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On September 13, 2021, Bristol Myers Squibb (Bristol Myers Squibb) announced the three-year follow-up data of the Phase 3 clinical trial CheckMate-743
Nivolumab (Nivolumab, the English trade name is Opdivo) targets PD-1, which can help the body restore the anti-tumor immune response
MPM is a rare but aggressive cancer that forms on the lining of the lungs
The multi-center, open-label CheckMate-743 trial enrolled 605 patients with unresectable MPM who had not been treated before
The results of the trial followed up for at least 3 years (35.
In the dual immune combination therapy group, 23% of patients were still alive at three years, compared to 15% in the chemotherapy control group
The combination therapy group continued to show a reduced risk of death (HR=0.
The safety characteristics of the combination therapy are consistent with the previously reported data, and no new safety signals have been found
In addition, at 3 years of follow-up (approximately 1 year after the patient ended treatment), regardless of the patient's tumor histological type, the dual immunotherapy combination had a longer duration of remission (DOR) than chemotherapy
28% of patients in the combination therapy group remained in remission at three years, compared with 0% in the chemotherapy group
The median DOR of patients in the combination therapy group was 11.
The objective response rate (ORR) of the combined treatment group was comparable to that of the chemotherapy group (39.
Reference materials:
[1] nivolumab Plus ipilimumab Demonstrates Durable Overall Survival at Three Years Compared to Chemotherapy in First-Line Unresectable Malignant Pleural Mesothelioma in Phase 3 CheckMate -743 Trial.
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