- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07661459
Optimizing Ancillary Therapies With Immune Checkpoint Inhibitors for Solid Tumors (OAT ICI) (OAT ICI)
2026년 8월 11일 업데이트: Val Adams
Optimizing Ancillary Therapies (Acetaminophen, Cannabis, Antihistamines, and NSAIDS) With Immune Checkpoint Inhibitors for Solid Tumors (OAT ICI)
This study evaluates whether optimization of ancillary therapies can improve the efficacy of immune checkpoint therapy in participants with solid tumors.
The ancillary therapies being optimized include the avoidance of daily acetaminophen and cannabis/THC/CBD while prescribing aspirin and loratadine.
The goal is to see if optimizing these four drugs can improve the efficacy of the treatment compared to a matched historical control.
연구 개요
상세 설명
There are multiple reports of ancillary drugs impacting the efficacy of immune checkpoint inhibitor therapy.
However, there are no prospective studies evaluating the potential benefit of optimizing multiple ancillary therapies in a prospective study.
To address this gap in knowledge the approach is to compare two groups; the first group is a prospective interventional population consisting of 98 solid tumor patients who have radiologically measurable cancer which are scheduled to receive immunotherapy as part of the participant's cancer treatment.
Enrolled patients will be asked to avoid daily acetaminophen and the use of cannabis/THC/CBD.
The participants will also be prescribed aspirin 162 mg (2 x 81 mg baby aspirin) and loratadine 10 mg to be taken once daily for 126 days.
Collectively, optimizing these 4 drugs is called the OAT protocol.
Once the prospective patient enrollment is complete, a historical control will be created to match patients based on their cancer, the treatment regimen, line of therapy, performance status, and age.
The control group will not have received the OAT protocol optimization.
The primary endpoint of the trial will be response rate at 18 weeks.
Other efficacy endpoints include progression free survival and overall survival at 12 months.
Safety and toxicity endpoints include those associated with aspirin and loratadine as well as the rate of immune-related adverse events.
The study will also capture drug discontinuation, including ICI therapy as a measure of toxicity.
Lastly, the study will explore the efficacy of the OAT protocol in different populations based on disease, smoking status, genetics, and cytokines.
The hypothesis is that optimizing these therapies will increase response rates by at least 15% compared to the controls.
연구 유형
중재적
등록 (추정된)
98
단계
- 2 단계
연락처 및 위치
이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.
연구 연락처
- 이름: Val Adams
- 전화번호: 8592575202
- 이메일: val.adams@uky.edu
연구 장소
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Kentucky
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Lexington, Kentucky, 미국, 40506
- 모병
- University of Kentucky Markey Cancer Center
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연락하다:
- Val Adams
- 전화번호: 859-257-5202
- 이메일: vadam0@uky.edu
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-
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:
- Solid tumor patients with measurable disease. Including patients with early stage and advanced stage cancer.
- Patients who are to get neoadjuvant or induction therapy prior to planned surgery or radiation are included if definitive therapy is planned to occur at least 18 weeks after ICI initiation.
- Treatment plan includes an immune checkpoint inhibitor (PD1 or PD-L1 inhibitor) as standard of care. Standard of care will be determined by referring to the NCCN guidelines. For rare situations where a disease is not found in the NCCN guideline, the treatment must be considered standard of care at the MCC.
- ECOG Performance Status 0-3.
- Life expectancy of at least 3 months.
- Adequate hematologic, renal and hepatic function based on institutional standards.
- Must be willing to stop/not start daily acetaminophen during the study period
- Must be willing to stop/not start THC-containing agent (e.g., medical or recreational marijuana, CBD) during the study period
- Patients willing to take a second-generation antihistamine (loratadine) and an NSAID (aspirin). Patients already taking a daily antihistamine and/or NSAID can participate and will continue the class of drug already being taken
- Ability to understand and the willingness to follow study procedures, including urine testing for THC.
- Ability to understand and the willingness to sign a written informed consent document.
Exclusion Criteria:
- Contraindication to immunotherapy, aspirin, or loratadine (including patients on blood thinners or antiplatelet agents that pose a high risk of bleeding based on the treating oncologist's opinion)
- History of allergic reactions attributed to loratadine or aspirin (true allergy, not intolerance)
- Known immunocompromised patients; defined as disease or drug related. This includes solid organ transplant patients, patients with active human immunodeficiency virus (detectable disease within the last 60 days), and those with autoimmune diseases on immune modulating drugs (disease modifying agents or steroids at a prednisone equivalent dose > 10 mg daily).
- Early-stage disease patients who are scheduled for definitive therapy in less than 126 days from treatment initiation
- Patients must not have had prior ICIs for advanced disease except as neoadjuvant + adjuvant therapy. Patients with recurrence after definitive therapy may have had prior ICIs for earlier stage disease if it was > 6 months since the last dose.
- Patients on an interventional cancer study
- History or evidence of any other clinically significant condition that, in the opinion of the investigator or treating physician, would pose a risk to subject safety or interfere with study procedures, evaluation or completion
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 |
|---|---|
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실험적: OAT ICI
Participants with solid tumors receiving standard-of-care immune checkpoint inhibitor therapy will follow the OAT ICI protocol, which includes use of loratadine and aspirin (or continuation of an equivalent antihistamine/NSAID), avoidance of acetaminophen, and avoidance of THC-containing products.
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Participants will receive Aspirin or continue an equivalent NSAID as part of the OAT ICI protocol while receiving standard-of-care immune checkpoint inhibitor therapy.
Participants will receive Loratadine or continue an equivalent antihistamine as part of the OAT ICI protocol while receiving standard-of-care immune checkpoint inhibitor therapy.
Participants will be instructed to avoid acetaminophen-containing products during immune checkpoint inhibitor therapy as part of the OAT ICI protocol.
Participants will be instructed to avoid THC-containing products during immune checkpoint inhibitor therapy as part of the OAT ICI protocol.
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간섭 없음: Matched Historical Control
Retrospective matched controls identified from UK Healthcare EHR and Kentucky Cancer Registry data.
Controls will be matched to enrolled participants by tumor type, disease stage, treatment regimen, line therapy, age group and ECOG performance status.
Historical controls will not receive the OAT ICI protocol.
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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18- Week Response Rate
기간: 18 Weeks
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To determine whether the OAT protocol improves therapeutic response to immune checkpoint inhibitor-containing regimens compared with matched historical controls, as measured by 18-week response rate.
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18 Weeks
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Progression-Free Survival by Disease Cohort
기간: 12 Months
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Progression-free survival among participants with lung cancer, head and neck cancer, bladder cancer, melanoma, and renal cell carcinoma compared with matched historical controls.
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12 Months
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Response Rate by Disease Cohort
기간: 18 Weeks
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Response rate (RECIST) at 18 weeks among participants with lung cancer, head and neck cancer, bladder cancer, melanoma, and renal cell carcinoma compared with matched historical controls
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18 Weeks
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Overall Survival
기간: 12 Months
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Overall survival at 12 months among participants receiving the OAT ICI protocol compared with matched historical controls.
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12 Months
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기타 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Changes in Immune Cell Populations
기간: Baseline, 9 Weeks and 18 Weeks
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T-cell subsets (including regulatory T cells [Tregs] and T-helper 17 [Th17] cells, monocytes, neutrophils at baseline, 9 and 18 weeks.
Associations between baseline values and changes over time with response rate will be evaluated.
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Baseline, 9 Weeks and 18 Weeks
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Changes in Cytokine Profile
기간: Baseline, 9 Weeks and 18 Weeks
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Cytokine profiles, including inerleukin-10 (IL-10) and histamine concentrations, measured at baseline, 9 and 18 weeks.
Associations between baseline values and changes over time with response rate will be evaluated.s.
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Baseline, 9 Weeks and 18 Weeks
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Response Rate by Tumor Histology
기간: 18 Weeks
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Response rate stratified by tumor histology including adenocarcinoma, squamous cell carcinoma, and other histologic subtypes.
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18 Weeks
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Response Rate by Smoking Status and Genetic Profile
기간: 18 Weeks
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Association of response rate with smoking status and genetic factors, including tumor mutational burden (TMB) and programmed death-ligand 1 (PD-L1) expression levels, using genetic data obtained from standard of care next-generation sequencing.
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18 Weeks
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Response Rate by Concurrent Ancillary Therapies
기간: 18 Weeks
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Association between response rate and use of other ancillary therapies that may affect immune checkpoint inhibitor effectiveness, including vaccines, proton pump inhibitors (PPIs), antibiotics and other concomitant treatments.
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18 Weeks
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공동 작업자 및 조사자
여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.
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 (실제)
2026년 6월 26일
기본 완료 (추정된)
2027년 7월 31일
연구 완료 (추정된)
2027년 7월 31일
연구 등록 날짜
최초 제출
2026년 6월 16일
QC 기준을 충족하는 최초 제출
2026년 6월 16일
처음 게시됨 (실제)
2026년 6월 22일
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
2026년 8월 14일
QC 기준을 충족하는 마지막 업데이트 제출
2026년 8월 11일
마지막으로 확인됨
2026년 8월 1일
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- 114969
약물 및 장치 정보, 연구 문서
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예
미국 FDA 규제 기기 제품 연구
아니
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예
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