Literature DB >> 29244173

Magnitude of Clinical Benefit of Cancer Drugs Approved by the US Food and Drug Administration.

Ariadna Tibau1, Consolación Molto1, Alberto Ocana2, Arnoud J Templeton3, Luis P Del Carpio1, Joseph C Del Paggio4, Agustí Barnadas1, Christopher M Booth5,6, Eitan Amir4.   

Abstract

Background: It is uncertain whether drugs approved by the US Food and Drug Administration (FDA) have clinically meaningful benefit as determined by validated scales such as the European Society for Medical Oncology Magnitude of Clinical Benefit Scale (ESMO-MCBS).
Methods: We searched the Drugs@FDA website for applications of anticancer drugs from January 2006 to December 2016. Study characteristics, outcomes, and regulatory pathways were collected from drug labels and reports of registration trials. For randomized controlled trials (RCTs), ESMO-MCBS grades were applied. Meaningful benefit was defined as a grade of A or B for (neo)adjuvant intent and 4 or 5 for palliative intent. All statistical tests were two-sided.
Results: We identified 63 individual drugs for 118 indications. These were supported by 135 studies, among which were 105 RCTs for which ESMO-MCBS could be applied. Only 46 (43.8%) met the ESMO-MCBS meaningful benefit threshold (100% of (neo)adjuvant trials and 38.8% of palliative trials). In palliative therapy trials, meaningful ESMO-MCBS grades were associated with phase III trials (compared with phase II; odds ratio [OR] = 38.45, 95% confidence interval [CI] = 3.27 to 452.00, P = .004), those with overall survival as their primary end point (compared with intermediate end points; OR = 8.28, 95% CI = 2.49 to 27.50, P = .001) and trials of targeted drugs with companion diagnostics (OR = 11.62, 95% CI = 2.95 to 45.78, P < .001). Over time, there has been an increase in the number of trials meeting the ESMO-MCBS threshold (Ptrend = .04). There were insufficient (neo)adjuvant studies to perform statistical analysis. Conclusions: The number of trials meeting the ESMO-MCBS threshold for clinical benefit has improved over time. However, fewer than half of RCTs supporting FDA approval meet the threshold for clinically meaningful benefit.

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Year:  2018        PMID: 29244173     DOI: 10.1093/jnci/djx232

Source DB:  PubMed          Journal:  J Natl Cancer Inst        ISSN: 0027-8874            Impact factor:   13.506


  16 in total

1.  Magnitude of Clinical Benefit of Cancer Drugs Approved by the US Food and Drug Administration Based on Single-Arm Trials.

Authors:  Ariadna Tibau; Consolación Molto; Maria Borrell; Joseph C Del Paggio; Agustí Barnadas; Christopher M Booth; Eitan Amir
Journal:  JAMA Oncol       Date:  2018-11-01       Impact factor: 31.777

2.  PP2A inhibition is a druggable MEK inhibitor resistance mechanism in KRAS-mutant lung cancer cells.

Authors:  Otto Kauko; Caitlin M O'Connor; Evgeny Kulesskiy; Jaya Sangodkar; Anna Aakula; Sudeh Izadmehr; Laxman Yetukuri; Bhagwan Yadav; Artur Padzik; Teemu Daniel Laajala; Pekka Haapaniemi; Majid Momeny; Taru Varila; Michael Ohlmeyer; Tero Aittokallio; Krister Wennerberg; Goutham Narla; Jukka Westermarck
Journal:  Sci Transl Med       Date:  2018-07-18       Impact factor: 17.956

Review 3.  Clinical Benefit Scales and Trial Design: Some Statistical Issues.

Authors:  Edward L Korn; Carmen J Allegra; Boris Freidlin
Journal:  J Natl Cancer Inst       Date:  2022-09-09       Impact factor: 11.816

4.  Comparison of Treatments for Nonmetastatic Castration-Resistant Prostate Cancer: Matching-Adjusted Indirect Comparison and Network Meta-Analysis.

Authors:  Lin Wang; Channing Paller; Hwanhee Hong; Lori Rosman; Anthony De Felice; Otis Brawley; G Caleb Alexander
Journal:  J Natl Cancer Inst       Date:  2022-02-07       Impact factor: 13.506

5.  Patient Participation in Clinical Trials of Oncology Drugs and Biologics Preceding Approval by the US Food and Drug Administration.

Authors:  Nora Hutchinson; Benjamin Carlisle; Adelaide Doussau; Rafia Bosan; Eli Gumnit; Amanda MacPherson; Dean A Fergusson; Jonathan Kimmelman
Journal:  JAMA Netw Open       Date:  2021-05-03

6.  The Comparative Effectiveness of Innovative Treatments for Cancer (CEIT-Cancer) project: Rationale and design of the database and the collection of evidence available at approval of novel drugs.

Authors:  Aviv Ladanie; Benjamin Speich; Florian Naudet; Arnav Agarwal; Tiago V Pereira; Francesco Sclafani; Juan Martin-Liberal; Thomas Schmid; Hannah Ewald; John P A Ioannidis; Heiner C Bucher; Benjamin Kasenda; Lars G Hemkens
Journal:  Trials       Date:  2018-09-19       Impact factor: 2.279

7.  Anticancer drugs approved by the Food and Drug Administration for gastrointestinal malignancies: Clinical benefit and price considerations.

Authors:  Di Maria Jiang; Kelvin K W Chan; Raymond W Jang; Christopher Booth; Geoffrey Liu; Eitan Amir; Robert Mason; Louis Everest; Elena Elimova
Journal:  Cancer Med       Date:  2019-03-07       Impact factor: 4.452

8.  Clinical Trial Evidence Supporting US Food and Drug Administration Approval of Novel Cancer Therapies Between 2000 and 2016.

Authors:  Aviv Ladanie; Andreas M Schmitt; Benjamin Speich; Florian Naudet; Arnav Agarwal; Tiago V Pereira; Francesco Sclafani; Amanda K Herbrand; Matthias Briel; Juan Martin-Liberal; Thomas Schmid; Hannah Ewald; John P A Ioannidis; Heiner C Bucher; Benjamin Kasenda; Lars G Hemkens
Journal:  JAMA Netw Open       Date:  2020-11-02

9.  The impacts of government reimbursement negotiation on targeted anticancer medication price, volume and spending in China.

Authors:  Yichen Zhang; Haishaerjiang Wushouer; Sheng Han; Mengyuan Fu; Xiaodong Guan; Luwen Shi; Anita Wagner
Journal:  BMJ Glob Health       Date:  2021-07

10.  Clinical benefit of immune checkpoint inhibitors approved by US Food and Drug Administration.

Authors:  Fei Liang; Sheng Zhang; Qin Wang; Wenfeng Li
Journal:  BMC Cancer       Date:  2020-08-31       Impact factor: 4.430

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