Clinical Study of Personalized mRNA Vaccine Encoding Neoantigen in Patients With Advanced Digestive System Neoplasms

Clinical Study of Personalized mRNA Tumor Vaccine Encoding Neoantigen in Patients With Advanced Esophageal Squamous Carcinoma, Gastric Adenocarcinoma, Pancreatic Adenocarcinoma and Colorectal Adenocarcinoma

A single arm, open-label pilot study is designed to determine the safety, tolerability and effectiveness of personalized mRNA tumor vaccine encoding neoantigen in Patients with advanced esophageal squamous carcinoma, gastric adenocarcinoma, pancreatic adenocarcinoma and colorectal adenocarcinoma

Study Overview

• Status: Unknown
• Conditions: Pancreatic Adenocarcinoma; Gastric Adenocarcinoma; Colorectal Adenocarcinoma; Advanced Esophageal Squamous Carcinoma
• Intervention / Treatment: Biological: Personalized mRNA Tumor Vaccine

Detailed Description

Dr. Bin Wang developed the investigational vaccine used in this clinical trial and designed the trial protocol.For patients with advanced esophageal squamous carcinoma, gastric adenocarcinoma, pancreatic adenocarcinoma and colorectal adenocarcinoma tumor who have disease progression with first line chemotherapy. Single or multiple doses of personalized mRNA tumor vaccine encoding neoantigen will be given to observe the safety and efficacy the mRNA tumor vaccine.

Primary objectives:

Determine the safety, tolerability and cytokinetics of the personalized mRNA tumor vaccine in patients with advanced esophageal squamous carcinoma, gastric adenocarcinoma, pancreatic adenocarcinoma and colorectal adenocarcinoma.

Secondary objectives:

Make a preliminary evaluation on the efficacy of personalized mRNA tumor vaccine in patients with advanced esophageal squamous carcinoma, gastric adenocarcinoma, pancreatic adenocarcinoma and colorectal adenocarcinoma with the following parameters:

Time of tumor progression (TTP);

Disease Control Rate (DCR);

Objective Remission Rate (ORR);

Overall Survival (OS).

• Study Type: Interventional
• Enrollment (Anticipated): 24
• Phase: Not Applicable

Contacts and Locations

Study Locations

• China
  • Shanghai
    • Shanghai, Shanghai, China
      • Recruiting
      • Changhai Hospital
      • Contact: Bin Wang, Dr.; Phone Number: +86 01231161448; Email: qcwangb@163.com
      • Contact: Xianbao Zhan, Dr.; Phone Number: +86 01231161441; Email: Zhanxianbao@126.com
      • Principal Investigator: Xianbao Zhan, Dr.
      • Sub-Investigator: Bin Wang, Dr.

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 75 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

1. Patients aged 18 - 75 with pathologically confirmed advanced Esophageal Squamous Carcinoma, Gastric Adenocarcinoma, Pancreatic Adenocarcinoma and Colorectal Adenocarcinoma.
2. Patients with advanced Esophageal Squamous Carcinoma, Gastric Adenocarcinoma, Pancreatic Adenocarcinoma and Colorectal Adenocarcinoma who have disease progression with first line chemotherapy. (1) Failure of treatment is defined as disease progression, recurrence or metastatic disease, or intolerable toxicities occurred after treatment. (2) Each line of treatment during the period of disease progression includes one or more chemotherapy drugs which are administered for not less than one cycle or even longer. Neoadjuvant/adjuvant therapy can be applied at an earlier stage of treatment. If patient has developed recurrence or metastatic disease within 24 weeks of neoadjuvant/adjuvant therapy, it is considered as one line of systemic chemotherapy. (3) Therapies that can be performed at an earlier stage are chemotherapy in conjunction with molecular targeted drugs.
3. Expected survival after first dose of study drug > 24 weeks.
4. At least one measurable lesion (≥ 10 mm) for imaging assessment.
5. ECOG scores 0 - 1.
6. Fresh pathological tissue specimens can be obtained

7. White blood cells (WBCs) ≥ 2.5×10^9/L

   • Platelets (PLT) ≥ 100×10^9/L
   • Hemoglobin, Blood (Hb) ≥ 9.0 g/dL
   • MID ≥ 1.5×10^9/L
   • Lymphocyte (LY) ≥ 0.47×10^9/L
   • LY% ≥ 15%
8. Serum albumin (Alb) ≥ 30 g/L
9. Serum lipase (LPS) and serum amylase < 1.5 ULN
10. Serum creatinine ≤ 1.5 ULN

11. Alanine aminotransferase (ALT) ≤ 2.5 ULN

    • Aspartate aminotransferase (AST) ≤ 2.5 ULN
    • If osseous metastasis or liver metastasis is developed and alkaline phosphatase • (ALP) > 2.5 ULN, ALT and AST < 1.5 ULN.
12. Serum total bilirubin (TBIL) ≤ 1.5 ULN

13. Prothrombin Time (PT): International Normalized Ratio (INR) < 1.7.

    • PT < (ULN + 4) s

All test results should be within their normal ranges, and the patient is not receiving continuous supportive care.

Exclusion Criteria:

Patients with any of the following conditions are not eligible for the study.

1. Pregnant or lactating women.
2. HIV positive, HCV positive, HBV DNA copies ≥ 10^3.
3. Uncontrolled active infection.
4. Concurrent use of systemic steroids. Recent or current use of inhaled steroids is not exclusionary.
5. Allergic to immunotherapies and related drugs.
6. Untreated brain metastases or having symptoms of brain metastases.
7. Metastases to the lung: central tumor or multiple metastases.
8. Patients with heart disease for which treatment is needed or with poorly controlled hypertension.
9. Patients with unstable or active peptic ulcer or with alimentary tract hemorrhage.
10. Patients with previous organ transplantation or in preparation for organ transplantation.
11. Patients have undertaken major surgeries or have been badly injured 4 weeks before the study (blood collection), or will undertake major surgeries during the study.
12. The judgment of investigators that the patient is not able to or not willing to follow the instructions of the protocol.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Personalized mRNA Tumor Vaccine; Personalized mRNA Tumor Vaccine Encoding Neoantigen in Patients with Advanced Esophageal Squamous Carcinoma, Gastric Adenocarcinoma, Pancreatic Adenocarcinoma and Colorectal Adenocarcinoma	Biological: Personalized mRNA Tumor Vaccine; subcutaneous injection with personalized mRNA tumor vaccine at least four times

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of participants with treatment-related adverse events as assessed by CTCAE v4.0	During the trial conduction, especially within the 24 weeks of treatment phase when mRNA tumor Vaccine administered, all adverse events (including laboratory abnormality and clinical events) will be closely monitored, and all ≥ grade 3 adverse events per CTCAE (v 3.0) will be recorded, including but not limited to the toxicities potentially suspected to relate to injection procedures and/or mRNA Tumor Vaccine therapy as listed below: Fever; Chills; Nausea, vomiting and other gastrointestinal symptoms; Fatigue; Hypotension; Respiratory distress; Tumor lysis syndrome; Neutropenia, thrombocytopenia; Liver and kidney dysfunction	24 weeks

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Disease Control Rate of Personalized mRNA Tumor Vaccine	Disease Control Rate (DCR)	1.5 years
Progression-free Survival of Personalized mRNA Tumor Vaccine	Progression-free Survival (PFS)	2 years
Time to Tumor Progression of Personalized mRNA Tumor Vaccine	Time to Tumor Progression (TTP)	2 years
Overall Survival of Personalized mRNA Tumor Vaccine	Overall Survival (OS)	3 years

Collaborators and Investigators

• Sponsor: Changhai Hospital
• Collaborators: Stemirna Therapeutics
• Investigators: Study Director: Xianbao Zhan, Dr., Chanhai hospital

Study record dates

Study Major Dates

• Study Start (Actual): May 1, 2018
• Primary Completion (Anticipated): December 31, 2019
• Study Completion (Anticipated): December 31, 2021

Study Registration Dates

• First Submitted: March 8, 2018
• First Submitted That Met QC Criteria: March 15, 2018
• First Posted (Actual): March 16, 2018

Study Record Updates

• Last Update Posted (Actual): February 26, 2019
• Last Update Submitted That Met QC Criteria: February 25, 2019
• Last Verified: February 1, 2019

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Neoplasms by Histologic Type; Neoplasms; Neoplasms, Glandular and Epithelial; Neoplasms, Squamous Cell; Carcinoma; Adenocarcinoma; Carcinoma, Squamous Cell
• Other Study ID Numbers: CHO-01002

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: Undecided

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No