Division of Hematology and Rheumatology, Faculty of Medicine, Kindai University Hospital, Osakasayama-shi, Osaka, Japan.
Department of Hematology, Perfect Liberty General Hospital, Tondabayashi-shi, Osaka, Japan.
Br J Haematol. 2022 Jul;198(2):360-372. doi: 10.1111/bjh.18208. Epub 2022 Apr 22.
We previously reported that a novel haemoglobin-platelet index (HPI) based on anaemia and thrombocytopenia was useful to predict the prognosis of patients with diffuse large B-cell lymphoma not otherwise specified (DLBCL NOS). Here, we analyse the utility of HPI in a new validation cohort with DLBCL NOS (n = 94). As a result, we confirm that HPI was effective for differentiating progression-free survival (PFS) and overall survival in this validation cohort. So, we further compare the utility of HPI with previously reported prognostic markers such as the National Comprehensive Center Network-International Prognostic Index (NCCN-IPI), Glasgow prognostic score (GPS), and platelet-albumin (PA) score, using a larger number of 160 patients consisting of the derivation cohort (n = 66) and a validation cohort (n = 94). As a result, the patients with a higher HPI score had significantly worse outcomes, and HPI predicted the prognosis of DLBCL NOS independently of NCCN-IPI. HPI was more sensitive than GPS and almost the same as PA score in predicting PFS. Moreover, the patients whose lymphoma cells were positive for interleukin-6 (IL-6) (75/111 cases) judged by immunohistochemical staining had significantly lower haemoglobin levels and platelet counts than IL-6-negative cases (36/111 cases), suggesting the involvement of IL-6 produced by lymphoma cells in anaemia and thrombocytopenia in DLBCL NOS patients.
我们之前报道过,一种基于贫血和血小板减少的新型血红蛋白-血小板指数(HPI)对于预测未特指弥漫性大 B 细胞淋巴瘤(DLBCL NOS)患者的预后是有用的。在这里,我们在一个新的包含 DLBCL NOS 的验证队列中分析了 HPI 的效用(n=94)。结果,我们证实 HPI 在该验证队列中对区分无进展生存期(PFS)和总生存期是有效的。因此,我们使用包含来自推导队列(n=66)和验证队列(n=94)的 160 名患者的更大样本量,进一步比较了 HPI 与之前报道的预后标志物的效用,如国家综合癌症网络-国际预后指数(NCCN-IPI)、格拉斯哥预后评分(GPS)和血小板-白蛋白(PA)评分。结果,HPI 评分较高的患者结局明显较差,HPI 独立于 NCCN-IPI 预测 DLBCL NOS 的预后。HPI 在预测 PFS 方面比 GPS 更敏感,与 PA 评分几乎相同。此外,通过免疫组织化学染色判断的白细胞介素-6(IL-6)阳性(75/111 例)的患者的血红蛋白水平和血小板计数明显低于 IL-6 阴性患者(36/111 例),提示淋巴瘤细胞产生的 IL-6 参与了 DLBCL NOS 患者的贫血和血小板减少。