- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07578727
A Multicenter, Prospective, Phase III Clinical Study of Proton Intensity-modulated Radiotherapy Versus Photon Intensity-modulated Radiotherapy for Untreated Non-metastatic Nasopharyngeal Carcinoma
연구 개요
상태
정황
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
등록 (추정된)
단계
- 해당 없음
연락처 및 위치
연구 연락처
- 이름: Taize Yuan
- 전화번호: 8620-32506195
- 이메일: taize.yuan@ccm.cn
참여기준
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
설명
Inclusion Criteria:
- 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.
Exclusion Criteria:
- 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.
공부 계획
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
|
공동 작업자 및 조사자
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .
비인두 암종(NPC)에 대한 임상 시험
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Sun Yat-sen University모병
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