HPV Molecular Genotyping as a Differential Diagnosis Tool in Cervical Cancer Metastasis

Author:

Montero-Macías Rosa12ORCID,Coronado Pluvio J.3ORCID,Robillard Nicolas4,Veyer David45,Villefranque Vincent1ORCID,Le Frére-Belda Marie-Aude6,Auberger Elisabeth7,Bitolog Pauline7,Stankovic Ivana6,Bélec Laurent48ORCID,Bats Anne-Sophie89,Lécuru Fabrice810,Péré Hélène48

Affiliation:

1. Obstetrics and Gynecology Department, Centre Hospitalier Simone Veil, 95602 Eaubonne, France

2. Complutense University of Madrid, 28223 Madrid, Spain

3. Women’s Health Institute José Botella Llusiá, Fundación de Investigación del Hospital Clínico San Carlos (IdISSC), Universidad Complutense, 28040 Madrid, Spain

4. Virology Laboratory, Georges Pompidou European Hospital, 75015 Paris, France

5. INSERM, Functional Genomics of Solid Tumors (FunGeST), Centre de Recherche des Cordeliers, Université de Paris and Sorbonne Université, 75013 Paris, France

6. Pathology Department, Georges Pompidou European Hospital, 75015 Paris, France

7. Pathology Department, Simone Veil Hospital, 95600 Eaubonne, France

8. Faculty of Medicine, Paris University, 75015 Paris, France

9. Gynecologic and Breast Oncologic Surgery Department, Georges Pompidou European Hospital, 75015 Paris, France

10. Breast, Gynecology and Reconstructive Surgery Unit, Curie Institute, 75005 Paris, France

Abstract

Background: Differentiating metastatic cervical cancer from another primary tumor can be difficult in patients with a history of cervical cancer and a distant lesion. The use of routine HPV molecular detection and genotyping tests could help in these cases. The objective of this study was to identify if an easy-to-use HPV molecular genotyping assay would allow differentiating between HPV tumor metastasis and a new independent primary non-HPV-induced tumor. Materials and Methods: Between 2010 and 2020, we identified patients with a primary cervical carcinoma who also had another secondary lesion. This identification included a clinical and histologic differential diagnosis of metastatic cervical cancer versus a new primary cancer or metastatic cancer from another site. We used a routine multiplex real-time PCR (rt-PCR) AnyplexTM II HPV28 (Seegene, Seoul, Republic of Korea) to detect the high-risk (HR)-HPV genome in the distant lesions in these patients. Results: Eight cases of cervical cancer with a new secondary lesion were identified. In seven, HR-HPV DNA was detected in the biopsy of the distant lesion, which confirmed the diagnosis of cervical cancer metastasis. In the remaining case, no HPV was detected in the secondary lung biopsy, confirming the diagnosis of new primary lung cancer. Conclusion: Our results pave the way for HPV molecular genotyping use in cases of newly diagnosed distant lesions in patients with a history of HPV cervical neoplasia by using a routine diagnosis process to complete the clinical and histologic differential diagnosis when confronted with ambiguous situations.

Publisher

MDPI AG

Subject

Medicine (miscellaneous)

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