The Clinical Value of Measuring Circulating HPV DNA during Chemo-Radiotherapy in Squamous Cell Carcinoma of the Anus.

anus neoplasms circulating tumor DNA human papillomavirus squamous cell carcinoma

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
18 May 2021
Historique:
received: 06 04 2021
revised: 07 05 2021
accepted: 14 05 2021
entrez: 2 6 2021
pubmed: 3 6 2021
medline: 3 6 2021
Statut: epublish

Résumé

Circulating tumor DNA (ctDNA) is investigated in various cancers. In squamous cell carcinoma of the anus (SCCA) infection with human papilloma virus (HPV) is found in around 90% of cases and here, plasma HPV (pHPV) can be used as ctDNA. Preliminary data have proved the ability to detect pHPV16 and -18 in SCCA. We have developed a highly sensitive method for measurement of six relevant pHPV subtypes, to investigate the elimination pattern of pHPV during chemo-radiotherapy (CRT) for SCCA and its clinical value. Patients treated at Aarhus University Hospital from 2016-2020 were included. P16 status in the primary biopsy was measured and 82% of patients had P16 positive tumor. Blood samples were collected prior to treatment (PT), mid treatment (MT), end of therapy (EOT), and during follow-up (FU). An in-house multiplex digital droplet PCR method measured pHPV subtypes 16, 18, 31, 33, 51, 58. Samples from 88 patients were drawn PT ( During CRT, pHPV can divide patients with SCCA into three groups with significantly different risk of failure. The use of pHPV can potentially assist in clinical treatment decision.

Sections du résumé

BACKGROUND AND PURPOSE OBJECTIVE
Circulating tumor DNA (ctDNA) is investigated in various cancers. In squamous cell carcinoma of the anus (SCCA) infection with human papilloma virus (HPV) is found in around 90% of cases and here, plasma HPV (pHPV) can be used as ctDNA. Preliminary data have proved the ability to detect pHPV16 and -18 in SCCA. We have developed a highly sensitive method for measurement of six relevant pHPV subtypes, to investigate the elimination pattern of pHPV during chemo-radiotherapy (CRT) for SCCA and its clinical value.
MATERIAL AND METHODS METHODS
Patients treated at Aarhus University Hospital from 2016-2020 were included. P16 status in the primary biopsy was measured and 82% of patients had P16 positive tumor. Blood samples were collected prior to treatment (PT), mid treatment (MT), end of therapy (EOT), and during follow-up (FU). An in-house multiplex digital droplet PCR method measured pHPV subtypes 16, 18, 31, 33, 51, 58.
RESULTS RESULTS
Samples from 88 patients were drawn PT (
CONCLUSION CONCLUSIONS
During CRT, pHPV can divide patients with SCCA into three groups with significantly different risk of failure. The use of pHPV can potentially assist in clinical treatment decision.

Identifiants

pubmed: 34070045
pii: cancers13102451
doi: 10.3390/cancers13102451
pmc: PMC8158133
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Danish Comprehensive Cancer Center - Radiotherapy
Organisme : Kræftens Bekæmpelse
Organisme : Aarhus Universitetshospital
Organisme : Bio- and Genome Bank Denmark

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Auteurs

Anna C Lefèvre (AC)

Experimental Clinical Oncology, Aarhus University Hospital, 8200 Aarhus N, Denmark.

Niels Pallisgaard (N)

Department of Pathology, Zealand University Hospital, 4000 Roskilde, Denmark.

Camilla Kronborg (C)

Danish Centre for Particle Therapy, 8200 Aarhus N, Denmark.

Karen L Wind (KL)

Experimental Clinical Oncology, Aarhus University Hospital, 8200 Aarhus N, Denmark.

Søren R P Krag (SRP)

Department of Pathology, Aarhus University Hospital, 8200 Aarhus N, Denmark.

Karen-Lise G Spindler (KG)

Experimental Clinical Oncology, Aarhus University Hospital, 8200 Aarhus N, Denmark.
Department of Oncology, Aarhus University Hospital, 8200 Aarhus N, Denmark.

Classifications MeSH