- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07647068
Autologous Tumor Infiltrating Lymphocytes With Interleukin-2 for the Treatment of Locally Advanced, Recurrent or Metastatic Gastrointestinal Stromal Tumors
A Phase 2 Study to Evaluate the Efficacy and Safety of Adoptive Transfer of Autologous Tumor Infiltrating Lymphocytes in Patients With Unresectable, Recurrent, or Metastatic Gastrointestinal Stromal Tumors
연구 개요
상태
정황
상세 설명
PRIMARY OBJECTIVE:
I. To evaluate the efficacy of a non-myeloablative lymphodepleting preparative regimen followed by infusion of autologous TIL and high-dose aldesleukin in patients with locally advanced, recurrent, or metastatic gastrointestinal stromal tumor (GIST) using the objective response rate (ORR).
SECONDARY OBJECTIVES:
I. To further evaluate the efficacy of this therapy using complete response (CR) rate, duration of response (DOR), disease control rate (DCR), progression-free survival (PFS), and overall survival (OS).
II. To characterize the safety profile of this therapy in patients with locally advanced, recurrent, or metastatic gastrointestinal stromal tumors (GIST).
OUTLINE:
Patients receive cyclophosphamide intravenously (IV) over 2 hours on days -8 and -7, fludarabine IV over 30 minutes on days -6 to -2 and TIL IV over 20-30 minutes on day 0 in the absence of disease progression or unacceptable toxicity. Starting within 24 hours of TIL infusion, patients receive aldesleukin IV over 15 minutes every 8 hours for up to 6 doses on days 0-3 in the absence of disease progression or unacceptable toxicity. Starting on day 1 or day 2, patients may receive filgrastim subcutaneously (SC) until neutrophil count > 1 x 10^9/L for 3 consecutive days or > 5 x 10^9/L. Patients with stable disease, partial response or recurrence may receive a second course of treatment. Patients also undergo chest x-ray at screening and urine and blood sample collection, computed tomography (CT), magnetic resonance imaging (MRI) or positron emission tomography (PET) throughout the study. Additionally, patients may also undergo echocardiography or multigated acquisition scan (MUGA) at screening and may also undergo a second surgery to collect cells on study.
After completion of study treatment, patients are followed up at 4-6 weeks, 12 weeks, every 3 months for 3 visits, then every 6 months up to month 24.
연구 유형
등록 (추정된)
단계
- 2 단계
연락처 및 위치
연구 연락처
- 이름: The Ohio State University Comprehensive Cancer Center
- 전화번호: 1-800-293-5066
- 이메일: OSUCCCClinicaltrials@osumc.edu
연구 장소
-
-
Ohio
-
Columbus, Ohio, 미국, 43210
- Ohio State University Comprehensive Cancer Center
-
수석 연구원:
- Joal Beane, MD
-
연락하다:
- Joal Beane, MD
- 전화번호: 812-453-6178
- 이메일: Joal.Beane@osumc.edu
-
-
참여기준
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
설명
Inclusion Criteria:
- Measurable locally advanced, recurrent, or metastatic GIST
- Patients with locally advanced disease should be unresectable by conventional surgical approaches
- Patients with distant metastatic spread must be refractory to approved standard systemic therapies (such as imatinib and sunitinib) if they are eligible to receive these treatments
- Patients must be co-enrolled on the companion protocol Cell Harvest and Preparation to Support Adoptive Cell Therapy Clinical Protocols and Pre-Clinical Studies (institutional review board [IRB] #2024C0043), and have available TIL cultures for therapy
- Patients with 3 or fewer brain metastases that are less than 1 cm in diameter and asymptomatic are eligible. Lesions that have been treated with stereotactic radiosurgery must be clinically stable for 1 month after treatment for the patient to be eligible. Patients with surgically resected brain metastases are eligible
- Greater than or equal to 18 years of age and less than or equal to age 75
- Able to understand and sign the informed consent document
- Clinical performance status of Eastern Cooperative Oncology Group (ECOG) 0 or 1
- Life expectancy of greater than three months
- Patients of both genders who are of child-bearing potential must be willing to practice birth control from the time of enrollment on this study and for up to four months after receiving the treatment
Serology:
- Seronegative for HIV antibody. (The experimental treatment being evaluated in this protocol depends on an intact immune system. Patients who are HIV seropositive can have decreased immune-competence and thus be less responsive to the experimental treatment and more susceptible to its toxicities.)
- Seronegative for hepatitis B antigen, and seronegative for hepatitis C antibody. If hepatitis C antibody test is positive, then patient must be tested for the presence of antigen by reverse transcriptase-polymerase chain reaction (RT-PCR) and be HCV ribonucleic acid (RNA) negative
- Women of child-bearing potential must have a negative pregnancy test because of the potentially dangerous effects of the treatment on the fetus
- Absolute neutrophil count greater than 1000/mm^3 without the support of filgrastim
- White blood cells (WBC) ≥ 3000/mm^3
- Platelet count ≥ 100,000/mm^3
- Hemoglobin > 8.0 g/dl
- Serum alanine aminotransferase (ALT)/aspartate aminotransferase (AST) ≤ to 3.5 times the upper limit of normal
- Serum creatinine ≤ to 1.6 mg/dl and calculated creatinine clearance (Crockcroft-Gault or 24-hour urine creatinine) ≥ 30 mL/min
- Total bilirubin ≤ to 2.0 mg/dl, except in patients with Gilbert's syndrome who must have a total bilirubin less than 3.0 mg/dl
More than four weeks must have elapsed since any prior systemic therapy at the time the patient receives the preparative regimen, and patients' toxicities must have recovered to a grade 1 or less (except for toxicities such as alopecia or vitiligo)
- Note: Patients may have undergone minor surgical procedures within the past 3 weeks, as long as all toxicities have recovered to grade 1 or less
Exclusion Criteria:
- Women of child-bearing potential who are pregnant or breastfeeding because of the potentially dangerous effects of the treatment on the fetus or infant
- Any form of primary immunodeficiency (such as severe combined immunodeficiency disease)
- Concurrent opportunistic infections (The experimental treatment being evaluated in this protocol depends on an intact immune system. Patients who have decreased immune competence may be less responsive to the experimental treatment and more susceptible to its toxicities)
- Active systemic infections (e.g.: requiring anti-infective treatment), coagulation disorders or any other active major medical illnesses
- History of major organ autoimmune disease
- Concurrent systemic steroid therapy including physiologic replacement dosing of systemic steroids (i.e. prednisone ≤ 10 mg/day or equivalent) as well as topical or inhaled corticosteroids are not allowed
- History of severe immediate hypersensitivity reaction to any of the agents used in this study
- History of active coronary or ischemic symptoms
Documented left ventricular ejection fraction (LVEF) of less than or equal to 45%
Note: testing is required in patients with:
- Age ≥ 65 years old
Clinically significant atrial and or ventricular arrhythmias including but not limited to:
- Atrial fibrillation, ventricular tachycardia, second or third degree heart block or have a history of ischemic heart disease, chest pain
Documented forced expiratory volume in 1 second (FEV1) less than or equal to 60% predicted tested in patients with:
- A prolonged history of cigarette smoking (20 pack [pk]/year of smoking within the past 2 years)
- Symptoms of respiratory dysfunction
- Patients who are receiving any other investigational agents
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 해당 없음
- 중재 모델: 단일 그룹 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
실험적: Treatment (TIL, aldesleukin)
Patients receive cyclophosphamide IV over 2 hours on days -8 and -7, fludarabine IV over 30 minutes on days -6 to -2 and TIL IV over 20-30 minutes on day 0 in the absence of disease progression or unacceptable toxicity.
Starting within 24 hours of TIL infusion, patients receive aldesleukin IV over 15 minutes every 8 hours for up to 6 doses on days 0-3 in the absence of disease progression or unacceptable toxicity.
Starting on day 1 or day 2, patients may receive filgrastim SC until neutrophil count > 1 x 10^9/L for 3 consecutive days or > 5 x 10^9/L.
Patients with stable disease, partial response or recurrence may receive a second course of treatment.
Patients also undergo chest x-ray at screening and urine and blood sample collection, CT, MRI or PET throughout the study.
Additionally, patients may also undergo echocardiography or MUGA at screening and may also undergo a second surgery to collect cells on study.
|
MRI를 받다
다른 이름들:
CT를 받다
다른 이름들:
주어진 IV
다른 이름들:
주어진 IV
다른 이름들:
주어진 SC
다른 이름들:
PET 받기
다른 이름들:
주어진 IV
다른 이름들:
무가를 겪다
다른 이름들:
흉부 엑스레이를 찍다
다른 이름들:
소변 및 혈액 샘플 수집을 수행합니다.
다른 이름들:
심 초음파 검사를받습니다
다른 이름들:
Undergo a second surgery
다른 이름들:
Given IV
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Objective response rate
기간: Up to 24 months
|
Will be estimated by the proportion of patients with a best response of complete response (CR) or partial response (PR) by Response Evaluation Criteria in Solid Tumors criteria, with corresponding exact 95% confidence limit being reported.
|
Up to 24 months
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
CR rate
기간: Up to 24 months
|
Will be estimated by the proportion of patients with a best response of complete response (CR) by Response Evaluation Criteria in Solid Tumors criteria
|
Up to 24 months
|
|
Duration of response
기간: Up to 24 months
|
The distribution among patients achieving CR or PR will be characterized by median and quartiles.
|
Up to 24 months
|
|
Disease control rate
기간: Up to 24 months
|
Up to 24 months
|
|
|
Progression-free survival
기간: From the initial date of treatment to the date of documented progression, or the date of death (in the absence of progression), assessed up to 24 months
|
Will be estimated by the Kaplan-Meier method.
The corresponding median survival times (with 95% confidence limits) will be determined, as will the cumulative percentage of patients remaining progression-free (and the cumulative percentage-alive) at selected time points after initial treatment (e.g., 3, 6,12, 18 months).
|
From the initial date of treatment to the date of documented progression, or the date of death (in the absence of progression), assessed up to 24 months
|
|
Overall survival
기간: From the initial date of treatment to the recorded date of death, assessed up to 24 months
|
Will be estimated by the Kaplan-Meier method.
The corresponding median survival times (with 95% confidence limits) will be determined, as will the cumulative percentage of patients remaining progression-free (and the cumulative percentage-alive) at selected time points after initial treatment (e.g., 3, 6,12, 18 months).
|
From the initial date of treatment to the recorded date of death, assessed up to 24 months
|
|
Incidence of adverse events
기간: Up to 30 days after treatment
|
Will be described and graded using the National Cancer Institute Common Terminology Criteria for Adverse Events version 5.0.
The maximum grade of toxicity for each category of interest will be recorded for each patient and the summary results will be tabulated by category and grade.
|
Up to 30 days after treatment
|
공동 작업자 및 조사자
스폰서
수사관
- 수석 연구원: Joal Beane, MD, Ohio State University Comprehensive Cancer Center
간행물 및 유용한 링크
유용한 링크
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 연구와 관련된 용어
추가 관련 MeSH 약관
- 신생물
- 조직학적 유형에 따른 신생물
- 위장관 신생물
- 소화계 신생물
- 소화기계 질환
- 위장병
- 신생물, 결합 및 연조직
- 신생물, 결합 조직
- 위장관 기질 종양
- 펩타이드
- 아미노산, 펩티드 및 단백질
- 단백질
- 유기 화학 물질
- 조사 기술
- 임상 실험실 기술
- 진단 기술 및 절차
- 진단
- 탄화수소
- 생물학적 요인
- 탄수화물
- 물리적 현상
- 화학 기술, 분석
- 스펙트럼 분석
- 포스 포 아미드 머스타드
- 질소 머스타드 화합물
- 겨자 화합물
- 탄화수소, 할로겐화
- 포스 포 아미드
- 유기 인 화합물
- 세포 간 신호 전달 펩티드 및 단백질
- 당 단백질
- Glycoconjugates
- 전자기 현상
- 자기 현상
- 전자기 방사선
- 방사
- 방사선, 이온화
- 식민지 자극 요인
- 조혈 세포 성장 인자
- 사이토 카인
- 시클로포스파미드
- 시편 처리
- 자기 공명 분광법
- fludarabine
- Aldesleukin
- 수술 절차, 수술
- 엑스선
- 육아 세포 콜로니 자극 인자
- 필 그라 스트 im
기타 연구 ID 번호
- OSU-22356 (기타 식별자: Ohio State University Comprehensive Cancer Center)
- NCI-2026-03863 (레지스트리 식별자: CTRP (Clinical Trial Reporting Program))
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
미국에서 제조되어 미국에서 수출되는 제품
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. .
자기 공명 영상에 대한 임상 시험
-
University of Wisconsin, MadisonNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK); Stanford University완전한
-
University Hospital, Bordeaux완전한
-
Centre hospitalier de l'Université de Montréal...Canadian Institutes of Health Research (CIHR); McGill University Health Centre/Research... 그리고 다른 협력자들모병
-
Biotronik SE & Co. KG완전한심장병독일, 체코 공화국, 스위스, 오스트리아, 영국
-
Beijing Anzhen Hospital아직 모집하지 않음다혈관 관상 동맥 질환 | ST 상승 심근 경색증(STEMI) | ACS(급성 관상동맥 증후군) | 미세혈관 폐쇄(MVO)중국
-
Shanghai Ninth People's Hospital Affiliated to...모병