Analysis of real-world data in patients with relapsed/refractory diffuse large B cell lymphoma who received salvage chemotherapy in the rituximab era

被引:8
|
作者
Fuji, Shigeo [1 ]
Kida, Shuhei [1 ]
Nakata, Kayo [2 ]
Morishima, Toshitaka [2 ]
Miyashiro, Isao [2 ]
Ishikawa, Jun [1 ]
机构
[1] Osaka Int Canc Inst, Dept Hematol, Chuo Ku, 3-1-69 Otemae, Osaka, Osaka, Japan
[2] Osaka Int Canc Inst, Canc Control Ctr, Osaka, Japan
关键词
Diffuse large B cell lymphoma; Salvage chemotherapy; Hematopoietic stem cell transplantation; INTERNATIONAL PROGNOSTIC INDEX; AUTOLOGOUS TRANSPLANTATION; OUTCOMES; REGIMENS; CHEMOIMMUNOTHERAPY; COMBINATION; EXPRESSION; REMISSION; THERAPY; FAILURE;
D O I
10.1007/s00277-020-04342-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although the overall clinical outcome of patients with diffuse large B cell lymphoma (DLBCL) has significantly improved, some patients still experience relapsed/refractory disease. In the rituximab era, real-world data about relapsed/refractory DLBCL are limited. To clarify the clinical outcome and prognostic factors in these patients, we conducted a retrospective analysis using data from the population-based Osaka Cancer Registry (OCR) from 2010 to 2015. In total, 189 adult patients aged up to 70 years who received CHOP or a CHOP-like regimen in combination with rituximab, as well as a subsequent second-line therapy, were included in the analysis. The median age was 63 years (range, 24-70). Age ( 63 years), the duration of first progression-free survival (PFS), and the use of rituximab in the second-line chemotherapy were prognostic factors for overall survival (OS) after the second-line treatment. In this cohort, 48 and 11 patients received autologous and allogeneic hematopoietic stem cell transplantation (HSCT), respectively. The probabilities of 3-year OS after autologous and allogeneic HSCT were 55.7% and 18.2%, respectively. In conclusion, we found that the clinical outcome of patients with relapsed/refractory DLBCL in the rituximab era was unsatisfactory. Further improvements in treatment strategies, including novel agents, are needed.
引用
收藏
页码:2253 / 2260
页数:8
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