Baseline Total Metabolic Tumor Volume is Prognostic for Refractoriness to Immunochemotherapy in DLBCL: Results From GOYA

被引:6
作者
Ruiz, Irene Canales [1 ]
Martelli, Maurizio [2 ]
Sehn, Laurie H. [3 ,4 ]
Vitolo, Umberto [5 ]
Nielsen, Tina G. [6 ]
Sellam, Gila [6 ]
Bottos, Alessia [6 ]
Klingbiel, Dirk [6 ]
Kostakoglu, Lale [7 ]
机构
[1] Univ Navarra, Clin Trial Unit, Pamplona, Spain
[2] Sapienza Univ, Hematol Inst, Dept Translat & Precis Med, Rome, Italy
[3] BC Canc Ctr Lymphoid Canc, Lymphoma Tumour Grp, Vancouver, BC, Canada
[4] Univ British Columbia, Vancouver, BC, Canada
[5] Fdn Piemonte Oncol, Candiolo Canc Inst, Dept Med Oncol, IRCCS, Candiolo, Italy
[6] F Hoffmann La Roche Ltd, Basel, Switzerland
[7] Univ Virginia, Dept Radiol & Med Imaging, Charlottesville, VA USA
关键词
Lymphoid malignancies; Primary chemorefractory disease; Prognostic indicators; Early relapse; Overall; B-CELL LYMPHOMA; CHOP; RITUXIMAB; CHEMOTHERAPY; DIAGNOSIS; TRIAL;
D O I
10.1016/j.clml.2022.04.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Prognostic indicators are required to identify patients with diffuse large B-cell lymphoma (DLBCL) who are at risk of early treatment failure. A secondary analysis of data from the GOYA study identified risk factors for primary chemorefractory disease and disease progression within 12 months (POD12). Total metabolic tumor volume has prognostic value in identifying patients at risk of early treatment failure. Introduction: A good response to initial therapy is key to maximizing survival in patients with diffuse large B-cell lymphoma (DLBCL), but patients with chemorefractory disease and early progression have poor outcomes. Patients and Methods: Data from the GOYA study in patients with DLBCL who received first-line rituximab or obinutuzumab plus cyclophosphamide, doxor ubicin, vincr istine, and prednisone (CHOP) were analyzed. Positron emission tomography/computed tomography (PET/CT)-derived characteristics associated with total metabolic tumor volume (TMTV) and clinical risk factors for primary chemorefractory disease and disease progression within 12 months (POD12) were explored. Results: Of those patients fulfilling the cr iter ia for analysis, 108/1126 (10%) were primary chemorefractory and 147/1106 (13%) had POD12. Primary chemorefractory and POD12 status were strongly associated with reduced overall survival. After multivariable analysis of clinical and imaging-based risk factors by backward elimination, only very high TMTV (quartile [Q] 1 vs. Q4 odds ratio [OR]: 0.45; P = .006) and serum albumin levels (low vs. normal OR of 1.86; P = .004) were associated with primary chemorefractoriness. After additionally accounting for BCL2/MYC translocation in a subset of patients, TMTV and BCL2/MYC double-hit status remained as significant predictors of primary chemorefractoriness (Q1 vs. Q4 OR: 0.32, P = .01 and double-hit vs. no-hit OR of 4.47, P = .02, respectively). Risk factors including very high TMTV, high sum of the product of the longest diameters (SPD), geographic region (Asia), short time since diagnosis, extranodal involvement and low serum albumin were retained for POD12. Conclusion: PET-derived TMTV has prognostic value in identifying patients at risk of early treatment failure.
引用
收藏
页码:E804 / E814
页数:11
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