Avoid common mistakes on your manuscript.
Dear Editor,
Recently, the largest prospective cohort of old and frail patients with aggressive B-cell lymphoma and bendamustine/rituximab (BR) as first-line treatment was reported (B-R-ENDA trial) [1]. B-R-ENDA was a multi-center, prospective, non-randomized trial on patients > 80 or 61–80 years not qualifying for CHOP (cyclophosphamide, doxorubicin, vincristine, prednisolone)-like therapy. Sixty-eight patients were included, with 39 patients (57%) > 80 years (target cohort; Table 1). However, due to slow recruitment, the trial was terminated before the planned target (50 patients > 80 years) was reached [1]. In line with four other bendamustine-based prospective trials (with only 14–49 patients) [1], it shows the difficulty of performing clinical trials in this patients’ population. These difficulties and the fact that standard treatment for old or frail patients not eligible for CHOP(-like) therapy has not been defined [1], retrospective studies are useful to answer important clinical questions [2].
To build more evidence on BR for older patients with aggressive B-cell lymphoma and to compare the results of a prospective clinical trial with real-world data, the aim was to compare the B-R-ENDA data with another study. However, it is difficult to compare different studies, e.g., multi-center vs. single-center analysis, prospective vs. retrospective design, differences in inclusion/exclusion criteria, study endpoints, or sample sizes. A retrospective study on 68 patients treated with BR for aggressive B-cell lymphoma (R-Benda study) [3] is useful for comparison with B-R-ENDA because that was also a multi-center study with the same sample size.
R-Benda was conducted on older or frail patients ≥ 65 years with ECOG performance score (PS) ≥ 2 or ≥ 75 years regardless of ECOG PS with de novo diffuse large B-cell lymphoma (DLBCL). The aim of this study was to compare the outcome of patients treated with BR vs. rituximab/CHOP. Sixty-eight patients treated with BR were analyzed within this study [3].
For direct comparison of both R-Benda and B-R-ENDA, the same parameters and endpoints, respectively, need to be analyzed. Therefore, the original R-Benda data set had to be re-evaluated according to the B-R-ENDA analyses (Table 1).
Regarding age, the whole R-Benda cohort was comparable with the whole B-R-ENDA cohort (median age 80 vs. 81 years). There were also no statistical differences in the portion of patients > 80 years (41% vs. 57%; P = 0.09). However, in R-Benda, in the subgroup of > 80 years (and the whole R-Benda cohort), there were fewer females than in B-R-ENDA. Regarding lymphoma specific parameters, in R-Benda, more patients > 80 years (and in the whole R-Benda cohort) had extranodal involvement compared to B-R-ENDA. According to the International Prognostic Index (IPI) score, in R-Benda, at least numeric more patients > 80 years (and in the whole cohort) had high-risk disease than in B-R-ENDA. The remission rates in the subgroup > 80 years (and in the whole cohort) were comparable between R-Benda and B-R-ENDA (Table 1). However, the overall response rate (sum of complete and partial remission) in the whole R-Benda cohort was higher compared to the whole B-R-ENDA cohort (62% vs. 41%; P = 0.03), caused by the higher complete remission (CR) rate in the cohort 61–80 years in R-Benda (44% vs. 10%; P = 0.005). The lower CR rate in B-R-ENDA, however, was expected based on the inclusion criteria for this age group [1].
The primary endpoint in B-R-ENDA was progression-free survival at 2 years (2y-PFS) [1]. After re-assessment of the R-Benda data set, it was possible to provide also the 2y-PFS rate. In the subgroup > 80 years, the 2y-PFS in R-Benda was markedly inferior compared to B-R-ENDA (21% vs. 45%), but less pronounced for the whole cohorts (36% vs. 40%). The same was true for 2-year overall survival rates, even for the whole cohorts the rates were equal (41% vs. 42%).
R-Benda and B-R-ENDA included older (≥ 75 years or > 80 years, respectively) or frail patients (≥ 65 years plus ECOG PS ≥ 2 or 61–80 years plus Cumulative Illness Rating Scale [CIRS] score > 6, respectively). Regarding ECOG PS, there were no differences between both studies. In R-Benda, the CIRS score was not considered, but the Charlson Comorbidity Index (CCI). CCI and CIRS score correlate in cancer patients [4, 5]. In B-R-ENDA, 72% of the whole cohort had a CIRS score > 6 indicating medical non-fit patients [1]. In the whole R-Benda cohort, 82% of the patients had an age-adjusted CCI ≥ 4 indicating intermediate-high risk patients [3], corresponding to medical non-fit patients. Therefore, taking age, CCI/CIRS score, and ECOG PS into account, the patients’ characteristics of the both cohorts were comparable. The survival differences between both studies may be attributed to sex differences, because the prognosis in patients with rituximab-based regimens for DLBCL is inferior in men [6]. High-risk disease according to IPI score as well as extranodal site involvement are also independent risk factors for survival [1, 7]. Because in R-Benda, at least for patients > 80 years, more men, more patients with high IPI score, and more extranodal sites involvement were included, the inferior survival can be explained.
Although patients in clinical trials often differ substantially from those in the general population, that was not true for R-Benda. Hence, daily clinical practice matches clinical trial data (Supplementary Table 1) [1, 8]—or vice versa—in this high-risk population. The results of the re-analysis of R-Benda confirm the 2y-PFS as a surrogate endpoint [1, 8, 9].
Data availability
The data that support the findings of this study are available from the corresponding author upon reasonable request.
References
Braulke F, Zettl F, Ziepert M, Viardot A, Kahl C, Prange-Krex G, Korfel A, Dreyling M, Bott A, Wedding U, Reichert D, de Wit M, Hartmann F, Poeschel V, Schmitz N, Witzens-Harig M, Klapper W, Rosenwald A, Wulf G, Altmann B, Trümper L (2022) First-line treatment with bendamustine and rituximab for old and frail patients with aggressive lymphoma: results of the B-R-ENDA trial. Hemasphere 6:e808. https://doi.org/10.1097/HS9.0000000000000808.
Talari K, Goyal M (2020) Retrospective studies – utility and caveats. J R Coll Physicians Edinb 50:398–402. https://doi.org/10.4997/JRCPE.2020.409
Zeremski V, Jentsch-Ullrich K, Kahl C, Mohren M, Eberhardt J, Fischer T, Schalk E (2019) Is bendamustine-rituximab a reasonable treatment in selected older patients with diffuse large B cell lymphoma? Results from a multicentre, retrospective study. Ann Hematol 98:2729–2737. https://doi.org/10.1007/s00277-019-03819-3
Extermann M, Overcash J, Lyman GH, Parr J, Balducci L (1998) Comorbidity and functional status are independent in older cancer patients. J Clin Oncol 16:1582–1587. https://doi.org/10.1200/JCO.1998.16.4.1582
Vitzthum LK, Feng CH, Noticewala S, Hines PJ, Nguyen C, Zakeri K, Sojourner EJ, Shen H, Mell LK (2018) Comparison of comorbidity and frailty indices in patients with head and neck cancer using an online tool. JCO Clin Cancer Inform 2:1–9. https://doi.org/10.1200/CCI.18.00082
Carella AM, de Souza CA, Luminari S, Marcheselli L, Chiappella A, di Rocco A, Cesaretti M, Rossi A, Rigacci L, Gaidano G, Merli F, Spina M, Stelitano C, Hohaus S, Barbui A, Puccini B, Miranda EC, Guida A, Federico M (2013) Prognostic role of gender in diffuse large B-cell lymphoma treated with rituximab containing regimens: a Fondazione Italiana Linfomi/Grupo de Estudos em Moléstias Onco-Hematológicas retrospective study. Leuk Lymphoma 54:53–57. https://doi.org/10.3109/10428194.2012.691482
Ziepert M, Hasenclever D, Kuhnt E, Glass B, Schmitz N, Pfreundschuh M, Loeffler L (2010) Standard International prognostic index remains a valid predictor of outcome for patients with aggressive CD20+ B-cell lymphoma in the rituximab era. J Clin Oncol 28:2373–2380. https://doi.org/10.1200/JCO.2009.26.2493
Storti S, Spina M, Pesce EA, Salvi F, Merli M, Ruffini A, Cabras G, Chiappella A, Angelucci E, Fabbri A, Liberati AM, Tani M, Musuraca G, Molinari A, Petrilli MP, Palladino C, Ciancia R, Ferrario A, Gasbarrino C, Monaco F, Fraticelli V, De Vellis A, Merli F, Luminari S (2018) Rituximab plus bendamustine as front-line treatment in frail elderly (>70 years) patients with diffuse large B-cell non-Hodgkin lymphoma: a phase II multicenter study of the Fondazione Italiana Linfomi. Haematologica 103:1345–1350. https://doi.org/10.3324/haematol.2017.186569
van der Galiën HT, Hoogendoorn M, Kibbelaar RE, van Meerten T, van Rijn RS (2019) Progression-free survival at 24 months (PFS24) and subsequent outcome for patients with diffuse large B-cell lymphoma (DLBCL) in the real-world setting. Ann Oncol 30:151–152. https://doi.org/10.1093/annonc/mdy482
Funding
Open Access funding enabled and organized by Projekt DEAL.
Author information
Authors and Affiliations
Contributions
E.S. was involved in initial patients’ management, initial data collection and data analysis, designed this current analysis, analyzed these data, and wrote the manuscript. K.J-U. was involved in initial patient’s management, interpreted the initial data, and revised the current manuscript. All authors approved the final version of the manuscript.
Corresponding author
Ethics declarations
Ethics approval
The initial study was approved by the central ethics committee (Magdeburg University Hospital, approval no. 15/19) as well as by respective local ethics committees.
Consent to participate
Given the nature of a retrospective chart review study and using routine clinical data, written informed consent was not required within the study.
Conflict of interest
The authors declare no competing interests.
Additional information
Trial registration
The retrospective chart review study was not registered within a clinical trial registry.
Publisher's note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Below is the link to the electronic supplementary material.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Schalk, E., Jentsch-Ullrich, K. Evidence of bendamustine plus rituximab for old and frail patients with aggressive B-cell lymphoma. Ann Hematol 102, 1617–1620 (2023). https://doi.org/10.1007/s00277-023-05166-w
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00277-023-05166-w