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Breast cancer drugs: FDA approval, development time, efficacy, clinical benefits, innovation, trials, endpoints, quality of life, value, and price.
Michaeli, Julia Caroline; Michaeli, Thomas; Trapani, Dario; Albers, Sebastian; Dannehl, Dominik; Würstlein, Rachel; Michaeli, Daniel Tobias.
Affiliation
  • Michaeli JC; Department of Obstetrics and Gynaecology, LMU University Hospital, LMU Munich, Munich, Germany.
  • Michaeli T; Department of Personalized Oncology, University Hospital Mannheim, Heidelberg University, Mannheim, Germany.
  • Trapani D; DKFZ-Hector Cancer Institute at the University Medical Center Mannheim, Mannheim, Germany.
  • Albers S; Division of Personalized Medical Oncology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Dannehl D; European Institute of Oncology, IRCCS, Milan, Italy.
  • Würstlein R; Department of Oncology and Hematology, University of Milan, Milan, Italy.
  • Michaeli DT; Department of Orthopaedics and Sport Orthopaedics, School of Medicine, Klinikum Rechts Der Isar, Technical University of Munich, Munich, Germany.
Breast Cancer ; 2024 Sep 25.
Article in En | MEDLINE | ID: mdl-39320645
ABSTRACT

OBJECTIVE:

This study analyzes the development, benefits, trial evidence, and price of new breast cancer drugs with US Food and Drug Administration (FDA) approval.

METHODS:

We identified 26 drugs with 42 FDA-approved indications for early and metastatic breast cancer (2000-2023). Data were collected from FDA labels, clinicaltrials.gov, and Medicare and Medicaid. Overall survival (OS) and progression-free survival (PFS) hazard ratios (HRs) and tumor response's relative risk (RR) alongside objective response rate (ORR) were meta-analyzed.

RESULTS:

The median development time for breast cancer drugs was 7.8 years (95% CI 6.2-10.8). 26% of treatments were considered innovative ("first-in-indication") with 88% acting via a targeted mechanism. 64% were small molecules, 19% antibodies, and 18% antibody-drug conjugates. 38% were approved for HR + and 31% for HER2 + breast cancer. 6 indications were for early and 36 for metastatic breast cancer. Indications utilized FDA's special programs orphan (2%), fast track (24%), accelerated approval (19%), priority review (74%), breakthrough therapy (44%). Approval was predominantly supported by phase 3 trials (88%) of randomized controlled design (66%), enrolling a median of 585 patients (IQR 417-752) at 181 centers (IQR 142-223) across 19 countries (IQR 17-20). New drugs' HR were 0.78 for OS (95% CI 0.74-0.82) and 0.59 for PFS (95% CI 0.54-0.64) with a RR for tumor response of 1.61 (95% CI 1.46-1.76). Median improvements of OS were 2.8 months (IQR 1.8-5.8) and PFS were 4.4 months (IQR 2.2-7.1). In single-arm trials, the average ORR was 31% (95% CI 10-53). In meta-regressions, the correlation between OS/PFS was 0.34 (p = 0.031) and OS/response was 0.01 (p = 0.435). 60% of treatments had a 'high-value' ESMO-MCBS score with 14% demonstrating improvements in quality of life. The median price was $16,013 per month (95% CI 13,097-17,617). There was no association between prices and patient benefit. The median value per life year gained was $62,419 (IQR 25,840-86,062).

CONCLUSIONS:

Over the past two decades, the development of innovative and effective drugs transformed the treatment landscape for breast cancer patients. Yet, investigators and regulators must safeguard that highly-priced new drugs demonstrate improvements in patient-centered clinical endpoints overall survival and quality of life.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Breast Cancer Journal subject: NEOPLASIAS Year: 2024 Document type: Article Affiliation country: Germany Country of publication: Japan

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Breast Cancer Journal subject: NEOPLASIAS Year: 2024 Document type: Article Affiliation country: Germany Country of publication: Japan