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UnknownNCT04134247

Study of PD-1 Monoclonal Antibody in Combination With Chemotherapy in Patients With RR NHL

Study of PD-1 Monoclonal Antibody in Combination With Chemotherapy in Patients With Relapsed or Refractory Non-Hodgkin Lymphoma

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
120 (estimated)
Sponsor
Shandong Provincial Hospital · Other Government
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Lymphoma is one of the fastest growing malignancies in the world, with an annual incidence rate of about 4%. Non-Hodgkin's lymphoma (NHL) is highly heterogeneous and can be broadly divided into two major categories, B-cell lymphoma and T/NK cell lymphoma. It is composed of diseases of different pathological types and malignant degrees, and the prognosis is not the same.The anti-PD-1 antibody may benefit patients with relapsed or refractory Hodgkin's lymphoma. At the same time, in non-Hodgkin's lymphoma, PD1 antibodies also show promising therapeutic prospects. We propose this research program, based on the previous research at home and abroad, to further clarify the role of PD-1 monoclonal antibody combined with chemotherapy in the treatment of relapsed and refractory NHL patients, evaluate its clinical efficacy and safety, and explore The best treatment strategy for patients with relapsed and refractory NHL in China.

Detailed description

Lymphoma is one of the fastest growing malignancies in the world, with an annual incidence rate of about 4%. In recent years, the incidence of malignant lymphoma in China has increased rapidly. It has risen to the ninth place among the top ten high-incidence tumors in men, and the female has risen to the eleventh place. In 2011, the incidence of lymphoma in the country has reached 6.43/100,000. According to the characteristics of clinicopathology, lymphoma is divided into two categories: Hodgkin's lymphoma (HL) and non-Hodgkin's lymphoma (NHL). HL is a single disease, relatively rare, but the prognosis is good, and patients with limited period have no progress for 5 years. The survival rate was 85-95%, and the 5-year progression-free survival rate of advanced patients was 30-85%. NHL is highly heterogeneous and can be broadly divided into two major categories, B-cell lymphoma and T/NK cell lymphoma. It is composed of diseases of different pathological types and malignant degrees, and the prognosis is not the same. In recent years, immunological checkpoint inhibitors have been the focus of research in the field of malignant tumor treatment. In clinical trials, PD-1/PD-L1 was found to be abnormally expressed in various lymphomas, including T-cell lymphoma, mediastinal large B-cell lymphoma, classical Hodgkin's lymphoma (CHL), and large variability. Cell lymphoma. Previous studies have evaluated the effects of antibody-based drugs against PD-1 (such as navobizumab and pabuleizumab) in patients with relapsed or refractory classic Hodgkin's lymphoma, and A higher response rate is shown and the security feature is acceptable. The domestic ORIENT-1 study showed that ididilimumab was highly active in patients with relapsed or refractory classic Hodgkin's lymphoma in China, and 80% (74/92) patients had an objective response. No patients died during the study. Of the 96 patients treated, 89 (93%) had treatment-related adverse events, including 17 (18%) patients with grade 3 or 4 treatment-related adverse events, and 11 patients (11%) experienced severe Adverse events, but no unexpected or off-target safety signals were found. Therefore, PD1 antibodies may benefit patients with relapsed or refractory Hodgkin's lymphoma. At the same time, in non-Hodgkin's lymphoma, PD1 antibodies also show promising therapeutic prospects. Clinical studies at home and abroad have shown that PD-1 inhibitors are effective in relapsed or refractory extranodal NKT lymphoma. The results of the Idiliumab ORIENT-4 test showed that 1 year OS 82.1%, ORR 67.9%, DCR 85.7%, and PD-1 inhibitor combined with citabin to treat relapsed or refractory extranodal NKT is underway; PD-1 inhibitor monotherapy for relapsed or refractory PTCL is generally effective (ORR 33%, 4 of them CR); PD-1 inhibitor monotherapy is effective in treating relapsed or refractory mycosis/Sezary syndrome (ORR) 37.5%) has been recommended by the NCCN guidelines; trials in combination with IFN γ-1b are underway. PD-1 inhibitor monotherapy for relapsed or refractory PMBCL or PCNSL is effective, and PD-1 inhibitors have been recommended by the NCCN guidelines for the former treatment. Therefore, we propose this research program, based on the previous research at home and abroad, to further clarify the role of PD-1 monoclonal antibody combined with chemotherapy in the treatment of relapsed and refractory NHL patients, evaluate its clinical efficacy and safety, and explore The best treatment strategy for patients with relapsed and refractory NHL in China.

Conditions

Interventions

TypeNameDescription
DRUGPD-1 combined with chemotherapyPD-1 200 mg,d1; Rituximab 375mg/m2,d0( the same as the chemotherapy group) The chemotherapy chooses one of the following: GDP:Gemcitabine 800-1000mg/m2, d1、8; Cisplatin 25mg/m2, d1-3; Dexamethasone 40mg, d1-4; GemOx:Gemcitabine 800-1000mg/m2, d1、8; Oxaliplatin 130mg/m2,d1; DA-EPOCH:Epirubicin 15mg/m2 ,d1-4; Etoposide 50mg/m2 ,d1-4; Vincristine 0.4mg/ m2 ,d1-4; Cyclophosphamide 750mg/ m2 , d5; Prednisone 60mg/m2/d, d1-5; ICE: Ifosfamide 1g/m2,d1-4; Cisplatin 25mg/m2, d1-4; Etoposide 60 mg/m2,d1-4; DICE: Ifosfamide 1 g/m2,dl-d4; Cisplatin 25mg/m2, d1-4; Etoposide 60 mg/m2,d1-4; Dexamethasone 10-20mg,d1-4; High dose MTX(Central recurrence):MTX 3.5g/m2,d1; Hyper CVAD(B):MTX 1g/m2, d1; Cytarabine 2-3g/m2, q12h, d2-3
DRUGchemotherapyRituximab 375mg/m2,d0( Except for patients who relapsed within12 months after the last application of rituximab) The chemotherapy chooses one of the following: GDP:Gemcitabine 800-1000mg/m2, d1、8; Cisplatin 25mg/m2, d1-3; Dexamethasone 40mg, d1-4; GemOx:Gemcitabine 800-1000mg/m2, d1、8; Oxaliplatin 130mg/m2,d1; DA-EPOCH:Epirubicin 15mg/m2 ,d1-4; Etoposide 50mg/m2 ,d1-4; Vincristine 0.4mg/ m2 ,d1-4; Cyclophosphamide 750mg/ m2 , d5; Prednisone 60mg/m2/d, d1-5; ICE: Ifosfamide 1g/m2,d1-4; Cisplatin 25mg/m2, d1-4; Etoposide 60 mg/m2,d1-4; DICE: Ifosfamide 1 g/m2,dl-d4; Cisplatin 25mg/m2, d1-4; Etoposide 60 mg/m2,d1-4; Dexamethasone 10-20mg,d1-4; High dose MTX(Central recurrence):MTX 3.5g/m2,d1; Hyper CVAD(B):MTX 1g/m2, d1; Cytarabine 2-3g/m2, q12h, d2-3

Timeline

Start date
2019-11-01
Primary completion
2021-11-01
Completion
2021-11-01
First posted
2019-10-22
Last updated
2019-10-22

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT04134247. Inclusion in this directory is not an endorsement.