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Integrating genetic subtypes with PET scan monitoring to predict outcome in diffuse large B-cell lymphoma
Integrating genetic subtypes with PET scan monitoring to predict outcome in diffuse large B-cell lymphoma
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Integrating genetic subtypes with PET scan monitoring to predict outcome in diffuse large B-cell lymphoma
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Integrating genetic subtypes with PET scan monitoring to predict outcome in diffuse large B-cell lymphoma
Integrating genetic subtypes with PET scan monitoring to predict outcome in diffuse large B-cell lymphoma

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Integrating genetic subtypes with PET scan monitoring to predict outcome in diffuse large B-cell lymphoma
Integrating genetic subtypes with PET scan monitoring to predict outcome in diffuse large B-cell lymphoma
Journal Article

Integrating genetic subtypes with PET scan monitoring to predict outcome in diffuse large B-cell lymphoma

2025
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Overview
Next Generation Sequencing-based subtyping and interim- and end of treatment positron emission tomography (i/eot-PET) monitoring have high potential for upfront and on-treatment risk assessment of diffuse large B-cell lymphoma patients. We performed Dana Farber Cancer Institute (DFCI) and LymphGen genetic subtyping for the HOVON84 (n = 208, EudraCT-2006-005174-42) and PETAL ( n  = 204, EudraCT-2006-001641-33) trials retrospectively combined with DFCI genetic data ( n  = 304). For all R-CHOP treated patients (n = 592), C5/MCD- and C2/A53-subtypes show significantly worse outcome independent of the international prognostic index. For all subtypes, adverse prognostic value of i/eot-PET-positive status is confirmed. Consistent with frequent primary refractory disease, only 67% C2 patients become eot-PET-negative versus 81-88% for other subtypes. Indicative of high relapse rates, outcome of C5 i/eot-PET-negative patients remains significantly worse in HOVON-84, which trend validates in the PETAL and SAKK38-07 trials (NCT00544219). These results show the added value of integrated genetic subtyping and PET monitoring for prognostic stratification and subtype-specific trial design. The prognostic impact of genetic subtypes in diffuse large B-cell lymphoma not otherwise specified (DLBCL-NOS) remains unclear. Here, the authors use data from multiple clinical trials to identify DLBCL-NOS genetic subtypes that are associated with patient outcomes, showing their potential value for prognostic stratification, trial design, and PET response monitoring.