Validation of POD24 as a robust early clinical end point of poor survival in FL from 5225 patients on 13 clinical trials

被引:108
作者
Casulo, Carla [1 ]
Dixon, Jesse G. [2 ]
Le-Rademacher, Jennifer [2 ]
Hoster, Eva [3 ]
Hochster, Howard S. [4 ]
Hiddemann, Wolfgang [5 ]
Marcus, Robert [6 ,7 ]
Kimby, Eva [8 ]
Herold, Michael [9 ]
Sebban, Catherine [10 ]
Gyan, Emmanuel [11 ]
Foon, Kenneth [12 ]
Nielsen, Tina [13 ]
Vitolo, Umberto [14 ]
Salles, Gilles A. [15 ]
Shi, Qian [2 ]
Flowers, Christopher R. [16 ]
机构
[1] Univ Rochester, Wilmot Canc Inst, Rochester, NY USA
[2] Mayo Clin, Div Biomed Stat & Informat, Rochester, MN USA
[3] Ludwig Maximilians Univ Hosp, Dept Internal Med 3, Campus Grosshadern, Munich, Germany
[4] Div Hematol Oncol & Transplantat, Munich, Germany
[5] Rutgers Canc Inst New Jersey, New Brunswick, NJ USA
[6] Addenbrookes Hosp, Dept Haematol, Cambridge, England
[7] Karolinska Univ Hosp, Karolinska Inst, Stockholm, Sweden
[8] Karolinska Univ Hosp, Hematol Ctr, Stockholm, Sweden
[9] Leiter Onkol Zentrum, Nordhauser Str 74, D-99089 Erfurt, Germany
[10] Ctr Leon Berard, Lyon, France
[11] Univ Tours, Dept Hematol & Cell Therapy, Tours, France
[12] Celgene Corp, Summit, NJ USA
[13] F Hoffmann Roche Ltd, Pharma Dev Clin Oncol, Basel, Switzerland
[14] IRCCS, FPO, Candiolo Canc Inst, Turin, Italy
[15] Mem Sloan Kettering Canc Ctr, New York, NY USA
[16] Univ Texas Houston, MD Anderson Canc Ctr, Dept Lymphoma Myeloma, Houston, TX USA
关键词
BURDEN FOLLICULAR LYMPHOMA; AUTOLOGOUS TRANSPLANTATION; RISK;
D O I
10.1182/blood.2020010263
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Observational studies and stand-alone trials indicate that patients with follicular lymphoma (FL) who experience disease progression within 24 months of front-line chemoimmunotherapy (POD24), have poor outcomes. We performed a pooled analysis of 13 randomized clinical trials of patients with FL in the pre- and postrituximab eras to identify clinical factors that predict POD24. Logistic regression models evaluated the association between clinical factors and POD24. Cox regression evaluated the association between POD24 as a time-dependent factor and subsequent overall survival (OS). A landmark analysis evaluated the association of POD24 with OS for the subset of patients who were alive at 24 months after trial registration. Patients without progression at 24 months at baseline had favorable performance status (PS), limited-stage (I/II) disease, low-risk FL International Prognostic Index (FLIPI) score, normal baseline hemoglobin, and normal baseline beta(2) microglobulin (B2M) level. In a multivariable logistic regression model, male sex (odds ratio [OR], 1.30), PS >= 2 (OR, 1.63), B2M (>= 3 mg/L; OR, 1.43), and high-risk FLIPI score (3-5; OR, 3.14) were associated with increased risk of progression before 24 months. In the time-dependent Cox model and the 24-month landmark analysis, POD24 was associated with poor subsequent OS (hazard ratio, 4.85 and 3.06, respectively). This is the largest pooled analysis of clinical trials data validating POD24 as a robust indicator of poor FL survival and identified clinical predictors of early death and progression that can aid in building comprehensive prognostic models incorporating clinical and molecular predictors of POD24.
引用
收藏
页码:1684 / 1693
页数:10
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