A Study of CAR-T Cells Therapy for Patients With Relapsed and/or Refractory Central Nervous System Hematological Malignancies

Trial statusRecruiting
Trial phaseEarly Phase 1
Trial typeInterventional
Biological sexAll
Age3-75
SponsorZhejiang University

About this trial

A Study of CAR-T Cells Therapy for Patients With Relapsed and/or Refractory Central Nervous System Hematological Malignancies

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Male or female aged 3-70 years;

Histologically confirmed diagnosis of B-ALL per the US National Comprehensive Cancer Network (NCCN) Clinical Practice Guidelines for Acute Lymphoblastic Leukemia (2016.v1);

CR not achieved after standardized chemotherapy;

CR achieved following the first induction, but CR duration isless than 12 months;

Disqualifiers

History of craniocerebral trauma, conscious disturbance,epilepsy,cerebrovascular ischemia, and cerebrovascular hemorrhagic diseases;

Electrocardiogram shows prolonged QT interval, severe heart diseases such as severe arrhythmia in the past;

Pregnant (or lactating) women;

Patients with severe active infections (excluding simple urinarytractinfectionand bacterial pharyngitis);

Trial design

Design model

Single group

Treatments tested in this trial

  • CAR-T cells

    Drug

    Each subject receive CAR T-cells by intravenous infusion

  • Ommaya Reservoir

    Procedure/Surgery

    Surgical catheter placement into the fourth ventricle of the brain

Treatment groups

72 Participants
are divided into 1 treatment group
Group A: Administration of CAR T-cellsExperimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

Dose-limiting toxicity (DLT)

Adverse events assessed according to NCI-CTCAE v5.0 criteria

Time frame
Baseline up to 28 days after CAR T-cells infusion
2

Incidence of treatment-emergent adverse events (TEAEs)

Incidence of treatment-emergent adverse events \[Safety and Tolerability\]

Time frame
Up to 2 years after CAR T-cells infusion

Secondary outcomes

1

B-cell acute lymphocytic leukemia(B-ALL), Overall response rate (ORR)

Assessment of ORR (ORR = CR + CRi) at Month 6, 12, 18 and 24

Time frame
At Month 1, 3, 6, 12, 18 and 24
2

B-ALL, Overall survival (OS)

From the first infusion of CAR-T cells to death or the last visit

Time frame
Up to 2 years after CAR-T cells infusion
3

B-ALL, Event-free survival (EFS)

From the first infusion of CAR-T cells to the occurrence of any event, including death, relapse orgene relapse, disease progression (any one occurs first), and the last visit

Time frame
Up to 2 years after CAR-T cells infusion
4

B cell non-hodgkin's lymphoma (B-NHL), Overall response rate (ORR)

Assessment of ORR (ORR = CR + PR) per Lugano 2014 criteria

Time frame
At Week 4, 12, and Month 6, 12, 18, 24

Other outcomes

Sponsors and contacts

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