Abstract 1181P
Background
Diagnosing cancer earlier can support timely treatment and improve patient prognosis. Innovative diagnostic tests need to appropriately respond to unmet needs. Target Product Profiles (TPPs) are specification documents that serve as demand-signalling tools to inform developing improved tests – in terms of scientific performance, fit with clinical pathways and patient needs. There is growing interest in their use. Commissioned by Cancer Research UK, RAND Europe and the Office of Health Economics conducted a study to establish a methodological process for developing robust diagnostic TPPs for cancer and identify the types of features TPPs should consider.
Methods
A mixed-methods approach combined international literature review, interviews, workshops with UK experts and developing an economic modelling tool for TPP requirements. 129 individuals contributed (academics, funders, healthcare professionals, industry, policy, regulatory and HTA experts, health economists, and patient and public voice).
Results
Establishing specifications for combinations of core features driving a test’s value is key to TPP development. Trade-offs between different requirements must be considered. Relevant features types fall into 9 categories (e.g. unmet need, analytical performance, clinical validity, clinical utility, human factors, infrastructure, cost/economic, regulation, environmental). Fit-for-purpose TPPs require input from diverse stakeholders through desk research, consultation and modelling methods. TPP development has 2 stages: inception (establishing core working group, governance, action plan) and implementation (scoping unmet need and key test requirements, TPP drafting, consensus building).
Conclusions
This internationally-relevant, tumour-site agnostic guide is an evidence-based resource for designing TPPs for specific cancer tests and use cases. It highlights multifaceted factors and practical tips for deciding which features to consider and methods to use in TPP development. Robust TPPs are an important tool for developing improved cancer diagnostic tests, but need to align with wider innovation and health system efforts.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
RAND Europe; Cancer Research UK.
Funding
Cancer Research UK.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
825P - Ultra-sensitive cfDNA analysis for minimally invasive measurable residual disease detection and profiling in multiple myeloma
Presenter: Natalia Buenache
Session: Poster session 09
826P - Efficacy of non-doxorubicin based regimens in severely G6PD deficient patients with DLBCL
Presenter: Shruti Prem Sudha
Session: Poster session 09
827P - Comparison of efficacy and safety between glofitamab and real-world regimens among Chinese patients with 3L+ relapsed/refractory diffuse large B-cell lymphoma: An external control study
Presenter: Keshu Zhou
Session: Poster session 09
828P - Translocation 11;14 is not associated with adverse prognosis in the era of novel anti-myeloma therapeutics
Presenter: Ioannis Ntanasis-Stathopoulos
Session: Poster session 09
829P - Flumatinib combined with chemotherapy for newly diagnosed adult with Ph-positive acute lymphoblastic leukemia: A single-center, retrospective observational study
Presenter: HAN SHUYU
Session: Poster session 09
830P - Prognostic model of pediatric AML patients with RUNX1-RUNX1T1 fusion gene
Presenter: Yang Xun
Session: Poster session 09
Resources:
Abstract
831P - Impact of chronic kidney disease on disease outcomes in hospitalized multiple myeloma patients: A National inpatient sample study from 2016 to 2020
Presenter: Marco Bermudez
Session: Poster session 09
Resources:
Abstract
832P - CLOMB: A validated scoring model to predict the relapse in the central nervous system of pediatric acute B-cell lymphoblastic leukemia
Presenter: Jiacheng Li
Session: Poster session 09
Resources:
Abstract
833P - Latest results of GVM±R regimen for the salvage therapy of patients with relapsed or refractory aggressive non-Hodgkin's lymphoma
Presenter: Wei Liu
Session: Poster session 09
834P - Treatment of DLBCL in HIV patient: Still a dilemma
Presenter: Devashish Desai
Session: Poster session 09