Neoadjuvant endocrine therapy with palbociclib in patients with high-risk breast cancer

التفاصيل البيبلوغرافية
العنوان: Neoadjuvant endocrine therapy with palbociclib in patients with high-risk breast cancer
المؤلفون: Steinar Lundgren, Egil S. Blix, Per Eystein Lønning, Hans Petter Eikesdal, C. Clausen, Emiel A. M. Janssen, Hildegunn Siv Aase, Jürgen Geisler, Turid Aas, Stian Knappskog, Helge Espelid, Bjørnar Gilje, G. Vagstad
المصدر: Annals of Oncology. 30:v59-v60
بيانات النشر: Elsevier BV, 2019.
سنة النشر: 2019
مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, business.industry, HER2 negative, Endocrine therapy, Hematology, Luminal a, Palbociclib, medicine.disease, University hospital, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, Breast cancer, Oncology, 030220 oncology & carcinogenesis, Family medicine, medicine, In patient, business, Complete response
الوصف: Background Optimal neoadjuvant therapy for luminal A breast cancer remains a topic of controversy. Methods In the phase 2 PETREMAC trial (NCT02624973), patients with large T2 (>4cm) or locally advanced breast cancers and luminal A characteristics (ER > 50%, HER2- and TP53 WT) received neoadjuvant endocrine therapy (NET) and CDK4/6 inhibition in concert. NET consisted of letrozole (postmenopausals) or tamoxifen + goserelin (premenopausals). Palbociclib (P) was added if Ki67 had decreased Results 88 patients were enrolled; mean tumor diameter 55 mm (range 20-95). 2 patients lacked Ki67 data for analysis, 1 was a screening failure. 47/85 (55%) had a drop >50% on NET alone. Among the remaining 38 patients, 31 had P added in concert, 5 had Ki67 50% in 22/31 patients (71%). NAC was required in 28/84 patients (33%) after NET +/- P. Thus far, 84 patients have completed neoadjuvant treatment, and 75 have surgery results ready. The clinical OR rate (ORR) before surgery was 24/32 for NET alone, 12/15 for NET + P and 24/28 for NAC after NET +/- P. The overall ORR before surgery was 85% (60/75, 13 w/missing data), and ORR 77% (36/47) for NET +/- P. Pathological complete response (pCR) has been observed in 4/75 patients at surgery, where 3/4 with pCR received NAC after NET +/- P. 40/88 tumors (45%) had mutations in the PI3K pathway; PIK3CA (33%), PTEN (6.8%) and AKT1 (4.5%). 5/15 lobular carcinomas (33%) and 16/73 other carcinomas (22%) harbored CDH1 mutations. CDH1 mutations were associated with a higher probability of Ki67 reduction >50% on NET alone (CDH1 mutated: 15/20 vs CDH1 WT: 32/66; p = 0.042). Conclusions NET +/- P was effective at reducing cell proliferation and yielded an ORR of 77% in these ER+, HER2 negative breast cancers. NAC was required only among 33% of the patients. CDH1 mutations seem predictive of response to NET in this setting. Clinical trial identification NCT02624973; 2015-002816-34. Legal entity responsible for the study Haukeland University Hospital, Bergen, Norway. Funding Det Regionale Samarbeidsorganet/Helse Vest, Pfizer. Disclosure P.E. Lonning: Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution): AstraZeneca; Honoraria (self), Travel / Accommodation / Expenses: Pierre Fabre; Honoraria (self): Roche; Advisory / Consultancy: Laboratorios Farmaceuticos Rovi; Research grant / Funding (self): Pfizer; Research grant / Funding (self): Novartis; Licensing / Royalties: Cytovation. E.S. Blix: Honoraria (self): Pfizer. B. Gilje: Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution): Roche; Honoraria (self), Research grant / Funding (institution): AstraZeneca; Advisory / Consultancy, Research grant / Funding (institution): Astellas Oncology; Research grant / Funding (institution): Cellgene; Research grant / Funding (institution): Pfizer; Travel / Accommodation / Expenses: Pierre Fabre. E.A. Janssen: Honoraria (self): AstraZeneca; Honoraria (self): Pfizer. J. Geisler: Honoraria (self), Advisory / Consultancy, Speaker Bureau / Expert testimony: Novartis; Honoraria (self), Advisory / Consultancy, Speaker Bureau / Expert testimony: MSD; Honoraria (self), Advisory / Consultancy: Lilly; Honoraria (self), Speaker Bureau / Expert testimony: Pierre Fabre; Honoraria (self), Speaker Bureau / Expert testimony: Brystol-Myers-Squibb; Advisory / Consultancy, Speaker Bureau / Expert testimony: AstraZeneca; Speaker Bureau / Expert testimony: Pfizer. T. Aas: Honoraria (self): AstraZenaca; Honoraria (self): Roche. S. Knappskog: Honoraria (self), Research grant / Funding (institution): AstraZenaca; Honoraria (self), Research grant / Funding (institution): Pfizer; Licensing / Royalties: Patent EP2389450 A1,Patent WO 2012/010661. H.P. Eikesdal: Honoraria (self), Research grant / Funding (institution), Travel / Accommodation / Expenses: AstraZenaca; Honoraria (self), Advisory / Consultancy, Research grant / Funding (institution): Novartis; Honoraria (self), Advisory / Consultancy, Speaker Bureau / Expert testimony, Research grant / Funding (institution): Pfizer; Honoraria (self), Travel / Accommodation / Expenses: Pierre Fabre; Honoraria (self): Amgen; Honoraria (self), Advisory / Consultancy: Roche; Honoraria (self): HAI Interaktiv AS; Honoraria (self): Dagens Medisin; Honoraria (self): Brystol-Myers-Squibb; Advisory / Consultancy: Lilly; Research grant / Funding (institution): Abbvie. All other authors have declared no conflicts of interest.
تدمد: 0923-7534
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::50ae5037c697f85d91241751ce0d4bc1
https://doi.org/10.1093/annonc/mdz240.009
حقوق: OPEN
رقم الأكسشن: edsair.doi...........50ae5037c697f85d91241751ce0d4bc1
قاعدة البيانات: OpenAIRE