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The survival prognosis of patients with advanced gastroesophageal junction cancer (GEJC) is poor; there is currently a lack of clinical trial data specific to GEJC, and most of the existing data are derived fromThe overall evaluation of gastric cancer (GC) treatment drugs.
Stomach cancer
This article reports the results of a subgroup analysis of the primary tumor type (GC or GEJC) in the TAGS trial.
This article reports the results of a subgroup analysis of the primary tumor type (GC or GEJC) in the TAGS trial.
The TAGS trial recruited mGC or mGEJC patients who had previously been treated with 2-line or above chemotherapy, and were randomized (2:1) to receive FTD/TPI or placebo treatment, while giving the best supportive treatment.
Baseline characteristics of the patient
Baseline characteristics of the patientA total of 507 patients were recruited, including 145 (29%) GEJC and 360 (71%) GC.
Efficacy prognosis in GEJC and GC groups
Efficacy prognosis in GEJC and GC groupsThe survival benefit of FTD/TPI treatment was observed in both subgroups.
Compared with placebo, in the GEJC and GC subgroups, the overall survival risk ratio of FTD/TPI was 0.
Time before deterioration
Time before deteriorationIn the GEJC and GC subgroups, 75 patients (77%) and 192 patients (81%) who received FTD/TPI treatment, respectively, reported adverse events ≥ Grade 3 caused by any cause.
No new security issues with FTD/TPI found
In summary, in the TAGS trial, as in GC patients, FTD/TPI also showed efficacy advantages and controllable safety in GEJC patients.
In the TAGS trial, as in GC patients, FTD/TPI also showed efficacy advantages and controllable safety in GEJC patients.
Original source:
Mansoor, W.
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