Abstract 103P
Background
The National Institute for Health and Care Excellence (NICE) develops recommendations for cancer therapeutics within the NHS by evaluating clinical evidence and cost-effectiveness. The ESMO-Magnitude of Clinical Benefit Scale (ESMO-MCBS) serves as a standardised, objective instrument to evaluate and quantify the clinical benefits of oncology treatments. The ESMO Scale for Clinical Actionability of Molecular Targets (ESCAT) provides a framework for assessing the clinical relevance and actionability of molecular targets identified through cancer genomics. This study looks at the NICE recommendation outcomes for solid tumour drugs and their corresponding ESMO-MCBS and ESCAT scores.
Methods
We reviewed NICE's solid cancer drug appraisals from the past five years, categorised as recommended, optimised, not recommended, or terminated approval. The corresponding ESMO-MCBS scores for each drug were identified, with numerical values assigned for metastatic settings and letter grades for curative contexts. Additionally, ESCAT scores were incorporated for drugs targeting specific genomic alterations. We look to assess the correspondance between ESMO-MCBS and ESCAT scores with the NICE recommendation outcomes.
Results
In the past five years, NICE has issued 131 recommendations for solid tumour drugs. Of these, 69 were categorised as recommended, 33 as optimised, 13 as not recommended, and 16 as terminated approvals. Of the 14 drugs used in curative settings, 12 received the highest ESMO-MCBS letter grade of A (indicating substantial benefit), while 2 were deemed to have no evaluable benefit. Among the 120 drugs used in metastatic settings, 6 received the highest ESMO-MCBS score of 5, 55 scored a 4, 43 scored a 3, 10 scored a 2, and 3 scored a 1. ESCAT scores were available for 49 drugs, with 33 achieving the top grading of I-A, 10 graded as I-B, and 6 as I-C.
Conclusions
We are conducting further assessments to evaluate correlation between ESMO assessment tools and NICE recommendation outcomes to ensure the decision-making processes employed by NICE are in alignment with evidence-based evaluation tools.
Editorial acknowledgement
Clinical trial identification
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
152P - Nanopore sequencing of cfDNA captures key copy number alterations in lung adenocarcinoma: A non-invasive approach for prognosis, therapy, and subtyping
Presenter: Khashayar Roohollahi
Session: Cocktail & Poster Display session
Resources:
Abstract
153P - Discovery of new BRCA1/2 mutations not described in the international breast consortium
Presenter: Wala Ben Kridis
Session: Cocktail & Poster Display session
Resources:
Abstract
154P - Alternative splicing in non-small cell lung cancer evolution
Presenter: Michelle Leung
Session: Cocktail & Poster Display session
Resources:
Abstract
155TiP - Exploring mechanisms of action and resistance to innovative therapeutic drugs: UNLOCK program
Presenter: Julieta Rodriguez
Session: Cocktail & Poster Display session
Resources:
Abstract
157P - Therapeutic potential of B7-H3 targeting in pediatric neuroblastoma
Presenter: Caroline E Nunes-Xavier
Session: Cocktail & Poster Display session
Resources:
Abstract
158P - E-JIB-04: An epigenetic targeted therapy for ovarian cancer with MECOM amplification
Presenter: Ibha Singh
Session: Cocktail & Poster Display session
Resources:
Abstract
159P - The impact of kisspeptin pre-treatment towards temozolomide resistance mechanisms and associated differently expressed proteins (DEPs) in human glioblastoma cells
Presenter: Isra Sati
Session: Cocktail & Poster Display session
Resources:
Abstract
160P - Clinical observation and immune effects of high-intensity focused ultrasound (HIFU) in the treatment of liver metastasis in colorectal cancer
Presenter: Shasha Wang
Session: Cocktail & Poster Display session
Resources:
Abstract
161P - Early phase cancer clinical trials: A viable treatment option for patients?
Presenter: Rhona Dawson
Session: Cocktail & Poster Display session
Resources:
Abstract
162P - Tailoring patient molecular selection for novel anti-MET therapies
Presenter: Lucia Notario Rincon
Session: Cocktail & Poster Display session
Resources:
Abstract