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| Name | Class |
|---|---|
| Xinqiao Hospital of Chongqing | OTHER |
| The First Affiliated Hospital of Anhui Medical University | OTHER |
| Harbin Hematology and Oncology Institute | OTHER |
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This multi-center clinical study will evaluate the efficacy and safety of Cladribine Combined With BEAC Pretreatment Regimen in the Treatment of Peripheral T-cell Lymphoma.
Peripheral T-cell lymphomas (PTCL) is a group of highly heterogeneous aggressive non-Hodgkin lymphomas originating from mature post-thymic T lymphocytes or NK/T cells. The treatment effect of patients receiving autologous hematopoietic stem cell transplantation (ASCT) is better than traditional chemotherapy, but the recurrence after transplantation is still as high as 50%. It is an urgent clinical problem to reduce the recurrence after PTCL transplantation. Cladribine can kill quiescent tumor cells, which is the main reason of tumor recurrence. Since 2018, our center has used cladribine combined with BEAC pretreatment regimen to treat 20 patients with PTCL. The PFS reached 68% at 2 years, which is about 15% higher than the previous classic BEAC regimen. This multi-center clinical study will further evaluate the efficacy and safety of Cladribine combined with BEAC pretreatment regimen in the Treatment of Peripheral T-cell Lymphoma.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| BEAC | Active Comparator | Patients in this arm will receive BEAC (Semustine, Etoposide, Cytarabine, Cyclophosphamide) as pretreatment regimen of ASCT |
|
| Cladribine combined with BEAC | Experimental | Patients in this arm will receive Cladribine combined with BEAC (Semustine, Etoposide, Cytarabine, Cyclophosphamide) as pretreatment regimen of ASCT |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| BEAC | Drug | Semustine, 300 mg/m2,-6d; Etoposide, 100 mg/m2,-5~-2d; Cytarabine, 100mg/m2,q12h,-5~-2d; Cyclophosphamide, 1.5g/m2,-5~-2d |
|
| Measure | Description | Time Frame |
|---|---|---|
| Progression free survival | Progression-free survival was defined as the time from the date of ASCT until the date of the first documented day of disease progression or relapse, using Revised Standards for Efficacy Evaluation of Malignant Lymphoma in 2007, or death from any cause, whichever occurred first. | Baseline up to data cut-off (up to approximately 2 years) |
| Measure | Description | Time Frame |
|---|---|---|
| Overall survival | Overall survival was defined as the time from the date of ASCT to the date of death from any cause. | Baseline up to data cut-off (up to approximately 2 years) |
| Overall remission rate |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Weili Zhao | Contact | +862164370045 | zwl_trial@163.com | |
| Pengpeng Xu | Contact | +862164370045 | pengpeng_xu@126.com |
| Name | Affiliation | Role |
|---|---|---|
| Weili Zhao | Ruijin Hospital | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Ruijin Hospital | Recruiting | Shanghai | Shanghai Municipality | China |
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| Affiliated Zhongshan Hospital of Dalian University |
| OTHER |
| Qilu Hospital of Shandong University | OTHER |
| Fujian Medical University Union Hospital | OTHER |
| Shanxi Province Cancer Hospital | OTHER |
| RenJi Hospital | OTHER |
| Xinhua Hospital, Shanghai Jiao Tong University School of Medicine | OTHER |
| Huashan Hospital | OTHER |
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| Cladribine combined with BEAC | Drug | Cladribine, 6mg/m2,-5~-2d, two hours before Cytarabine Semustine, 300 mg/m2,-6d; Etoposide, 100 mg/m2,-5~-2d; Cytarabine, 100mg/m2,q12h,-5~-2d; Cyclophosphamide, 1.5g/m2,-5~-2d |
|
Percentage of participants with overall response was determined on the basis of Revised Standards for Efficacy Evaluation of Malignant Lymphoma in 2007.
| 3 months after the transplantation |
| Transplantation-related adverse reactions | Transplantation-related adverse reactions are any untoward medical occurrence in a participant which is related to ASCT | Baseline up to data cut-off (up to approximately 5 years) |
| Patient tolerance | Percentage of participants who can tolerate the whole treatment of ASCT | Through the whole course of ASCT, an average of one month |
| Relapse rate | Percentage of participants who relapse determined on the basis of Revised Standards for Efficacy Evaluation of Malignant Lymphoma in 2007. | Baseline up to data cut-off (up to approximately 5 years) |
| ID | Term |
|---|---|
| D016411 | Lymphoma, T-Cell, Peripheral |
| ID | Term |
|---|---|
| D016399 | Lymphoma, T-Cell |
| D008228 | Lymphoma, Non-Hodgkin |
| D008223 | Lymphoma |
| D009370 | Neoplasms by Histologic Type |
| D009369 | Neoplasms |
| D008232 | Lymphoproliferative Disorders |
| D008206 | Lymphatic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
| D007160 | Immunoproliferative Disorders |
| D007154 | Immune System Diseases |
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| ID | Term |
|---|---|
| C051019 | BAEC protocol |
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