UV signature, and high tumor mutational burden with positive PD-L1 staining. Accordingly, we report a durable radiologic and molecular complete response upon nivolumab plus IVC and antiretroviral therapy (ART). We demonstrated the safety and efficacy of ICIs, and feasibility of managing adverse events caused by antitumor, antiviral, and integrative therapies.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>38781626</pmid><doi>10.1016/j.oraloncology.2024.106859</doi><orcidid>https://orcid.org/0000-0003-2501-3097</orcidid></addata></record>
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source Elsevier ScienceDirect Journals
subjects HNSCC (head and neck squamous cell carcinoma)
Immune checkpoint inhibitor (ICI)
Nivolumab
People living with HIV (PLWH)
Precision immunotherapy
Precision oncology
UV signature
title Durable radiologic and molecular complete response following nivolumab in an HNSCC patient with UV signature and HIV
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