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DOI 10.1186/s12885-019-5535-2

Медицинская библиотека · BMC cancer · 2019

Cytology material is equivalent to tumor tissue in determining mutations of BRCA 1/2 genes in patients with tubo-ovarian high grade serous carcinoma.

Gornjec Andreja, Novakovic Srdjan, Stegel Vida, Hocevar Marko, Pohar Marinsek Ziva, Gazic Barbara, Krajc Mateja, Skof Erik

Клиническое исследованиеСравнительное исследованиеСтатьяПеревод в очереди

Аннотация

BACKGROUND

High-grade serous ovarian cancer is a detrimental disease. Treatment options in patients with a recurrent disease are dependent on BRCA1/2 mutation status since only patients with known BRCA mutation are eligible for treatment with poly(ADP-ribose) polymerase inhibitors (PARPi). The aim of this study was to compare concordance of BRCA mutation analyses from cytological samples (CS) with BRCA mutation analyses from histological formalin fixed paraffin embedded (FFPE) samples.

METHODS

Mutation analysis of BRCA1 and BRCA2 genes was performed in 44 women diagnosed with primary or recurrent high-grade ovarian cancer from three different samples: blood, cytological sample (ascites, pleural effusion and enlarged lymph nodes) and tumor tissue. Results from all three samples were compared.

RESULTS

Among 44 patients, there were 15 germline mutations and two somatic mutations. A 100% concordance was found between cytological and histologic samples.

CONCLUSION

There is a 100% concordance in BRCA mutation testing between cytological and histologic samples. BRCA mutation testing from CS could replace testing from FFPE tissue in clinical decision making in ovarian cancer patients.

TRIAL REGISTRATION: The study was retrospectively registered at ISRCTN registry on 24/11/2015 - ISRCTN42408038 .

Для цитирования: Gornjec Andreja, Novakovic Srdjan, Stegel Vida, Hocevar Marko, Pohar Marinsek Ziva, Gazic Barbara, Krajc Mateja, Skof Erik. Cytology material is equivalent to tumor tissue in determining mutations of BRCA 1/2 genes in patients with tubo-ovarian high grade serous carcinoma.. BMC cancer. 2019. DOI: 10.1186/s12885-019-5535-2.

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