AB801 in Combination With Chemotherapy and Immunotherapy for the Treatment of Patients With Borderline Resectable, Locally Advanced or Metastatic Cholangiocarcinoma or Pancreatic Cancer
A Phase 1/1b Trial of AB801 in Combination With Chemotherapy and PD-1/PD-L1 Blockade in Patients With Cholangiocarcinoma or Pancreatic Adenocarcinoma
調査の概要
状態
条件
詳細な説明
PRIMARY OBJECTIVE:
I. Assess safety and tolerability of ligritinib (AB801) in combination with chemotherapy and immunotherapy in patients with cholangiocarcinoma and pancreatic adenocarcinoma.
SECONDARY OBJECTIVES:
I. Objective response rate. II. Progression free survival. III. Duration of response. IV. Proportion of patients taken to curative intent surgery after neoadjuvant therapy.
EXPLORATORY OBJECTIVES:
I. To evaluate the effect on AXL expression by comparing pre-treatment core biopsies with post-therapy operative specimens or biopsies taken at time of progression.
II. To evaluate the effects of study treatment on tumor microenvironment by comparing pre-treatment core biopsies with operative specimens or biopsies taken at time of progression via multiple modalities including immunohistochemistry (IHC), cytometry by time-of-flight (CyTOF), ribonucleic acid sequencing (RNA Seq)/spatial transcriptomics.
III. To assess for changes in peripheral blood throughout treatment including but not limited to soluble AXL, immune cell populations and change in systemic cytokines.
IV. To explore changes in gene alterations via whole exome sequencing.
OUTLINE: This is a dose-escalation study of AB801 followed by a dose-expansion study. Patients are assigned to 1 of 2 cohorts.
COHORT I: Patients with cholangiocarcinoma receive AB801 orally (PO) once daily (QD), gemcitabine and cisplatin intravenously (IV) over 30 minutes on days 1 and 8 and durvalumab IV over 60 minutes on day 1 of each cycle. Cycles repeat every 21 days for 24 weeks in the absence of disease progression or unacceptable toxicity.
COHORT II: Patients with pancreatic cancer receive AB801 PO QD and zimberelimab IV over 60 minutes on day 1 of each cycle. Patients receive oxaliplatin IV over 120 minutes, leucovorin IV, and irinotecan IV on days 1 and 15 of each cycle and fluorouracil IV over 46 hours on days 1 and 15 of each cycle. Cycles repeat every 28 days for 24 weeks in the absence of disease progression or unacceptable toxicity.
All patients undergo computed tomography (CT) or magnetic resonance imaging (MRI) throughout the trial as well as tissue biopsy on trial.
After completion of study treatment, patients are followed up at 30 and 90 days and then every 3 months.
研究の種類
入学 (推定)
段階
- フェーズ 1
連絡先と場所
研究場所
-
-
California
-
Los Angeles、California、アメリカ、90095
- 募集
- UCLA / Jonsson Comprehensive Cancer Center
-
主任研究者:
- Lee S. Rosen, MD
-
コンタクト:
- Christopher Lim
- 電話番号:310-633-8400
- メール:ChristopherLim@mednet.ucla.edu
-
-
参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- Male or female ≥ 18 years of age and willing and able to provide informed consent
Previously untreated cytologically or histologically confirmed, at least one measurable lesion via Response Evaluation Criteria in Solid Tumors (RECIST 1.1) of cholangiocarcinoma or pancreatic adenocarcinoma meeting following criteria:
Cholangiocarcinoma
- Borderline resectable/locally advanced cholangiocarcinoma: to be defined as unresectable disease on evaluation by a hepatobiliary multi-disciplinary tumor board/surgeon based on tumor size/location, vascular involvement, and absence of extrahepatic metastasis.
- Metastatic cholangiocarcinoma: Patients with metastatic cholangiocarcinoma patient who have not received prior systemic therapy
Pancreatic adenocarcinoma
Borderline resectable pancreatic adenocarcinoma: There are multiple definitions of borderline resectable pancreatic ductal adenocarcinoma (PDAC). For the purposes of this study, borderline resectable disease will be identified per the National Comprehensive Cancer Network (NCCN) criteria. Per this definition, borderline resectable PDAC is defined as the presence of any one or more of the following on CT:
- An interface between the tumor and superior mesenteric artery (SMA) or celiac axis (CA) measuring < 180º of the circumference of the vessel wall.
- An interface between the tumor with the common hepatic artery without extension into the celiac axis or hepatic artery bifurcation allowing for safe and complete resection and reconstruction.
- An interface between the primary tumor and the superior mesenteric vein or portal vein (SMV-PV) measuring ≥ 180° of the circumference of the vessel wall
- Short-segment occlusion of the SMV-PV with normal vein above and below the level of obstruction that is amenable to resection and venous reconstruction
- An interface between the primary tumor and the inferior vena cava (IVC)
Locally advanced pancreatic adenocarcinoma: Multiple guidelines defining locally advanced PDAC have been developed. For the purposes of this study, locally advanced PDAC cases will be identified per the definition developed by the NCCN. Per this definition, locally advanced PDAC is defined as presence of any one or more of the following on CT:
- Interface between the tumor and SMA or CV measuring > 180º of the circumference of the vessel wall or solid tumor contact with the CA and aortic involvement.
- Occlusion of the SMV-PV that is not amenable to resection and venous reconstruction
- Metastatic pancreatic adenocarcinoma: Patients with metastatic pancreatic adenocarcinoma who have not received prior systemic therapy
- Eastern Cooperative Oncology Group (ECOG) performance status of 0-1
- Absolute neutrophil count (ANC) ≥ 1.5x10^9/L
- Platelets ≥ 100x10^9/L
- Hemoglobin ≥ 9 g/dL
- Creatinine clearance (Ccr) ≥ 50 mL/min (as calculated by Modified Cockcroft-Gault formula)
- Serum total bilirubin ≤ 2x upper limit of normal (ULN) or < 3x ULN if Gilbert's syndrome
- Aspartate aminotransferase (AST) (serum glutamic-oxaloacetic transaminase [SGOT]) and alanine aminotransferase (ALT) (serum glutamic-pyruvic transaminase [SGPT]) ≤ 2.5 X ULN; < 5x ULN in patients with liver metastases
- Women with no childbearing potential because of surgery or who are at least 1 year postmenopausal (ie, 12 months post last menstrual period) or with menopause confirmed by follicle-stimulating hormone testing, OR
- Women of childbearing potential (defined as any female who has experienced menarche and is not permanently sterile or post-menopausal) must use an effective nonhormonal method of contraception (intrauterine device or intrauterine system; condom or occlusive cap [diaphragm or cervical or vault caps] with spermicidal foam or gel or film or cream or suppository; or vasectomized male partner if he is the sole partner of that participant) or practice true abstinence for the duration of the study and for up to 14 months after the last systemic treatment
- Male participants must use an effective method of contraception (condom or occlusive cap [diaphragm or cervical or vault caps] with spermicidal foam or gel or film or cream or suppository; or vasectomy) or practice true abstinence as defined throughout the study and for up to 11 months after the systemic treatment
- Immunosuppressive doses of systemic medications, such as corticosteroids or absorbed topical corticosteroids (doses > 10 mg/day prednisone or equivalent) must be discontinued at least 2 weeks (14 days) before study treatment administration. Physiologic doses of corticosteroids (≤ 10 mg/day of prednisone or its equivalent) or short pulses of corticosteroids (≤ 3 days) may be permitted
- Products with known potential to prolong the corrected QT (QTc) interval should be avoided when possible. When able will replace non-prolonging QTc acting drug when available and if medically necessary
- Major surgery as defined by the Investigator must be completed at least 4 weeks before study treatment administration. Participants should have recovered from the surgical procedure prior to the first dose being administered
- Adequate baseline tumor tissue sample for correlative studies
Exclusion Criteria:
- Previous treatment with any of planned study drugs in cholangiocarcinoma, though patients with one cycle of gemcitabine/cisplatin/durvalumab will be considered eligible
- Previous treatment with any of planned study drugs in pancreatic adenocarcinoma, though patients with one cycle of FOLFIRINOX will be considered eligible
- Peripheral neuropathy > grade 2
- Known status of HIV which is not well-controlled (CD4 < 300) at the time of study eligibility. Patients with controlled and treated HIV/hepatitis C virus (HCV) and an undetectable viral load are allowed
Untreated hepatitis B infection; Patient has known active hepatitis B virus (HBV) or hepatitis C virus (HCV), or human immunodeficiency virus (HIV) infection (testing is not mandatory, unless known active or known history of infection or required by local regulation):
- Participants with resolved or treated HCV (ie, HCV antibody positive but undetectable HCV ribonucleic acid [RNA]) will not be excluded from this study
Underlying medical conditions that, in the Investigator's opinion, will make the administration of investigational product (IP)(s) hazardous, including but not limited to:
- Interstitial lung disease, including history of interstitial lung disease or non-infectious pneumonitis
- Active viral, bacterial, or fungal infections requiring parenteral treatment within 14 days of the initiation of the IP,
- Active infection or antibiotics within 48 hours prior to study screening;
- A condition or unresolved adverse event (AE) from a prior investigational drug that may obscure the interpretation of toxicity determination or AEs,
- History of prior solid-organ transplantation
- Any history of malignancy less than 5 years prior to the time of study eligibility (Patients with history of skin cancers excluding melanoma and cancers with a very low risk of recurrence i.e., low grade prostate cancer, thyroid cancer and low risk cervical cancer will be eligible for participation)
- Serious medical comorbidities such as New York Heart Association Class III/IV cardiac disease, uncontrolled cardiac arrhythmias, myocardial infarction over the past 12 months
- Known family history or personal history of long QTc syndrome or previous drug-induced QTc prolongation of at least grade 3 (QTc > 500 ms)
- Screening 12-lead electrocardiogram (ECG), in triplicate, with a measurable QTc interval of > 450ms
- Known, existing uncontrolled coagulopathy. Patients who have had a venous thromboembolic event (e.g., pulmonary embolism or deep vein thrombosis) requiring anticoagulation are eligible IF: they are appropriately anticoagulated and have not had a grade 2 or greater bleeding episode in the 3 weeks before day 1
- Known pregnancy, nursing women or positive pregnancy test. Requirement for women of childbearing potential (WOCBP): Negative serum pregnancy test at screening and serum or urine prior to dosing on cycle 1 day 1, within 24 hours prior to the start of treatment (minimum sensitivity 25 IU/L or equivalent units of human chorionic gonadotropin [HCG]). WOCBP must also have a negative serum or urine pregnancy test every 3 weeks, within 24 hours prior to the start of treatment
- Any condition (concurrent disease, infection, or comorbidity) that interferes with ability to participate in the study, causes undue risk, or complicates the interpretation of safety data, in the opinion of the investigator
- History of trauma or major surgery within 28 days prior to the first dose of IP
- Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial
Any active or documented history of autoimmune disease, including but not limited to inflammatory bowel disease, celiac disease, Wegner syndrome, Hashimoto syndrome, systemic lupus erythematosus, scleroderma, sarcoidosis, or autoimmune hepatitis, within 3 years of the first dose of study treatment, except for the following:
- Type I diabetes mellitus, hypothyroidism only requiring hormone replacement, skin disorders such as vitiligo, or alopecia not requiring systemic therapy, or conditions not expected to recur in the absence of an external trigger.
- Endocrinopathies where the participant is stable on hormone replacement therapy
- History of Hashimoto syndrome within 3 years of the first of study treatment that resolved to hypothyroidism alone
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:非ランダム化
- 介入モデル:並列代入
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:Cohort I (AB801, gemcitabine, cisplatin, durvalumab)
Patients with cholangiocarcinoma receive AB801 PO QD, gemcitabine and cisplatin IV over 30 minutes on days 1 and 8 and durvalumab IV over 60 minutes on day 1 of each cycle.
Cycles repeat every 21 days for 24 weeks in the absence of disease progression or unacceptable toxicity.
Patients undergo CT or MRI throughout the trial as well as tissue biopsy on trial.
|
MRIを受ける
他の名前:
与えられた IV
他の名前:
与えられた IV
他の名前:
CTを受ける
他の名前:
与えられた IV
他の名前:
組織生検を受けます
他の名前:
Given PO
他の名前:
|
|
実験的:Cohort II (AB801, zimberelimab, FOLFIRINOX)
Patients with pancreatic cancer receive AB801 PO QD and zimberelimab IV over 60 minutes on day 1 of each cycle.
Patients receive oxaliplatin IV over 120 minutes, leucovorin IV, and irinotecan IV on days 1 and 15 of each cycle and fluorouracil IV over 46 hours on days 1 and 15 of each cycle.
Cycles repeat every 28 days for 24 weeks in the absence of disease progression or unacceptable toxicity.
Patients undergo CT or MRI throughout the trial as well as tissue biopsy on trial.
|
MRIを受ける
他の名前:
CTを受ける
他の名前:
与えられた IV
他の名前:
与えられた IV
他の名前:
与えられた IV
他の名前:
与えられた IV
組織生検を受けます
他の名前:
Given PO
他の名前:
Give IV
他の名前:
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Incidence of dose limiting toxicities
時間枠:During first cycle of the dose escalation phase (cycle length = 21 days for cohort I and 28 days for cohort II)
|
Overall exposure to study drug, the numbers of participants completing each cycle, and the dose intensity will be summarized using descriptive statistics.
The number of participants with any dose adjustment will be presented for entire treatment period as well as for each cycle.
The number of participants with dose reductions, dose delays, or dose omissions will also be summarized, as will the reasons for dose adjustments.
Adverse events and serious adverse events will be reported using Common Terminology Criteria for Adverse Events version 5 terminology and severity.
|
During first cycle of the dose escalation phase (cycle length = 21 days for cohort I and 28 days for cohort II)
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Overall response rate (ORR)
時間枠:Up to 2 years
|
Will be defined as proportion of patients with complete response (CR) or partial response (PR) at time of data analysis.
ORR and their corresponding exact 2-sided 95% confidence interval will be calculated.
|
Up to 2 years
|
|
Overall survival
時間枠:Up to 2 years
|
Will be estimated using Kaplan-Meier method.
|
Up to 2 years
|
|
Proportion of patients take to curative surgery
時間枠:Up to 2 years
|
Will be analyzed using descriptive statistics.
|
Up to 2 years
|
|
Duration of response
時間枠:up to 2 years
|
Will be summarized and plotted over time by Kaplan-Meier method.
Time from the first documentation of CR or PR to the date of first documentation of disease progression or death (whichever occurs first).
|
up to 2 years
|
|
Progression-free survival
時間枠:up to 2 years
|
Will be estimated using Kaplan-Meier method.
Time from first study dose date to the date of first documentation of disease progression or death (whichever comes first)
|
up to 2 years
|
協力者と研究者
捜査官
- 主任研究者:Lee S Rosen、UCLA / Jonsson Comprehensive Cancer Center
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
- 内分泌系疾患
- 部位別新生物
- 新生物
- 組織型別の新生物
- 消化器系腫瘍
- 消化器系疾患
- 内分泌腺腫瘍
- 膵臓の病気
- 新生物、腺および上皮
- 腺癌
- がん
- 膵臓の新生物
- 胆管癌
- アミノ酸、ペプチド、およびタンパク質
- タンパク質
- 硫黄化合物
- 有機化学物質
- 複素環化化合物、1リング
- 複素環化化合物
- 複素環化化合物、2リング
- 複素環化化合物、融合リング
- 調査手法
- 標本処理
- 臨床検査技術
- 診断技術と手順
- 診断
- 外科的処置、手術
- 細胞学的技術
- 細胞診断
- カムプトテシン
- アルカロイド
- 酵素と補酵素
- 抗体
- 免疫グロブリン
- 免疫タンパク質
- 血液タンパク質
- 血清グロブリン
- グロブリン
- 無機化学物質
- 塩素化合物
- 窒素化合物
- 調整錯体
- デオキシシチジン
- シチジン
- ピリミジンヌクレオシド
- ピリミジン
- 要素
- 金属
- 診断技術、外科的
- 化学技術、分析
- スペクトル分析
- ホルミルテトラヒドロフォレート
- テトラヒドロフォレート
- 葉酸
- 羽毛
- プテリジン
- ウラシル
- ピリミジノン
- 金属、重い
- コエンザイム
- 免疫グロブリンアイソタイプ
- 硫化物
- 陰イオン
- イオン
- 電解質
- 硫化水素
- プラチナ化合物
- 遷移要素
- オキサリプラチン
- イリノテカン
- ゲムシタビン
- フルオロウラシル
- ロイコボリン
- 免疫グロブリンG
- シスプラチン
- クエン酸1,2-ジアミノシクロヘキサン白金II
- 生検
- 磁気共鳴分光法
- Durvalumab
- ジスルフィド
- 白金
- zimberelimab
- Dehydroftorafur
その他の研究ID番号
- 25-2512
- NCI-2026-03183 (レジストリ識別子:CTRP (Clinical Trial Reporting Program))
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
米国で製造され、米国から輸出された製品。
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