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Nasopharyngeal Carcinoma (NPC)NCT07578727

A Multicenter, Prospective, Phase III Clinical Study of Proton Intensity-modulated Radiotherapy Versus Photon Intensity-modulated Radiotherapy for Untreated Non-metastatic Nasopharyngeal Carcinoma

A study testing Proton Therapy System (ProBeam) and Photon Therapy System (TrueBeam) in people with Nasopharyngeal Carcinoma (NPC), run by Guangzhou Concord Cancer Center at 2 sites in China.

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

Proton therapy for nasopharyngeal carcinoma can reduce radiotherapy-related toxic reactions, and some retrospective studies have found that proton therapy improves the survival of patients with nasopharyngeal carcinoma. However, high-level prospective clinical evidence is still lacking. Read more about this study

Who is it for?
Ages 18 to 70 years
Conditions the study is for
Nasopharyngeal Carcinoma (NPC)
What is being tested?
Proton Therapy System (ProBeam) and Photon Therapy System (TrueBeam)
Type of treatment
Surgery or procedure
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
504 participants
Where
2 sitesChina
Study dates
1 Jul 2026to 30 Dec 2028
Phase
Interventional
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 to 70 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Diagnosed by histology and/or cytology as non-keratinizing carcinoma of the nasopharynx (differentiated or undifferentiated type, i.e., WHO type II or III).
  • Clinical stage: T1-4N0-3M0, I-III stage (AJCC 9th edition).
  • Age: ≥ 18 years old, ≤ 70 years old.
  • Gender: No restrictions.
  • ECOG ≤ 1.
  • Good organ function:
  • Normal bone marrow function: WBC ≥ 4×109/L, Platelet ≥ 100×109/L, HGB ≥ 90g/L Total bilirubin, AST, ALT ≤ 2.0× upper limit of normal value; Creatinine clearance rate ≥ 60ml/min or Creatinine ≤ 1.5× upper limit of normal value.
  • The patient has signed the informed consent form and is willing and able to comply with the study visit schedule, treatment plan, laboratory tests and other research procedures.

Who cannot join

  • The patient has a poor general condition and is in a state of poor health; or the patient has already experienced metastasis.
  • The patient has an uncontrolled severe infectious disease.
  • The patient has severe diseases or complications in the heart, lungs, liver, kidneys or other systems, and the investigator judges that they cannot complete the clinical trial.
  • There are implants such as artificial ears or dentures within the radiotherapy range, and the investigator judges that they are not suitable for proton therapy.
  • The patient has a history of radiotherapy in the head and neck region.
  • The patient has mental illness, drug abuse or alcohol dependence.

Trial locations and contacts

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

China2 sites
  • Varian Probeam

    Guangzhou, Guangdong

  • Varian Probeam

    Guangzhou, Guangdong

    Yuan Taize, 86-13512786950, Taize.yuan@ccm.cn

Other trials in China

About this study

Proton therapy for nasopharyngeal carcinoma can reduce radiotherapy-related toxic reactions, and some retrospective studies have found that proton therapy improves the survival of patients with nasopharyngeal carcinoma. However, high-level prospective clinical evidence is still lacking. This study aims to investigate the efficacy and side effects of proton therapy compared with photon intensity-modulated radiotherapy for nasopharyngeal carcinoma through a multicenter, prospective, phase III clinical trial, providing more high-quality evidence-based medical evidence for proton therapy of nasopharyngeal carcinoma.

Read the detailed description

Nasopharyngeal carcinoma (NPC) is a common malignant tumor of the head and neck. The incidence of nasopharyngeal carcinoma is high in China, accounting for 47% of cases worldwide, and the incidence in southern China is 20 times the global rate. Among these, the incidence in Guangdong is one of the highest in the world, which is why nasopharyngeal carcinoma is also referred to as the 'Guangdong tumor'. Because the growth site of nasopharyngeal carcinoma is adjacent to the base of the skull, it easily invades the skull base. Its pathology is mainly moderately to poorly differentiated squamous cell carcinoma, which is sensitive to radiation; therefore, radiotherapy is the first-choice treatment for nasopharyngeal carcinoma.

In recent years, with the widespread application of intensity-modulated radiotherapy (IMRT) technology and the development of targeted therapy and immunotherapy, the 5-year survival rate of patients with nasopharyngeal carcinoma has exceeded 80%, and many patients survive long-term. Therefore, while further attention is paid to improving efficacy, it is even more important to focus on the long-term quality of life of nasopharyngeal carcinoma patients. Due to the dosimetric limitations of conventional photon radiotherapy, patients treated with IMRT often experience some late complications that seriously affect quality of life, such as dry mouth, restricted mouth opening, radiation-induced caries, radiation-induced cranial nerve injury, brain injury, spinal cord injury, and pituitary dysfunction. In addition, due to the large area of low-dose irradiation, the incidence of second primary tumors in the head and neck caused by radiotherapy is approximately 0.5-3%.

Proton therapy is a new technology that uses the unique 'Bragg peak' characteristic of proton beams to treat tumors, and it has been widely applied in many developed countries in Europe and America. Photon beams gradually lose energy after penetrating to a certain depth in the human body. By the time they reach the lesion, the dose intensity has already significantly decreased, while surrounding normal tissues (OARs) such as the brainstem, spinal cord, salivary glands, and skin are exposed to relatively high doses of radiation, leading to radiotherapy side effects. In contrast, proton therapy, due to its special 'Bragg peak' characteristic, maintains a roughly stable dose after entering the body, then increases and reaches a peak to release all its energy when irradiating the lesion, achieving a 'targeted blast' on the tumor, and rapidly decreases after passing through the lesion, resulting in minimal radiation to the surrounding normal tissues and thus reducing the occurrence of long-term adverse reactions. An early study explored the clinical outcomes of 17 T4 stage NPC patients treated with a combination of proton and photon therapy. At three years, patients had a local control (LC) rate of 92%, disease-free survival rate of 75%, and overall survival (OS) rate of 74%. Late toxic reactions included one patient with temporal lobe imaging changes, one patient with mandibular radiation osteonecrosis, and two patients with endocrine dysfunction. Researchers indicated that combined proton and photon therapy could achieve good local control in T4 NPC patients, regardless of whether chemotherapy was also used. A case-control study on NPC patients published in 2015 showed that 20% of patients receiving intensity-modulated proton therapy (IMPT) required gastric tube insertion, while 65% of patients receiving intensity-modulated radiation therapy (IMRT) with photons required it. Additionally, the incidence of vomiting, nausea, gastrointestinal, and other radiotherapy side effects in the IMPT group was much lower than in the IMRT group.The Trento Proton Therapy Center in Italy published in 2019 the efficacy and toxicity of proton plus photon radiotherapy for locally advanced NPC. The study included 17 previously untreated patients with stage III-IVa NPC, who received photon radiotherapy with dose-escalated proton therapy combined with concurrent chemotherapy. The results showed 2-year, 5-year, and 10-year local recurrence-free rates of 94%, 86%, and 86%, respectively. Regarding acute toxicities, one patient required parenteral nutrition due to difficulty swallowing (16% weight loss) and was hospitalized for a short period (10 days). Two other patients experienced treatment interruptions of 5 and 6 days due to acute mucositis and having to undergo tympanostomy for otitis media. Regarding late toxicities, six patients showed temporal lobe necrosis on brain MRI, and one of them developed corresponding symptoms. A 2023 study on the use of photon and proton radiotherapy in definitive treatment of nasopharyngeal carcinoma included 80 non-metastatic NPC patients treated at their institution from 2012 to 2022; 48 received photon radiotherapy, and 32 received proton therapy. The photon and proton cohorts were compared. The median follow-up was 30 months. The results showed that the 2-year progression-free survival was 63.9% in the photon group and 90.3% in the proton group; the 2-year overall survival was 86.8% in the photon group and as high as 96.8% in the proton group. A 2025 retrospective study from Taiwan, China showed that compared with intensity-modulated photon radiotherapy, proton therapy improved survival in patients with nasopharyngeal carcinoma.

Being tested
Proton Therapy System (ProBeam), Photon Therapy System (TrueBeam)
Keywords
proton therapy, nasopharyngeal carcinoma
Medical subject headings
Nasopharyngeal Carcinoma

What participants receive

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

  • Proton Therapy System (ProBeam)Radiation

    Treatment planning and target delineation: All patients were in the supine position with the head extended backward, with the mask fixed, and enhanced computed tomography (CT) scans were performed for positioning. The slice thickness was 1.25mm. The gross tumor volume (GTV) included the recurrent primary lesion. The clinical target volume (CTV) included the anatomical expansion of the tumor and the suspicious lesions visible under the microscope. CTV specific delineation refers to the Chinese Nasopharyngeal Carcinoma Radiotherapy Guidelines (2022 edition).Radiation dose and treatment plan: The prescribed dose was 70 Gray (Gy) delivered in 33 fractions. Physicists design intensity-modulated proton therapy plans according to the physician's requirements. After the radiotherapy plan was designed, it was evaluated and repeatedly optimized by the physician and the physicist until satisfactory results were achieved. Treatment: was required for each treatment session.

  • Photon Therapy System (TrueBeam)Radiation

    Treatment planning and target delineation: All patients were in the supine position with the head extended backward, with the mask fixed, and enhanced computed tomography (CT) scans were performed for positioning. The slice thickness was 1.25mm. The gross tumor volume (GTV) included the recurrent primary lesion. The clinical target volume (CTV) included the anatomical expansion of the tumor and the suspicious lesions visible under the microscope. CTV specific delineation refers to the Chinese Nasopharyngeal Carcinoma Radiotherapy Guidelines (2022 edition).Radiation dose and treatment plan: The prescribed dose was 70 Gray (Gy) delivered in 33 fractions. Physicists design intensity-modulated photon therapy plans according to the physician's requirements. After the radiotherapy plan was designed, it was evaluated and repeatedly optimized by the physician and the physicist until satisfactory results were achieved. Treatment: was required for each treatment session.

Study groups in NCT07578727
Study groupRoleWhat they receive
Proton therapy groupExperimentalAll patients received proton therapy, with a prescribed dose of 70Gy in 33 fractions, 5 days per week, for a total of 6.5 weeks.
Receives: Radiation: Proton Therapy System (ProBeam)
Photon therapy groupPlacebo comparatorAll patients received photon therapy, with a prescribed dose of 70Gy in 33 fractions, 5 days per week, for a total of 6.5 weeks.
Receives: Radiation: Photon Therapy System (TrueBeam)

What is being measured

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

  1. 3-year progression-free survival time

    Defined as the time interval from the start of treatment to tumor progression or death for any reason; if there is no tumor progression, it is until the time of the last follow-up.

    Measured: From enrollment to the three-year follow-up period

  2. Incidence of severe oral mucositis

    Grade III or higher oral mucositis occurring during radiotherapy

    Measured: during radiotherapy

Secondary outcomes (5)
  1. Overall survival time

    Defined as the time interval from the start of treatment to death from any cause; if no death occurs, it is until the date of the last follow-up.

    Measured: From enrollment to the three-year follow-up period

  2. Distance-free metastasis-free survival time (DMFS)

    The definition is the time interval from the start of treatment to the occurrence of distant metastasis. If there is no distant metastasis, it is the time until the last follow-up.

    Measured: From enrollment to the three-year follow-up period

  3. No local region recurrence-free survival time (LRFS)

    It is defined as the time interval from the start of treatment to the occurrence of local regional recurrence. If there is no local regional recurrence, it is the time until the last follow-up.

    Measured: From enrollment to the three-year follow-up period

  4. Incidence of severe late complications

    The proportion of subjects whose toxicity reaction is level 3 during the clinical trial period. The researchers record AE that appeared during the clinical trial cycle and grade it according to Common Terminology Criteria for Adverse Events (CTCAE) version 5.0.

    Measured: From enrollment to the three-year follow-up period

  5. Short-term treatment responses

    The proportion of patients who achieved treatment response at the end of neoadjuvant chemotherapy and 3 months after the radiotherapy to evaluate the short-term therapeutic effect. Treatment response will be assessed according to the The Response Evaluation Criteria in Solid Tumors (RECIST) criteria, and categorized as Complete Response (CR), Partial Response (PR), Stable Disease (SD), or Progressive Disease (PD).

    Measured: From enrollment to the three-month follow-up period

Timeline

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

  1. First posted11 May 2026
  2. Study start1 Jul 2026 (estimated)
  3. Primary completion30 Dec 2028 (estimated)
  4. Study completion30 Dec 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
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Non-randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
504 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07578727
Sponsor's protocol ID
2026-IIT-003
Status last verified
Jul 2026
First submitted
5 May 2026
Last updated
8 Jul 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Proton Therapy System (ProBeam) and Photon Therapy System (TrueBeam) in people with Nasopharyngeal Carcinoma (NPC), run by Guangzhou Concord Cancer Center at 2 sites in China.

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 8 inclusion and 6 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 8 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in China. 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. Some participants in this study may receive a placebo. 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 Taize Yuan (8620-32506195, taize.yuan@ccm.cn), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

3-year progression-free survival time (time frame: From enrollment to the three-year follow-up period). The study lists 2 primary outcomes in all. 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 8 Jul 2026.

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