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Palbociclib in HR-Positive, HER2-Negative Advanced/Metastatic Breast Cancer: A Systematic Scoping Review of Real-World Evidence from Countries Outside of Western Regions that Are Underrepresented in Clinical Trials.
Rauthan, Amit; Jain, Ankita; Singh, Manmohan; Sendur, Mehmet A N.
Affiliation
  • Rauthan A; Department of Medical Oncology, Manipal Hospital, Bengaluru, India.
  • Jain A; Medical Affairs Oncology and Field Medical Excellence, Regional Medical Affairs, Pfizer Healthcare India Private Limited, The Capital, 1802/1901, Plot No. C-70, G-Block, Bandra Kurla Complex, Bandra (E), Mumbai, 400 051, India. Ankita.Jain@pfizer.com.
  • Singh M; Regional Medical Affairs, Pfizer Corporation Hong Kong Limited, Hong Kong, Hong Kong.
  • Sendur MAN; Department of Medical Oncology, Faculty of Medicine and Ankara Bilkent City Hospital, Ankara Yildirim Beyazit University, Ankara, Turkey.
Oncol Ther ; 12(3): 395-418, 2024 Sep.
Article de En | MEDLINE | ID: mdl-39095679
ABSTRACT

INTRODUCTION:

Limited awareness exists regarding real-world data (RWD) for palbociclib in patients with hormone receptor-positive, human epidermal growth factor receptor 2-negative advanced/metastatic breast cancer in populations from certain countries outside of Western regions.

METHODS:

A systematic scoping review was conducted using PubMed and Embase to evaluate RWD for palbociclib from countries outside of Western regions that are underrepresented in clinical trials. Search criteria were aligned with our research question for relevant English-language publications, without restrictions on publication date, followed by Phase 1 (title and abstract) and Phase 2 (full-text) screening of retrieved citations as per Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Data analyses of eligible studies were done separately for abstracts and full-text publications to enhance the precision and reliability of the results.

RESULTS:

Database search yielded 1485 non-duplicate records, 46 qualified for inclusion, of which 47.8% were published as full text. The analysis of outcomes, based exclusively on full-text publications that collectively included 2048 patients treated with palbociclib, revealed the median progression-free survival (PFS) of 20.2-36.7 months, overall survival (OS) of 39.9 months (reported in one publication) and objective response rate (ORR) of 45.3-80.0% with first-line treatment. In ≥ second line, the median PFS, OS and ORR ranged from 7.0 to 24.2 months, 11 to 19.6 months, and 13.9% to 47.9%, respectively. The safety profile of palbociclib was similar to that reported in pivotal clinical studies, and no new safety concerns were identified.

CONCLUSIONS:

A comprehensive volume of evidence demonstrates that palbociclib's effectiveness and safety profile in real-world settings align with those observed in clinical trials, offering valuable insights for clinical decision-making in countries outside of Western regions underrepresented in clinical trials.
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Oncol Ther Année: 2024 Type de document: Article Pays d'affiliation: Inde Pays de publication: Nouvelle-Zélande

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Oncol Ther Année: 2024 Type de document: Article Pays d'affiliation: Inde Pays de publication: Nouvelle-Zélande