Optimization and validation of the international metabolic prognostic index for CD19 CAR-T in large B-cell lymphoma

淋巴瘤 国际预后指标 索引(排版) 医学 内科学 CD19 肿瘤科 免疫学 计算生物学 弥漫性大B细胞淋巴瘤 计算机科学 生物 万维网 外周血
作者
Michael Winkelmann,Sandeep Raj,Michael D. Jain,Gloria Iacoboni,Fabian Müller,Leo Hansmann,Magdalena Corona,Alejandro Luna,Khushali Jhaveri,Gunjan L. Shah,Michael Scordo,Turab Mohammad,Erin Dean,Gabriel T. Sheikh,Wolfgang G. Kunz,Tobias Tix,Veit Bücklein,Akshay Bedmutha,Doris Leithner,Marion Subklewe
出处
期刊:Blood Cancer Journal [Springer Nature]
卷期号:15 (1)
标识
DOI:10.1038/s41408-025-01338-1
摘要

While CD19-directed CAR T-cell therapy represents a transformative immunotherapy for relapsed/refractory large B-cell lymphoma (r/r LBCL), more than 50% of patients ultimately progress or relapse. Recently, the International Metabolic Prognostic Index (IMPI) - incorporating age, stage, and metabolic tumor volume (MTV) - was shown to improve prognostication for LBCL frontline treatment. Here, we examine its utility to predict toxicity and survival in CAR-T recipients. This multicenter observational study spanning six international sites included 504 patients with available 18FDG-PET/CT imaging at last response assessment prior to lymphodepletion. Optimal CAR-adapted MTV thresholds were identified in a development cohort (n = 256) and incorporated into a CAR-T-specific IMPI ("CAR-IMPI"). The prognostic performance of CAR-IMPI was validated in an independent cohort (n = 248). CAR-IMPI risk categories, defined by the median (1.35) and terciles (1.07, 1.58), demonstrated significant discrimination for progression-free survival (PFS; p < 0.0001) and overall survival (OS; p < 0.0001) in both cohorts. Multivariate Cox regression confirmed CAR-IMPI as an independent predictor of survival, accounting for pre-lymphodepletion LDH and CRP, performance status, treatment center, and CAR-T product. Patients in the CAR-IMPI high-risk category experienced increased severity of CRS and ICANS, and higher rates of intensive care unit (ICU) admissions. In an exploratory analysis, combining CAR-IMPI with established indices of high-risk systemic inflammation (CAR-HEMATOTOX, InflaMix) further enhanced survival stratification. The CAR-IMPI may provide a potent and validated PET-based tool for risk stratification of clinical outcomes in patients with r/r LBCL receiving CD19 CAR-T therapy. Our data highlight the utility of combining clinical and radiological modalities, with implications for patient selection and the anticipated level-of-care for toxicity management.
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