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Targeted next-generation sequencing has incremental value in the diagnostic work-up of patients with suspect pancreatic masses; a multi-center prospective cross sectional study.
Achterberg, Friso B; Mulder, Babs G Sibinga; Janssen, Quisette P; Koerkamp, Bas Groot; Hol, Lieke; Quispel, Rutger; Bonsing, Bert A; Vahrmeijer, Alexander L; van Eijck, Casper H J; Roos, Daphne; Perk, Lars E; van der Harst, Erwin; Coene, Peter-Paul L O; Doukas, Michail; Smedts, Frank M M; Kliffen, Mike; van Velthuysen, Marie-Louise F; Terpstra, Valeska; Sarasqueta, Arantza Farina; Morreau, Hans; Mieog, J Sven D.
Afiliación
  • Achterberg FB; Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands.
  • Mulder BGS; Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands.
  • Janssen QP; Department of Surgery, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.
  • Koerkamp BG; Department of Surgery, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.
  • Hol L; Department of Gastro-Enterology, Maasstad Hospital, Rotterdam, The Netherlands.
  • Quispel R; Department of Gastro-Enterology, Reinier de Graaf Gasthuis, Delft, The Netherlands.
  • Bonsing BA; Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands.
  • Vahrmeijer AL; Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands.
  • van Eijck CHJ; Department of Surgery, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.
  • Roos D; Department of Surgery, Reinier de Graaf Gasthuis, Delft, The Netherlands.
  • Perk LE; Department of Gastro-Enterology, Haaglanden Medical Center, The Hague, The Netherlands.
  • van der Harst E; Department of Surgery, Maasstad Hospital, Rotterdam, The Netherlands.
  • Coene PLO; Department of Surgery, Maasstad Hospital, Rotterdam, The Netherlands.
  • Doukas M; Department of Pathology, Erasmus Medical MC, University Medical Center, Rotterdam, The Netherlands.
  • Smedts FMM; Department of Pathology, Reinier de Graaf Gasthuis, Delft, The Netherlands.
  • Kliffen M; Department of Pathology, Maasstad Hospital, Rotterdam, The Netherlands.
  • van Velthuysen MF; Department of Pathology, Erasmus Medical MC, University Medical Center, Rotterdam, The Netherlands.
  • Terpstra V; Department of Pathology, Haaglanden Medical Center, The Hague, The Netherlands.
  • Sarasqueta AF; Department of Pathology, Amsterdam University Medical Centers, Amsterdam, The Netherlands.
  • Morreau H; Department of Pathology, Leiden University Medical Center, Leiden, The Netherlands.
  • Mieog JSD; Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands.
PLoS One ; 18(1): e0280939, 2023.
Article en En | MEDLINE | ID: mdl-36696439
ABSTRACT

BACKGROUND:

The diagnostic process of patients with suspect pancreatic lesions is often lengthy and prone to repeated diagnostic procedures due to inconclusive results. Targeted Next-Generation Sequencing (NGS) performed on cytological material obtained with fine needle aspiration (FNA) or biliary duct brushing can speed up this process. Here, we study the incremental value of NGS for establishing the correct diagnosis, and subsequent treatment plan in patients with inconclusive diagnosis after regular diagnostic work-up for suspect pancreatic lesions.

METHODS:

In this prospective cross-sectional cohort study, patients were screened for inclusion in four hospitals. NGS was performed with AmpliSeq Cancer Hotspot Panel v2 and v4b in patients with inconclusive cytology results or with an uncertain diagnosis. Diagnostic results were evaluated by the oncology pancreatic multidisciplinary team. The added value of NGS was determined by comparing diagnosis (malignancy, cystic lesion or benign condition) and proposed treatment plan (exploration/resection, neoadjuvant chemotherapy, follow-up, palliation or repeated FNA) before and after integration of NGS results. Final histopathological analysis or a 6-month follow-up period were used as the reference standard in case of surgical intervention or non-invasive treatment, respectively.

RESULTS:

In 50 of the 53 included patients, cytology material was sufficient for NGS analysis. Diagnosis before and after integration of NGS results differed in 24% of the patients. The treatment plan was changed in 32% and the diagnosis was substantiated by the NGS data in 44%. Repetition of FNA/brushing was prevented in 14% of patients. All changes in treatment plan were correctly made after integration of NGS. Integration of NGS increased overall diagnostic accuracy from 68% to 94%.

INTERPRETATION:

This study demonstrates the incremental diagnostic value of NGS in patients with an initial inconclusive diagnosis. Integration of NGS results can prevent repeated EUS/FNA, and can also rigorously change the final diagnosis and treatment plan.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Pancreáticas Tipo de estudio: Clinical_trials / Diagnostic_studies / Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2023 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Pancreáticas Tipo de estudio: Clinical_trials / Diagnostic_studies / Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2023 Tipo del documento: Article País de afiliación: Países Bajos