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Poster

What Are the Likely PICOs for Tovorafenib and Lifileucel as the First Products to go Through the JCA?

15/10/2025

Objectives: 

EUHTA regulation has applied from the 1st January 2025 for oncology products and ATMPs. The first ones reportedly undertaking JCA are tovorafenib and lifileucel (search as of 03/06/2025). The aim of this study is to predict the scope (PICOs) of those first JCAs.  

Methods: 

A TLR including the following, was conducted to align with the resources that assessors are likely to use: 

  1. ​Phase 2/3 clinical trials for the products under assessment, giving their likely positioning 
  1. ​Two most recent HTAs, in relevant indications, performed by lead assessors, co-assessors and 2 others  
  1. ​Relevant clinical practice guidelines in those countries where HTAs are gathered   

​Consolidation used a 4-step process to ensure that member state needs are translated in the lowest possible number of PICOs. 

Results: 

For tovorafenib, indicated in the treatment of paediatric low-grade glioma (LGG), Ireland, Germany, France and Sweden were the markets of interest. Where 2 clinical practice guidelines were identified from the European society for Paediatric Oncology and German Society for Paediatric Oncology and Haematology, along with 3 HTAs resulting in 5 potential sets of PICOs. There were broadly consistent Populations, Comparators (standard of care chemotherapy) and relevant Outcomes.  

​For lifileucel, indicated for the treatment of melanoma, France, Poland, Spain and Sweden were markets of interest. Where 4 clinical practice guidelines have been identified, along with 6 HTAs, primarily for Keytruda, Opdivo and nivolumab-relatlimab combination therapy, resulting in 9 potential sets of PICOs. 

Conclusion: 

​​Based on the clinical trials of tovorafenib and lifileucel, predicting the PICOs in tovorafenib will be easier for the manufacturer than for lifileucel, primarily due to the lack of treatment options in LGG. The PICOs used in the tovorafenib trial are therefore closer to our predictions, however this study did not look at all member states, which is a limitation.   

​Basic.(1, 2) 

​Tovorafenib.(3-10) 

​Lifileucel. (11-14)

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References

  1. Member State Coordination Group on Health Technology Assessment. Guidance on the scoping process 2024 [Available from: https://health.ec.europa.eu/document/download/7be11d76-9a78-426c-8e32-79d30a115a64_en?filename=hta_jca_scoping-process_en.pdf
  2. European Commission. Joint Clinical Assessments 2025 [Available from: https://health.ec.europa.eu/health-technology-assessment/implementation-regulation-health-technology-assessment/joint-clinical-assessments_en
  3. Gnekow AK, Kandels D, van Tilburg C, Azizi AA, Opocher E, Stokland T, et al. SIOP-E-BTG and GPOH Guidelines for Diagnosis and Treatment of Children and Adolescents with Low Grade Glioma  Clinical Paediatrics. 2019;231(3):107-35. 
  4. Roka K, Scheinemann K, Avula S, Maduro JH, Thomale UW, Sehested A, et al. European standard clinical practice recommendations for primary pediatric  low-grade gliomas  EJC Paediatric Oncology. 2024;4. 
  5. TLV. Finlee (dabrafenib) i kombination med Spexotras (trametinib) 2024 [Available from: https://www.tlv.se/download/18.158aaf7f192711c69bb3cd49/1729170226478/241017_finlee_spexotras_1328-2024_underlag.pdf
  6. Transparency Committee. FINLEE/SPEXOTRAS (dabrafenib/trametinib) – Glioma 2024 [Available from: https://www.has-sante.fr/jcms/p_3530986/fr/finlee-/-spexotras-dabrafenib-/-trametinib-gliome
  7. G-BA. Benefit assessment method for the active ingredient trametinib (malignant glioma, BRAF V600E mutation, ≥ 1 year, low-grade (LGG)/higher-grade (HGG) after at least 1 prior therapy; combination with dabrafenib)  2024. 
  8. Botella-Estrada R, Boada-García A, Carrera-Álvarez C, Fernández-Figueras M, González-Cao M, Moreno-Ramírez D, et al. Clinical Practice Guideline on Melanoma From the  Spanish Academy of Dermatology and Venereology (AEDV) ACTAS Dermo-Sifiliográficas. 2021;112:142-52. 
  9. Márquez-Rodas I, Muñoz Couselo E, Rodríguez Moreno JF, M A, Fernández A, Berciano Guerrero MÁ, et al. SEOM-GEM clinical guidelines for cutaneous melanoma. Clinical & Translational Oncology. 2024;26(11):2841-55. 
  10. Rutkowski P, Wysocki PJ, Nasierowska-Guttmejer A, Jeziorski A, Wysocki WM, Kalinka-Warzocha E, et al. Guidelines for Diagnostic and Therapeutic Management: Cutaneous melanomas. Oncology in Clinical Practice. 2019;15. 
  11. Amaral T, Ottaviano M, Arance A, Chiarion-Sileni V, Donia M, Dummer R, et al. Cutaneous melanoma: ESMO Clinical Practice Guideline for diagnosis,  treatment and follow-up Annals of Oncology. 2024;30(12):1884-901. 
  12. Guillot B, Dalac S, Denis MG, Dupuy A, Emile JF, De La Fouchardiere A, et al. French updated recommendations in Stage I to III melanoma treatment and management  JEADV. 2017;31(4):567-747. 
  13. Transparency Committee. KEYTRUDA (pembrolizumab) – Stage IIB, IIC, or III melanoma 2022 [Available from: https://www.has-sante.fr/jcms/p_3395770/fr/keytruda-pembrolizumab-melanome-de-stade-iib-iic-ou-iii
  14. Transparency Committee. OPDIVO/YERVOY (nivolumab/ipilimumab) – Advanced melanoma  2023 [Available from: https://www.has-sante.fr/jcms/p_3481898/fr/opdivo/yervoy-nivolumab/ipilimumab-melanome-avance

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