Effectiveness of Adjuvant Radiotherapy in Small Oropharyngeal Squamous Cell Cancer and Single Lymph Node Metastasis.
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|ClinicalTrials.gov Identifier: NCT00964977|
Recruitment Status : Recruiting
First Posted : August 25, 2009
Last Update Posted : November 16, 2012
|First Submitted Date ICMJE||August 24, 2009|
|First Posted Date ICMJE||August 25, 2009|
|Last Update Posted Date||November 16, 2012|
|Start Date ICMJE||October 2009|
|Estimated Primary Completion Date||December 2013 (Final data collection date for primary outcome measure)|
|Current Primary Outcome Measures ICMJE
||Primary study object: overall survival [ Time Frame: 9 years ]
The objective of the clinical study will be to investigate two different patient groups (irradiated/unirradiated) with pT1/2 primary and verification of a singular ipsilateral lymph node metastasis in parallel design in order to evaluate the possible benefit of radiation therapy. The following null hypothesis forms the basis of the present study: Radiation therapy will have no influence on the overall survival in patients with pT1/2, pN1 primary tumor. First patients will be observed for 9 years, last patient in will be followed-up for 5 years.
|Original Primary Outcome Measures ICMJE
||Primary study object: overall survival [ Time Frame: 9 years ]|
|Change History||Complete list of historical versions of study NCT00964977 on ClinicalTrials.gov Archive Site|
|Current Secondary Outcome Measures ICMJE
|Original Secondary Outcome Measures ICMJE
||Time to occurrence of lymphatic metastases Time to occurrence of local relapse Time to occurrence of distant metastases Tumor related death due to local tumor progression or metastatic spread Life Quality [ Time Frame: 9 years ]|
|Current Other Outcome Measures ICMJE||Not Provided|
|Original Other Outcome Measures ICMJE||Not Provided|
|Brief Title ICMJE||Effectiveness of Adjuvant Radiotherapy in Small Oropharyngeal Squamous Cell Cancer and Single Lymph Node Metastasis.|
|Official Title ICMJE||Effectiveness of Adjuvant Radiotherapy in Patients With Oropharyngeal and Floor of Mouth Squamous Cell Carcinoma and Concomitant Histological Verification of Singular Ipsilateral Cervical Lymph Node Metastasis (pN1-state)|
|Brief Summary||Radiotherapy with or without adjuvant chemotherapy represents an important column of modern therapy in advanced squamous cell originated tumours of the head and neck. However to date no studies are available which study the effectiveness of radiotherapy in patients with resected small tumours (T1, T2) and concomitant ipsilateral metastasis of a single lymph node (pN1) for general treatment recommendation. The present study is designed as non-blinded, prospective, multicenter randomized controlled trial (RCT) for comparison of overall-survival as primary clinical target in patients receiving radiation therapy vs. patients without adjuvant radiation following curative intended surgery. Aim of the study is to enroll 560 adult males and females for 1:1 randomization to one of the two treatment arms (radiation/non-radiation. Secondary clinical endpoints are as follows: Incidence and time to tumor relapse (locoregional relapse, lymph node involvement and metastatic spread), Quality of life as reported by EORTC (QLQ-C30 with H&N 35 module) and time from operation to orofacial rehabilitation.|
Prevailing curative intended therapeutic strategies combine radical resection of the tumor mass with a safety margin followed by radiation of the original tumor site and adjacent locoregional lymphatic drainage areas. To date selection of the individual therapeutic pattern is essentially guided by pre- and post-therapeutic TNM staging parameters. Exceptionally for advanced tumors postoperative radiotherapy and optional combination with (radiosensitizing) chemotherapeutic agents is favorable and recommended. Interdisciplinary guidelines stated the following detailed recommendations for application of adjuvant radiation therapy:
The methodological key problems which had to be addressed in the protocol were the following:
Methods/Design Study Design The study is designed as a non-blinded, prospective, randomized controlled clinical trial.
Study objectives Objective of the clinical study will be the investigation of two different patient collectives (irradiated/unirradiated) with pT1/2 primary and verification of a singular ipsilateral lymph node metastasis in parallel design in order to evaluate a possible significant benefit of radiation therapy. Investigation of further biological parameters will be concomitantly performed to assess a possible prediction of tumor progression and to evaluate surrogate markers of radioresistance. The following null hypothesis forms the basis of the present study: Radiation therapy will have no influence on the overall survival in patients with pT1/2, pN1 primary tumor. Secondary outcome variables include incidence and time to tumor relapse (locoregional relapse, lymph node involvement and metastatic spread), Quality of life as reported by EORTC (QLQ-C30 with H&N 35 module) and time from operation to orofacial rehabilitation.
Males and females with histological verified diagnosis of a primary squamous cell carcinoma of the oral cavity or the oropharynx are eligible. Inclusion criteria are as follows:
Study interventions Radiotherapy should begin within 6 weeks after the last surgical intervention, whereas a minimal postoperative healing period of at least 8 days should be respected. Causes for delay of intervention are to be documented. Application of radiotherapy defines group 1 versus the non irradiated group (group 2).
Surgical treatment The primary is considered radically resected if macroscopic and histologic evaluation approved resection margins without tumor residuals (R0 status). For surgical proceeding a safety margin of at least 1cm is established. For surgical considerations of lymph node resection the tumor localization is divided in level I (below occlusional plane) and level II (above occlusional plane) respecting pre-, postcanine or retromolar finding in addition. Classification of cervical regions follows the recommendations of Robbins from 2002. Hence, the neck is divided into 6 different sections.
Ipsilateral N0 state of cervical lymph nodes Pre- and postcanine localized tumors of level I require a selective neck dissection of the cervical level 1-3. In level I tumours of the retromolar triangle selective neck dissection of ipsilateral level 1-5 is proceeded. In level II tumors no selective neck dissection is considered.
Contralateral N0 state No neck dissection is performed Ipsilateral N1- N2 state For retromolar localized level I tumors a modified radical neck dissection is performed. If the tumor is localized pre- or postcanine intraoperative frozen sections of level 1 lymph nodes are evaluated. Positive intraoperative results lead to modified radical resection of level 1-5 lymph nodes. In case of negative results resection of the lymph nodes within level 1-3 is affiliated. Negative instantaneous sections in level II tumors require no lymph node dissection. All metastatic affection of level II-III lymph nodes necessitates modified radical neck dissection.
Contralateral N1-N2 state Instantaneous section is performed for level 1 lymph nodes. Modified radical neck dissection is performed in positive, resection of level 1-3 lymph nodes is conducted in negative results. Metastases spread in level 2-3 lymph nodes acquire modified radical neck dissection.
Lymph node therapy of midline tumors Midline tumors may require bilateral resection of lymph node echelons at risk. Bilateral modified neck dissection is performed for staging purposes if indicated. Contralateral lymph node dissection of the level 1-3 in precanine localized tumors is mandatory.
Technical conditions and practical execution of radiation therapy Radiotherapy is performed by photons of 4 to10 MeV or/and electrons of 6 to 15 MeV maximum energy. Individual 3 dimensional dose distribution calculation is mandatory and has to be made on the basis of a postoperative native computer tomogram. All patients are to be treated while immobilized by a custom made face mask made of thermoplast or equivalent. Clinical target volume definition compasses the original tumor site with a safety margin of 2 cm in each direction.
Floor of mouth, anterior tongue Irradiation of the anterior two third of the tongue as well as the anterior floor of mouth is irradiated by lateral opposing beams, while the maxilla is separated by insertion of a bite block.
Oropharynx, buccal plane, soft palate confined to one side For tumors of the buccal plane, the tonsilla, the soft palate and the retromolar triangle two types of planning target volume may be applied.
In case of negative contralateral cervical nodes an ipsilateral target volume for the primary is defined including the lymph nodes of group IB, IIA and IIB. Irradiation technique recommended is a two wedge fields typically angulated by 90 to 120 degrees. The ipsilateral node levels III-V are treated by an anterior portal down to clavicle. The contralateral neck is spared.
Tumors of the lateral and dorsal pharyngeal wall and their lymphatic drainage (levels II, III, IV and V) are irradiated bilaterally with opposing beams. Irrespective of technique used 3 D conformal dose shaping is highly recommended.
Dosage and fractionation Target volume definition and dosage has to be performed according to the rules of ICRU report 50. At the primary tumor site and at involved lymph node levels a total dose of 59.4 Gy in 33 fractions within 45 days is scheduled. At electively irradiated volumes a total dose of 50.4 Gy in 28 fractions is scheduled. All fractions of 1.8 Gy each are given five times per week. In case of machine break down an additional fraction per week is recommended with an at least 6 h interval between two fractions on the same day or on Saturday. Total treatment duration (including planned/unplanned interruptions) is to be documented in days. Any patient must be available for intent to treat analysis.
Instead of the classical portal arrangements and dose distributions intensity modulated radiotherapy using an inverse calculation algorithm may be used in experienced centers. Dose constraints for normal tissues are at the discretion of the participating centers. Dose specification according to the RTOG protocol H 0022 is recommended. Details are given in a standard operation procedure.
Follow-Up Recruitment phase will be 4 years with physical examination, ECOG index, and quality of life questionnaire will be performed 3, 6 and 12 months after end of radiation. Further follow up will be performed annually up to 5 years to obtain sufficient clinical data.
Randomization and Sample Size The present study setup consists of a two armed randomized controlled trial (RCT) as primary study aim. Patients rejecting their participation to a randomized approach and preference to a certain procedure (radiation/no radiation) will be included into a prospective observational study after given informed consent. This parallel constructed observational trial will be performed with a maximum of consistency to treatment and observation compared to the RCT. In case of positive attendance the patients will be randomized, stratified by the criteria of adequate lymph node therapy (yes/no) as formulated by the DOESAK. Randomization to both groups (radiation group/control group) will be 1 to1. Patients will be recruited over a period of 4 years and follow-up will be annually until the trial ends, i.e. at least for 5 years for each patient. Sample size calculation will be performed for the two-sided log rank test at a significance level of 5%. Assuming an exponential distributed survival with survival probabilities after 5 years of 45% within the control group and of 55% within the radiation group (results observed from the DOESAK collective) and a drop-out rate of 5% per year, 280 patients per group are required to detect a significant difference in overall survival with a power of 70%. In case of impaired patient recruitment within the randomized trial, it is intended to recruit at least 280 patients per group in the observational study.
Analysis of RCT and observational trial
Initiation of this trial is only arguable with a realistic chance of statistical evaluation of an adequate count of randomized patients. Hence an intermediate assessment of attendance to randomization will be performed after the first and the second year of recruitment. If less than 5% of patients agreed to randomization within the first and 10% within the second year RCT will be stopped and the study is continued solely as observational trial (see table 1). Intermediate assessment is performed with presumption of accelerating involvement to achieve a minimum of 20% randomized patients after the recruitment phase. As consequence to the study design two different collectives (randomized collective/ collective with preferred form of therapy) will exist. The following scenarios of analysis are possible:
Outcome measurements Primary clinical endpoint Overall survival Secondary clinical endpoints Incidence of tumor relapse
Overall survival will be evaluated in a Cox proportional hazard model with treatment and adequate lymph node therapy (yes/no) as covariates. Further covariates may be considered if they affect survival.
|Study Type ICMJE||Interventional|
|Study Phase||Phase 3|
|Study Design ICMJE||Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
|Intervention ICMJE||Radiation: Radiation therapy
Patients receive radiation within 6 weeks after surgery. At primary tumour site and involved lymph node level a total dose of 59.4 Gy in 33 fractions within 45 days is scheduled according to the rules of ICRU report 50.
|Publications *||Moergel M, Jahn-Eimermacher A, Krummenauer F, Reichert TE, Wagner W, Wendt TG, Werner JA, Al-Nawas B. Effectiveness of adjuvant radiotherapy in patients with oropharyngeal and floor of mouth squamous cell carcinoma and concomitant histological verification of singular ipsilateral cervical lymph node metastasis (pN1-state)--a prospective multicenter randomized controlled clinical trial using a comprehensive cohort design. Trials. 2009 Dec 23;10:118. doi: 10.1186/1745-6215-10-118.|
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
|Recruitment Status ICMJE||Recruiting|
|Estimated Enrollment ICMJE||560|
|Estimated Completion Date||December 2018|
|Estimated Primary Completion Date||December 2013 (Final data collection date for primary outcome measure)|
|Eligibility Criteria ICMJE||
|Ages||18 Years and older (Adult, Senior)|
|Accepts Healthy Volunteers||No|
|Listed Location Countries ICMJE||Germany, Netherlands, Switzerland|
|Removed Location Countries|
|NCT Number ICMJE||NCT00964977|
|Other Study ID Numbers ICMJE||DOESAK-pN1-108399|
|Has Data Monitoring Committee||Yes|
|U.S. FDA-regulated Product||Not Provided|
|IPD Sharing Statement||Not Provided|
|Responsible Party||Prof. Dr. Dr. Wilfried Wagner, Johannes Gutenberg University Mainz|
|Study Sponsor ICMJE||Johannes Gutenberg University Mainz|
|Collaborators ICMJE||Deutsche Krebshilfe e.V., Bonn (Germany)|
|PRS Account||Johannes Gutenberg University Mainz|
|Verification Date||November 2012|
ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP