Radiotherapy delays do not predict survival, recurrence in oropharynx carcinoma

15 Mar 2022
Radiotherapy delays do not predict survival, recurrence in oropharynx carcinoma

Treatment delays do not necessarily contribute to cancer-specific survival (CSS) or locoregional recurrence (LRR) in patients with oropharynx carcinoma, reveals a study. However, time on treatment (TOT) of 1 to 3 days is associated with lower CSS.

A team of researchers performed a retrospective analysis to examine the prognostic significance of treatment delays for oropharynx carcinoma patients treated with definitive radiotherapy (RT), comparing p16+ with p16 disease. A total of 763 patients treated between 2012 and 2016 were included in the analysis.

Treatment delay was defined as the time from pathologic diagnosis to RT initiation; to stratify outcomes, the following thresholds were used: ≤60, 61 to 90, and >90 days. TOT delays were estimated based on the RT fractionation, and TOT delay of 1 to 3 days was compared with >3 days. Finally, the researchers performed multivariable analysis to determine the predictors of CSS and LRR.

Of the patients, 650 (85 percent) had p16+ disease. Multivariable analysis revealed the association of a TOT delay of 1 to 3 days with inferior CSS (hazard ratio [HR], 1.81, 95 percent confidence interval [CI], 1.02‒3.22) compared with <1 day.

On the other hand, treatment delay >90 vs ≤60 days (HR, 1.68, 95 percent CI, 0.98‒3.04) and 61 to 90 vs ≤60 days (HR, 0.94, 95 percent CI, 0.60‒1.48) showed no association with CSS.

Furthermore, treatment delay >90 versus ≤60 days (HR, 1.29; 95 percent CI, 0.66‒2.52), 61 to 90 vs ≤60 days (HR, 0.98, 95 percent CI, 0.64‒1.52), TOT 1 to 3 vs <1 day (HR, 0.91, 95 percent CI, 0.39‒2.11), and TOT >3 vs <1 day (HR, 1.79, 95 percent CI, 0.80‒3.99) did not correlate with LRR. Treatment delay also showed no interaction with p16 status in relation to LRR (p=0.27) or CSS (p=0.17).

“[A] p16 status should not be a significant factor when triaging RT start dates,” the researchers said.

Am J Clin Oncol 2022;45:122-128