Geburtshilfe Frauenheilkd 2020; 80(06): e46
DOI: 10.1055/s-0040-1714588
Abstracts
Senologie

Awareness and availability of routine germline BRCA1/2 (gBRCA1/2) mutation testing in patients with Advanced Breast Cancer (ABC) in the outpatient oncology setting in Germany

MP Lux
1   Kooperatives Brustzentrum Paderborn, Paderborn, Deutschland
2   Frauen- und Kinderklinik St. Louise, Paderborn, Deutschland
3   St. Josefs-Krankenhaus, Salzkotten, Deutschland
,
T Decker
4   Onkologie Ravensburg, Ravensburg, Deutschland
,
ED Runkel
5   Pfizer Pharma GmbH, Berlin, Deutschland
,
A Niyazov
6   Pfizer Inc., , New York, Vereinigte Staaten von Amerika
,
RGW Quek
7   Pfizer Inc., , San Francisco, Vereinigte Staaten von Amerika
,
E Glastetter
5   Pfizer Pharma GmbH, Berlin, Deutschland
,
N Marschner
8   iOMEDICO AG, Freiburg, Deutschland
,
N Harbeck
9   Brustzentrum, Frauenklinik der Universität München (LMU), München, Deutschland
› Institutsangaben
 
 

    Introduction We investigated clinical practice, awareness, and availability of routine gBRCA1/2 testing in German outpatient oncology setting.

    Material 23-item online survey.

    Methods Completed by 50 office-based oncologists (medical/gynecologic), October 2019-February 2020.

    Results Known family history (FH) of gBRCA1/2-related cancer(s) and hormone receptor status influences gBRCA1/2 testing (Table). Most oncologists routinely test ABC patients with triple-negative breast cancer (TNBC) independent of FH; only reason for not testing TNBC patients (n=3) was reimbursement difficulties. Testing rates for HR+/HER2- ABC patients were generally lower and depended on FH. Reasons for not testing HR+/HER2- ABC patients (n; with FH 7, without 33): available therapy alternatives [rate (%); with FH 100.0, without 54.5], reimbursement difficulties [rate (%); with FH 28.6, without 24.2] or other [rate (%); with FH 0, without 24.2]. Other factors included guideline recommendations and age at BC onset. Test turnaround time [median (range); 4.0 (1.0-21.0) weeks] and availability of genetic counseling influenced when oncologists routinely initiate gBRCA1/2 testing (46.0 %; 36.0 %, respectively). Most oncologists reported access to gBRCA1/2 testing as satisfactory (30.0 %) or good (36.0 %).

    Conclusion gBRCA1/2 testing seems established in Germany’s outpatient oncology setting. Opportunities exist to improve testing of HR+ ABC patients without family history given gBRCA1/2-targeted therapy options. Funding: Pfizer.

    Tab. 1

    gBRCA1/2 testing rates [% (n/N)] in ABC patients by subtype and family history (n=number of physicians who replied yes; N=number of physicians asked)

    ABC Subtype

    ABC patients WITH known family history of gBRCA1/2-related cancer(s): Testing Rate in % (n/N)

    ABC patients WITHOUT known family history of gBRCA1/2-related cancer(s): Testing Rate in % (n/N)

    TNBC

    98.0 (49/50)

    92.0 (46/50)

    HR+/HER2-

    82.0 (41/50)

    30.0 (15/50)

    HR+/HER2+

    76.0 (38/50)

    10.0 (5/50)

    HR-/HER2+

    82.0 (41/50)

    16.0 (8/50)


    #

    Interessenkonflikt siehe unter

    https://www.abstractserver.com/seno2020/uploads/115-COI-1581866408.pdf

    Publikationsverlauf

    Artikel online veröffentlicht:
    16. Juli 2020

    © Georg Thieme Verlag KG
    Stuttgart · New York