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The potential benefit of adding palbociclib to fulvestrant as first-line therapy in patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative endocrine-sensitive advanced breast cancer (ABC) is unclear
.
Therefore, Spanish scholars carried out a phase II clinical study GEICAM/2014-12 (FLIPPER) to evaluate the efficacy of fulvestrant combined with CDK4/6 inhibitor palbociclib in patients with HR+/HER2- advanced breast cancer
The potential benefit of adding palbociclib to fulvestrant as first-line therapy in patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative endocrine-sensitive advanced breast cancer (ABC) is unclear
A total of 189 patients were included in the study, including 94 in the fulvestrant + palbociclib group and 95 in the fulvestrant + placebo group
.
The cutoff date (January 11, 2020), and the median follow-up time was 28.
A total of 189 patients were included in the study, including 94 in the fulvestrant + palbociclib group and 95 in the fulvestrant + placebo group
PFS
PFSThe ORR was 68.
3% in the fulvestrant + palbociclib group and 42.
2% in the fulvestrant + placebo group (OR 2.
9; 80% CI, 1.
8-4.
6, p=0.
004)
.
The 24-week CBR in the two groups was 90.
The ORR was 68.
Efficacy assessment
Efficacy assessmentIn subgroup analysis, among patients with visceral metastases, the median PFS in the fulvestrant + palbociclib group and fulvestrant + placebo group was 30.
9 and 19.
4 months, respectively (p=0.
003); Median PFS was 33.
4 and 25.
6 months in the strontium+palbociclib group and fulvestrant+placebo group, respectively (p=0.
176); among patients with newly diagnosed metastases, fulvestrant+palbociclib and fulvestrant+ The median PFS in the placebo group was 33.
4 and 16.
4 months, respectively (p<0.
001); among patients with recurrence and metastasis, the median PFS in the fulvestrant + palbociclib group and the fulvestrant + placebo group were 30.
5 and 27.
3, respectively months (p=0.
370)
.
9 and 19.
4 months, respectively (p=0.
003); Median PFS was 33.
4 and 25.
6 months in the strontium+palbociclib group and fulvestrant+placebo group, respectively (p=0.
176); among patients with newly diagnosed metastases, fulvestrant+palbociclib and fulvestrant+ The median PFS in the placebo group was 33.
4 and 16.
4 months, respectively (p<0.
001); among patients with recurrence and metastasis, the median PFS in the fulvestrant + palbociclib group and the fulvestrant + placebo group were 30.
5 and 27.
3, respectively months (p=0.
370)
.
In subgroup analysis, among patients with visceral metastases, the median PFS in the fulvestrant + palbociclib group and fulvestrant + placebo group was 30.
PFS subgroup analysis
PFS subgroup analysis
In conclusion, the study showed that fulvestrant + palbociclib improved PFS in patients compared with fulvestrant + placebo
.
.
Studies have shown that fulvestrant + palbociclib improves patients' PFS compared to fulvestrant + placebo treatment
Original source:
Original source:Albanell J, Martínez MT, Ramos M, O'Connor M, de la Cruz-Merino L, Santaballa A, Martínez-Jañez N, Moreno F, Fernández I, Alarcón J, Virizuela JA, de la Haba-Rodríguez J, Sánchez- Rovira P, González-Cortijo L, Margelí M, Sánchez-Muñoz A, Antón A, Casas M, Bezares S, Rojo F.
Albanell J, Martínez MT, Ramos M, O'Connor M, de la Cruz-Merino L, Santaballa A, Martínez-Jañez N, Moreno F, Fernández I, Alarcón J, Virizuela JA, de la Haba-Rodríguez J, Sánchez- Rovira P, González-Cortijo L, Margelí M, Sánchez-Muñoz A, Antón A, Casas M, Bezares S, Rojo F.
Randomized phase II study of fulvestrant plus palbociclib or placebo in endocrine-sensitive, hormone receptor-positive/HER2- advanced breast cancer: GEICAM/2014-12 (FLIPPER).
Eur J Cancer.
2022 Jan;161:26-37.
doi: 10.
1016/j.
ejca.
2021.
11.
010.
Epub 2021 Dec 11.
PMID: 34902765.
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