Study of Eryaspase in Combination With Chemotherapy Versus Chemotherapy Alone as 2nd-Line Treatment in PAC

Pancreatic Adenocarcinoma Clinical Trial

— Trybeca-1  

Official title:

A Randomized, Phase 3 Study of Eryaspase in Combination With Chemotherapy Versus Chemotherapy Alone as 2nd-Line Treatment of Patients With Pancreatic Adenocarcinoma

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03665441
• Other study ID #: GRASPANC 2018-01
• Status: Completed
• Phase: Phase 3
• Start date: September 15, 2018
• Est. completion date: January 18, 2022

Study information

• Verified date: January 2021
• Source: ERYtech Pharma
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is an open-label, multicenter, randomized, Phase 3 study in patients with ductal adenocarcinoma of the pancreas who have failed only one prior line of systemic anti-cancer therapy for advanced pancreatic cancer and have measurable disease.

Description:

Patients who meet all inclusion and exclusion criteria will be randomized in a 1:1 ratio to one of the following treatment arms (see figure below): - Arm A (investigational arm): eryaspase in combination with either gemcitabine/Abraxane or irinotecan-based therapy (FOLFIRI [FOLinic acid-Fluorouracil-IRInotecan regimen] or Onivyde®/5 fluorouracil/leucovorin), or - Arm B (control arm): gemcitabine/Abraxane or irinotecan-based therapy (FOLFIRI or Onivyde/5-FU/leucovorin) The chemotherapy will be investigator's choice and based on what patient has received in first line treatment. Treatment will continue until disease progression, unacceptable toxicity, or the patient's withdrawal of consent. An End of Treatment visit should occur within approximately 30 days from last dose of eryaspase or chemotherapy regimen. A survival follow-up period will include the collection of survival, progression of disease if applicable, treatment updates, and quality of life assessments every 8 weeks.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 512
• Est. completion date: January 18, 2022
• Est. primary completion date: August 30, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

A patient will be eligible for the study if all the following criteria are met:

1. Must be 18 years of age or older.

2. Must have histologically confirmed pancreatic adenocarcinoma.

3. Must have Stage III or IV disease.

4. Must have received one line of systemic chemotherapy in the advanced setting with or without targeted agents, immunotherapy, or radiotherapy for treatment of advanced pancreatic adenocarcinoma.

5. Must have radiological evidence of disease progression following most recent prior treatment, defined as appearance of any new lesion or increase of >20% of one or more existing lesions.

6. Must have measurable lesion(s) per RECIST version 1.1 by CT scan with contrast (or MRI, if the patient is allergic to CT contrast media). NOTE: Bone disease consisting of blastic lesion only is not measurable.

7. Archival or fresh tumor tissue must be available for evaluating relevant biomarkers. Formalin-fixed paraffin-embedded [FFPE] block preferred, or a minimum of 10 unstained FFPE slides of one archived block is required. NOTE: Cytology samples from fine needle aspirates or brushing biopsies are not sufficient. If archival tissue is unavailable and an elective biopsy can't be scheduled due to COVID, this will be waived.

8. Must have adequate performance status:

1. ECOG Performance Status (PS) score of 0, or

2. ECOG PS score one and score =80 on Karnofsky Performance Status (KPS) scale. NOTE: Must have body mass index (BMI) =18.5 kg/m2 (obtained <14 days prior to randomization.

9. Must have life expectancy of >12 weeks according to the investigator's clinical judgment.

10. Females of childbearing potential must have a negative pregnancy test at screening and additional negative pregnancy test prior to first dose. Males and females of childbearing potential must agree to use a highly effective method of contraception during treatment and for at least 6 months after the last dose of study treatment.

11. Must have adequate laboratory parameters at baseline (obtained <14 days prior to randomization). Laboratory parameters outside of these ranges that are deemed

clinically insignificant should be discussed with the medical monitor:

1. Absolute neutrophil count =1.5 x 109/L.

2. Hemoglobin =9 g/dL. Patients with a baseline Hemoglobin =13 g/dL should be discussed with the medical monitor.

3. Platelet count =100,000/mm3 (100 x 109/L).

4. Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) =2.5 x upper limit of normal (ULN) (=5 x ULN in presence of liver metastases).

5. Total bilirubin = 1.5 x institutional ULN.

6. Serum creatinine within normal limits or calculated clearance >60 mL/min/1.73 m2 for patients with serum creatinine levels above or below the institutional normal range.

7. Acceptable coagulation parameters: plasma antithrombin III >70% and fibrinogen =1.5 g/L

8. Serum albumin =3.0 g/dL.

12. Patients requiring biliary stent placement must have the biliary stent placed >7 days prior to screening and must have normalization of bilirubin level after stenting.

13. Must not be receiving therapy in a concurrent clinical study and must agree not to participate in any other interventional clinical studies during their participation in this trial while on study treatment. Patients taking part in surveys or observational studies are eligible to participate in this study.

14. Must be able to understand and comply with the conditions of the protocol and must have read and understood the consent form and provided written informed consent. Exclusion Criteria: A patient is not eligible to participate in the study if any of the following criteria are

met:

1. Resectable or borderline resectable pancreatic adenocarcinoma at the time of signing the informed consent.

2. Histology other than pancreatic adenocarcinoma (for example, but not inclusive:

neuroendocrine, adenosquamous, etc.).

3. More than one line of prior treatment in advanced or metastatic setting.

4. Patient has experienced medically significant acute decline in clinical status including

1. Decline in ECOG PS to >1 (or KPS <70) between baseline visit and within 72 hours prior to randomization.

2. Weight loss of =10% during screening.

5. Presence of active or symptomatic untreated central nervous system (CNS) metastases. NOTE: Patients with asymptomatic or stable CNS metastases are eligible, provided that the CNS metastases are radiologically and clinically stable, and the patient is off high-dose steroid treatment for at least one month prior to randomization.

6. Prior radiotherapy to the only area of measurable disease. NOTE: Patients must have completed treatment and recovered from all acute treatment-related toxicities prior to administration of the first dose of eryaspase or chemotherapy.

7. Bone as the only site of metastatic disease from pancreatic cancer (bone only disease).

8. History of recent clinical pancreatitis, according to revised Atlanta criteria, within 3 months of randomization. NOTE: The revised Atlanta classification [1] requires that two or more of the following criteria be met for the diagnosis of acute pancreatitis: (a) abdominal pain suggestive of pancreatitis, (b) serum amylase or lipase level =3 x ULN, or (c) characteristic imaging findings using CT or MRI.

9. Neurosensory neuropathy > Grade 2 at baseline.

10. Pregnancy or breastfeeding.

11. History of infection with human immunodeficiency virus (HIV) and/or active infection with hepatitis B or hepatitis C. NOTE: Patients with unknown status of hepatitis B or C must be tested and declared negative before randomization.

12. Hypersensitivity to any of the components of the chemotherapy or ASNase.

13. Patients who have received live or live attenuated vaccines within 3 weeks of randomization.

14. History of other malignancies NOTE: Adequately treated non-melanoma skin cancer or curatively treated in-situ cancer of the cervix may be eligible. NOTE: Patients successfully treated for other malignancies and are disease-free for at least 5 years may be eligible.

15. Any other severe acute or chronic condition/treatments that may increase the risk of

study participation including:

1. History of abdominal fistula, gastrointestinal perforation, peptic ulcer, or intra-abdominal abscess within 6 months prior to randomization.

2. Current or history within 6 months prior to randomization of medically significant cardiovascular disease including symptomatic congestive heart failure >New York Heart Association (NYHA) Class II, unstable angina pectoris, clinically significant cardiac arrhythmia.

3. Patients with pre-existing coagulopathy (e.g. hemophilia).

4. Psychiatric illness/social situations or any other serious uncontrolled medical disorders in the opinion of the Investigator that would limit compliance with study requirements.

Related Conditions & MeSH terms

• Adenocarcinoma
• Pancreatic Adenocarcinoma

Intervention

Drug:
• eryaspase
L-asparaginase encapsulated in erythrocytes (red blood cells)
• Gemcitabine plus Abraxane
gemcitabine, Abraxane
• Irinotecan plus 5-FU plus leucovorin
irinotecan, 5-FU, leucovorin

Locations

Country	Name	City	State
France	Institut de Cancerologie	Brest
United Kingdom	Hammersmith Hospital	London
United States	Boca Raton Regional Hospital	Boca Raton	Florida
United States	Beth Israel Deaconess Medical Center	Boston	Massachusetts
United States	Roswell Park Cancer Institute	Buffalo	New York
United States	Duke University	Durham	North Carolina
United States	St. Joseph Heritage Healthcare	Fullerton	California
United States	University of Minnesota Health Clinics and Surgery Center	Minneapolis	Minnesota
United States	Ochsner Clinic Foundation	New Orleans	Louisiana
United States	Weill Cornell Medicine	New York	New York
United States	University of Rochester Medical Center	Rochester	New York
United States	University of California Davis Medical Center	Sacramento	California
United States	Arizona Cancer Center	Scottsdale	Arizona
United States	Medical Oncology Associates	Spokane	Washington
United States	Stony Brook University	Stony Brook	New York
United States	Georgetown University Hospital	Washington	District of Columbia

Sponsors (1)

Lead Sponsor	Collaborator
ERYtech Pharma

Countries where clinical trial is conducted

United States,  France,  United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Overall Survival (OS)	To determine whether the addition of eryaspase to chemotherapy improves OS when compared to chemotherapy alone	~12 months
Secondary	Progression Free Survival (PFS)	To compare PFS between the 2 treatment arm. Progression is determined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.1), as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions.	~24 weeks
Secondary	Objective Response Rate (ORR)	To compare the ORR between the 2 treatment arms. ORR is defined as the proportion of patients who achieve objective tumor response (CR or PR) per modified RECIST 1.1: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions.	~24 weeks
Secondary	Duration of Response (DoR)	To compare the DoR between the 2 treatment arms	~24 weeks
Secondary	Disease Control Rate (DCR)	To compare the between the 2 treatment arms	~24 weeks
Secondary	Incidence of Treatment Emergent Adverse Events as Assessed by CTCAE v5.0	To evaluate the safety and tolerability of eryaspase in combination with chemotherapy versus chemotherapy alone by assessing the number of patients with with treatment emergent adverse events per CTCAE v5.0	~9 months
Secondary	Time to Quality of Life Questionnaire EORTC QLQ-C30 First Worsening in Global Health Status Analysis	The time to first Worsening was defined as the date of randomization to the date of first Worsening occurred in patient score on their global health status. Patients who did not have any worsening were censored at date of last measurement or at baseline if no measurement is available post-baseline.	~1 year