Abstract

ObjectivesEven though frequent, it is not known how HIV infection and treatment impact in the consolidation by radiotherapy of non-Hodgkin diffuse large B-cell lymphomas (DBCL). This article aim to assess that difference that HIV makes on radiation treatment.Patients and methodsA retrospective cohort of all DBCL patients treated with chemotherapy and consolidative radiotherapy at a single institution between 2010 and 2018 was assessed. All patients had biopsy-proven lymphoma and were included if radiation was part of the treatment and had at least 6 months of follow-up or were followed until death.ResultsThree-hundred fifty-nine (359) patients were selected, with a median age at diagnosis of 57.7 years (13–90 years). Twenty-eight patients (7.8%) were HIV positive. Median follow-up was 48.0 months. Female patients were 51.3% and most had a good performance in the ECOG scale (78.8% are ECOG 0–1). Median overall survival was not reached, but mean OS was 50.1 months with 86 deaths. Median progression-free survival was 48.7 months. HIV infection had no impact on OS (p = 0.580) or PFS (p = 0.347) among patients treated with RT. HIV positive patients were more frequently staged only with CT (p > 0.05) with no impact on PFS (p = 0.191). No HIV positive patient received rituximab due to local policy restrictions and HIV positive patients were more prone to receive CHOP-like chemotherapy (p < 0.05), specially ones with etoposide (CHOEP). CHOP was associated with better survival (p = 0.015) in the overall population and in the HIV negative population (p = 0.002), but not in the HIV positive population (p = 0.982). RT toxicities were not overall more frequent in the HIV positive population (p = 0.567), except for fatigue (p < 0.05) and hematological toxicities (p = 0.022).ConclusionHIV status did not influence on survival when patients were treated with consolidative radiotherapy. HIV infection was a bias on our sample for staging methods and chemotherapy regimens choices. For HIV positive patients there was an increase in fatigue and hematological toxicities of any grade with radiation.

Highlights

  • The role of radiotherapy (RT) in the treatment of non-Hodgkin diffuse large B-cell lymphomas (DLBCL) has been tested over the years

  • human immunodeficiency virus (HIV) infection had no impact on Overall survival (OS) (p = 0.580) or Progression-free survival (PFS) (p = 0.347) among patients treated with RT

  • HIV status did not influence on survival when patients were treated with consolidative radiotherapy

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Summary

Introduction

The role of radiotherapy (RT) in the treatment of non-Hodgkin diffuse large B-cell lymphomas (DLBCL) has been tested over the years. After the MabThera [1] trial, radiation as a consolidative treatment was not a consensus. Compared [2] the no-inferiority between RT and no consolidative therapy in initial very low-risk DLBCL and reveal positive findings [2], even though that trial can be criticized by the low threshold given to the no-RT arm for the 5-year event free survival (EFS) and for accepting a difference of EFS between the two groups larger than the difference usually seen between low-IPI no bulky disease and high-risk disease. The International Lymphoma Radiation Oncology Group (ILROG) has proposed guidelines to its use [4]. RT is an accepted option for consolidation in DLBCL

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