Salvage immuno-chemotherapy with a combination of rituximab, high-dose cytarabine, mitoxantrone and dexamethasone for patients with primary CNS lymphoma: A preliminary study

2007 ◽  
Vol 48 (7) ◽  
pp. 1429-1433 ◽  
Author(s):  
Ryuya Yamanaka ◽  
Junpei Homma ◽  
Masakazu Sano ◽  
Naoto Tsuchiya ◽  
Naoki Yajima ◽  
...  
Blood ◽  
2013 ◽  
Vol 122 (21) ◽  
pp. 3051-3051
Author(s):  
Beata Ostrowska ◽  
Michal Osowiecki ◽  
Katarzyna Domanska-Czyz ◽  
Joanna Romejko-Jarosinska ◽  
Ewa Paszkiewicz-Kozik ◽  
...  

Abstract Background Currently recommended treatment for the primary CNS lymphoma (PCNSL) involves high-dose methotrexate (HM) preferably in combination with high-dose cytarabine (HA). However, nearly half of the patients present with locally advanced disease and poor performance status (PS) prohibiting the use of this biologically challenging therapy. On the other hand, CHOP±Rituximab with or without HM is considered suboptimal due to generaly negative, if any, published results, and a strong belief in the existence of blood-brain barrier preventing bioavailability of doxorubicin to CNS tissue. In effect, patients with DLBCL of the CNS which is the most common type of PCNSL miss the benefits of the optimal treatment for DLBCL. We evaluated the outcome of patients treated at our institution with variety of regimens evolving over time including CHOP/CHOP-like + HM, HM ± HA, and CHOP-R (rituximab) + HM. Varying proportion of patients received whole brain radiotherapy (WBRT) as well. Patients and Methods Between 2000 and 2011, 92 patients diagnosed with PCNSL were treated. Median age (range) was 59 (19 – 79) years, female: 55%, ECOG performance score (PS) 0-1: 30%, 2: 21%, 3-4: 49%. Most common symptoms at diagnosis were: memory loss (56%), focal symptoms (54%), confusion (36%), depression (20%), seizures (20%), agitation (13%). Diagnosis was established by stereotactic biopsy (50%), craniotomy (48%), and cerebro-spinal fluid flow cytometry in two cases. Total resection of tumor was done in 22%, tumor gross resection (debulking) in 27%, and biopsy only in 51% of patients. Cerebral / spinal parenchyma was involved in 52%, deep brain sites - in 48%. Mass effect and brain edema were present in 70% and 81%, respectively. Multiple brain lesions were present in 39% of patients. Patients were treated on 3 consecutive protocols: 2000-2006 (n=27): CHOP/CHOP-like+HM [median (range) HM total dose: 6.3 g (1.9-21)] with WBRT in 67%, 2006-2010 (n=13): HM±HA including „Bonn“ protocol [median (range) HM total dose 16.8 g (3-25.3) and median (range) HA total dose: 12 g(8-41)] with WBRT in 23%, 2009-2011 (n=19): CHOP-R + HM [median (range) HM total dose: 20 g (3-42)] with WBRT in 26% of patients. 33 patients (36%) received variety of treatments with a palliative intent. Results In all 92 patients, 1-, 2-, and 4-year overall survival (OS) was 50%, 41%, and 24% respectively. In patients treated with a radical approach including intended HM dose of 3 g/m2 per cycle (n=59): 1-, 2-, and 4-year OS was 63%, 59%, and 35%, respectively. In this group, event-free survival (EFS) was 58%, 49%, and 32%, respectively. In patients with PS 0-1, 2, and 3-4, 3-year OS was 67%, 26%, and 8%, respectively. 3-year EFS in these patients was 56%, 27%, and 8%, respectivly (p=0.00). Two-year OS in patients with total tumor resection, debulking, or biopsy only, was 78%, 62%, and 14%, respectively (p=0.00). Deep structure involvement vs cerebral parenchyma was not predictive of OS or EFS (p=0.33). In patients treated with CHOP/CHOP-like+HM with a median follow-up (FU) of 122 months, 1-, 2-, and 4-year OS was 59%, 55%, and 37%, and corresponding EFS was 52%, 48%, and 29%, respectively. 4 patients (15%) died of treatment-related toxicity (TRT). In patients treated with HM±HA, with a median FU of 39 months, 1-, 2-, and 4-year OS was 61%, 54%, and 18%, and corresponding EFS was 53%, 38%, and 20%, respectively. 2 patients (15%) died of TRT. In patients treated with CHOP-R+HM, with a median FU of 30 months, 1-, 2-, and 4-year OS was 68%, 68%, and 49%, and corresponding EFS was 68%, 57%, and 57%, respectively. 12 of 19 patients in this group are alive with no evidence of disease.7 patients died, 3 from disease progression, and 3 (16%) from TRT. Conclusion Outcome of PCNSL patients was highly dependent on the baseline performance score with only few patients with PS 3-4 surviving 3 years. Extent of primary surgery was also predictive of survival. In our series of 92 patients treated on consecutive clincal protocols over a period of 10 years, no benefit to methotreaxte dose escalation or addition of high-dose cytarabine could be demonstrated. The most favorable outcome was achieved with CHOP-R combined with HM at a dose of 3 g/m² per cycle. Disclosures: No relevant conflicts of interest to declare.


The Lancet ◽  
2009 ◽  
Vol 374 (9700) ◽  
pp. 1512-1520 ◽  
Author(s):  
Andrés JM Ferreri ◽  
Michele Reni ◽  
Marco Foppoli ◽  
Maurizio Martelli ◽  
Gerasimus A Pangalis ◽  
...  

Blood ◽  
2016 ◽  
Vol 128 (22) ◽  
pp. 781-781
Author(s):  
Benjamin Kasenda ◽  
Gabriele Ihorst ◽  
Roland Schroers ◽  
Agnieszka Korfel ◽  
Ingo GH Schmidt-Wolf ◽  
...  

Abstract Purpose To investigate safety and efficacy of high-dose chemotherapy followed by autologous stem cell transplantation (HCT-ASCT) in patients with relapsed or refractory primary CNS lymphoma (PCNSL). Patients and methods We conducted a single-arm multicentre phase 2 study for immunocompetent patients (<66 years of age) with PCNSL failing prior HD-MTX based chemotherapy. Induction treatment consisted of 2 courses of rituximab (rituximab 375mg/m2), high-dose cytarabine (2 x 3g/m2) and thiotepa (40mg/m2) with collection of autologous stem cells in between. Conditioning treatment for HCT-ASCT consisted of rituximab 375mg/m2, carmustine 400mg/m2 and thiotepa (4 x 5mg/kg). Patients commenced HCT-ASCT irrespective of response status after induction. Only patients not achieving complete remission (CR) after HCT-ASCT received whole brain radiotherapy (WBRT). The primary endpoint was CR after HCT-ASCT by intention-to-treat (ITT). Secondary endpoints included safety, progression free survival (PFS, time to progression or death) and overall survival (OS, time to death due to any cause). Results Between May 2007 and July 2012, we enrolled 39 patients from 12 German centres. The median age and Karnofsky performance score was 57 years (range 37 to 65) and 90% (range 60% to 100%), respectively. 28 (71.8%) patients had relapsed and 8 (28.2%) refractory disease. 22 (56.4%) patients responded to induction (4 CR, 18 partial remissions [PR]) and 32 (82.1%) patients commenced HCT-ASCT. 22 patients (56.4%, 95% CI 39.6% to 72.2%) achieved CR after HCT-ASCT, 6 (15.4%) achieved PR, and 1 (2.6%) had stable disease. In 9 (17.8%) patients the final scan was not done, because 7 (18.0%) did not undergo HCT-ASCT and 2 died (5.1%) during HCT-ASCT procedure. After a median follow-up of 45.2 months, the respective 2-year PFS and OS rates were 46.0% (95% CI 30.3% to 61.7%, median PFS 12.4 months, Figure 1) and 56.4% (95% CI 40.8% to 72.0%); median OS not reached (Figure 2). The non-relapse mortality rate was 10.3% (95% CI 4.1% to 26.0%) at 1 year without any further increase afterwards. In the subset of 32 patients who received HCT-ASCT, 14 (56.3%) experienced progression or died translating into 1 and 2-year PFS rates (calculated from date of HCT-ASCT) of 62.5% (95% CI 45.7% to 79.3%) and 56.1% (95% CI 38.8% to 73.3%) with no further decrease afterwards. Main grade 3 or higher toxicities were hematological as expected. We recorded four (10.3%) treatment-related deaths, 2 during induction and 2 during HCT-ASCT. Conclusions In eligible PCNSL patients failing HD-MTX based chemotherapy, a short induction with high-dose cytarabine and thiotepa followed by HCT-ASCT is an effective treatment option. Our data provide a reliable benchmark for future comparative studies needed to further scrutinize the role of HCT-ASCT in the salvage setting for PCNSL. Figure 1. Progression free survival Figure 1. Progression free survival Figure 2. Overall survival Figure 2. Overall survival Disclosures Kasenda: Riemser: Other: Travel Support. Schmidt-Wolf:Janssen: Research Funding; Novartis: Research Funding. Röth:Alexion Pharmaceuticals: Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Novartis: Honoraria. Stilgenbauer:Amgen: Consultancy, Honoraria, Other: Travel grants, Research Funding; Genentech: Consultancy, Honoraria, Other: Travel grants , Research Funding; Boehringer Ingelheim: Consultancy, Honoraria, Other: Travel grants , Research Funding; Janssen: Consultancy, Honoraria, Other: Travel grants , Research Funding; Hoffmann-La Roche: Consultancy, Honoraria, Other: Travel grants , Research Funding; Pharmacyclics: Consultancy, Honoraria, Other: Travel grants , Research Funding; Novartis: Consultancy, Honoraria, Other: Travel grants , Research Funding; Sanofi: Consultancy, Honoraria, Other: Travel grants , Research Funding; Gilead: Consultancy, Honoraria, Other: Travel grants , Research Funding; AbbVie: Consultancy, Honoraria, Other: Travel grants, Research Funding; Mundipharma: Consultancy, Honoraria, Other: Travel grants , Research Funding; Genzyme: Consultancy, Honoraria, Other: Travel grants , Research Funding; GSK: Consultancy, Honoraria, Other: Travel grants , Research Funding; Celgene: Consultancy, Honoraria, Other: Travel grants , Research Funding. Illerhaus:Riemser: Honoraria; Amgen: Honoraria.


2020 ◽  
Vol 2 (Supplement_3) ◽  
pp. ii2-ii2
Author(s):  
Eisei Kondo

Abstract High-dose chemotherapy followed by autologous hematopoietic stem cell transplantation (HDT-ASCT) is listed as a consolidation therapy option for primary central nervous system (CNS) lymphoma in the guidelines of western countries. The advantages of HDT-ASCT for primary CNS lymphoma as consolidation are believed to be high rates of long-term remission and lower neurotoxicity, even though its eligibility is limited to younger fit patients. In the Japanese guideline, HDT-ASCT for primary CNS lymphoma is however not recommended in daily practice, mainly because thiotepa was unavailable since 2011. The Japanese registry data for hematopoietic transplantation have shown that primary CNS lymphoma patients were treated with various HDT regimens and thiotepa-containing HDT was associated with better progression free survival (P=.019), lower relapse (P=.042) and a trend toward a survival benefit (Kondo E et al, Biol Blood Marrow Transplant 2019). A pharmacokinetic study of thiotepa(DSP-1958) in HDT-ASCT for lymphoma was conducted in 2017, and thiotepa was approved for HDT-ASCT in lymphoma this March, meaning that optimal HDT regimen for CNS lymphoma is now available in Japan. The treatment strategy of CNS lymphoma needs further development to improve survival and reduce toxicity.


Blood ◽  
2020 ◽  
Vol 136 (19) ◽  
pp. 2229-2232
Author(s):  
Kathryn Lurain ◽  
Thomas S. Uldrick ◽  
Ramya Ramaswami ◽  
Mark N. Polizzotto ◽  
Priscila H. Goncalves ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Junyao Yu ◽  
Huaping Du ◽  
Xueshi Ye ◽  
Lifei Zhang ◽  
Haowen Xiao

AbstractWith the exception of high-dose methotrexate (HD-MTX), there is currently no defined standard treatment for newly diagnosed primary central nervous system lymphoma (PCNSL). This review focused on first-line induction and consolidation treatment of PCNSL and aimed to determine the optimal combination of HD-MTX and the long-term beneficial consolidation methods. A comprehensive literature search of MEDLINE identified 1407 studies, among which 31 studies met the inclusion criteria. The meta-analysis was performed by using Stata SE version 15. Forest plots were generated to report combined outcomes like the complete response rate (CRR), overall survival, and progression-free survival. We also conducted univariate regression analyses of the baseline characteristics to identify the source of heterogeneity. Pooled analysis showed a CRR of 41% across all HD-MTX-based regimens, and three- and four-drug regimens had better CRRs than HD-MTX monotherapy. In all combinations based on HD-MTX, the HD-MTX + procarbazine + vincristine (MPV) regimen showed pooled CRRs of 63% and 58% with and without rituximab, respectively, followed by the rituximab + HD-MTX + temozolomide regimen, which showed a pooled CRR of 60%. Pooled PFS and OS showed that post-remission consolidation with autologous stem cell transplantation (ASCT) was associated with the best survival outcome, with a pooled 2-year OS of 80%, a 2-year PFS of 74%, a 5-year OS of 77%, and a 5-year PFS of 63%. Next, whole-brain radiation therapy (WBRT) + chemotherapy showed a pooled 2-year OS of 72%, 2-year PFS of 56%, 5-year OS of 55%, and 5-year PFS of 41%, with no detectable CR heterogeneity throughout the entire treatment process. In HD-MTX-based therapy of newly diagnosed PCNSL, MPV with or without rituximab can be chosen as the inductive regimen, and the rituximab + HD-MTX + temozolomide regimen is also a practical choice. Based on our study, high-dose chemotherapy supported by ASCT is an efficacious approach for consolidation. Consolidation with WBRT + chemotherapy can be another feasible approach.


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