Comparison of Four Clinical Prognostic Scores in Patients with Advanced Gastric and Esophageal Cancer
03 medical and health sciences
Treatment Outcome
0302 clinical medicine
Esophageal Neoplasms
Stomach Neoplasms
Gastrointestinal Cancer
Humans
Prognosis
Proportional Hazards Models
Retrospective Studies
3. Good health
DOI:
10.1093/oncolo/oyac235
Publication Date:
2022-11-15T17:40:12Z
AUTHORS (17)
ABSTRACT
AbstractBackgroundPrognostic scores that can identify patients at risk for early death are needed to aid treatment decision-making and patient selection for clinical trials. We compared the accuracy of four scores to predict early death (within 90 days) and overall survival (OS) in patients with metastatic gastric and esophageal (GE) cancer.MethodsAdvanced GE cancer patients receiving first-line systemic therapy were included. Prognostic risks were calculated using: Royal Marsden Hospital (RMH), MD Anderson Cancer Centre (MDACC), Gustave Roussy Immune (GRIm-Score), and MD Anderson Immune Checkpoint Inhibitor (MDA-ICI) scores. Overall survival (OS) was estimated using the Kaplan-Meier method. Cox proportional hazards models were used to analyze associations between prognostic scores and OS. The predictive discrimination was estimated using Harrell’s c-index. Predictive ability for early death was measured using time-dependent AUCs.ResultsIn total, 451 patients with metastatic GE cancer were included. High risk patients had shorter OS for all scores (RMH high- vs. low–risk median OS 7.9 vs. 12.2 months, P < .001; MDACC 6.8 vs. 11.9 months P < .001; GRIm-Score 5.3 vs. 13 months, P < .001; MDA-ICI 8.2 vs. 12.2 months, P < .001). On multivariable analysis, each prognostic score was significantly associated with OS. The GRIm-Score had the highest predictive discrimination and predictive ability for early death.ConclusionsThe GRIm-Score had the highest accuracy in predicting early death and OS. Clinicians may use this score to identify patients at higher risk of early death to guide treatment decisions including clinical trial enrolment. This score could also be used as a stratification factor in future clinical trial designs.
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