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Head and Neck CancerNCT07066878

This Protocol Focuses on the Factors That Influence Survival, the Development of Complications and the Quality of Life Based on the Treatment Received in the Group of Patients Suffering From Malignant Lesions of the Head and Neck

An observational study of Head and Neck Cancer, run by IRCCS San Raffaele at 1 site in Italy.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

This protocol focuses on a retrospective, single-center analysis, analyzing the factors that influence survival as the main objective, and secondarily the development of complications and the quality of life based on the treatment received in the group of patients suffering from malignant lesions of the head and neck. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Head and Neck Cancer
What is being tested?
treatment received in the group of patients suffering from malignant lesions of the head and neck.
Type of treatment
Surgery or procedure
How many people
400 participants
Where
1 siteItaly
Study dates
1 May 2026to 20 Jun 2028
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: The study population consists of patients who have been diagnosed with a malignant lesion of the head and neck district (specifically at the level of the oral cavity, oropharynx, larynx, hypopharynx or parotid gland) and underwent treatment with curative purpose (specifically the treatment may be surgical alone, surgical followed by radiotherapy treatment and possible chemotherapy, or radiotherapy, in possible association with chemotherapy in an upfront setting).

Who may be able to join

  • Participant is willing and able to provide informed consent for study participation
  • Age 18 years or older
  • Histological diagnosis of head and neck cancer (any site, any histology)
  • Treatment (surgical and/or radiotherapy and/or medical) received at San Raffaele Hospital between January 2014 and January 2024
  • Consent for use of personal data for scientific purposes

Who cannot join

  • Age under 18 years
  • No histological diagnosis of head and neck cancer
  • Treatment not performed at San Raffaele Hospital (surgical and/or radiotherapy and/or medical)
  • Lack of signed consent for use of personal data for scientific purposes
  • Severe comorbidities interfering with study participation or treatment protocols
  • Inability to understand or provide informed consent due to cognitive or psychiatric disorders
  • Concurrent participation in another clinical trial that may interfere with study outcomes

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Italy1 site
  • Ospedale San Raffaele

    Milan

Other trials in Italy

About this study

Official title: Survival, Complications and Quality of Life in Patients Affected by Head and Neck Cancer: a Retrospective Analysis

This protocol focuses on a retrospective, single-center analysis, analyzing the factors that influence survival as the main objective, and secondarily the development of complications and the quality of life based on the treatment received in the group of patients suffering from malignant lesions of the head and neck.

Read the detailed description

Head and neck cancers (HNCs) comprise a heterogeneous group of malignancies arising from the mucosal epithelium of the upper aerodigestive tract, including the oral cavity, pharynx (nasopharynx, oropharynx, and hypopharynx), and larynx. These tumors are predominantly squamous cell carcinomas (HNSCC), although salivary gland malignancies and other histologic subtypes such as neuroendocrine tumors or sarcomas are also included in this anatomical classification. Globally, HNCs account for nearly 900,000 new cases and over 400,000 deaths annually, representing a significant burden in both high- and low-income countries.

Over the past decades, improvements in diagnostic imaging (e.g., PET/CT, MRI), surgical techniques (including transoral robotic surgery [TORS] and transoral laser microsurgery [TLM]), radiotherapy modalities (e.g., intensity-modulated radiotherapy [IMRT]), and systemic therapies (platinum-based chemotherapy, targeted agents such as cetuximab, and, more recently, immune checkpoint inhibitors like nivolumab and pembrolizumab) have reshaped the therapeutic landscape. Nevertheless, survival outcomes remain highly variable and largely dependent on tumor site, T and N classification, extranodal extension (ENE), perineural and lymphovascular invasion, margin status, HPV status (particularly in oropharyngeal carcinomas), and patient-related factors such as age, performance status, and comorbidities.

For early-stage tumors (Stage I-II), single-modality treatment-typically surgery or radiotherapy-achieves excellent oncologic outcomes with 5-year overall survival (OS) rates ranging from 70% to 90%. In contrast, patients with locally advanced disease (Stage III-IVB), particularly with hypopharyngeal or advanced laryngeal tumors, face significantly worse prognoses, with 5-year OS rates often below 40%, despite aggressive multimodality treatment. A notable exception is HPV-positive oropharyngeal squamous cell carcinoma (OPSCC), which exhibits favorable biology and enhanced responsiveness to chemoradiation, leading to OS rates exceeding 80-90%, even in advanced stages.

Treatment planning must balance oncologic control with functional preservation. While surgical resection (with or without microvascular reconstruction) remains a mainstay for many subsites, organ-preservation protocols based on concurrent chemoradiotherapy are often preferred for tumors of the oropharynx, hypopharynx, and larynx, particularly in functionally critical areas. However, definitive chemoradiation is associated with substantial acute and late toxicities, including mucositis, dysphagia, xerostomia, aspiration, and long-term dependence on feeding tubes or tracheostomy, which may severely impact health-related quality of life (HRQoL).

In this context, robust comparative analyses of different treatment modalities-taking into account tumor subsite, stage, treatment-related morbidity, complications (e.g., graded by the Clavien-Dindo classification), and validated patient-reported outcome measures such as the EORTC QLQ-H\&N35 and the FACT-H\&N-are critical for guiding evidence-based, patient-centered care. Understanding the oncologic efficacy, complication profile, and quality of life outcomes across treatment strategies is essential to inform multidisciplinary decision-making and optimize long-term survivorship.

Being tested
treatment received in the group of patients suffering from malignant lesions of the head and neck.
Medical subject headings
Head and Neck Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • treatment received in the group of patients suffering from malignant lesions of the head and neck.Procedure or surgery

    This protocol focuses on a retrospective, single-center analysis, analyzing the factors that influence survival as the main objective, and secondarily the development of complications and the quality of life based on the treatment received in the group of patients suffering from malignant lesions of the head and neck.

Study groups in NCT07066878
Study groupRoleWhat they receive
Oral cavity cancer patientsNot described
Receives: Procedure: treatment received in the group of patients suffering from malignant lesions of the head and neck.
Oropharyngeal cancer patiensNot described
Receives: Procedure: treatment received in the group of patients suffering from malignant lesions of the head and neck.
Laryngeal/Hypopharyngeal cancer patientsNot described
Receives: Procedure: treatment received in the group of patients suffering from malignant lesions of the head and neck.
Major salivary glands cancer patientsNot described
Receives: Procedure: treatment received in the group of patients suffering from malignant lesions of the head and neck.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Overall Survival (OS) in Patients with Head and Neck Malignancies Treated with Curative Intent

    To assess overall survival in patients with malignant lesions of the head and neck (oral cavity, oropharynx, hypopharynx, larynx) undergoing curative treatment. Treatment modalities include major oncological surgery (alone or followed by adjuvant radiotherapy ± chemotherapy), definitive radiotherapy, definitive chemoradiotherapy, or induction chemotherapy followed by surgery or radiotherapy.

    Time Frame: 5 years from treatment initiation

    Unit of Measure: Time (months)

    Measured: 5 years

Secondary outcomes (1)
  1. Incidence and Severity of Treatment-Related Complications Classified by Clavien-Dindo Scale

    To evaluate postoperative and post-therapy complications related to surgery, radiotherapy, and chemotherapy. Complications include hemorrhage, wound dehiscence, pharyngocutaneous fistula, flap necrosis, radiodermatitis, xerostomia, mucositis, cytopenia, sepsis, and organ dysfunction.

    Classification: Clavien-Dindo Classification of Surgical Complications (Grade I to V; higher grades indicate more severe complications)

    Time Frame: Assessed short-term (≤30 days) and medium-term (up to 12 months) post-treatment, with overall follow-up to 5 years

    Unit of Measure: Clavien-Dindo Grade (Ordinal scale: Grade I [minor] to Grade V [death])

    Measured: 5 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Jul 2025
  2. Study start1 May 2026 (estimated)
  3. Primary completion1 Jun 2027 (estimated)
  4. Study completion20 Jun 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Retrospective
Enrolment
400 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07066878
Sponsor's protocol ID
RETRO-HN
Status last verified
Jun 2025
First submitted
21 Jun 2025
Last updated
15 Jul 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Head and Neck Cancer, run by IRCCS San Raffaele at 1 site in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 15 Jul 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Andrea Galli (+390226438446, salerno.emilio@hsr.it), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Overall Survival (OS) in Patients with Head and Neck Malignancies Treated with Curative Intent (time frame: 5 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Jul 2025.

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