Continuing Adjuvant Tamoxifen to 10 Years

Slides:



Advertisements
Similar presentations
Obesity at Diagnosis Is Associated with Inferior Outcomes in Hormone Receptor Positive Breast Cancer 1 The Impact of Body Mass Index (BMI) on the Efficacy.
Advertisements

Protecting the heart and the kidney: Implications from the SHARP trial Dr. Christina Reith University of Oxford United Kingdom.
Integration of Capecitabine into Anthracycline- and Taxane-Based Adjuvant Therapy for Triple Negative Early Breast Cancer: Final Subgroup Analysis of the.
History of the randomized evidence on early breast cancer overall survival: Radiation vs no radiation after mastectomy L. Vakaet 2006.
ATLAS Steering Committee: 24 September 2005 Steering Committee meeting, 24 th September 2005 University of Oxford Examination Schools.
Time to Distant Metastases (ITT) Cumulative incidence of distant metastases (ITT) Adapted from Jones et al. SABCS 2008, abstract /477169/465253/454771/ /4146.
Jack Cuzick, Ph.D. Wolfson Institute of Preventive Medicine St Bartholomew’s Medical School London, United Kingdom Implementation Issues for Chemoprevention.
Meta-analysis of trials of radiotherapy in DCIS Early Breast Cancer Trialists’ Collaborative Group (EBCTCG)
Long-Term Effects of Continuing Adjuvant Tamoxifen to 10 Years versus Stopping at 5 Years After Diagnosis of Oestrogen Receptor- Positive Breast Cancer:
These slides were released by the speaker for internal use by Novartis.
Wildiers H, et al. Lancet Oncol. 2007;8:1101. Breast Cancer in Elderly (>65 Years) Recommendations of the International Society of Geriatric Oncology Surgical.
These slides were released by the speaker for internal use by Novartis.
Slide Source: Lipids Online Slide Library Women’s Health Initiative: Trial of Estrogen plus Progestin 16,608 women randomized 16,608.
These slides were released by the speaker for internal use by Novartis
Randomized Comparison of Adjuvant Aromatase Inhibitor Exemestane plus Ovarian Function Suppression vs Tamoxifen plus Ovarian Function Suppression in Premenopausal.
Best first ? The ATAC completed treatment analysis Professor Jack Cuzick Wolfson Institute of Preventive Medicine, London, UK.
A systematic meta-analysis of randomized controlled trials for adjuvant chemotherapy for localized resectable soft-tissue sarcoma Nabeel Pervaiz Nigel.
San Antonio Breast Cancer Symposium 2012 Helen K. Chew, MD, FACP Professor of Medicine.
Early Breast Cancer Trialists' Collaborative Group (EBCTCG). Effects of chemotherapy and hormonal therapy for early breast cancer on recurrence and 15-year.
Start or Switch?: Latest data from ABCSG/ARNO
T Andre, E Quinaux, C Louvet, E Gamelin, O Bouche, E Achille, P Piedbois, N Tubiana-Mathieu, M Buyse and A de Gramont. Updated results at 6 year of the.
Published online July 24, Aromatase inhibitors versus tamoxifen in early breast.
DL Wickerham MD Deputy Chairman NRG Oncology Oct 5, 2015
Breast cancer 5 year survival rates (UK, 1975) by stage at diagnosis.
A Comparison of Fulvestrant 500 mg with Anastrozole as First-line Treatment for Advanced Breast Cancer: Follow-up Analysis from the FIRST Study Robertson.
Adjuvant chemotherapy – When should surgeons recommend? Joint Hospital Surgical Grand Round Dr Lorraine Chow Ruttonjee Hospital.
Extended adjuvant treatment with anastrozole: results from the ABCSG Trial 6a R Jakesz, H Samonigg, R Greil, M Gnant, M Schmid, W Kwasny, E Kubista, B.
Anastrozole (‘Arimidex’): a new standard of care?
Breast cancer affects 1 in 8 women during their lives. 1 Population Statistics.
‘Arimidex’, Tamoxifen, Alone or in Combination (ATAC) trial: Completed Treatment Analysis.
Lectures inEarly Breast Cancer A PowerPoint slide set based on images from: Lectures in Early Breast Cancer Part 3: Adjuvant Therapy in Early Breast Cancer.
1 Risk Benefit and Conclusions George Sledge, MD Indiana University School of Medicine.
2 years versus 1 year of adjuvant trastuzumab for HER2-positive breast cancer (HERA): an open-label, randomised controlled trial Aron Goldhirsch, Richard.
Breast Cancer Screening 1. 2 Methods 3 Mammography.
J Clin Oncol 30: R2 윤경한 / Prof. 김시영 Huan Jin, Dongsheng Tu, Naiqing Zhao, Lois E. Shepherd, and Paul E. Goss.
Angelo Di Leo “Sandro Pitigliani” Medical Oncology Department Hospital of Prato Istituto Toscano Tumori, Prato, Italy Adjuvant hormone therapy in post-menopausal.
Mamounas EP et al. Proc SABCS 2012;Abstract S1-10.
Figure 1. Raw mean scores of the MFI subscales ‘mental fatigue’ and ‘reduction in motivation’ (range 4–20, the higher the score the more mental fatigue.
JOURNAL OF CLINICAL ONCOLOGY 25:
Efficacy and safety of more intensive lowering of LDL cholesterol: a meta-analysis of data from 170 000 participants in 26 randomised trials  Cholesterol.
Prognostic and Predictive Value of the 21-Gene Recurrence Score Assay in Postmenopausal Women with Node-Positive, Estrogen- Receptor-Positive Breast Cancer.
THBT neoadjuvant endocrine therapy is to be used in post-menopausal breast cancer woman Antonino Grassadonia Università «G. D’Annunzio» – Chieti-Pescara.
Early Breast Cancer Clinical Trialists’ Collaborative Group
San Antonio Breast Cancer Symposium, December 6-10, 2016
سرطان الثدي Breast Cancer
Figure 5 Schematic illustration of different clinical trial designs
Intellectual property of the EBCTCG trialists.
Volume 378, Issue 9804, Pages (November 2011)
Nat. Rev. Clin. Oncol. doi: /nrclinonc
Volume 366, Issue 9503, Pages (December 2005)
Figure 1 Underreporting of treatment-related toxicities by physicians, relative to patients with either advanced-stage lung cancer, or early-stage breast.
Treatment of HR+ Breast Cancer: A Clinical Update
Untch M et al. Proc SABCS 2010;Abstract P
Figure 2 Examples of histopathological validation
Effect of Obesity on Prognosis after Early Breast Cancer
Volume 381, Issue 9869, Pages (March 2013)
RIDDLE-NSTEMI Trial design: Patients with NSTEMI were randomized to either immediate (within 2 hours) intervention or delayed (within 72 hours) intervention.
ABSTRACT ABCSG 6a MA17-1 MA.17R NSABP B-33. Extended Adjuvant Therapy With Aromatase Inhibitor Among Postmenopausal Breast Cancer.
Volume 386, Issue 10001, Pages (October 2015)
MAINTENANCE THERAPY WITH PARP INHIBITORS
Volume 386, Issue 10001, Pages (October 2015)
ONCOLOGYEDUCATION.COM ARTICLE SUMMARIES
Adjuvant Ovarian Suppression in Premenopausal Breast Cancer
Badwe RA et al. SABCS 2009;Abstract 72.
Relevance of breast cancer hormone receptors and other factors to the efficacy of adjuvant tamoxifen: patient-level meta-analysis of randomised trials 
20-Year Risks of Breast-Cancer Recurrence
Published online Feb 7, 2019 Increasing the dose intensity of chemotherapy by more frequent administration or sequential scheduling:
Time to Recurrence (Hormone Receptor-positive Patients)
THE LANCET Oncology Volume 19, No. 1, p27–39, January 2018
NOAH: pCR Results Patients (%) P=0.002 P=0.003 P=0.29 P=0.43 With T
Presentation transcript:

Continuing Adjuvant Tamoxifen to 10 Years

ATLAS Christina Davies,et al. Lancet 2013; 381: 805–16

Figure 3A: Recurrence by treatment allocation for 6846 women with ER-positive disease

Figure 3B: Breast cancer mortality by treatment allocation for 6846 women with ER-positive disease

Figure 4: Recurrence by treatment allocation for 6846 women with ER-positive disease, subdivided by patient or tumour characteristics and location or time of first recurrence

Conclusions aTTom confirms that, in ER+ disease, continuing tamoxifen to year 10 rather than just to year 5 produces further reductions in recurrence, from year 7 onward, and breast cancer mortality after year 10. 10 years of adjuvant tamoxifen, compared to no tamoxifen, reduces breast cancer mortality by about one third in the first 10 years following diagnosis and by a half subsequently.

aTTom During 1991-2005, 6,953 women with ER+ (n=2755), or ER untested (4198, estimated 80% ER+ if status known) invasive breast cancer were, after 5 years of tamoxifen, randomized to stop tamoxifen or continue to year 10. Richard G. Gray, et al. J Clin Oncol, 2013, 31 (suppl)

RESULT OF aTTOM Allocation to continue tamoxifen reduced breast cancer recurrence (580/3468 vs 672/3485, p=0.003). Longer treatment also reduced breast cancer mortality (392 vs 443 deaths after recurrence, p=0.05) Non-breast-cancer mortality was little affected (457 vs 467 deaths, rate ratio 0.94 [0.82-1.07]). There were 102 vs 45 endometrial cancers RR=2.20 (1.31-2.34, p<0.0001) with 37 (1.1%) vs 20 (0.6%) deaths (absolute hazard 0.5%, p=0.02).