RecruitingRecruiting
Gemcitabine, Nab-Paclitaxel, and Bosentan for the Treatment of Unresectable Pancreatic Cancer
NCT04158635 · City of Hope Medical Center
In plain English
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Official title
A Phase 1 Study of Gemcitabine, Nab-Paclitaxel, and Bosentan in Patients With Unresectable Pancreatic Cancer
About this study
PRIMARY OBJECTIVE:
I. To assess the safety, toxicity and feasibility of administering bosentan with nab-paclitaxel and gemcitabine.
SECONDARY OBJECTIVES:
I. To assess the response rate associated with this combination therapy in first line pancreatic cancer patients.
II. To assess the progression-free survival and overall survival of all patients who start protocol therapy, and describe the outcomes based on measures of compliance during the lead-in week, and compliance with supplement during chemotherapy.
EXPLORATORY OBJECTIVES:
I. To determine the impact of bosentan on the mass transport in the tumor (surrogate of alterations in tumor stroma and blood flow). (Pharmacodynamic Investigations) II. To describe the pharmacokinetic profile of nab-paclitaxel and bosentan and compare to historic single-agent profile. (Pharmacokinetic Investigations) III. To explore the association between hepatotoxicity to study agents and organic anion-transporting polypeptide (OATP) polymorphisms. (Pharmacogenomic Investigations) IV. To explore biomarkers on pre-treatment biopsy samples and peripheral blood samples for correlations of predictive of response.
V. To describe quality of life utilizing the Functional Assessment of Cancer Therapy: General (FACT-G) questionnaire.
OUTLINE:
Patients receive bosentan orally (PO) twice daily (BID) on days -7 to 21 or 8-21 of cycle 1 and days 1-21 of subsequent cycles. Patients also receive nab-paclitaxel intravenously (IV) over 30 minutes and gemcitabine IV over 30 minutes on days 1, 8, and 15. Cycles repeat every 21 days in the absence of disease progression or unacceptable toxicity.
After completion of study treatment, patients are followed up at 30 days. Patients who complete study treatment without disease progression are followed up every 2 months until disease progression and then biannually thereafter. Patients who complete study treatment with disease progression are followed up biannually.
Eligibility criteria
Main Inclusion Criteria
* Adult patients with unresectable pancreatic carcinoma
* Patients must be a candidate to receive one of the following chemotherapy combinations as determined by the treating physician:
Arm A2: gemcitabine plus nab-paclitaxel given every 2 weeks (arm A1 is closed per this amendment)
Arm B: mFOLFIRINOX given every 2 weeks
* Willingness to permit study team to obtain and use archival tissue, if already existing, or, be willing to undergo a fresh tumor biopsy if clinically possible (exceptions may be provided by study PI if medically unsafe to perform biopsy).
* Weight ≥ 40 kg
* ANC ≥ 1500/mm3; platelets ≥ 100,000/mm3
* AST, ALT ≤ 1.5 x ULN. Patients with liver metastases ≤ 3 x ULN
* Total serum bilirubin ≤ 1.5 x ULN
* Creatinine clearence ≥ 60 mL/min
Main Exclusion Criteria
* Current or planned use of Warfarin, Cyclosporine A, Rifampicin, Glyburide (other diabetic medications are allowed)
* Current or planned use of agents contraindicated for use with strong CYP3A4 inducers
* Strong inhibitors or inducers of CYP2C9
* Strong inhibitors or inducers of CYP3A
* Agent or agents that moderately inhibit both CYP2C9 and CYP3A (via a single concomitant agent, or co-administration of concomitant agents)
* No other prior malignancy is allowed except for the following: adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, adequately treated Stage I or II cancer from which the patient is currently in complete remission, or any other cancer from which the patient has been disease free for five years.
* Current or history of ≥ Grade 2 peripheral neuropathy
* Known allergy to eggs or any of the components within the study agents and/or their excipients.
Study design
Enrollment target: 21 participants
Allocation: non_randomized
Masking: none
Age groups: adult, older_adult
Timeline
Starts: 2021-09-01
Estimated completion: 2027-03-09
Last updated: 2026-04-17
Interventions
Drug: BosentanDrug: GemcitabineDrug: Nab-paclitaxelOther: Quality-of-Life AssessmentOther: Questionnaire Administration
Primary outcomes
- • Incidence of adverse events (Up to 30 days after last dose of protocol therapy)
- • Dose limiting toxicities (DLTs) (Up to 21 days (Cycle 1))
- • Compliance (During the first week)
Sponsor
City of Hope Medical Center · other
With: National Cancer Institute (NCI)
Contacts & investigators
InvestigatorRavi Salgia · principal_investigator, City of Hope Medical Center
All locations (1)
City of Hope Medical CenterRecruiting
Duarte, California, United States