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

2026년 5월 13일 업데이트: Guangzhou Concord Cancer Center
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.

연구 개요

상세 설명

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.

연구 유형

중재적

등록 (추정된)

504

단계

  • 해당 없음

연락처 및 위치

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연구 연락처

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

설명

Inclusion Criteria:

  1. Diagnosed by histology and/or cytology as non-keratinizing carcinoma of the nasopharynx (differentiated or undifferentiated type, i.e., WHO type II or III).
  2. Clinical stage: T1-4N0-3M0, I-III stage (AJCC 9th edition).
  3. Age: ≥ 18 years old, ≤ 70 years old.
  4. Gender: No restrictions.
  5. ECOG ≤ 1.
  6. 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.

  7. 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.

Exclusion Criteria:

  1. The patient has a poor general condition and is in a state of poor health; or the patient has already experienced metastasis.
  2. The patient has an uncontrolled severe infectious disease.
  3. 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.
  4. 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.
  5. The patient has a history of radiotherapy in the head and neck region.
  6. The patient has mental illness, drug abuse or alcohol dependence.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위화되지 않음
  • 중재 모델: 병렬 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Proton therapy group
All patients received proton therapy, with a prescribed dose of 70Gy in 33 fractions, 5 days per week, for a total of 6.5 weeks.
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.
위약 비교기: Photon therapy group
All patients received photon therapy, with a prescribed dose of 70Gy in 33 fractions, 5 days per week, for a total of 6.5 weeks.
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.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
3-year progression-free survival time
기간: From enrollment to the three-year follow-up period
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.
From enrollment to the three-year follow-up period

2차 결과 측정

결과 측정
측정값 설명
기간
심각한 후기 합병증 발생률
기간: 등록부터 3년 추적 관찰 기간까지
임상 시험 기간 동안 독성 반응이 3단계인 피험자의 비율입니다. 연구자들은 임상 시험 주기 동안 발생한 이상반응(AE)을 기록하고, 이를 Common Terminology Criteria for Adverse Events (CTCAE) version 5.0에 따라 등급을 매깁니다.
등록부터 3년 추적 관찰 기간까지
단기 치료 반응
기간: 등록부터 3개월 추적 관찰 기간까지
신보조 화학요법 종료 시점 및 방사선 치료 3개월 후에 치료 반응을 달성한 환자의 비율을 통해 단기 치료 효과를 평가한다. 치료 반응은 고형 종양 반응 평가 기준(RECIST)에 따라 완전 관해(CR), 부분 관해(PR), 질병 안정(SD), 질병 진행(PD)으로 평가 및 분류된다.
등록부터 3개월 추적 관찰 기간까지
Overall survival time
기간: From enrollment to the three-year follow-up period
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.
From enrollment to the three-year follow-up period
Distance-free metastasis-free survival time (DMFS)
기간: From enrollment to the three-year follow-up period
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.
From enrollment to the three-year follow-up period
No local region recurrence-free survival time (LRFS)
기간: From enrollment to the three-year follow-up period
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.
From enrollment to the three-year follow-up period

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연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 5월 1일

기본 완료 (추정된)

2028년 12월 30일

연구 완료 (추정된)

2028년 12월 30일

연구 등록 날짜

최초 제출

2026년 5월 5일

QC 기준을 충족하는 최초 제출

2026년 5월 5일

처음 게시됨 (실제)

2026년 5월 11일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 5월 15일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 5월 13일

마지막으로 확인됨

2026년 5월 1일

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비인두 암종(NPC)에 대한 임상 시험

Proton Therapy System (ProBeam)에 대한 임상 시험

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