Moon Joon Ho, Hamad Nada, Sohn Sang Kyun, Uhm Jieun, Alam Naheed, Gupta Vikas, Lipton Jeffrey H, Messner Hans A, Seftel Matthew, Kuruvilla John, Kim Dennis Dong Hwan
Department of Hematology/Oncology, Kyungpook National University Hospital, 130 Dongduk-ro, Jung-gu, Daegu, 41944, Korea.
Allogeneic Blood and Marrow Transplantation Program, Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Department of Medicine, University of Toronto, 610 University Ave, Toronto, ON, M5G2M9, Canada.
Ann Hematol. 2017 May;96(5):805-815. doi: 10.1007/s00277-017-2939-4. Epub 2017 Feb 18.
The CIBMTR chronic graft-versus-host disease (cGVHD) risk score can be refined and improved for better prognostic stratification. Three hundred and seven consecutive patients diagnosed with cGVHD by the NIH consensus criteria were retrospectively reviewed and had the CIBMTR risk score applied and analyzed. The CIBMTR risk score was successfully validated in our cohort (n = 307). The 3-year overall survival (OS) rates in each risk group (RG) were 82.5 ± 11.3% (RG1), 79.4 ± 3.0% (RG2), 71.8 ± 6.3% (RG3), and 27.3 ± 13.4% (RG4). A significantly lower OS rate and higher non-relapse mortality (NRM) were noted in RG4 compared to the other RGs. However, there were no differences in OS or NRM among RG1 to 3. To improve prognostic stratification power of the CIBMTR risk score, we incorporated the absolute lymphocyte (ALC) and eosinophil count (EC) at time of cGVHD into the CIBMTR risk score. Lower ALC (<1.0 × 10/L, HR 1.94, p = 0.014) and lower EC (<0.5 × 10/L, HR 3.27, p = 0.014) were confirmed as adverse risk factors for OS. Patients were stratified into four revised risk groups (rRG). The 3-year OS rates were 93.3 ± 6.4% (rRG1, score 0-3), 84.9 ± 3.4% (rRG2, score 4-6), 70.9 ± 4.4% (rRG3, score 7-9), and 32.0 ± 1.1% (rRG4, score ≥ 10) (p < 0.001). The 3-year NRM rates were 0.0% (rRG1), 6.7 ± 0.4% (rRG2), 18.4 ± 0.7% (rRG3), and 57.7 ± 5.1% (rRG4) (p < 0.001). The revised CIBMTR risk score was superior to the original CIBMTR risk score for OS (p < 0.001). The revised CIBMTR risk score including ALC and EC at the onset of cGVHD improved the prognostic stratification power of the CIBMTR risk score for long-term outcomes.
国际骨髓移植登记处(CIBMTR)的慢性移植物抗宿主病(cGVHD)风险评分可以进一步优化和改进,以实现更好的预后分层。对307例根据美国国立卫生研究院(NIH)共识标准确诊为cGVHD的连续患者进行回顾性分析,并应用和分析CIBMTR风险评分。CIBMTR风险评分在我们的队列(n = 307)中得到成功验证。各风险组(RG)的3年总生存率(OS)分别为82.5±11.(RG1)、79.4±3.0%(RG2)、71.8±6.3%(RG3)和27.3±13.4%(RG4)。与其他风险组相比,RG4的OS率显著更低,非复发死亡率(NRM)更高。然而,RG1至3之间的OS或NRM没有差异。为提高CIBMTR风险评分的预后分层能力,我们将cGVHD发生时的绝对淋巴细胞计数(ALC)和嗜酸性粒细胞计数(EC)纳入CIBMTR风险评分。较低的ALC(<1.0×10/L,HR 1.94,p = 0.014)和较低的EC(<0.5×10/L,HR 3.27,p = 0.014)被确认为OS的不良风险因素。患者被分为四个修订风险组(rRG)。3年OS率分别为93.3±6.4%(rRG1,评分0 - 3)、84.9±3.4%(rRG2,评分4 - 6)、70.9±4.4%(rRG3,评分7 - 9)和32.±1.1%(rRG4,评分≥10)(p < 0.001)。3年NRM率分别为0.0%(rRG1)、6.7±0.4%(rRG2)、18.4±0.7%(rRG3)和57.7±5.1%(rRG4)(p < 0.001)。修订后的CIBMTR风险评分在OS方面优于原始CIBMTR风险评分(p < 0.001)。纳入cGVHD发生时ALC和EC的修订CIBMTR风险评分提高了CIBMTR风险评分对长期预后的分层能力。