Pressurized Intraperitoneal Aerosolized Nab-Paclitaxel in Combination With Gemcitabine and Cisplatin for the Treatment of Biliary Tract Cancer Patients With Peritoneal Metastases

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18+
SponsorCity of Hope Medical Center

About this trial

This phase I trial studies the side effects of pressurized intraperitoneal aerosolized chemotherapy (PIPAC) nab-paclitaxel in combination with gemcitabine and cisplatin in treating patients with biliary tract cancer that has spread to the peritoneum (peritoneal metastases). PIPAC involves the administration of intraperitoneal chemotherapy (anticancer drugs given directly to the lining of the abdomen). PIPAC uses a nebulizer (a device that turns liquids into a fine mist) which is connected to a high-pressure injector and inserted into the abdomen (part of the body that contains the digestive organs) during a laparoscopic procedure (a surgery using small incisions to introduce air and insert a camera and other instruments into the abdominal cavity for diagnosis and/or to perform routine surgical procedures). Pressurization of the liquid chemotherapy through the study device results in aerosolization (a fine mist or spray) of the chemotherapy intra-abdominally (into the abdomen), which results in the drug reaching more of the tissue as well as reaching deeper into the tissue, which reduces the amount of chemotherapy that needs to be used and potentially reduces side effect. Chemotherapy drugs, such as nab-paclitaxel, gemcitabine, and cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving nab-paclitaxel via PIPAC in combination with standard of care gemcitabine and cisplatin may reduce side effects and make this chemotherapy regimen more tolerable in patients with biliary tract cancer that has spread to the spread to the peritoneum.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Documented informed consent of the participant and/or legally authorized representative

Assent, when appropriate, will be obtained per institutional guidelines

Agreement to allow the use of archival tissue from diagnostic tumor biopsies

If unavailable, exceptions may be granted with study principal investigator (PI) approval

Disqualifiers

Any prior systemic therapy treatment for advanced cholangiocarcinoma or gallbladder cancer

Any prior adjuvant therapy (chemotherapy, radiation therapy, biological therapy, immunotherapy) completed < 6 months prior to registration

Strong CYP3A4 inducers/inhibitors within 14 days prior to day 1 of protocol therapy

Bowel obstruction requiring nasogastric tube, percutaneous endoscopic gastrostomy, or exclusive total parenteral nutrition

Trial design

Design model

Single group

Treatments tested in this trial

  • Cisplatin

    Drug

    Given IV

  • Gemcitabine

    Drug

    Given IV

  • Nab-paclitaxel

    Drug

    Given via PIPAC

  • Quality-of-Life Assessment

    Other intervention

    Ancillary studies

  • Questionnaire Administration

    Other intervention

    Ancillary studies

Treatment groups

12 Participants
are divided into 1 treatment group
Group A: Treatment (gemcitabine, cisplatin, nab-paclitaxel PIPAC)Experimental treatment 5 interventions

Trial outcomes

Primary outcomes

1

Incidence of adverse events

Measured by National Cancer Institute Common Terminology Criteria for Adverse Events version 5.0. Toxicities observed during the first 6 weeks after the first cycle will be summarized by type (organ affected or laboratory determination), severity, time of onset, duration, probable association with the study treatment, and reversibility or outcome.

Time frame
Up to 6 weeks after cycle 1 (1 cycle = 21 days)

Secondary outcomes

1

Efficacy - RECIST

Measured by Response Evaluation Criteria in Solid Tumors (RECIST) via computerized tomography (CT) scan.

Time frame
Up to 1 year after completion of chemotherapy
2

Efficacy - PGRS

Measured by Peritoneal Regression Grading Score (PGRS) via biopsy at each Pressurized Intraperitoneal Aerosolized Chemotherapy (PIPAC) cycle.

Time frame
Up to 1 year after completion of chemotherapy
3

Efficacy - PCI

Measured by Peritoneal Carcinomatosis Index (PCI) at the time of laproscopy.

Time frame
Up to 1 year after completion of chemotherapy
4

Post-operative surgical complications

Measured by Clavien-Dindo classification. Results will be strictly descriptive in nature.

Time frame
Up to 4 weeks after each pressurized intraperitoneal aerosolized chemotherapy treatment

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

City of Hope Medical Center

Lead sponsor

National Cancer Institute (NCI)

Collaborator