PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
March 3, 2026EJC Skin Cancer0 citationsOpen Access

Comparative analysis of progression free survival and treatment maintenance in patients with advanced melanoma responding to first-line treatment

View Full Paper
MRMargot RicartLMLaurent MortierSDStéphane Dalle

Key Points

  • Median progression-free survival was 10.7 months for BRAF and MEK inhibitors, and 84.6 months for anti-PD1 immunotherapy.
  • Patients receiving anti-PD1 monotherapy had a treatment maintenance duration exceeding progression-free survival.
  • Analysis was conducted using data from the Melbase database, comparing treatment responses in patients with advanced melanoma.
  • First-line combined anti-PD1/Anti-CTLA4 immunotherapy provided the most durable response, particularly in patients without brain metastases.

Abstract

AbstractBackground Specific data regarding Progression-Free Survival (PFS) and treatment maintenance estimated by Time To Next Treatment (TTNT) in patients with advanced melanoma responding to first-line treatments are scarce. Objective To evaluate and compare in a real-life setting PFS and overall TTNT in patients with advanced melanoma responding to first-line treatment within three therapeutic subsets: BRAF and MEK inhibitors (group 1), anti-PD1 (group 2) and anti-PD1/Anti-CTLA4 immunotherapies (group 3); and to perform comparative analyses of PFS and TTNT according to response depth (complete or partial response), brain metastases (BM), and per-treatment disease progression. Patients and Methods Patients with unresectable stage III or IV melanoma registered in the French nationwide multicenter Melbase database and responding to first-line immunotherapy or targeted therapy were retrospectively included. Overall and situation-specific PFS and TTNT were assessed and compared within and between therapeutic groups. Results Median PFS was 10.7 months, 84.6 months, and not reached in group 1, 2 and 3 respectively. No obvious difference was observed between PFS and TTNT for patients receiving targeted therapies (TT) and combined anti-PD1/CTLA4 immunotherapy. Conversely, TTNT largely exceeded PFS in patients receiving anti-PD1 alone, with an increasing gap over time. Similar trends were observed in patients with BM and in those experiencing per-treatment disease progression. Conclusion First-line combined anti-PD1/Anti-CTLA4 immunotherapy was associated with the most durable response in patients with advanced melanoma considered as responders, compared with anti-PD1 alone or targeted therapy, independently of BM status. Anti-PD1 monotherapy was frequently maintained beyond disease progression, in contrast to targeted therapy.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Ricart et al. (2026) studied this question.

synapsesocial.com/papers/69a7615cc6e9836116a2f338https://doi.org/10.1016/j.ejcskn.2026.100782
Ask AI
Helpful
Bookmark
Share
View Full Paper