Abstract

Simple SummaryTreatment of oropharynx cancers usually requires radiation, chemotherapy, surgery, or a combination of all three. Although these treatments are effective, they can cause both short- and long-term side effects, particularly when more than one treatment option is used. Robotic surgery is now an option for patients with oropharynx cancers, but it is not clear how many patients will require additional treatment with radiation, or combined chemotherapy and radiation, after surgical treatment. In this study we used a large national database of oropharynx cancer patients and found that two-thirds of patients who were treated with robotic surgery required radiation therapy and one-third required chemotherapy with radiation. In addition, we found that the true tumor stage of the patients in this study was often higher than was initially thought prior to surgery. Finally, patients treated at high volume surgical centers were more likely to have more of their tumor removed compared to those at low volume facilities. Better survival quality of oropharynx cancer patients could be achieved by improving pre-surgical selection of patients so that the number of treatment modalities is reduced. Trans-oral robotic surgery (TORS) has emerged as an important surgical treatment option in the management of human papillomavirus (HPV)-positive and -negative oropharynx cancer. However, treatment selection is paramount to ensure that patients will not require multimodality adjuvant therapy. In this study, we determined predictors of adjuvant therapy in TORS-treated patients. The National Cancer Database (NCDB) was used to identify patients with newly diagnosed clinical T1-T4, N0-N3 oropharyngeal squamous cell carcinoma who underwent TORS between 2010–2016. Kaplan–Meier survival analysis was used to estimate overall survival (OS). A total of 2999 patients were studied, and the five-year OS for the entire cohort was 82.5%, and for HPV-positive and -negative cohorts it was 88.3% and 67.9%, respectively (p < 0.001). Among all patients treated with TORS, 35.1% of patients received no additional treatment, 33.5% received adjuvant radiation alone (RT), and 31.3% received adjuvant chemoradiation. The N stage was pathologically upstaged in 629 (20.9%) patients after TORS. Patients treated at higher-volume centers were more likely to have negative surgical margins (OR: 0.96, 95% CI: 0.94, 0.98, p < 0.001), but this did not influence the receipt of adjuvant therapy. The high rate of adjuvant multimodality treatment after TORS suggests a need for improved patient selection. Limitations of this study, including lack of data on loco-regional control, progression free survival, acute and late toxicities, and utilization of pretreatment PET/CT imaging, should be addressed in future studies.

Highlights

  • The incidence of oropharynx cancers has steadily increased in the last decade, likely driven by a concomitant rise in the incidence of human papillomavirus (HPV)-associated oropharyngeal squamous cell carcinoma (OPSCC) [1]

  • We identified 4954 nonmetastatic OPSCC patients who were treated with Trans-oral robotic surgery (TORS) from 2010–2016, which formed our initial data set

  • The receipt of adjuvant radiation therapy (Hazard ratio: (HR): 0.65, 95% CI: 0.48, 0.87), adjuvant chemoradiation (HR: 0.81, 95% CI: 0.62, 1.07), HPV status (HR: 0.31, 95% CI: 0.24, 0.42), Charlson comorbidity score (HR: 1.56, 95% CI: 1.18, 2.0), clinical Tumor (T) stage (T3/4 vs. T1, HR: 1.75, 95% CI:1.16, 2.64), clinical N stage (N2c+ vs. N0, HR: 1.29, 95% CI: 0.8, 2.07), surgical margin status, Extracapsular extension (ECE)

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Summary

Introduction

The incidence of oropharynx cancers has steadily increased in the last decade, likely driven by a concomitant rise in the incidence of human papillomavirus (HPV)-associated oropharyngeal squamous cell carcinoma (OPSCC) [1]. Several landmark studies have demonstrated superior survival outcomes for HPV-associated OPSCC compared to tobacco- and alcohol-driven OPSCC [2,3]. As outcomes continue to improve in OPSCC, de-intensification of treatment has emerged as an attractive strategy in this favorable subset of patients. TransOral Robotic Surgery (TORS) is a promising, minimally invasive surgical strategy for treatment de-intensification in the management of OPSCC. Recent studies have shown excellent quality-of-life, functional, and oncologic outcomes in patients treated with TORS [4,5]. We demonstrated excellent overall survival (OS), but high rates of adjuvant therapy for patients undergoing TORS for T1-T2, N0-N2b OPSCC treated between

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