Minimal residual disease monitoring in early stage follicular lymphoma can predict prognosis and drive treatment with rituximab after radiotherapy

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Pulsoni A., Della Starza I., Cappelli L. V., Tosti M. E., Annechini G., Cavalli M., De Novi L. A., D', Elia G. M., Grapulin L., Guarini A., Del Giudice I., Foa R.
ISSN: 0007-1048

Since 2000, we have investigated 67 consecutive patients with stage I/II follicular lymphoma (FL) for the presence of BCL2/IGH rearrangements by polymerase chain reaction (PCR), real time quantitative PCR (RQ-PCR) and digital droplet PCR (ddPCR). All patients were treated with involved-field radiotherapy (IF-RT) (24–30 Gy). From 2005, patients with minimal residual disease (MRD) after IF-RT received rituximab (R) (375 mg/m2, 4 weekly administrations). The median follow-up is 82 months (17–196). At diagnosis, 72% of patients were BCL2/IGH+. Progression-free survival (PFS) was significantly better in patients with undetectable/low levels (<10?5) of circulating BCL2/IGH+ cells at diagnosis and in those who were persistently MRD? during follow-up (P = 0·0038). IF-RT induced an MRD? status in 50% of cases; 16/19 (84%) MRD+ patients after IF-RT became MRD? after R treatment. A significantly longer PFS was observed in MRD+ patients treated with R compared to untreated MRD+ patients (P = 0·049). In early stage FL, both circulating levels of BCL2/IGH+ cells at diagnosis and MRD status during follow-up bear prognostic implications. Standard IF-RT fails to induce an MRD-negative status in half of patients. Most patients become MRD? following treatment with R and this is associated with a significantly better PFS.

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