PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
March 28, 2026Current Oncology1 citationsOpen Access

Real-World Outcomes of First-Line Cetuximab and Platinum-Based Chemotherapy in Recurrent and/or Metastatic Head and Neck Squamous Cell Carcinoma: A Multicenter Observational Study and Literature Review

View Full Paper
ZRZoran RakušićVBVesna BišofSVSanja Vušković

Key Points

  • To evaluate the real-world effectiveness of the EXTREME regimen for recurrent and metastatic head and neck squamous cell carcinoma.
  • Conducted a retrospective multicenter study across six oncology centers in Croatia.
  • Included 217 patients with recurrent and/or metastatic head and neck squamous cell carcinoma.
  • Analyzed overall survival, progression-free survival, response rates, and safety.
  • 91% of patients received the EXTREME regimen.
  • Median overall survival was 14 months (95% CI, 12–17).
  • Median progression-free survival was 6.2 months (95% CI, 6.0–7.2).
  • Objective response rate was 21%, and disease control rate was 63%.
  • Grade ≥ 3 toxicity occurred in 18.9% of patients without any treatment-related deaths.

Abstract

Background: The EXTREME regimen (cetuximab with cisplatin/carboplatin and 5-fluorouracil) has long been a standard first-line treatment for recurrent and/or metastatic head and neck squamous cell carcinoma (R/M HNSCC), particularly in patients ineligible for immunotherapy. However, real-world evidence remains limited, especially in regions with delayed access to novel therapies. Methods: We conducted a retrospective, multicenter study of 217 patients with R/M HNSCC treated with cetuximab-based chemotherapy at six Croatian oncology centers between 2016 and 2022, prior to reimbursement of pembrolizumab. The primary endpoint was overall survival (OS); secondary endpoints included progression-free survival (PFS), response rates, and safety. Results: The majority (91%) received the EXTREME regimen. Median OS was 14 months (95% CI, 12–17), and median PFS was 6.2 months (95% CI, 6.0–7.2). Objective response rate was 21%, and disease control rate was 63%. Cetuximab-induced rash correlated with longer PFS. Grade ≥ 3 toxicity occurred in 18.9% of patients. No treatment-related deaths were observed. Conclusion: In routine clinical practice, cetuximab combined with platinum-based chemotherapy remains an effective and well-tolerated first-line treatment for R/M HNSCC, particularly in patients who are ineligible for immunotherapy or with PD-L1–negative tumors. These findings support its continued use in appropriately selected patients.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Rakušić et al. (2026) studied this question.

synapsesocial.com/papers/69c772058bbfbc51511e2230https://doi.org/10.3390/curroncol33040183
Ask AI
Helpful
Bookmark
Share
View Full Paper