Abstract 272P
Background
High rate of clinical fractures was reported during adjuvant HT trials (9-14% in BIG 1-98, ATAC, IES). Since 2015, in Italy, bisphosphonates and denosumab are reimbursed for prevention of bone fractures in EBC HR+ postmenopausal pts receiving HT, regardless of T-score values (Note 79 of AIFA-Agenzia Italiana del Farmaco). In 2019, these drugs were administered only in 25% of potentially beneficiary pts. The P&P is a nationwide Bone Health (BH) management project designed to improve adherence to recommendations regarding fracture risk assessment and risk prevention measures in pts receiving HT for HR+ EBC.
Methods
The BH management model P&P was developed in 10 Italian cancer centres and includes: 1- training of multidisciplinary team and presentation of a BH management model by the oncologist (with referral to the Bone Specialist if osteoporosis); 2- implementation of this model in every centre; 3- evaluation, after 12 months, of rate of EBC HR+ pts in postmenopausal status (natural, surgical, secondary to chemotherapy or hormonal blockage) assessed for BH within 30 days from the start of adjuvant HT; 4- evaluation, after 12 months, of rate of EBC HR+ pts receiving therapy within 90 days from the start of adjuvant HT, according to the criteria for reimbursement by AIFA.
Results
At 12 months after implementation of P&P, data are available from 6 centres (IRCCS Negrar, Ancona Hospital, IRCCS San Martino Genova, Poliambulanza Brescia, Cardarelli Napoli, Papa Giovanni XXIII Bergamo) in 1,551 postmenopausal EBC HR+ pts. The first analysis reports that 83% of EBC HR+ patients who started adjuvant HT were assessed for BH within 30 days compared to 43% in the 2019 national survey and 68% of pts started bisphosphonates/denosumab compared to 25% in the 2019 national survey.
Conclusions
Implementation of the P&P model has been shown to increase the rate of postmenopausal EBC HR+ pts on adjuvant HT assessed for BH and treated with bisphosphonate/denosumab to reduce the risk of bone fractures. A new project is ongoing to assess the rate of fractures in Italian pts after the approval of Note 79 by AIFA.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
S. Gori.
Funding
Amgen.
Disclosure
C. Bighin: Financial Interests, Personal, Research Grant: Novartis, Roche, Lilly, Eisai, Gilead, Italfarmaco. F. Puglisi: Financial Interests, Personal, Advisory Board: Amgen, AstraZeneca, Daiichi Sankyo, Celgene, Eisai, Eli Lilly, Exact Sciences, Gilead, Ipsen, Menarini, MSD, Novartis, Pierre Fabre, Roche, Pfizer, Seagen, Takeda, Viatris; Financial Interests, Personal, Research Grant: AstraZeneca, Eisai, Roche. A. Fabi: Financial Interests, Personal, Advisory Board: Roche, Pfizer, Novartis, Lilly, Seagen, Gilead, Exact Science, Dompè Biotech. All other authors have declared no conflicts of interest.
Resources from the same session
252P - Adjuvant chemotherapy in T1a/bN0 breast cancer patients with high oncotype DX recurrence scores (RS>25)
Presenter: Daniela Katz
Session: Poster session 02
253P - Is 6-weekly administration of pembrolizumab in combination with chemotherapy for early triple-negative breast cancer safe? A real-world early comparison of q6w versus q3w administration of pembrolizumab in two large cancer centres in the UK
Presenter: Vasileios Angelis
Session: Poster session 02
254P - Effects of delaying adjuvant chemotherapy initiation on clinical outcomes in early triple-negative breast cancer patients
Presenter: Maria Eleni Hatzipanagiotou
Session: Poster session 02
255P - Prognostic stratification capacity of the CPS+EG scoring system in HER2-low and HER2-zero early breast cancer treated with neoadjuvant chemotherapy
Presenter: Nicolas Roussot
Session: Poster session 02
256P - Evolution and risk stratification of adjuvant treatment strategies for early breast cancer: A Chinese perspective based on a national cancer database
Presenter: Ying Fan
Session: Poster session 02
257P - The characteristics of HER2-positive microinvasive breast cancer and the necessity of chemotherapy and anti-HER2 therapy in these patients: A real-world study
Presenter: Bo Lan
Session: Poster session 02
258P - Cost-effectiveness of neoadjuvant pembrolizumab plus chemotherapy followed by adjuvant pembrolizumab for high-risk early-stage triple-negative breast cancer in Colombia
Presenter: Ricardo Brugés Maya
Session: Poster session 02
259P - Adjuvant doxorubicin-cyclophosphamide in early-stage breast cancer provides long-term cardiac safety
Presenter: Thiti Susiriwatananont
Session: Poster session 02
260P - Oncology efficacy of gonadotropin-releasing hormone agonist in hormone receptor-positive very young breast cancer patients treated with neoadjuvant chemotherapy
Presenter: Hee Jun Choi
Session: Poster session 02
261P - Dysregulation of immune checkpoint proteins in newly- diagnosed early breast cancer patients undergoing neoadjuvant chemotherapy: A comparison between TNBC and non-TNBC patients
Presenter: Bernardo Rapoport
Session: Poster session 02