Molecular Guided Treatments in Gynecologic Oncology: Analysis of a Real-World Precision Cancer Medicine Platform

被引:6
|
作者
Taghizadeh, Hossein [1 ,4 ]
Mader, Robert M. [1 ,4 ]
Muellauer, Leonhard [2 ]
Aust, Stefanie [3 ,4 ]
Polterauer, Stephan [3 ,4 ]
Koelbl, Heinz [3 ,4 ]
Seebacher, Veronika [3 ,4 ]
Grimm, Christoph [3 ,4 ]
Reinthaller, Alexander [3 ,4 ]
Prager, Gerald W. [1 ,4 ]
机构
[1] Med Univ Vienna, Dept Med 1, Clin Div Oncol, Vienna, Austria
[2] Med Univ Vienna, Clin Inst Pathol, Vienna, Austria
[3] Med Univ Vienna, Dept Obstet & Gynecol, Vienna, Austria
[4] Comprehens Canc Ctr Vienna, Vienna, Austria
来源
ONCOLOGIST | 2020年 / 25卷 / 07期
关键词
Precision medicine; Gynecologic oncology; Molecular aberrations; Molecular profiling; Immunohistochemistry; Targeted agents; OVARIAN-CANCER; 1ST-LINE CHEMOTHERAPY; PHASE-II; EFFICACY; SAFETY; HETEROGENEITY; EVEROLIMUS; EXEMESTANE; THERAPY; TRIAL;
D O I
10.1634/theoncologist.2019-0904
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction Advanced gynecologic cancers have a poor prognosis and constitute a major challenge for adequate treatment strategies. By analyzing and targeting molecular alterations, molecular guided treatments may be a viable option for the treatment of advanced gynecologic cancers. Patients and Methods In this single-center, real-world retrospective analysis of our platform for precision cancer medicine (PCM), we describe the molecular profiling of 72 patients diagnosed with different types of advanced gynecologic malignancies. Tumor samples of the patients were examined by next-generation sequencing panel and immunohistochemistry (IHC). Results In total, we identified 209 genetic aberrations in 72 patients. The ten most frequent alterations were TP53 (n = 42, 20%), KRAS (n = 14, 6.6%), PIK3CA (n = 11, 5.2%), PIK3R1 (n = 9, 4.3%), ATR (n = 8, 3.8%), PTEN (n = 8, 3.8%), BRCA1 (n = 6, 2.8%), NF1 (n = 4, 1.9%), NOTCH1 (n = 4, 1.9%), and POLE (n = 4, 1.9%), which account for more than half of all molecular alterations (52.6%). In 21 (29.1%) patients only one mutation could be detected, and 44 (61.1%) patients had more than one mutation. No molecular alterations were detected in seven (9.7%) patients. IHC detected expression of phosphorylated mammalian target of rapamycin and epidermal growth factor receptor in 58 (80.6%) and 53 (73.6%) patients, respectively. In over two thirds (n = 49, 68.1%), a targeted therapy was suggested, based on the identified genetic aberrations. The most frequently recommended specific treatment was the combination of everolimus with exemestane (n = 18, 25 %). Conclusion Based on our observations, it seems that PCM might be a feasible approach for advanced gynecologic cancers with limited treatment options. Implications for Practice Nowadays molecular profiling of advanced gynecologic malignancies is feasible in the clinical routine. A molecular portrait should be done for every patient with an advanced therapy-refractory gynecologic malignancy to offer molecular-based treatment concepts.
引用
收藏
页码:E1060 / E1069
页数:10
相关论文
共 50 条
  • [1] Interim analysis of a real-world precision medicine platform for molecular profiling of metastatic or advanced cancers: MONDTI
    Kieler, Markus
    Unseld, Matthias
    Bianconi, Daniela
    Waneck, Fredrik
    Mader, Robert
    Wrba, Fritz
    Fuereder, Thorsten
    Marosi, Christine
    Raderer, Markus
    Staber, Philipp
    Berger, Walter
    Sibilia, Maria
    Polterauer, Stephan
    Muellauer, Leonhard
    Preusser, Matthias
    Zielinski, Christoph C.
    Prager, Gerald W.
    ESMO OPEN, 2019, 4 (04)
  • [2] Real-world data from a Molecular Tumor Board: improved outcomes in gynecologic and breast cancer patients with precision medicine
    Charo, Lindsey
    Eskander, Ramez
    Sicklick, Jason
    Kim, Ki Hwan
    Kim, Hyo Jeong
    Okamura, Ryosuke
    Schwab, Richard
    Lee, Suzanna
    Subramanian, Rupa
    Shatsky, Rebecca
    Plaxe, Steven
    Kato, Shumei
    Kurzrock, Razelle
    GYNECOLOGIC ONCOLOGY, 2021, 162 : S257 - S258
  • [3] Precision oncology for pancreatic cancer in real-world settings
    Kleeff, Joerg
    Michalski, Christoph W.
    LANCET ONCOLOGY, 2020, 21 (04): : 469 - 471
  • [4] Real-World Evidence and Precision Medicine in Cancer Research
    Zhou, Wei
    Carson, Ken
    Freeman, Andy
    Liu, Geoffrey
    Carleton, Bruce
    PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2017, 26 : 458 - 458
  • [5] Real-world evidence of precision medicine for biliary tract cancer
    Hayashi, Hideyuki
    Tanishima, Shigeki
    Fujikura, Tomoka
    Nakamura, Kohei
    Ishikawa, Marin
    Kato, Yasutaka
    Kawano, Ryutaro
    Hirata, Kenro
    Hamamoto, Yasuo
    Nishihara, Hiroshi
    ANNALS OF ONCOLOGY, 2023, 34 : S1417 - S1417
  • [6] Real-World Data From a Molecular Tumor Board: Improved Outcomes in Breast and Gynecologic Cancers Patients With Precision Medicine
    Charo, Lindsey M.
    Eskander, Ramez N.
    Sicklick, Jason
    Kim, Ki Hwan
    Lim, Hyo Jeong
    Okamura, Ryosuke
    Lee, Suzanna
    Subramanian, Rupa
    Schwab, Richard
    Shatsky, Rebecca
    Plaxe, Steven
    Kato, Shumei
    Kurzrock, Razelle
    JCO PRECISION ONCOLOGY, 2022, 6
  • [7] The importance of real-world data to precision medicine
    Kalra, Dipak
    PERSONALIZED MEDICINE, 2019, 16 (02) : 79 - 82
  • [8] Real-world data for precision cancer medicine-A European perspective
    Christopoulos, Petros
    Schlenk, Richard
    Kazdal, Daniel
    Blasi, Miriam
    Lennerz, Jochen
    Shah, Rajiv
    Budczies, Jan
    Malek, Nisar
    Froehling, Stefan
    Rosenquist, Richard
    Schirmacher, Peter
    Bozorgmehr, Farastuk
    Kuon, Jonas
    Reck, Martin
    Thomas, Michael
    Stenzinger, Albrecht
    GENES CHROMOSOMES & CANCER, 2023, 62 (09): : 557 - 563
  • [9] Building towards Precision Oncology for Pancreatic Cancer: Real-World Challenges and Opportunities
    Wang, Yifan
    Lakoma, Anna
    Zogopoulos, George
    GENES, 2020, 11 (09) : 1 - 18
  • [10] Real-world surgical treatment of thoracic cancer in the era of precision medicine Editorial
    Wei, Guobang
    Chen, Yongbing
    FRONTIERS IN SURGERY, 2022, 9