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Clinical and Morphological Features of ER-Positive HER2-Negative Breast Tumors with PIK3CA Mutations in Russian Patients
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Background: Several targeted drugs have been recently approved for the treatment of PIK3CA-mutated hormone receptor-positive (HR+)/HER2-negative (HER2−) breast cancer (BC). This study aimed at a comprehensive evaluation of the spectrum of PIK3CA alterations in Russian BC patients. Methods: The tumor material from 1872 patients with ER+/HER2− BC was tested by a combination of PCR-based methods. Results: Mutations were detected in 693/1872 (37%) cases, including 46 BC with two PIK3CA lesions. The three most common substitutions (E542K, E545K, and H1047R) were identified in 542/693 (78%) PIK3CA-mutated cases, while as many as 5.5–12% of identified mutations were not potentially detectable by common commercial kits. The study included patients of Slavic and non-Slavic ethnicities residing in regions with different climate conditions, however, these factors did not influence the distribution of PIK3CA mutations. The presence of PIK3CA variants was associated with older patient age at diagnosis (p = 0.0002), smaller tumor size (p = 0.005), lower grade (p = 0.005), Ki67 <20% (p = 0.0001) and progesterone receptor-positive status (p = 0.002) at the initial disease diagnosis, and fewer distant metastases at the time of the detection of BC spread (p = 0.0001). In a subgroup of 413 BC patients who received adjuvant tamoxifen or aromatase inhibitors, PIK3CA mutations were not associated with resistance to either type of treatment. Conclusions: The results of this study highlight the need to extend the PIK3CA testing beyond the hotspot regions of this gene. Although PIK3CA alterations contribute to the pathogenesis of HR+/HER2− BC and represent a target for several novel drugs, they are not intrinsically associated with unfavorable clinical characteristics of this subtype of cancer disease.
MDPI AG
Tatyana N. Sokolova
Grigory A. Yanus
Svetlana N. Aleksakhina
Yana V. Belysheva
Aleksandra P. Chernyakova
Yulia S. Zharnakova
Alisa S. Nikitina
Tatyana M. Stebneva
Aleksandr S. Martianov
Alla Yu. Goryainova
Mark I. Gluzman
Rashida V. Orlova
Anastasiya I. Stukan’
Alena V. Zyuzyukina
Ruslan A. Zukov
Polina R. Korzun
Jeyla O. Binnatova
Anastasia S. Abuzova
Yulia N. Murunova
Aleksandr V. Sultanbaev
Elena N. Vorobeva
Leonid M. Mikhaevich
Victoria N. Pyliv
Anna N. Lysenko
Zarema K. Khachmamuk
Andrey E. Kozlov
Sergey Yu. Bakharev
Shagen G. Parsyan
Elena I. Rossokha
Leri D. Osidze
Irina S. Shumskaya
Anna V. Agaeva
Tatyana A. Kasmynina
Veronika V. Klimenko
Kamila T. Akhmetgareeva
Almira A. Vakhitova
Madina D. Chakhkieva
Vadim N. Dmitriev
Yana I. Bakshun
Alexey E. Vasiliev
Dunya D. Gasimly
Nadezhda A. Kravchenko
Dmitriy A. Maksimov
Alfia I. Nesterova
Ineza O. Sharvashidze
Christina Kh. Gadzaova
Galina G. Rakhmankulova
Zaur M. Khamgokov
Irina K. Amirkhanova
Ludmila V. Bembeeva
Vladimir I. Vladimirov
Oleg L. Petrenko
Natalia G. Ruskova
Ekaterina L. Serikova
Ksenia S. Subbotina
Svetlana A. Tkachenko
Victor L. Chang
Sanal P. Erdniev
Victoria S. Barbara
Anna V. Vasilevskaya
Yulia V. Mikheeva
Natalia O. Popova
Anastasia V. Fateeva
Denis Yu. Yukalchuk
Anna A. Grechkina
Khedi S. Musayeva
Svetlana V. Odintsova
Petimat I. Khabibulaeva
Alina G. Khlobystina
Kseniya A. Shvaiko
Elena A. Basova
Irina A. Bogomolova
Marina B. Bolieva
Viktor E. Goldberg
Marianna V. Kibisheva
Konstantin V. Menshikov
Dmitriy V. Ryazanov
Yana A. Udalova
Aleksandr V. Shkradyuk
Idris M. Khabriev
Dmitriy V. Kirtbaya
Alexey M. Degtyarev
Aleksandr A. Epkhiev
Yana A. Tyugina
Mirza A. Murachuev
Alena S. Stelmakh
Aglaya G. Iyevleva
Evgeny N. Imyanitov
Title: Clinical and Morphological Features of ER-Positive HER2-Negative Breast Tumors with PIK3CA Mutations in Russian Patients
Description:
Background: Several targeted drugs have been recently approved for the treatment of PIK3CA-mutated hormone receptor-positive (HR+)/HER2-negative (HER2−) breast cancer (BC).
This study aimed at a comprehensive evaluation of the spectrum of PIK3CA alterations in Russian BC patients.
Methods: The tumor material from 1872 patients with ER+/HER2− BC was tested by a combination of PCR-based methods.
Results: Mutations were detected in 693/1872 (37%) cases, including 46 BC with two PIK3CA lesions.
The three most common substitutions (E542K, E545K, and H1047R) were identified in 542/693 (78%) PIK3CA-mutated cases, while as many as 5.
5–12% of identified mutations were not potentially detectable by common commercial kits.
The study included patients of Slavic and non-Slavic ethnicities residing in regions with different climate conditions, however, these factors did not influence the distribution of PIK3CA mutations.
The presence of PIK3CA variants was associated with older patient age at diagnosis (p = 0.
0002), smaller tumor size (p = 0.
005), lower grade (p = 0.
005), Ki67 <20% (p = 0.
0001) and progesterone receptor-positive status (p = 0.
002) at the initial disease diagnosis, and fewer distant metastases at the time of the detection of BC spread (p = 0.
0001).
In a subgroup of 413 BC patients who received adjuvant tamoxifen or aromatase inhibitors, PIK3CA mutations were not associated with resistance to either type of treatment.
Conclusions: The results of this study highlight the need to extend the PIK3CA testing beyond the hotspot regions of this gene.
Although PIK3CA alterations contribute to the pathogenesis of HR+/HER2− BC and represent a target for several novel drugs, they are not intrinsically associated with unfavorable clinical characteristics of this subtype of cancer disease.
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