scholarly journals Case Report: Bortezomib Plus CDOP Followed by Sequential Autologous Hematopoietic Stem Cell Transplantation and Lenalidomide-Based Maintenance Therapy in Plasmablastic Lymphoma

2021 ◽  
Vol 8 ◽  
Author(s):  
Jiao Cai ◽  
Ling Qiu ◽  
Lei Ma ◽  
Nan Zhang ◽  
Fang-yi Fan

The standardized treatment plan for patients with plasmablastic lymphoma (PBL) remains controversial. Taking morphological characteristics and immunophenotypes into consideration may provide superior options for the treatment of PBL. In this case, we report that a myeloma-type regimen containing bortezomib plus cyclophosphamide, epirubicin, vindesine and prednisolone (CDOP) followed by sequential autologous hematopoietic stem cell transplantation (ASCT) and lenalidomide-based maintenance therapy to treat PBL may represent a promising regimen to improve the prognosis.

Blood ◽  
2007 ◽  
Vol 110 (11) ◽  
pp. 2812-2812 ◽  
Author(s):  
Philippe Rousselot ◽  
Françoise Huguet ◽  
Norbert Vey ◽  
Kamal Bouabdallah ◽  
Jacques Delaunay ◽  
...  

Abstract We previously reported a 93% CR rate in patients with Philadelphia positive acute lymphoblastic leukemias (Ph+ ALL) treated with an imatinib (Glivec®) based induction (DIV regimen) (Rea et al. Leukemia, 2006;20:400–3). We decided to further confirm these results in a larger prospective cohort of patients and to evaluate the combination of imatinib and Pegasys® for patients in CR not eligible for hematopoietic stem cell transplantation (HSCT). Patients not previously exposed to imatinib and with resistant or refractory Ph+ ALL, lymphoid blast crisis CML (LBC CML) or with de novo Ph+ ALL and aged over 55y were eligible. The DIV regimen consisted in one IV injection of vincristine 2 mg combined with 2 days of dexamethasone 40 mg PO repeated weekly for 4 weeks as induction and then monthly for 4 months as consolidation. Imatinib was administered at 800 mg per day during the induction period and at 600 mg/d continuously with 6 mercaptopurine during consolidation. Patients in CR not eligible for HSCT were allocated to maintenance therapy consisting in weekly SC injection of Pegasys® 45 μg and continuous administration of imatinib 400 mg per day for 2 years. 54 patients (median age 62y, 22 to 83) were included (22 resistant or refractory Ph+ ALL, 3 relapsed Ph+ ALL, 4 LBC CML and 25 elderly Ph+ ALL). The median follow up was 18 months. The overall CR rate after induction was 85%. 42 patients were eligible for post consolidation therapy: 18 patients received HSCT (10 allogenic HSCT including 9 out of the 15 patients aged under 55y and 8 autologous HSCT). 18 out of 24 patients (75%) without HSCT started the maintenance therapy. Reasons for not being in maintenance were relapse in one case, septic death in 3 cases and toxicity in 2 cases. The interval from CR to HSCT was 5.8 months in median (2.6 to 11.3). The medain interval from CR to maintenance was 5.4 months (5.2 to 6.7). The median survival of the transplanted group of patients was 29.9 months compared to 27.9 months for patients treated with the maintenance schedule (p=0,98). Six patients (33%) relapsed in the HSCT group and 7 (38.8%) in the maintenance group. Grade 2 to 4 neutropenia and/or thrombocytopenia were observed in 33% of cases during maintenance therapy leading to transient interruption of Pegasys® injections. Extra haematological grade 3 to 4 toxicities were infrequent (1 papillary oedema and two infections). We confirm here the high CR rate obtained in Ph+ acute lymphocytic leukemias with the DIV regimen, without the need of intensive chemotherapy. Maintenance therapy with Pegasys® and imatinib represents an alternative approach for patients not eligible for HSCT and was associated with a median survival of 27.9 months in this study.


Blood ◽  
2016 ◽  
Vol 128 (22) ◽  
pp. 5833-5833
Author(s):  
Chengcheng Fu ◽  
Yun Xu ◽  
Juan Wang ◽  
Jin Zhou ◽  
Ling Ma ◽  
...  

Abstract Though a large number of studies have confirmed that large dose chemotherapy combined with autologous transplantation can improve the OS and PFS in patients with multiple myeloma, the suitable time for transplantation is not yet conclusive. The impact of treatment depth on survival and the essentiality of maintenance therapy after autologous transplantation because of the maintenance-related side effects is also inconclusive. To evaluate the efficacy of autologous hematopoietic stem cell transplantation (ASCT) in the treatment of multiple myeloma (MM), the effects of transplantation timing, depth of treatment and maintenance therapy on survival in patients with multiple myeloma (MM). The data of 111 patients with multiple myeloma who received autologous hematopoietic stem cell transplantation (ASCT) from April 30, 2004 to June 30, 2015 were retrospectively analyzed. The median follow-up period was 31 (6-139) months. 109 of the 111 patients successfully underwent hematopoietic reconstruction,2 patients died of transplantation-related mortality. The overall response rates(ORR)rate increased from 82.9%(92/111)at pre-ASCT to 91.9%(102/111)at post-ASCT. The median progress free survival(PFS)was 50 months. The median overall survival(OS)was not reached. The median PFS and median OS in the sequential transplantation group were significantly better than those in the non sequential transplantation group (86 months vs33 months, P=0.001,not reached vs 43 months, P=0.000).The median PFS of patients achieving a nCR at pre-ASCT was longer than those not achieving a nCR group (62 months vs 34 months, P=0.023).OS showed any significance(not reached vs 47 months, P=0.094).The median PFS of patients achieving a nCR at post-ASCT was longer than those not achieving a nCR group (54 months vs 26 months, P=0.004).OS showed any significance(not reached vs 53 months, P=0.128).Regarding maintenance therapy:the group of patients achieving post-ASCT nCR:The median PFS of patients with maintenance therapy was longer than those without maintenance treatment(86 months vs 33 months, P=0.009).The median OS in maintenance therapy group was not reached,the median OS in the maintenance free treatment group was 47 months (P=0.004).The group of patients achieving less than nCR at post-ASCT:In the maintenance group, the median PFS was 26 months,the median PFS for maintenance free treatment group was 9 months (P=0.518).The median OS of patients with maintenance therapy was longer than those without maintenance treatment(53 months vs 28 months, P=0.011). Autologous transplantation after induction chemotherapy, with maintenance therapy is the preferred treatment for patients with MM.The depth of treatment has a great influence on the survival time of patients,Patients with nCR at any time during the therapy (pre-ASCT,post-ASCT) had longer OS.Maintenance therapy is associated with an extended OS, no matter whether a nCR is reached or not at post-ASCT. Disclosures No relevant conflicts of interest to declare.


Sign in / Sign up

Export Citation Format

Share Document