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Osimertinib (Osimertinib) is the standard second-line treatment for patients with EGFR-mutant NSCLC who acquire the T790M mutation, and the efficacy of its combination with bevacizumab is unclear
.
Therefore, the results of a phase II study, BOOSTER, were published in Annals of Oncology, evaluating second-line Osimertinib (osimertinib) combined with bevacizumab versus Osimertinib (osimertinib) monotherapy in patients with EGFR T790M-mutated advanced NSCLC.
Osimertinib (Osimertinib) is the standard second-line treatment for patients with EGFR-mutant NSCLC who acquire the T790M mutation, and the efficacy of its combination with bevacizumab is unclear
The BOOSTER study is an open-label, randomized Phase II clinical study
.
The primary study endpoint was investigator-assessed progression-free survival (PFS)
The BOOSTER study is an open-label, randomized Phase II clinical study
Between May 2017 and February 2019, 155 patients were randomized (combination arm: 78; single-agent arm: 77)
The median follow-up time was 33.
PFS
PFSIn subgroup analysis, the combination group improved median PFS in current and former smokers [HR: 0.
57 (0.
33-0.
98); Wald's test P=0.
043], but not in non-smokers (HR: 1.
29 ( 0.
82-2.
02); Wald's test P=0.
28)
.
57 (0.
33-0.
98); Wald's test P=0.
043], but not in non-smokers (HR: 1.
29 ( 0.
82-2.
02); Wald's test P=0.
28)
.
In subgroup analysis, the combination group improved median PFS in current and former smokers [HR: 0.
Differences in PFS treated with different smoking status
Differences in PFS treated with different smoking statusMedian OS was 24.
0 months (95% CI 17.
8-32.
1) in the combination arm versus 24.
3 months (95% CI 16.
9-37.
0) in the monotherapy arm, with no significant difference in OS [log-rank P =0.
89; HR: 1.
03 (0.
68-1.
56)
.
The combination group numerically prolonged median OS in current and former smokers [HR: 0.
Median OS was 24.
OS
OSDifferences in OS between different smoking statuses
Differences in OS between different smoking statusesORR was 55% (95% CI 43%-66%) in both treatment arms and DCR was 90% (95% CI 81%-95%) and 82% (95%) in the combination arm and monotherapy arm, respectively CI 71%-90%) (P=0.
17)
.
17)
.
ORR was 55% (95% CI 43%-66%) in both treatment arms and DCR was 90% (95% CI 81%-95%) and 82% (95%) in the combination arm and monotherapy arm, respectively CI 71%-90%) (P=0.
In the safety cohort, 152 of 153 patients (99%) experienced at least one AE of any grade (76 in each group)
In conclusion, the study showed that Osimertinib (osimertinib) combined with bevacizumab second-line therapy did not significantly improve the prognosis of patients with T790M mutation in EGFR-mutant advanced NSCLC
.
.
Studies have shown that Osimertinib (osimertinib) combined with bevacizumab second-line therapy does not significantly improve the prognosis of patients with T790M mutation in EGFR-mutant advanced NSCLC
.
Studies have shown that Osimertinib (osimertinib) combined with bevacizumab second-line therapy does not significantly improve the prognosis of patients with T790M mutation in EGFR-mutant advanced NSCLC
.
Original source:
Original source:Soo RA, Han JY, Dafni U, et al.
A randomised phase II study of osimertinib and bevacizumab versus osimertinib alone as second-line targeted treatment in advanced NSCLC with confirmed EGFR and acquired T790M mutations: the European Thoracic Oncology Platform (ETOP 10- 16) BOOSTER trial.
Ann Oncol.
2022 Feb;33(2):181-192.
doi: 10.
1016/j.
annonc.
2021.
11.
010.
Epub 2021 Nov 26.
PMID: 34839016.
A randomised phase II study of osimertinib and bevacizumab versus osimertinib alone as second-line targeted treatment in advanced NSCLC with confirmed EGFR and acquired T790M mutations: the European Thoracic Oncology Platform (ETOP 10- 16) BOOSTER trial.
Ann Oncol.
2022 Feb;33(2):181-192.
doi: 10.
1016/j.
annonc.
2021.
11.
010.
Epub 2021 Nov 26.
PMID: 34839016.
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