TY - JOUR
T1 - Radiotherapy Versus Transoral Robotic Surgery for Oropharyngeal Squamous Cell Carcinoma
T2 - Final Results of the ORATOR Randomized Trial
AU - Nichols, Anthony C.
AU - Theurer, Julie
AU - Prisman, Eitan
AU - Read, Nancy
AU - Berthelet, Eric
AU - Tran, Eric
AU - Fung, Kevin
AU - De Almeida, John R.
AU - Bayley, Andrew
AU - Goldstein, David P.
AU - Hier, Michael
AU - Sultanem, Khalil
AU - Richardson, Keith
AU - Mlynarek, Alex
AU - Krishnan, Suren
AU - Le, Hien
AU - Yoo, John
AU - MacNeil, S. Danielle
AU - Winquist, Eric
AU - Hammond, J. Alex
AU - Venkatesan, Varagur
AU - Kuruvilla, Sara
AU - Warner, Andrew
AU - Mitchell, Sylvia
AU - Chen, Jeff
AU - Johnson-Obaseki, Stephanie
AU - Odell, Michael
AU - Corsten, Martin
AU - Parker, Christina
AU - Wehrli, Bret
AU - Kwan, Keith
AU - Palma, David A.
N1 - Publisher Copyright:
© 2024 American Society of Clinical Oncology.
PY - 2024/12/1
Y1 - 2024/12/1
N2 - Radiotherapy (RT) and transoral robotic surgery (TORS) are both curative-intent treatment options for oropharyngeal squamous cell carcinoma (OPSCC). Herein, we report the final outcomes of the ORATOR trial comparing these modalities, 5 years after enrollment completion. We randomly assigned 68 patients with T1-2N0-2 OPSCC to RT (with chemotherapy if node-positive) versus TORS plus neck dissection (± adjuvant RT/chemoradiation). The primary end point was swallowing quality of life (QOL) assessed with the MD Anderson Dysphagia Inventory (MDADI). Secondary end points included overall and progression-free survival (OS, PFS), adverse events (AEs), and other QOL metrics. The primary end point has been previously reported (Nichols 2019). In this report, the median follow-up was 5.1 years (IQR, 5.0-5.3 years). MDADI total scores converged by 5 years and were not significantly different across the follow-up period (P =.11). EORTC QLQ-C30 and H&N35 scores demonstrated differing profiles, including worse dry mouth in the RT arm (P =.032) and worse pain in the TORS arm (P =.002). Grade 2-5 AE rates did not differ between arms (91% [n = 31] v 97% [n = 33] respectively, P =.61), with more neutropenia and hearing loss in the RT arm, and more dysphagia and other pain in the TORS arm based on grades 2-5 (all P <.05). There were no differences in OS or PFS. In conclusion, toxicity and QOL profiles differ in some domains between RT and TORS, but oncologic outcomes were excellent in both arms. Choice of treatment should remain a shared decision between the patient and their providers.
AB - Radiotherapy (RT) and transoral robotic surgery (TORS) are both curative-intent treatment options for oropharyngeal squamous cell carcinoma (OPSCC). Herein, we report the final outcomes of the ORATOR trial comparing these modalities, 5 years after enrollment completion. We randomly assigned 68 patients with T1-2N0-2 OPSCC to RT (with chemotherapy if node-positive) versus TORS plus neck dissection (± adjuvant RT/chemoradiation). The primary end point was swallowing quality of life (QOL) assessed with the MD Anderson Dysphagia Inventory (MDADI). Secondary end points included overall and progression-free survival (OS, PFS), adverse events (AEs), and other QOL metrics. The primary end point has been previously reported (Nichols 2019). In this report, the median follow-up was 5.1 years (IQR, 5.0-5.3 years). MDADI total scores converged by 5 years and were not significantly different across the follow-up period (P =.11). EORTC QLQ-C30 and H&N35 scores demonstrated differing profiles, including worse dry mouth in the RT arm (P =.032) and worse pain in the TORS arm (P =.002). Grade 2-5 AE rates did not differ between arms (91% [n = 31] v 97% [n = 33] respectively, P =.61), with more neutropenia and hearing loss in the RT arm, and more dysphagia and other pain in the TORS arm based on grades 2-5 (all P <.05). There were no differences in OS or PFS. In conclusion, toxicity and QOL profiles differ in some domains between RT and TORS, but oncologic outcomes were excellent in both arms. Choice of treatment should remain a shared decision between the patient and their providers.
UR - https://www.scopus.com/pages/publications/85205302434
U2 - 10.1200/JCO.24.00119
DO - 10.1200/JCO.24.00119
M3 - Article
C2 - 39303189
AN - SCOPUS:85205302434
SN - 0732-183X
VL - 42
SP - 4023
EP - 4028
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 34
ER -