Triple Negative Breast cancer New treatment options arenowhere?
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1 Triple Negative Breast cancer New treatment options arenowhere? Ofer Rotem, M.D., B.Sc. Breast Unit, Davidoff center Rabin Medical center October 2017
2 Case 6/ M.D., 38 years old woman, healthy, no family Hx Palpated mass in her right breast O/E & Imaging 3cm mass in Rt breast UOQ and a 2cm mobile LN in the right axilla. CNBx Rt breast & axilla IDC Grade 2-3, LN-Pos ER/PR/HER2-Neg, Ki67-40% Systemic work-up no evidence of Met disease TNBC Stage II T2N1M0
3 Case After consulting with her surgeon, the Mrs. D refers to your clinic for Preoperative treatment. Mrs. D is married + 3, works as a pilot in EL-AL.
4 Which regimen would you prefer? 1- DD AC Weekly Taxol 2- DD AC Taxol-Carbo 3- DD AC-Bev Taxol-Carbo-Bev 4- AC Weekly Taxol
5
6 GeparSixto: Study Design Randomized phase IIb study in 51 German centers Pts with centrally confirmed TNBC* or HER2+ BC with ct2 - T4a-d or ct1 with N+ disease (N = 588) PMCb Myocet 20 mg/m² Q1W + Paclitaxel 80 mg/m² Q1W Carboplatin AUC 2 Q1W q.18w (n = 295) PM Myocet 20 mg/m² Q1W + Paclitaxel 80 mg/m² Q1W q.18w (n = 293) Surgery Primary endpoint: pcr Secondary endpoints: RFS, DFS, OS *TNBC pts also received bevacizumab 15 mg/kg IV Q3W. HER2+ BC pts also received trastuzumab 8 mg/kg IV (initial dose), then 6 mg/kg IV Q3D (subsequent doses) and lapatinib 750 mg QD. Dose reduced to AUC 1.5 after 330 pts enrolled. von Minckwitz G, et al. SABCS Abstract S2-04.
7 GeparSixto: pcr Outcomes SABCS 2015 pcr, % ypt0/is ypn0 PMCb PM Odds Ratio P Value All pts (n = 588) * HER2+ BC (n = 273) TNBC (n = 315) gbrca wild type (n = 241)* gbrca mutant (n = 50)* *Level for significance = 0.2 Test for interaction, P = * Germline Mutation Status, Pathological Complete Response, and Disease-Free Survival in Triple-Negative Breast Cancer Secondary Analysis of the GeparSixto Randomized Clinical Trial Eric Hahnen. JAMA Oncology, Oct von Minckwitz G, et al. SABCS Abstract S2-04. von Minckwitz G, et al. Lancet Oncol. 2014;15: von Minckwitz G, et al. ASCO Abstract 1005.
8 Pts With DFS (%) GeparSixto: DFS by gbrca Status and Regimen in TNBC BRCA wt PM BRCA wt PMCb BRCA mt PM BRCA mt PMCb BRCA wt PM BRCA wt PMCb BRCA mt PM BRCA mt PMCb yDFS (%) 85.3 Vs Vs 82.5 HR, CI 0.53, Non-Significant WT Mos BRCA1/2 Mut
9 CALGB 40603
10 CALGB pcr breast/axilla No Carbo Carbo 41% 54% OR-1.71, p No Bev Bev 44% 52% OR-1.36, p Control With Bev With Carbo With Bev & Carbo 39% 43% 49% 60% William M. Sikov, et al. JCO, Jan 2015
11 San Antonio Breast Cancer Symposium, December 8-12, 2015 CALGB EFS and OS by Factor Carboplatin Bevacizumab Yes No Yes No EFS OS 3-year 76% 71% 75% 72% HR 0.84 ( ) 0.80 ( ) 3-year 81% 85% 85% 81% HR 1.15 ( ) 0.76 ( )
12 ESMO Guidelines. 2015: Addition of carboplatin to neoadj chemotherapy in TNBC - For BRCA 1/2 or RAD mutations it is acceptable to add a platinum compound, after discussion with the patient. NCCN Guidelines version : The NCCN panel does not recommend addition of carboplatin to neoadj standard chemotherapy for patients with TNBC outside a clinical trial setting.
13 ASCO 2017: I-SPY 2 Trial: Combination of Pembrolizumab Plus Standard Neoadjuvant Therapy in High-Risk Breast Cancer
14 ASCO 2017: I-SPY 2 Trial 69 pts were randomized to Pembro (HER2- subsets only) from Dec 2015 until it graduated in Nov pts (25 HR+, 21 TN) have undergone surgery.
15 Case cont Mrs. D decided she wants it all! DD AC Carbo-Taxol + Bev Rt Breast Lumpectomy + ALND Pathology report: IDC Grade II, 0.5cm, LN-3/17
16 Next step? 1- Adj xeloda 2- RTx and cont FU 3- NGS 4- Clinical trial OlympiA (In case of Germline BRCA Mut)
17 CREATE-X NEJM, Jun 2017 Stratified by ER status, age, neoadjuvant chemotherapy, use of 5-FU, institution, node status Wk 24 Pts yrs of age with stage I-IIIB HER2- BC and residual disease (non-pcr, N+) after neoadjuvant chemotherapy* and surgery; ECOG PS 0 or 1; no previous oral fluoropyrimidines Japan & South Korea (N = 910) Capecitabine 2500 mg/m²/day PO Days 1-14 Q3W for 8 cycles Hormonal therapy if ER/PgR+ (n = 455) Hormonal therapy if ER/PgR+ No further therapy if ER/PgR- (n = 455) *Anthracycline/taxane, anthracycline containing, or docetaxel/cyclophosphamide. 25 pts were removed from treatment (n = 10) and control (n = 15) arms due to failure to meet eligibility criteria. IDMC recommended extension to 8 cycles following interim safety analysis of first 50 pts receiving 6 cycles. [2] 1. Toi M, et al. SABCS Abstract S Ohtani S, et al. SABCS Abstract P
18 CREATE X PEP DFS SEP OS, time from first day of preoperative chemotherapy to recurrence or death, safety, cost-effectiveness The result of the prespecified interim analysis met the PEP, so the trial was terminated.
19 CREATE X - TN Pts 5yDFS 70% Vs 56% 5yOS 79% Vs 70%
20 Case cont Mrs. D was found to be BRCA1/2 WT, and decided to get Capecitabine Lower back pain, fatigue. PET scan - metastatic dis Bones, liver. ECOG 1 Blood test Normal
21 WWUD? 1- NGS 2- Chemotherapy (+/- Bev) 3- PARPi 4- Immunotherapy
22 Immunotherapy
23 Somatic mutation prevalence (number of mutations per megabase) Somatic mutations in cancers Breast Cancer and mutations: Lower median rate detected compared to the most immune-sensitive cancers but wide range of mutations detected 1, Alexandrov L,B. Nature 2013
24 TNBC - The best of what s left... Luen, The Breast, 2016
25
26
27 1L 2L
28 Results<br />BOR per RECIST v1.1 by line of therapy
29 KEYNOTE An Open-Label, Single-Arm Multicenter Phase 1b/2 Study to Evaluate the Efficacy and Safety of Eribulin Mesylate in Combination With Pembrolizumab in Subjects With Metastatic Triple-Negative Breast Cancer (mtnbc) SABCS 2016
30 Case Cont Single agent Pembrolizumab Clinical and radiographic PD. NGS: Somatic BRCA1 Mut
31 OlympiAD ASCO 2017 NEJM
32 OlympiAD
33 OlympiAD
34 OlympiAD No crossover
35 Case Cont Olaparib Clinical and radiographic PD. New Liver Biopsy TN, AR > 10%
36 11%
37
38 TNBC subtypes comparison with intrinsic PAM50 subtypes (Unsupervised Vs supervised clustering) 374 TNBC GE profiles were subtyped using PAM50 or TNBCtype
39 Anti Androgen therapy Bicalutamide Enzalutamide Abiraterone acetate
40 RR-0-8%
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