Abstract 240P
Background
In NATALEE, RIB + NSAI yielded a statistically significant benefit in invasive disease-free survival (iDFS, using STEEP criteria by investigator assessment) vs NSAI alone (hazard ratio [HR], 0.749; 95% CI, 0.628-0.892; P=.0006) in a broad age range of pts with HR+/HER2− EBC. We report outcomes with RIB + NSAI in older pts (≥65 y).
Methods
Pts were treated with RIB + NSAI or NSAI alone. Efficacy, safety, and quality of life were assessed in pts ≥65 vs <65 y (data cutoff: July 21, 2023).
Results
Of 5101 pts in NATALEE, 773 (15.2%) were ≥65 and 4328 (84.8%) were
Conclusions
RIB + NSAI showed similar benefit regardless of age, with no new safety signals. The rate of RIB discontinuation without dose reduction in older pts highlights an opportunity to optimize AE management. These results further support RIB efficacy and tolerability in pts with HR+/HER2− EBC regardless of age.
Clinical trial identification
NATALEE: CLEE011O12301C, The release date is: NATALEE: 2018-09-21.
Editorial acknowledgement
Editorial assistance in the writing of the abstract was provided by Molly Amador, PhD of Nucleus Global.
Legal entity responsible for the study
Novartis Pharmaceuticals Corporation.
Funding
Novartis Pharmaceuticals Corporation.
Disclosure
M. Untch: Financial Interests, Institutional, Advisory Board, Advisory board, lectures; all fees and honoraria to the employer/institution: AstraZeneca, Amgen, Daiichi Sankyo, Lilly, Roche, Pfizer, MSD Oncology, Seagen, Pierre Fabre, Sanofi Aventis, Myriad, Gilead, Novartis, Stemline, Genzyme, Medac. D. Yardley: Financial Interests, Institutional, Research Grant, Research Funding to Institution: Ambrx, Amgen, AstraZeneca, Biomarin, Biothera Pharmaceuticals, Clovis Pharma, Dana Farber Cancer Institute, Lilly, Roche/Genentech, G1 Therapeutics, Gilead Therapeutics, Incyte, Innocrin Pharmaceuticals, MacroGenics, MedImmune, Medivation, Merck, Merrimac; Financial Interests, Institutional, Advisory Board, Consulting/Advisory Role (Payment to inst): AstraZeneca, G1 Therapeutics, Gilead Sciences, Immunomedics, Integra Connect, Novartis, Sanofi-Aventis, Stemline Therapeutics. S. Im: Financial Interests, Personal, Advisory Board, no payment: AstraZeneca, Novartis, Eisai, Roche, Hanmi, Pfizer, Lilly, MSD, GSK, Daiichi Sankyo; Financial Interests, Institutional, Advisory Board: Bertis; Financial Interests, Personal, Advisory Board: Idience; Financial Interests, Institutional, Research Grant: AstraZeneca, Pfizer, Roche, Eisai, Dae Woong; Financial Interests, Institutional, Local PI, Clinical Trial Budget: AstraZeneca, Hanmi, Novartis, Roche, Pfizer, Daiichi Sankyo, MSD, Lilly; Financial Interests, Institutional, Coordinating PI, Clinical Trial Budget: Eisai; Financial Interests, Institutional, Research Grant, Clinical Trial Budget: Boryung Pharm. T. Pluard: Financial Interests, Personal and Institutional, Research Grant: Novartis, Pfizer, Scorpion Therapeutics, Gilead, AstraZeneca, Sermonix, Carrick; Financial Interests, Personal, Advisory Board: Novartis; Financial Interests, Personal, Speaker, Consultant, Advisor: Gilead, Stemline, AstraZeneca. L. Hart: Financial Interests, Institutional, Research Grant, Research support for my institution: Novartis; Financial Interests, Personal, Speaker’s Bureau, 2019 Speaker's Bureau: Novartis. J.P. Crown: Financial Interests, Personal, Other: Pierre Fabre, Novartis, AstraZeneca, Regeneron, Immunocore; Other, Personal, Other, Travel support to meetings: Novartis, MSD Oncology, Pfizer, Roche, AstraZeneca, Regeneron; Financial Interests, Personal, Stocks/Shares: Oncoassure, Akkure; Other, Personal, Other, WO2020011770 (A1) - A method of predicting response to treatment in cancer patients: Pending Patent. C. Zamagni: Financial Interests, Personal, Advisory Board: Roche, EISAI, Novartis, AstraZeneca, Pfizer, Lilly, Daiichi Sankyo, Exact Sciences, MSD, GSK, Gilead, Seagen; Financial Interests, Institutional, Local PI: Roche, Novartis, AstraZeneca, Pfizer, Seagen, Medivation, AbbVie, Array BioPharma, Morphotek, Synthon, Daichii-Sankyo, MSD, GSK, Gilead; Financial Interests, Personal, Other, Member of an Independent Data Monitoring Committee for an international clinical trial: AstraZeneca; Non-Financial Interests, Other, member of the Scientific Committee: LOTO Onlus, Susan J Komen Emilia-Romagna, Mamazone Sudtirol; Other, travel accomodation and partecipation expenses for scientific congresses: Roche, Novartis, Pfizer, Daichii-Sankyo, MSD, GSK, Gilead, AstraZeneca. I. Blancas López-Barajas: Financial Interests, Personal, Advisory Board: AstraZeneca, Bristol-Myers Squibb, Celgene, Daiichi Sankyo, Eisai, Gilead, Grünenthal, GSK, Lilly, MSD, Novartis, Pfizer, Pierre-Fabre, Roche, Seagen; Financial Interests, Personal, Other, Medical monitor: Medical Science Innovation Research (MEDSIR); Financial Interests, Institutional, Funding: AstraZeneca, Lilly, Roche, Agendia; Financial Interests, Institutional, Research Grant: Pfizer; Other, Support for attending meetings and/or travel: AstraZeneca, Bristol-Myers Squibb, Daiichi Sankyo, Gilead, Lilly, Novartis, Pfizer, Roche, Pierre Fabre. F. Parnizari: Other, Personal and Institutional, Other, Translational Research In Oncology is contracted by Novartis as CRO conducting the NATALEE trial.: Novartis. M. Gao; K. Amin; H. Hu: Financial Interests, Personal and Institutional, Full or part-time Employment: Novartis; Financial Interests, Personal and Institutional, Stocks or ownership: Novartis. H.S. Rugo: Financial Interests, Personal, Advisory Board, Consultancy/advisory support: NAPO; Financial Interests, Personal, Invited Speaker, Honoraria: Mylan/Viatris, Chugai; Financial Interests, Personal, Advisory Board, Advisory/Consultancy: PUMA, Sanofi; Financial Interests, Institutional, Local PI: Novartis, Lilly, Pfizer, Daiichi, AstraZeneca, Gilead Sciences, Inc.; Financial Interests, Institutional, Coordinating PI: OBI Pharma, F. Hoffmann-La Roche AG/Genentech, Inc., Merck; Financial Interests, Institutional, Research Grant: Stemline Therapeutics, Ambryx. All other authors have declared no conflicts of interest.
Resources from the same session
1978P - Accurate detection of urothelial carcinoma by whole-genome methylation profiling of urinary cell-free DNA
Presenter: Huiqin Guo
Session: Poster session 13
1979P - Disitamab vedotin (DV) plus toripalimab (T) in unresectable locally advanced or metastatic urothelial carcinoma (la/mUC): Long-term outcomes from a phase Ib/II study
Presenter: Li Zhou
Session: Poster session 13
1980P - Association of PD-L1 expression with clinical response to TAR-200 in the phase IIb SunRISe-1 trial
Presenter: Evanguelos Xylinas
Session: Poster session 13
1981P - Cabozantinib plus durvalumab in patients with advanced and chemotherapy-treated urothelial carcinoma (UC) and variant histology (VH): An open-label, phase II, single-arm proof-of-concept trial: ARCADIA study. Subgroup analysis for bone metastasis
Presenter: Marco Stellato
Session: Poster session 13
1982P - Post hoc analysis of outcomes according to prior chemotherapy (CT) response and platinum agent in the international SAUL study of atezolizumab (atezo) for urinary tract carcinoma (UTC)
Presenter: Begona Perez Valderrama
Session: Poster session 13
1983P - Feasibility and efficacy of split-dose cisplatin with atezolizumab for cisplatin-ineligible urothelial carcinoma (SOGUG-AUREA): Final results
Presenter: Guillermo Antonio De Velasco Oria
Session: Poster session 13
1984P - Efficacy and safety of disitamab vedotin combined with gemcitabine as neoadjuvant therapy for muscle-invasive bladder cancer: A multi-center, single-arm, phase II trial
Presenter: Chu Yang
Session: Poster session 13
1985P - Retrospective database analysis of real-world treatment patterns and sequencing in locally advanced or metastatic urothelial carcinoma patients receiving sacituzumab govitecan
Presenter: Ronac Mamtani
Session: Poster session 13
1986P - Prospective evaluation of BCG unresponsive bladder cancer carcinoma in situ identifies genetic mechanisms of immunotherapy resistance and targeted therapy using an ultra-sensitive next generation sequencing minimal residual disease (MRD) assay
Presenter: Joshua Meeks
Session: Poster session 13
1987P - TROP-2 as a promising ADC target in penile squamous cell carcinoma that promotes cell proliferation by activating AKT through PKCα pathway
Presenter: Yi Tang
Session: Poster session 13