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Phase III Study Assessing the "Best of" Radiotherapy Compared to the "Best of" Surgery (Trans-oral Surgery (TOS)) in Patients With T1-T2, N0-N1 Oropharyngeal, Supraglottic Carcinoma and With T1, N0 Hypopharyngeal Carcinoma
Oropharyngeal Squamous Cell Carcinoma (OPSCC) arises in the soft palate, tonsils, base of tongue, pharyngeal wall, and the vallecula. Most of the patients with early stage OPSCC are usually cured. Treatment of early stage OPSCC can be successfully achieved with primary surgery including neck dissection, as indicated, or with definitive radiotherapy. The current standard treatment for OPSCC is therefore based on either surgery and/or radiotherapy, both associated with comparable, high tumor control rates but with different side effects profiles and technical constraints. In order to decrease the potential morbidity of surgery, transoral approaches have been developed within the last decades, including transoral robotic surgery (TORS), transoral laser microsurgery (TLM) or conventional transoral techniques. On the other hand, patients with head and neck cancer treated with IMRT experienced significant improvements in cause specific survival (CSS) compared with patients treated with non-IMRT techniques thus suggesting that IMRT may be beneficial in terms of patient's outcomes and toxicity profile. It is as yet unclear however, which one of the new techniques is superior to the other in terms of function preservation. Given that the functional outcome of most importance is swallowing function, the preservation of swallowing is thus of major importance. The main objective of the study is to assess and compare the patient-reported swallowing function over the first year after randomization to either IMRT or TOS among patients with early stage OPSCC, SGSCC, and HPSCC.
Eligible patients will be randomized 1 to 1 to surgery (Arm 1) or radiotherapy (Arm 2). ARM 1: Surgery Trans-oral surgery (any trans-oral approach such as trans-oral laser microsurgery conventional trans-oral surgery or trans-oral robotic surgery) will be applied to all patients in this arm. A surgical margin is defined to be clear (R0), if found to be \>/=3mm in the final specimen (except deep margin for tonsillar resection, that is either R1 or R0), is defined to be close, if 1-\<3mm, and considered to be involved (R1), if \<1mm in the final specimen. Clearly defined marginal biopsies are required for each TOS-technique. Trans-oral re-resections are required in case of R1 or close-margin to convert the patient to an R0-status.Postoperative RT or chemo-RT will be given within 5-6 weeks of surgery in case of positive. ARM 2: Radiotherapy Intensity modulated radiation therapy (IMRT) with Simultaneous integrated boost (SIB) will be applied to all patients in this arm. PTV prescription to tumor and high risk areas will be delivered daily for 5 days per week to a total dose of 66-70Gy in 2 Gy/fraction over 6 weeks, elective/prophylactic mucosal and nodal areas will receive a total dose of 54.25- 54.45 Gy in 33-35 fractions of 1.55-1.65 Gy over 6 weeks.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
CHU-UCL Namur - CHU Mont Godinne
Namur, Yvoir, Belgium
Cliniques Universitaires Saint-Luc
Brussels, Belgium
Institut Jules Bordet-Hopital Universitaire ULB
Brussels, Belgium
U.Z. Leuven - Campus Gasthuisberg
Leuven, Belgium
Hopitaux Universitaires de Strasbourg - Hautepierre
Strasbourg, France
Universitaetsklinikum Koeln
Cologne, Germany
Universitaetklinikum Halle - Martin Luther Universitaet
Halle, Germany
Universitaets Krankenhaus Eppendorf - UKE - University Cancer Center
Hamburg, Germany
Universitaetsklinikum Jena
Jena, Germany
Staedtisches Klinikum Leipzig - Klinikum St Georg
Leipzig, Germany
Start Date
November 27, 2017
Primary Completion Date
June 30, 2025
Completion Date
June 30, 2029
Last Updated
August 14, 2025
112
ESTIMATED participants
Intensity-Modulated Radiation Therapy (IMRT)
RADIATION
Trans Oral Surgery (TOS)
PROCEDURE
Lead Sponsor
European Organisation for Research and Treatment of Cancer - EORTC
NCT06980038
NCT02734537
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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