Comparative efficacy & safety of buparlisib plus fulvestrant, fulvestrant plus dalpiciclib, and ribociclib plus letrozole for postmenopausal, hormone receptor-positive, and HER2-negative breast cancer

•Dalpiciclib + fulvestrant is effective in hormone (+) and HER2 (−) breast cancers.•Dalpiciclib and buparlisib cause neutropenia.•Gastrointestinal tract-related adverse effects while treatment with fulvestrant.•Liver function monitoring is recommended for ribociclib + letrozole treatment.•Women shou...

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Veröffentlicht in:Clinics (São Paulo, Brazil) Brazil), 2023-01, Vol.78, p.100291, Article 100291
Hauptverfasser: Liu, Qi, Hou, Lingli, Zhao, Ying, Yang, Hongwei, Mo, Zhengying, Yu, Fei
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Sprache:eng
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Zusammenfassung:•Dalpiciclib + fulvestrant is effective in hormone (+) and HER2 (−) breast cancers.•Dalpiciclib and buparlisib cause neutropenia.•Gastrointestinal tract-related adverse effects while treatment with fulvestrant.•Liver function monitoring is recommended for ribociclib + letrozole treatment.•Women should be under the supervision of a consultant while 100 mg/day of buparlisib. This study aimed to compare progression-free survival, overall survival, clinical benefits, and adverse effects in postmenopausal women with hormone receptor-positive and HER2-negative breast cancer who received buparlisib plus fulvestrant against those of women who received dalpiciclib plus fulvestrant, considering ribociclib plus letrozole treatment as the reference standard. Women received buparlisib plus fulvestrant (BF cohort, n = 108), dalpiciclib plus fulvestrant (DF cohort, n = 132), or ribociclib plus letrozole (RL cohort, n = 150) until unacceptable toxicity was observed. A total of 117 (89 %), 80 (74 %), and 84 (56 %) women in the BF, DF, and RL cohorts, respectively, had clinical benefits. After treatment, the clinical benefits for women and after 42 months of follow-up progression-free survival and overall survival were higher in the DF cohort than in the BF and RL cohorts (p 
ISSN:1807-5932
1980-5322
1980-5322
DOI:10.1016/j.clinsp.2023.100291