Clinical Study of Pabolizumab for Neoadjuvant Immunotherapy of Locally Advanced Microsatellite-unstable Gastric Adenocarcinoma

NCT05816863 | Unknown FDA Drug

• 1 other identifier: LGH2021374
• Study Type: observational
• Target: 32
• Locations: 1 country
• Sites: 1

Brief Summary

Our study is aim to evaluate the efficacy and safety of pabolizumab in neoadjuvant immunotherapy of locally advanced microsatellite-unstable gastric adenocarcinoma.

Conditions

Gastric Cancer; Gastric Adenocarcinoma

Keywords

PD-1; immuno-oncology; pabolizumab; neoadjuvant; immunotherapy

Outcome Measures

Primary Outcomes (1)

• Pathologic Complete Response (pCR) Rate

  pCR is defined as absence of viable tumor (pT0pT0N0) in examined tissue

  Up to approximately 15 Weeks (Time of surgery)

Secondary Outcomes (3)

• Overall Survival (OS)

  Up to approximately 71 months.

• Progression free survival (PFS)

  3 years.

• R0 resection rate

  Within 4 weeks following the operation.

Study Arms (1)

Experimental

pabolizumab

Drug: pabolizumab

Interventions

pabolizumab DRUG

pabolizumab IV every 3 weeks (q3w)

Experimental

Eligibility Criteria

• Age: 18 Years - 75 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Probability Sample

Study Population

Patients with locally advanced microsatellite-unstable gastric adenocarcinoma

You may qualify if:

• ECOG 0-1.
• Gastroscopy confirmed adenocarcinoma of the gastroesophageal junction or stomach and biopsy pathology confirmed adenocarcinoma of the stomach.
• Advanced gastric cancer as assessed by ultrasonography and/or gastric CT (cT3-T4b, Nany, M0).
• Biopsy tissues with IHC indicates deficient mismatch repair(dMMR),that is, the loss of at least one of the four proteins ,MSH1, MSH2, MSH6, PMS2; or gene detection implies MSI-H;
• Subjects must have at least one measurable lesion in accordance with RECIST v1.1. A lesion previously treated with local therapies such as radiotherapy can be considered a target lesion if there is objective evidence of progression in the lesion.
• Is willing to provide tissue from a tumor lesion at baseline and at time of surgery.
• Has life expectancy of greater than 6 months.
• Adequate organ function.

You may not qualify if:

• Female participants who are pregnant or breastfeeding or expecting to conceive children within the projected duration of the study, starting with the screening visit through180 days after the last dose of chemotherapy or through 120 days after the last dose of pembrolizumab, whichever is greater.
• Uncontrolled pleural effusion, pericardial effusion, or ascites requiring repeated drainage.
• as a known additional malignancy that is progressing or has required active treatment within the past 5 years. Note: Participants with basal cell carcinoma of the skin, squamous cell carcinoma of the skin, or carcinoma in situ that have undergone potentially curative therapy are not excluded.
• Any disease requiring systemic treatment. Local replacement steroids are permitted
• Subjects with active, known or suspected autoimmune disease, or a medical history of autoimmune disease, with the exceptions of the following: vitiligo, alopecia, Grave disease, psoriasis or eczema not requiring systemic treatment within the last 2 years, hypothyroidism (caused by autoimmune thyroiditis) only requiring steady doses of hormone replacement therapy and type I diabetes only requiring steady doses of insulin replacement therapy, or completely relieved childhood asthma that requires no intervention in adulthood, or primary diseases that will not relapse unless triggered by external factors.
• Known history of allogeneic organ transplantation or allogeneic hematopoietic stem cell transplantation.
• Known history of active tuberculosis (TB).
• Serious infections within 4 weeks prior to the first dose of study drug, including but not limited to complications requiring hospitalization, sepsis or severe pneumonia.
• An active infection requiring systemic therapy.
• Subjects with untreated chronic hepatitis B or chronic hepatitis B virus (HBV) DNA exceeding 2000 IU/ mL or active hepatitis C virus (HCV) should be excluded. Subjects with non-active HBsAg carriers, treated and stable hepatitis B (HBV DNA \<500 IU/ mL) , and cured hepatitis C can be enrolled. Subjects with positive HCV antibodies are eligible only if the HCV RNA test results are negative.
• Known history of testing positive for human immunodeficiency virus (HIV).
• Any conditions that, in the investigator's opinion, may put subjects treated with the study drug at risks, or interfere with the evaluation of study drug or subject safety, or the interpretation of results.
• Known history of allergy or hypersensitivity to Pabolizumab or any of its components

Sponsors & Collaborators

• Peking University Cancer Hospital & Institute: lead

Study Sites (1)

Beijing Cancer Hospital

Beijing, Beijing Municipality, 100142, China

RECRUITING

MeSH Terms

Conditions

Stomach Neoplasms

Condition Hierarchy (Ancestors)

Gastrointestinal Neoplasms; Digestive System Neoplasms; Neoplasms by Site; Neoplasms; Digestive System Diseases; Gastrointestinal Diseases; Stomach Diseases

Central Study Contacts

Jialin Li, MD

CONTACT

8601088196970; ljldoc@163.com

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Zhaode Bu. MD

Study Record Dates

• First Submitted: April 4, 2023
• First Posted: April 18, 2023
• Study Start: March 1, 2023
• Primary Completion: March 1, 2024
• Study Completion: March 1, 2024
• Last Updated: April 18, 2023

Record last verified: 2023-04

Locations

CN (1)