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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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