NCT04688528Recruiting
Dose De-escalation and Sentinel LN Mapping Driven Radiotherapy of Contralateral Neck in Ipsilateral Node Positive HNSCC
A Prospective Randomized Phase 2 Study of Dose and Volume De-escalation Radiotherapy With Sentinel Lymph Nodes Mapping for Contralateral Irradiation in Unilaterally Node Positive Head and Neck Squamous Cell Carcinomas (SEMIRAHN)
Source: ClinicalTrials.gov · Last updated 1 Jul 2024 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
The study involves head and neck squamous cell carcinomas (HNSCC) of the oral cavity, oropharynx, larynx or hypopharynx with positive nodes on only one side of the neck and no distant metastasis treated by primary (chemo)radiotherapy. The elective node irradiation on the contralateral side is not always mandatory and the dose may be too high. In this study, we evaluate two strategies: the impact of sentinel lymph node mapping to tailor the volumes to irradiate and the dose reduction.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 147 (estimated)
- First submitted
- 18 Dec 2020
- Start date
- 10 Jun 2021
- Primary completion date
- Jan 2027
- Lead sponsor
- Universitaire Ziekenhuizen KU Leuven
- Diseases
- Head and neck cancer
- NCT number
- NCT04688528
What you commit to
- Study type: Interventional
- Planned participants: 147
- From 10 Jun 2021 to the primary completion date, Jan 2027
- 10 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Patient has history of:
- radiotherapy or surgery in the neck with potential impact on lymphatic drainage ("violated neck");
- cancer in the last five years (excluding skin basal cell carcinoma, in situ cervix carcinoma and T1 of glottis or lip, completely chirurgically resected (R0) without intervention disturbing cervical lymph drainage);
- Absolute contra-indication to iodine contrast injection, even after proper cortisone and cetirizine pre-medication.
- Synchronous second malignancy.
- Any psychological disorder or familial, sociological or geographical condition which, in the investigator's opinion, might jeopardise participant's safety or compliance with the protocol.
- Female who is pregnant, breast-feeding or intends to become pregnant or is of child-bearing potential and not using an adequate contraceptive method.
- Highly effective methods of birth control are defined as those, alone or in combination, that result in a low failure rate (i.e., less than 1% per year) when used consistently and correctly; such as implants, injectables, combined oral contraceptives, some IUDs, true sexual abstinence (i.e. refraining from heterosexual intercourse during the entire period of risk associated with the Trial treatments) or vasectomised partner.
Other
- HNSCC from nose, sinuses, oesophagus, salivary glands or nasopharynx.
- Non-HNSCC histology.
- Positive contralateral neck by node size or positive US-FNAC in dubious nodes.
- Distant metastasis.
- Tumor crossing the midline without contralateral mapping after 99mTc-nanocolloïd injection.
- Tumor too large to be safely injected, as deemed by the surgeon. In case of doubt, contact may always be taken with the national coordinating investigator to discuss the situation and take a final decision.
Who the study is looking for
- Written informed consent given according to ICH/GCP and national/local regulations must be obtained prior to any screening procedures.
- World Health Organization (WHO) performance status 0-1.
- Age ≥ 18 years.
- Patients with a pathologically proven invasive HNSCC, including oral cavity, oropharynx (independently of HPV status), larynx or hypopharynx.
- Decision by Multidisciplinary Tumor Board of primary treatment with radical radiotherapy with or without concurrent chemotherapy (according to the local guidelines).
- Baseline imaging of the neck:
- ≤ 2.5 mm slices CT with iodine injection (independently or during the FDG-PET/CT examination IF acquired in normal diagnostic conditions, i.e. arms along the thorax with diagnostic quality);
- MRI not mandatory but allowed, performed according to centres guidelines;
- FDG-PET/CT.
- Tumor characteristics:
- cT-classification (8th TNM staging): T1(except T1 of glottis)-T4a (or, for p16+ oropharyngeal tumors classified cT4, if criteria are compatible with cT4a-stage of p16- tumors).
- cN-classification (8th TNM staging), as assessed by iodine contrasted CT (or MRI) and FDG-PET:
- i. mandatorily cN0 contralaterally to the primary tumor (or on one side of the neck for midline primary tumors):
- 1\. smallest diameter \< 5 mm in retropharyngeal level (VIIa);
- 2\. smallest diameter of Küttner node (level IIa) \< 12 mm;
- 3\. smallest diameter \< 10 mm or sum of smallest and largest diameters \< 17 mm in any other level;
- 4\. no central necrosis ;
- 5\. maximal standardized uptake value (SUVmax) ≤ 2.2;
- 6\. in dubious cases (typically 2.2 \< SUVmax \< 4.5 and inconclusive CT or MRI), US-guided FNAC may be required to exclude positive node contralaterally.
- ii. ipsilaterally positive (if any of the above mentioned criteria is met), i.e. cN1, cN2a, cN2b, ipsilateral cN3b; or cN1 for oropharyngeal p16+ tumors.
- No distant metastasis.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (10)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| OLV Aalst Coordinator of this site? Confirm its status | Aalst | Belgium | Recruiting |
| Institute Jules Bordet Coordinator of this site? Confirm its status | Brussels | Belgium | Recruiting |
| UCL - Saint Luc Coordinator of this site? Confirm its status | Brussels | Belgium | Recruiting |
| ZOL Coordinator of this site? Confirm its status | Genk | Belgium | Recruiting |
| University Hospital Gent Coordinator of this site? Confirm its status | Ghent | Belgium | Recruiting |
| JESSA Ziekenhuis Coordinator of this site? Confirm its status | Hasselt | Belgium | Recruiting |
| Universitaire Ziekenhuizen Leuven Coordinator of this site? Confirm its status | Leuven | Belgium | Recruiting |
| AZ Sint Maarten Coordinator of this site? Confirm its status | Mechelen | Belgium | Recruiting |
| CHU UCL Namur Coordinator of this site? Confirm its status | Namur | Belgium | Recruiting |
| AZ Turnhout Coordinator of this site? Confirm its status | Turnhout | Belgium | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.