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PREDIX HER2 trial : Event-free survival and pathologic complete response in clinical subgroups and stromal TILs levels

Authors :
Hatschek, T.
Andersson, A.
Bjöhle, J.
Bosch, A.
Carlsson, L.
Dreifaldt, Ann Charlotte
Einbeigi, Z.
Elinder, E.
Fredholm, H.
Isaksson-Friman, E.
Hellström, M.
Johansson, H.
Lekberg, T.
Lindman, H.
Zerdes, I.
Foukakis, T.
Hartman, J.
Brandberg, Y.
Bergh, J.
Hatschek, T.
Andersson, A.
Bjöhle, J.
Bosch, A.
Carlsson, L.
Dreifaldt, Ann Charlotte
Einbeigi, Z.
Elinder, E.
Fredholm, H.
Isaksson-Friman, E.
Hellström, M.
Johansson, H.
Lekberg, T.
Lindman, H.
Zerdes, I.
Foukakis, T.
Hartman, J.
Brandberg, Y.
Bergh, J.
Publication Year :
2020

Abstract

Background: Neoadjuvant treatment with Trastuzumab-emtansine was associated with similar rates of pathological complete remission (pCR) as standard therapy withd ocetaxel, trastuzumab and pertuzumab in the PREDIX HER2 trial. Here, results of event-free survival (EFS), and pCR rates in key clinical-pathological subgroups and biomarkers including the abundance of stromal tumor infiltrating lymphocytes (TILs) are presented. Methods: PREDIX HER2 is a randomized, multicenter, open-label, phase 2 study involving 9 Swedish sites. Patients with HER2 positive breast cancer, verified by ISH, T>20 mm and/or verified lymph node metastases were randomized to six three-weekly courses of either docetaxel, trastuzumab SC and pertuzumab (group A), or trastuzumab emtansine (T-DM1, group B). Switch of treatment to the opposite arm was allowed in case of lack of response or severe toxicity. Radiological evaluation included 18F-FDG PET/CT. Patients in both groups received adjuvant chemotherapy with epirubicin and cyclophosphamide. TILs were evaluated using standard methodology, median 10%. Results: In total 197 pts. were evaluable, 99 in group A, and 98 in group B. pCR (ypT0/is ypN0) was achieved in 90 pts, 45.7%, with no significant difference between the two treatment groups. pCR rates were lower in the group of patients with hormone receptor (HR)epositive compared with HR-negative tumors but similar in both treatment groups. pCR rates did not differ between the two treatments in subgroups defined by age, menopausal status, tumor grade, T size, node status, HR-status, HER2 status and Ki67. Progressive disease was observed in 3 pts. (3%) during treatment with T-DM1, none in group A. After a median follow-up of 2.4 years 13 EFS events occurred, with no significant differences between the treatment groups. The presence of 10% TILs predicted pCR significantly (p¼0.009), similar in both treatment groups. We also found that a decrease of SUVmax by more than 80% was highly predictive of p<br />Funding Agencies:Research funds at RadiumhemmetRegion Stockholm Roche Sweden AB

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1234076681
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1016.j.annonc.2020.03.037