scholarly journals Impact of relative dose intensity of standard regimens on survival in elderly patients aged 80 years and older with diffuse large B-cell lymphoma

Haematologica ◽  
2020 ◽  
Vol 105 (8) ◽  
pp. e415-e418 ◽  
Author(s):  
Shin Lee ◽  
Kei Fujita ◽  
Eiju Negoro ◽  
Tetsuji Morishita ◽  
Kana Oiwa ◽  
...  
2016 ◽  
Vol 58 (3) ◽  
pp. 736-739 ◽  
Author(s):  
Yusuke Kanemasa ◽  
Tatsu Shimoyama ◽  
Yuki Sasaki ◽  
Miho Tamura ◽  
Takeshi Sawada ◽  
...  

Blood ◽  
2007 ◽  
Vol 110 (11) ◽  
pp. 4456-4456
Author(s):  
Yoshiki Terada ◽  
Hirohisa Nakamae ◽  
Takahiko Nakane ◽  
Hideo Koh ◽  
Yasunobu Takeoka ◽  
...  

Abstract Introduction: The achievement of a clinical response to the first induction chemotherapy has been considered for predicting survival in patients (pts) with aggressive non-Hodgkin lymphoma (NHL). Reduced dose intensity of chemotherapy has been likely to compromise long-term outcome of the patients with aggressive NHL treated with a standard chemotherapy of cyclophosphamide (CY), doxorubicin (ADR), vincristine and prednisone (CHOP). In particular, recent studies have revealed the relevance of relative dose intensity (RDI) to clinical outcomes, with reduced RDI leading to a poor survival, as well as the impact of RDI<85% for aggressive NHL with detailed analysis of risk factors influencing reduce RDI<85% (Gary H. Lyman, J. Clin Oncol22: 4302, 2004). This study was conducted to investigate the impact of RDI<85% of CHOP on outcomes of the pts with diffuse large B-Cell lymphoma (DLCL). Methods: Data were retrospectively collected on 100 pts with DLCL who had been initially treated with more than 3 courses of CHOP (n=70) or CHOP plus rituximab (CHOP-R, n=30) at our institution between 1995 and 2006. We evaluated whether RDI might affect clinical outcomes, including complete response (CR) and event free survival (EFS). The average RDI derived from CY and ADR (referred to as RDI-CY/ADR) was determined for each patient, with classified into 2 populations according to the differences from the value of 85%, including RDI-CY/ADR<85% (n=60), and RDI-CY/ADR≥85% (n=40). Results: The median age of the study population was 54 years (range, 17 to 76), with 36 pts older than 60 years (yrs) of age. According to International Prognostic Index (IPI) score, pts were classified into 2 groups of low/ low-intermediate (n=46) and high/ high-intermediate (n=54). The overall CR rate reached 62%, and the probability of overall survival (OS) or EFS at 5 years estimated 77% or 43%, respectively with a median follow-up of 13.3 months. Multivariate analysis identified RDI-CY/ADR<85%, as well as IPI score to be associated with CR rate and EFS. Thus, RDI-CY/ADR<85% and IPI score of high/ high-intermediate were significant factors for lower CR rate (as RDI-CY/ADR≥85%, HR=0.3, 95% CI 0.1 to 0.7, p=0.009, and HR=5.5, 95% CI 2.2 to 14, p<0.001, respectively), and for reduced EFS (HR=1.9, 95% CI 1.0 to 3.7, p=0.048, and as IPI score of low/ low-intermediate HR=0.3, 95% CI 0.2 to 0.6, p<0.001, respectively). Furthermore, logrank analysis revealed that CY/ADR-RDI<85% was the significant factor for reduced EFS in non elderly pts (≤60 yrs of age), or in pts with IPI score of low/ low-intermediate (p=0.01, p=0.02, respectively). Conclusion: These data thus suggested the impact of RDI-CY/ADR<85% in influencing outcomes of the pts with DLCL, in terms of CR rate and EFS. Further investigation is currently planned to confirm this promising results with longer follow-up in larger numbers of pts with NHL.


2019 ◽  
Vol 8 (3) ◽  
pp. 1103-1109 ◽  
Author(s):  
Monika Długosz‐Danecka ◽  
Sebastian Szmit ◽  
Tomasz Ogórka ◽  
Aleksander B. Skotnicki ◽  
Wojciech Jurczak

Blood ◽  
2009 ◽  
Vol 114 (22) ◽  
pp. 406-406 ◽  
Author(s):  
Richard Delarue ◽  
Herve Tilly ◽  
Gilles Salles ◽  
Christian Gisselbrecht ◽  
Nicolas Mounier ◽  
...  

Abstract Abstract 406 Introduction: In 2000, the Gela demonstrated the survival advantage of adding Rituximab to CHOP21 over CHOP21 in the treatment of diffuse large B-cell lymphoma (DLBCL) in elderly patients. Two consecutive studies from the German group have shown an improvement of survival with CHOP14 compared to CHOP21, and then after with R-CHOP14 compared to CHOP14. Here, we report the results of the planned interim analysis of the LNH03-6B, a multicentric, phase III open-label, randomized trial evaluating the efficacy of R-CHOP given every 14 days compared to R-CHOP given every 21 days, held after the inclusion of the first 202 patients, with a median follow-up of 24 months. Patients and methods: Patients between 60 and 80 years old with DLBCL and aaIPI ≥ 1 were eligible. They were randomized between two immunochemotherapy regimens combining Rituximab and CHOP given every 2 (R-CHOP14, arm A) or 3 weeks (R-CHOP21, arm B) for 8 cycles. They were subsequently randomized between a prophylactic treatment with Darbepoetin alfa and a conventional treatment of chemotherapy-induced anemia. G-CSF was given according to physician decision. The primary objective was to evaluate the efficacy of R-CHOP14 compared to R-CHOP 21 as measured by the EFS, events being defined as death from any cause, relapse for complete responders and unconfirmed complete responders, progression during or after treatment and changes of therapy during allocated treatment. Secondary objectives were OS, PFS, DFS, response rate and analysis of dose-intensity and toxicity. According to previous LNH98-5 protocol, sample size was calculated to demonstrate an improvement of 2-year EFS from 55% to 65% with R-CHOP14. Six-hundred patients, randomized 1:1 between the two treatment groups recruited over 4 years and followed for a minimum of one year, will provide 80% power at the overall 5% (2-sided) significance level to detect the expected difference. Results: In this planned interim analysis, 202 patients were randomized and 201 received study treatment, 103 with R-CHOP14 and 98 with R-CHOP21. Median age was 72 years. Patients' characteristics were similar in both groups with a slightly higher proportion of patients with aaIPI 2-3 in R-CHOP14 arm (67% vs 59%) whereas a higher proportion of patients in R-CHOP21 arm presented with B symptoms (43% vs 37%). The median interval between cycles was 15 days in R-CHOP14 group and 21 days in R-CHOP21 group; 73 patients (71%) in R-CHOP14 group and 74 patients (76%) in R-CHOP21 group completed 8 cycles without progression. In the R-CHOP14 group, the increase of dose-intensity at the end of treatment, calculated according to 3-week interval as a reference, was 125% for cyclophosphamide and doxorubicin. Ninety percent of patients treated with R-CHOP14 received G-CSF, whereas only 66% in R-CHOP21 group. Response rate (CR+CRu) was 67% in R-CHOP14 arm and 75% in R-CHOP21 arm (p=NS). The 2-year EFS was 48% in R-CHOP14 arm compared with 61% in R-CHOP21 (p=NS). A similar trend was observed for 2-year PFS (49% vs 63%), 2-year DFS (57% vs 70%) and 2-year OS (67% vs 70%) (p=NS for all). Grade 3-4 hematological toxicity was more frequent in R-CHOP14 group, with a higher proportion of patients receiving red cell or platelet transfusions and/or experiencing febrile neutropenia, resulting in higher proportion of patients hospitalized for adverse events. In contrast, there was no difference for extra-hematological grade 3-4 toxicities. Conclusions: The results of this interim analysis of the LNH03-6B trial favor treatment with R-CHOP21 in elderly patients with DLBCL, with trends toward higher efficacy and lower toxicity compared to R-CHOP14. These results should be confirmed by the final analysis, concerning the 602 patients included, planned in 2010. Disclosures: No relevant conflicts of interest to declare.


PLoS ONE ◽  
2015 ◽  
Vol 10 (4) ◽  
pp. e0123978 ◽  
Author(s):  
Antonio Gutiérrez ◽  
Leyre Bento ◽  
Antonia Maria Bautista-Gili ◽  
Francesc Garcia ◽  
Jordi Martinez-Serra ◽  
...  

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