TY - JOUR
T1 - Validation of POD24 as a robust early clinical end point of poor survival in FL from 5225 patients on 13 clinical trials
AU - for the FLASH (Follicular Lymphoma Analysis of Surrogacy Hypothesis) Group
AU - Casulo, Carla
AU - Dixon, Jesse G.
AU - Le-Rademacher, Jennifer
AU - Hoster, Eva
AU - Hochster, Howard S.
AU - Hiddemann, Wolfgang
AU - Marcus, Robert
AU - Kimby, Eva
AU - Herold, Michael
AU - Sebban, Catherine
AU - Gyan, Emmanuel
AU - Foon, Kenneth
AU - Nielsen, Tina
AU - Vitolo, Umberto
AU - Salles, Gilles A.
AU - Shi, Qian
AU - Flowers, Christopher R.
N1 - Funding Information:
This work was supported by Celgene and Roche.
Funding Information:
Conflict-of-interest disclosure: C.C. received research funding from Verastem and Gilead. E.H. received institutional research funding and personal travel expense from Roche. M.L. declares, in the past 5 years, consultancy, participation on advisory boards, invitation to scientific meetings, institutional research support, and contracts with AbbVie, Acerta, Amgen, Archigen, ADC Therapeutics, BeiGene, Celgene, Gilead, Johnson & Johnson, Jazz, Roche, Sandoz, and Takeda; nonfinancial interests including serving as principal or strategic investigator in studies supported by Celgene, Johnson and Johnson, and BeiGene; and leadership roles as a board member of Fondazione Italiana Linfomi, a member of the European Hematology Association (EHA) Guideline Committee; membership on the Euro-MRD Board and the ESMO (European Society for Medical Oncology) Guidelines Committee up to December 2018; and holding office as Vice President of the Associazione Italiana Leucemie (Alessandria section). W.H. has received honoraria and research support from Roche, Celgene, Bayer, and Janssen. E.K. has received grants and other support from Roche and Genentech, during the conduct of the study; personal fees from Bayer, and Genmab, personal Janssen, Gilead/Roche, and AbbVie; and nonfinancial support from MEI Pharma, outside the submitted work. T.N. is an executive committee member, and was employed by and held stock ownership in F. Hoffman La Roche. F.M. served on the advisory board of Celgene, Roche, Giead, Epizyme, and Verasteem and received honoraria for scientific lectures from Celgene, Roche, Janssen and AbbVie. U.V., S.G., Q.S., and C.R.F. are executive committee members. J.G.D., O.F.-S., H.S.H., R.M., and M.H. declare no competing financial interests.
Publisher Copyright:
© 2022 American Society of Hematology
PY - 2022/3/17
Y1 - 2022/3/17
N2 - 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 β2 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.
AB - 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 β2 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.
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U2 - 10.1182/blood.2020010263
DO - 10.1182/blood.2020010263
M3 - Article
C2 - 34614146
AN - SCOPUS:85126374374
SN - 0006-4971
VL - 139
SP - 1684
EP - 1693
JO - Blood
JF - Blood
IS - 11
ER -