Abstract 105P
Background
Anti-angiogenesis inhibitors have shown enhanced antitumor activity when combined with PD-1 inhibitors in patients with metastatic colorectal cancer (mCRC). The study aimed to forecast the prognosis and identify the influential factors associated with the therapeutic combination of VEGFR-TKIs and PD-1 inhibitors in patients with microsatellite-stable (MSS) mCRC.
Methods
We conducted a retrospective study of MSS mCRC patients treated with VEGFR-TKI coupled with PD-1 inhibitors from January 2020 to April 2024. Kaplan-Meier curves were generated for OS. Boruta algorithm and LASSO-Cox regression model were applied to identify key features associated with OS in our clinical dataset, which comprises 34 features including age, sex, primary location, differentiation, RAS status, metastatic sites, treatment lines, the treatment duration of VEGFR-TKIs and the treatment cycles of PD-1 inhibitors, etc. Restricted cubic splines (RCS) were used to estimate the effects of key features on OS.
Results
The study enrolled 79 eligible patients, with a median age of 57 years (range, 24-81), and 65.8% were male. The most frequently utilized VEGFR-TKI was fruquintinib. The median number of previous treatment lines was two. Median OS was 27.1 months (95% CI 20.6–NA). Median PFS was 5.7 months (95% CI 4.3–7.9). LASSO-Cox regression identified four signature features: sex, primary location, differentiation, and the treatment duration of VEGFR-TKIs, which highly influenced the OS. Boruta algorithm identified the treatment duration of VEGFR-TKIs as the only key feature influencing the OS of patients. RCS results suggested an approximately linear relationship between the hazard ratio (HR) for OS and the treatment duration of VEGFR-TKIs (P = 0.0234, P for non-linearity = 0.630), and the treatment duration of fruquintinib longer than 2.8 months was significantly associated with longer OS.
Conclusions
The machine learning findings indicate that the duration of VEGFR-TKI treatment impacts OS in patients with MSS mCRC, a treatment duration of fruquintinib exceeding 2.8 months was found to have a significant positive influence on OS for patients with MSS mCRC.
Legal entity responsible for the study
Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
195P - Anti-CTLA4 therapy leads to early expansion of peripheral Th17 population and induction of Th1 cytokines
Presenter: Mari Nakazawa
Session: Poster Display session
Resources:
Abstract
196P - Single-cell analysis of stage-I high-grade serous ovarian carcinoma reveals the essential role of regulatory T cells in early tumor establishment
Presenter: Joanna Mikulak
Session: Poster Display session
Resources:
Abstract
197P - Comprehensive immunoprofiling of the intratumoral and peripheral T cell receptor gene repertoire in triple-negative breast cancer patients
Presenter: Antonios Mingos
Session: Poster Display session
Resources:
Abstract
198P - Association of types of treatment modalities with expression of T Lymphocytes (CD4, CD8, Treg) in breast cancer patients and their clinical outcome
Presenter: Arshi Rizwan
Session: Poster Display session
Resources:
Abstract
199P - Cancer neutrophil encyclopedia: A deep dive into antigen-presenting warriors
Presenter: Yingcheng Wu
Session: Poster Display session
Resources:
Abstract
200P - CXCR1+ neutrophil infiltration orchestrates response to third-generation EGFR-TKI in EGFR mutant NSCLC
Presenter: Haowei Wang
Session: Poster Display session
Resources:
Abstract
201P - Underlying mechanisms of neutrophil-mediated immunosuppression and resistance to treatment in breast cancer: Further evidence that these cells matter
Presenter: Bruna Filipa Correia
Session: Poster Display session
Resources:
Abstract
202P - Mining tumor infiltrating B cells to discover antibody-target pairs and develop novel therapies
Presenter: Matthieu Delince
Session: Poster Display session
Resources:
Abstract
203P - Targeting IL-33 reprograms tumor microenvironment and potentiates antitumor response to anti-PD-L1 immunotherapy
Presenter: Xuyao Zhang
Session: Poster Display session
Resources:
Abstract
204P - Deciphering the crosstalk between tumor and circulating immune microenvironment in advanced NSCLC patients undergoing immunotherapy
Presenter: Prisca Tamarozzi
Session: Poster Display session
Resources:
Abstract