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Integrin β7, BCMA, CS1, CD38 and CD138 as the Single or Compound Targets for the Fourth Genenation of CAR-T Cells

Integrin β7, BCMA, CS1, CD38 and CD138 as the Single or Compound Targets for the Fourth Genenation of CAR-T Cells

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03778346
Enrollment
30
Registered
2018-12-19
Start date
2018-11-15
Completion date
2022-12-31
Last updated
2020-11-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

RRMM

Brief summary

According to the high expression of tumor cell-associated antigen CD138, integrin β7, CS1, CD38 and BCMA in patients with refractory/recurrent multiple myeloma, the fourth generation of CAR-T cells(simultaneously expressing IL7 and CCL19) with 10 different dual target combinations are used to minimize the tumor burden in the patient individually and precisely and improve the immunosuppressive microenvironment of the tumor , thereby effectively treating refractory/recurrent multiple myeloma .

Detailed description

Multiple myeloma(MM) is one of the most common malignant diseases in the blood system.There is still no cure for the disease which only control the development of the disease in various ways including proteasome inhibitors and immune regulator and hematopoietic stem cell transplantation . Combined with the advantages of multiple therapies, chimeric antigen receptor T cells (CAR-T) have gradually becoming one of the strongest and most powerful weapons against multiple myeloma.The basic principle is to use the patient's own immune cells to clear cancer cells. MM is genetically and phenotypically heterogeneous,Antigen escape and relapse after CAR-T treatment is a global problem, so the effective treatment of refractory/relapsing multiple myeloma with CAR-T cells usually requires targeting multiple antigens. The investigators use Integrin β7(a large family of molecules that are central regulators in multicellular biology and orchestrating cell-cell and cell-extracellular matrix (ECM) adhesive interactions from embryonic development to mature tissue function), BCMA(highly expressed on malignant MM plasma cells and providing a substantial antiapoptotic signal making it an encouraging target for BCMA-directed immunotherapy),CS1(encoded by the SLAMF7 gene,a robust marker of normal plasma cells and malignant plasma),CD38(encoded by the CD38 gene and functioning in cell adhesion, signal transduction and calcium signaling) and CD138(known as syndecan 1, a surface protein expressed on most healthy and malignant plasma cells as an adhesion protein, binding collagen and fibronectin molecules located in the extracellular matrix. ) as the Single or Compound Targets for the Fourth Genenation of CAR-T Cells ,thereby effectively treating refractory/recurrent multiple myeloma .

Interventions

BIOLOGICALCAR-T therapy in Relapsed/Refractory multiple myeloma

Integrin β7, BCMA, CS1, CD38 and CD138 as the Single or Compound Targets for the Fourth Genenation of CAR-T Cells to treat Relapsed/Refractory multiple myeloma

Sponsors

Zhejiang Qixin Biotech
CollaboratorUNKNOWN
The Sixth Affiliated Hospital of Wenzhou Medical University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Patients who meet the requirements voluntarily participate in the study and sign the Informed Consent Form. 2. Age is 18 to 80 years old, gender is not limited. 3. Patients with relapsed or refractory myeloma who meet the following criteria for multiple myeloma diagnostic criteria defined by the IMWG (2017): Subjects have received adequate prior treatment of at least 2 regimens; during the most recent treatment or after treatment , the disease progresses or recurs. 4. The Eastern Cancer Cooperative Group (ECOG) scores 0 to 2 (the tumor causes bone pain). 5. The expected survival period is more than 12 weeks. 6. No other malignant tumors, severe autoimmune diseases or congenital immunodeficiency, serious progressive infection, cranial nerve disorder or mental illness.

Exclusion criteria

1. Pregnant or lactating women. 2. Patients with uncontrollable active infections. 3. Patients with systemic steroids; recent or current use of inhaled steroids is not excluded. 4. Previously involved CAR-T cell therapies produced any uncontrolled disease.

Design outcomes

Primary

MeasureTime frameDescription
Adverse events that are related to treatment2 yearsSafety and tolerability measured by occurrence of study related adverse effects defined by NCI-CTCAE v4.03

Secondary

MeasureTime frameDescription
2 year overall survival(OS)2 yaersTo estimate 2 year overall survival(OS) after BCMA/CD138/CD38/Integrinβ7/CS1-CART infusion and sequential treatment with Relapsed/Refractory MM
3 year progression free survival (PFS)3 yaersTo estimate 3 year progression free survival after BCMA/CD138/CD38/Integrinβ7/CS1 CART infusion and sequential treatment with Relapsed/Refractory MM

Countries

China

Contacts

Primary ContactBingmu Fang, M.D
fbm636@163.com0578-2780108
Backup ContactYonghua Liu, M.D
liuyonghua2010@163.com

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 15, 2026