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
25P - Feasibility of digital spatial profiling as a diagnostic: Comparison to immunohistochemistry (IHC)
Presenter: Hannah Hibbs
Session: Cocktail & Poster Display session
Resources:
Abstract
26P - Predictive biomarker discovery for ICI treatment response in metastatic MMRd endometrial cancer through deep proteomic profiling of FFPE tissue samples
Presenter: Juan Francisco Grau-Béjar
Session: Cocktail & Poster Display session
Resources:
Abstract
27P - Analytical validation of a small amplicon NGS panel for MSI detection
Presenter: Alexandra Lebedeva
Session: Cocktail & Poster Display session
Resources:
Abstract
28P - Clinical significance of TROP2 expression in lung adenocarcinomas
Presenter: Kazuya Takamochi
Session: Cocktail & Poster Display session
Resources:
Abstract
29P - PTEN/CREBBP/NOTCH1 co-alterations with TP53/RB1 define molecular subtypes associated with primary therapy resistance in small cell lung cancer (SCLC)
Presenter: Louisa Hempel
Session: Cocktail & Poster Display session
Resources:
Abstract
30P - Role of suppressor of cytokine signalling 6 (SOCS6) in colorectal cancer pathogenesis: Integrating clinical and molecular perspectives
Presenter: Asma Al- Bahri
Session: Cocktail & Poster Display session
Resources:
Abstract
31P - Adult granulosa cell tumours of ovary: Analysis of 227 non-recurrent and recurrent cases
Presenter: Jan Hojný
Session: Cocktail & Poster Display session
Resources:
Abstract
32P - Clinical evaluation cancer testis antigen 45 (CT45) expression in ovarian cancer
Presenter: Harshita Dubey
Session: Cocktail & Poster Display session
Resources:
Abstract
33P - Molecular-genetic concordance of the primary tumor and brain metastases of colorectal cancer (GENCONCOR-1)
Presenter: David Halafyan
Session: Cocktail & Poster Display session
Resources:
Abstract
34P - A prognostic signature to predict recurrence in patients with residual disease in triple-negative breast cancer: NACATRINE trial
Presenter: Ana Julia de Freitas
Session: Cocktail & Poster Display session
Resources:
Abstract