AI Article Synopsis

  • The study compared weekly paclitaxel and cetuximab against the EXTREME regimen in patients with recurrent/metastatic squamous cell carcinoma of the head and neck (R/M SCCHN).
  • Both treatment groups had similar response rates, but weekly paclitaxel and cetuximab showed significantly better progression-free survival (6.0 months vs. 5.0 months).
  • Factors such as male gender, older age, good performance status, and no history of platinum chemotherapy were associated with better outcomes in the paclitaxel group.

Article Abstract

Background: The effectiveness of the combination chemotherapy of weekly paclitaxel and cetuximab has not yet been compared to that of the current standard regimen, EXTREME (combination of 5-fluorouracil, cisplatin and cetuximab).

Methods: We retrospectively reviewed the clinical records of R/M SCCHN patients who received cetuximab-containing chemotherapy as a first-line therapy; from these, patients receiving a weekly paclitaxel and cetuximab regimen (cohort A) and the EXTREME regimen (cohort B) were extracted. The responses, prognoses and adverse events of these two cohorts were evaluated.

Results: A total of 86 patients were included (cohort A, 49; cohort B, 36). Patients with histories of platinum-based chemotherapy were more frequently given the cohort A treatment. Though the response rates were similar in the two cohorts (45% in cohort A and 51% in cohort B; p=0.83), the progression-free survival (PFS) was significantly more favorable in cohort A by the log-rank test (6.0monthsvs 5.0months; p=0.027). In the Cox-regression hazard analyses, male gender (hazard ratio [HR]=2.1, p=0.010), older age (≥ 70 yo) (HR=5.0, p=0.018), PS 0 (HR=2.2, p=0.027), no history of platinum chemotherapy (HR=3.2, p=0.003) and the presence of a tracheostomy (HR=2.3, p=0.039) were favorable factors within cohort A.

Conclusion: In selected R/M SCCHN patients, the combination of weekly paclitaxel and cetuximab could be the better treatment option than the EXTREME regimen.

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http://dx.doi.org/10.1016/j.oraloncology.2017.07.022DOI Listing

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