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2nd-line Therapy With Nal-IRI After Gem/Nab-pac in Advanced Pancreatic Cancer - Predictive Role of 1st-line Therapy (PREDICT)

A

AIO-Studien

Status and phase

Active, not recruiting
Phase 3

Conditions

Locally Advanced Pancreatic Cancer
Metastatic Pancreatic Cancer

Treatments

Drug: Irinotecan Liposomal Injection [Onivyde]

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT03468335
AIO-PAK-0216

Details and patient eligibility

About

Second-line therapy with Nal-IRI after failure gemcitabine/nab-paclitaxel in advanced pancreatic cancer - predictive role of 1st-line therapy

Full description

Research hypothesis:

Patients profit from 2nd-line therapy with Nal-IRI if they also had a benefit from 1st-line treatment. Benefit from treatment (either 1st or 2nd-line) will be defined as a patient specific Time-To-Treatment Failure (TTF) which is in the upper third of the distribution of TTF values of the studied population.

Enrollment

270 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Written informed consent including participation in translational research and any locally-required authorization (EU Data Privacy Directive in the EU) obtained from the subject prior to performing any protocol-related procedures, including screening evaluations

  2. Clinical indication for a 2nd-line systemic therapy according to current standard-of-care.

  3. Age ≥ 18 years at time of study entry

  4. Patients with histologically or cytologically confirmed pancreatic ductal adenocarcinoma

  5. Imaging of evaluable lesions within 2 weeks of inclusion (either sonography, X-ray, CT scans, MRI)

  6. ECOG performance status 0-2

  7. One line of systemic gemcitabine/Nab-paclitaxel -based therapy for advanced disease (irrespective of prior adjuvant therapy) OR Previous adjuvant gemcitabine/Nab-paclitaxel-based chemotherapy with documented progression less than 6 months after termination

  8. Detailed documentation of prior therapy (duration, dose-intensity, maximum toxicity, reason for discontinuation)

  9. Adequate blood count, liver-enzymes, and renal function:

    • neutrophil count > 1.5 x 10^6/mL
    • Platelet count ≥ 100 x 10^9/L (≥100,000 per mm^3)
    • AST (SGOT)/ALT (SGPT) ≤ 5 x institutional upper limit of normal
    • bilirubin ≤1.5 ULN (<3 x ULN in patients with confirmed mechanical cholestasis)
    • Creatinine Clearance CLcr ≥ 30 mL/min
  10. Subject is willing and able to comply with the protocol for the duration of the study including undergoing treatment and scheduled visits and examinations including follow up.

Exclusion criteria

Medical criteria:

  1. Any condition or comorbidity that, in the opinion of the investigator, would interfere with evaluation of study treatment or interpretation of patient safety or study results, including but not limited to:

    1. Active uncontrolled infection, chronic infectious diseases, immune deficiency syndromes

    2. Premalignant hematologic disorders, e.g. myelodysplastic syndrome

    3. Clinically significant cardiovascular disease in (incl. myocardial infarction, unstable angina, symptomatic congestive heart failure, serious uncontrolled cardiac arrhythmia) 6 months before enrollment

    4. Prior (<3 years) or concurrent malignancy (other than biliary-tract cancer) which either progresses or requires active treatment. Exceptions are: basal cell cancer of the skin, pre-invasive cancer of the cervix, T1a or T1b prostate carcinoma, or superficial urinary bladder tumor [Ta, Tis and T1].

    5. Pre-existing lung disease of clinical significance or with impact on performance status

    6. History or clinical evidence of CNS metastases

      Exceptions are: Subjects who have completed local therapy and who meet both of the following criteria:

      I. are asymptomatic and II. have no requirement for steroids 6 weeks prior to start of study treament. Screening with CNS imaging (CT or MRI) is required only if clinically indicated or if the subject has a history of CNS metastases

    7. Allogeneic transplantation requiring immunosuppressive therapy or other major immunosuppressive therapy

    8. Severe non-healing wounds, ulcers or bone fractions

    9. Evidence of bleeding diathesis or coagulopathy

    10. Major surgical procedures, except open biopsy, or significant traumatic injury within 28 days prior to star of study treatment, or anticipation of the need for major surgical procedure during the course of the study except for surgery of central intravenous line placement for chemotherapy administration.

    11. Known Gilbert-Meulengracht syndrome

    12. Known chronic hypoacusis, tinnitus or vertigo

    13. Bone marrow depression (e.g., after radiation therapy)

    14. Pernicious anemia and other megaloblastic anemias secondary to vitamin B12 deficiency

    15. Severe impairment of hepatic function

    16. Diarrhea

    Drug related criteria:

  2. Medication that is known to interfere with any of the agents applied in the trial.

  3. Known dihydropyrimidine dehydrogenase (DPD) deficiency

  4. History of hypersensitivity to any of the study drugs or any of the constituents of the products.

  5. Any other efficacious cancer treatment except protocol specified treatment at study start.

    Safety criteria:

  6. Female subjects who are pregnant, breast-feeding or male or female patients of reproductive potential who are not employing an effective method of birth control (failure rate of less than 1% per year). [Acceptable methods of contraception are: implants, injectable contraceptives, combined oral contraceptives, intrauterine pessars (only hormonal devices), sexual abstinence or vasectomy of the partner]. Women of childbearing potential must have a negative pregnancy test (urine or serum β-HCG acc. to SOC) at Screening.

    Methodological criteria:

  7. Any experimental pretreatment for advanced disease

  8. Participation in another clinical study with an investigational product during the last 30 days before inclusion or 7 half-lifes of previously used trial medication, whichever is longer.

  9. Previous enrollment in the present study (does not include screening failure).

    Regulatory and ethical criteria:

  10. Patient who might be dependent on the sponsor, site or the investigator

  11. Patients who are unable to consent because they do not understand the nature, significance and implications of the clinical trial and therefore cannot form a rational intention in the light of the facts [§ 40 Abs. 1 S. 3 Nr. 3a AMG].

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

270 participants in 1 patient group

Single Arm
Other group
Description:
Cancer treatment for PDAC: * Nal-IRI (4.3 mg/ml) 70 mg/m2 as 1.5 hour infusion * 5-FU 2400 mg/m2 as 46 hour infusion * Folinic acid 400 mg/m2 as 0.5 hour infusion * all on D1 of each cycle; Cycle q2w ± 5 days Treatment until progressive disease or intolerable toxicity or withdrawal of consent.
Treatment:
Drug: Irinotecan Liposomal Injection [Onivyde]

Trial contacts and locations

35

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Data sourced from clinicaltrials.gov

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