Abstract 20P
Background
In China, new breast cancer (BC) patients (pts) in county regions (including rural areas) account for more than 40% of all BC cases each year. No studies have reported the disease characteristics and treatment patterns of BC pts in China counties. This study aimed to explore the treatment patterns of BC pts in county-level hospitals in China.
Methods
CHASE001 was an observational, multicenter study assessing real-world treatment patterns among pts with HER2+ or HR+/HER2- BC conducted at 26 sites in county areas of China, including four cohorts (HER2+ early BC (eBC), HR+/HER2- eBC, HER2+ advanced BC (aBC), and HR+/HER2- aBC). The primary endpoint was treatment patterns within each cohort. The interim results for HER2+ eBC and HR+/HER2- eBC are described here.
Results
628 pts were included (302 in HER2+ eBC and 326 in HR+/HER2- eBC cohort): for HER2+ and HR+/HER2- cohort respectively, median age, 53/51 years; clinical T2, 41.39%/37.73%; clinical N0, 41.72%/45.40%. Of 584 pts who underwent breast cancer surgery, only 10.53% (30/285) received breast-conserving surgery (BCS) in HER2+ and 12.71% (38/299) in HR+/HER2- cohort. Notably, the proportions of adjuvant radiotherapy (RT) following BCS were 46.67% (14/30) in HER2+ and 47.37% (18/38) in HR+/HER2- cohort. In HER2+ cohort, 20.20% (61/302) received neoadjuvant therapy (NAT) while 94.70% (286/302) received adjuvant therapy. 81.97% (50/61) of NAT were HER2 targeted regimens, of which 84.00% (42/50) received dual anti-HER2 target therapy (trastuzumab/pertuzumab). 80.77% (231/286) of adjuvant therapies were HER2 targeted regimens, of which 53.68% (124/231) were dual-targeted. Of pts with positive lymph nodes who received HER2 targeted adjuvant therapy, 75.90% applied dual anti-HER2 target therapy. In HR+/HER2- cohort, 13.50% (44/326) received NAT while 92.02% (300/326) received adjuvant therapy. The most common neoadjuvant and adjuvant chemotherapy regimens were both AC-T (41.67% and 51.79%, respectively).
Conclusions
This analysis showed unsatisfactory adherence to guidelines for BCS, RT, and NAT, but higher adherence for adjuvant anti-HER2 therapy. Further action was needed to ensure that patients in Chinese county had access to high quality and guideline centric care.
Clinical trial identification
NCT05544123.
Editorial acknowledgement
Legal entity responsible for the study
P. Lu.
Funding
AstraZeneca.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
78P - First-in-human phase I study of TT-00434, an orally available FGFR (1-3) inhibitor in patients with advanced solid tumors
Presenter: Chia Jui Yen
Session: Poster Display
Resources:
Abstract
79P - Accelerated identification of recurrent neoantigens for the development of off-the-shelf cancer vaccines
Presenter: Le Son Tran
Session: Poster Display
Resources:
Abstract
80P - Safety, preliminary efficacy, and pharmacokinetics of HLX26 plus serplulimab in advanced solid tumours: An open-label, dose-escalation phase I study
Presenter: Yanmin Wu
Session: Poster Display
Resources:
Abstract
81P - A first-in-human, multiple dose and dose escalation phase I study to investigate the safety, tolerability and antitumor activity of SmarT cells plus PD-1 blocking antibodies in patients with far advanced/metastatic solid tumors
Presenter: Qin Liu
Session: Poster Display
Resources:
Abstract
82P - NEXUS: A phase I dose escalation study of selinexor plus nivolumab and ipilimumab in Asian patients with advanced/metastatic solid malignancies
Presenter: Gloria Chan
Session: Poster Display
Resources:
Abstract
83P - The updated report of phase I trial of VG2025, a non-attenuated HSV-1 oncolytic virus expressing IL-12 and IL-15/RA payloads, in patients with advanced solid tumors
Presenter: Yinan Shen
Session: Poster Display
Resources:
Abstract
84P - T cell receptor repertoire profiles of tumor -infiltrating lymphocytes improves neoantigen prioritization for personalized cancer immunotherapy
Presenter: Tran Nguyen
Session: Poster Display
Resources:
Abstract
85P - Oligometastatic solid tumors: Disease characteristics and role of local therapies
Presenter: Alshimaa Al Hanafy
Session: Poster Display
Resources:
Abstract
86P - Efficacy and safety of HLX07 monotherapy in advanced cutaneous squamous cell carcinoma: An open-label, multicentre phase II study
Presenter: Changxing Li
Session: Poster Display
Resources:
Abstract
87TiP - Phase I expansion study of the tissue factor (TF)–targeting antibody-drug conjugate (ADC) XB002 as a single-agent and combination therapy in patients with advanced solid tumors (JEWEL-101)
Presenter: Mustafa Syed
Session: Poster Display
Resources:
Abstract