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The Neoadjuvant Treatment of Locally Advanced Thoracic Esophageal Squamous Cell Carcinoma

2021년 6월 23일 업데이트: Shen Lin, Peking University

Camrelizumab Combined With Chemotherapy for Neoadjuvant Treatment of Locally Advanced Thoracic Esophageal Squamous Cell Carcinoma:A Phase II Clinical Study to Explore the Relationship Between Biomarkers and Efficacy

This is a randomized, open, two arm phase II clinical study. 40 patients are included in the exploratory study. The dominant population with higher biomarker positive / IO score was identified to provide the basis for the later phase III study. The subjects were randomly divided into the group of camrelizumab combined with paclitaxel and cisplatin or the group of camrelizumab combined with albumin bound paclitaxel and cisplatin according to the ratio of 1:1. The treatment cycle was every 3 weeks. The curative effect was evaluated when the treatment cycle was 2, and the resection of esophageal cancer was considered after 3 cycles. Postoperative adjuvant therapy was based on the patient's condition and surgical results; For patients with R0 resection, postoperative adjuvant treatment is not recommended. For patients with R1 / R2 resection, multi-disciplinary joint discussion and consultation are recommended to propose individualized comprehensive treatment.

연구 개요

연구 유형

중재적

등록 (예상)

40

단계

  • 2 단계

연락처 및 위치

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연구 장소

    • Beijing
      • Beijing, Beijing, 중국, 100142
        • Department of GI Oncology, Peking University Cancer Hospital,

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

18년 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

Inclusion Criteria:

  1. Age: 18-75 years old, male or female;
  2. Esophageal squamous cell carcinoma was confirmed by pathology (except for cervical and Suprathoracic tumors that could not be operated);
  3. Patients with resectable esophageal squamous cell carcinoma with clinical stage T3-T4a or TxN + M0 (except T4b);
  4. ECOG PS score was 0-1;
  5. There was at least one measurable lesion (according to recist1.1) or unmeasurable lesion that could be evaluated, and the imaging diagnosis time was ≤ 21 days;
  6. The expected survival time was more than 3 months;
  7. The function of the main organs was normal, and there were no serious blood, heart, lung, liver, kidney, bone marrow and other functional abnormalities and immunodeficiency diseases. The laboratory examination meets the following requirements:

    1. Hemoglobin (Hb) ≥ 90g / L;
    2. WBC ≥ 3.0 × 109/L; Neutrophil count (NEUT) ≥ 1.5 × 109/L;
    3. Platelet count (PLT) ≥ 100 × 109/L;
    4. Serum creatinine (SCr) ≤ 1.5 times the upper limit of normal (ULN) or creatinine clearance rate ≥ 50 ml / min (Cockcroft Gault formula);
    5. Total bilirubin (TBIL) ≤ 1.5 times the upper limit of normal (ULN);
    6. The levels of AST and ALT were less than 2.5 times the upper limit of normal (ULN);
  8. There was no active bleeding or thrombosis

    1. International normalized ratio INR ≤ 1.5 × ULN;
    2. Partial thromboplastin time APTT ≤ 1.5 × ULN;
    3. Prothrombin time Pt ≤ 1.5ULN;
  9. The patients with normal or mild to moderate abnormal lung function (VC% > 60%, FEV1 > 1.2L, FEV1% > 40%, DLco> 40%) could tolerate esophagectomy;
  10. The fertile female subjects were required to conduct blood pregnancy test within 72 hours before the first administration, and the result was negative, and voluntarily used appropriate contraceptive methods during the observation period and within 90 days after the last administration of the study drug; For men, surgical sterilization or consent to appropriate contraceptive methods during the observation period and within 90 days after the last administration of the study drug should be used.
  11. The subjects voluntarily joined the study and signed the informed consent form (ICF);
  12. The patients with good compliance were expected to follow up the efficacy and adverse events / reactions according to the protocol requirements.

Exclusion Criteria:

  1. Subjects who have received or are receiving additional chemotherapy, radiotherapy, targeted or immunotherapy;
  2. Any active autoimmune disease or history of autoimmune disease (such as interstitial pneumonia, uveitis, enteritis, hepatitis, hypophysitis, vasculitis, myocarditis, nephritis, hyperthyroidism, hypothyroidism (can be included after hormone replacement therapy)); The subjects with childhood asthma who had been completely relieved and did not need any intervention or vitiligo in adulthood could be included, but the subjects who needed bronchodilator for medical intervention could not be included;
  3. Patients with congenital or acquired immune deficiency, such as human immunodeficiency virus (HIV) infection, active hepatitis B (HBV DNA ≥ 500 IU / ml), hepatitis C (HCV antibody positive and HCV-RNA higher than the detection limit of the analytical method), or co infection of hepatitis B and hepatitis C;
  4. Immunosuppressive drugs were used within 14 days before the first use of the study drug, excluding nasal and inhaled corticosteroids or physiological doses of systemic corticosteroids;
  5. Live attenuated vaccine was inoculated within 4 weeks before the first administration or during the study period;
  6. Patients with hypertension who can not be reduced to normal range after antihypertensive drug treatment (systolic blood pressure ≤ 140 mmHg / diastolic blood pressure ≤ 90 mmHg);
  7. Subjects with uncontrollable clinical cardiac symptoms or diseases, such as (1) heart failure of NYHA II or above (2) unstable angina pectoris (3) myocardial infarction within 1 year (4) clinically significant supraventricular or ventricular arrhythmia requiring clinical intervention;
  8. Severe infection (e.g. need for intravenous antibiotics, antifungal or antiviral drugs) occurred within 4 weeks before the first administration, or fever of unknown origin > 38.5% occurred during the screening period / before the first administration;
  9. History of allogeneic organ transplantation or allogeneic hematopoietic stem cell transplantation is known;
  10. Pregnant or lactating women; The fertile subjects were unwilling or unable to take effective contraceptive measures;
  11. Other malignant tumors were found in the past or at the same time, but the cured basal cell carcinoma of skin, carcinoma in situ of cervix and carcinoma in situ of breast were excluded;
  12. Known to have allergic history to the drug components of this protocol;
  13. Other situations considered unsuitable by the researchers.

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: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Camrelizumab+ Paclitaxel+ Cisplatin
The subjects were randomly divided into the group of camrelizumab combined with paclitaxel and cisplatin or the group of camrelizumab combined with albumin bound paclitaxel and cisplatin according to the ratio of 1:1. Esophageal cancer resection was performed after 3 cycles of medication (the researchers decided the follow-up treatment according to the postoperative pathological situation). At the end of the treatment, the patients were followed up for safety and effectiveness.

Camrelizumab: intravenous drip, fixed dose 200 mg, D1, repeated once every 3 weeks.

Paclitaxel: 80 mg / m2, intravenous drip for 180 minutes, D1, D8, repeated every 3 weeks.

Cisplatin: 75 mg / m2, intravenous drip for 120 minutes, D1, repeated every 3 weeks.

실험적: Camrelizumab+ Albumin bound paclitaxel+ Cisplatin
The subjects were randomly divided into the group of camrelizumab combined with paclitaxel and cisplatin or the group of camrelizumab combined with albumin bound paclitaxel and cisplatin according to the ratio of 1:1. Esophageal cancer resection was performed after 3 cycles of medication (the researchers decided the follow-up treatment according to the postoperative pathological situation). At the end of the treatment, the patients were followed up for safety and effectiveness.

Camrelizumab: intravenous drip, fixed dose 200 mg, D1, repeated once every 3 weeks.

Albumin bound paclitaxel: 130 mg / m2, intravenous drip for 30 minutes, D1, D8, repeated every 3 weeks.

Cisplatin: 75 mg / m2, intravenous drip for 120 minutes, D1, repeated every 3 weeks.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
biomarkers related to pCR
기간: 9 weeks
t has a good value in predicting the efficacy of immunotherapy, and is helpful for the accurate formulation of treatment plan and the accurate evaluation of prognosis of patients with esophageal cancer.
9 weeks

2차 결과 측정

결과 측정
측정값 설명
기간
Objective Response Rate
기간: 9 weeks
Assess ORR, defined as Investigator-assessed CR + PR, per RECIST 1.1.
9 weeks
Disease Control Rate
기간: 9 weeks
Percentage of patients with CR/PR/SD in the number of patients that whose tumour can be evaluated.
9 weeks
Disease free survival
기간: Time from randomization to patient's tumor progression or death
The DFS will be defined as the time of patients alive without local recurrence or distant metastasis of disease from the date of the administration of treatment.
Time from randomization to patient's tumor progression or death
Overall Survival
기간: The time from the beginning of randomization to death due to any cause.
OS is defined as the time from registration to death due to any cause, or censored at date last known alive. Measured by the method of Kaplan and Meier
The time from the beginning of randomization to death due to any cause.
Safety
기간: from first treatment to 90 days after esophagectomy
Adverse events
from first treatment to 90 days after esophagectomy

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스폰서

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 (예상)

2021년 7월 1일

기본 완료 (예상)

2022년 9월 1일

연구 완료 (예상)

2022년 12월 1일

연구 등록 날짜

최초 제출

2021년 5월 28일

QC 기준을 충족하는 최초 제출

2021년 6월 23일

처음 게시됨 (실제)

2021년 6월 24일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2021년 6월 24일

QC 기준을 충족하는 마지막 업데이트 제출

2021년 6월 23일

마지막으로 확인됨

2021년 6월 1일

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Camrelizumab+ Paclitaxel+ Cisplatin에 대한 임상 시험

3
구독하다