4.3 Article

Association between treatment-related lymphopenia and survival in glioblastoma patients following postoperative chemoradiotherapy

Journal

STRAHLENTHERAPIE UND ONKOLOGIE
Volume 198, Issue 5, Pages 448-457

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00066-021-01855-5

Keywords

Lymphopenia; Immunosuppression; Glioblastoma; Radiotherapy; Temozolomide

Funding

  1. Universita degli Studi di Milano -Bicocca within the CRUI-CARE Agreement

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This study found that treatment-related lymphopenia does not adversely affect overall survival in glioblastoma patients. Factors affecting survival included age, sex, extent of surgery, access to chemotherapy, and certain dose parameters. Prospective studies are needed to confirm these findings.
Purpose Our study investigated the association between treatment-related lymphopenia and overall survival (OS) in a series of glioblastoma (GBM) patients. We also explored clinical and dosimetric predictors of lymphocytes depletion. Methods Between 2015 and 2019, 64 patients were treated at the same institution with postoperative chemoradiotherapy. Peripheral lymphocyte count (PLC) data and dose-volume histogram parameters were collected. Radiotherapy (RT) schedule consisted in standard total dose of 60 Gy in 30 daily fractions, with concomitant and adjuvant temozolomide (TMZ). Posttreatment acute absolute lymphopenia (nadir AAL) was calculated as a PLC lower than 1.0 x 10(3)/mm(3). Acute relative lymphopenia (ARL) was expressed by the nadir-PLC/baseline-PLC ratio Results A total of 57 patients were eligible and included in the analyses. The median PLC was significantly decreased following chemoradiotherapy (2180/mm(3) vs 900/mm(3)). Median OS was 16 months (range 5-55 months), with no significant difference between patients who developed nadir AAL and those who did not (16 months vs 16.5 months; p = 0.304). When considering ARL vs non-ARL, median OS was 14 months vs 26 months (p = 0.013), respectively. In multivariate Cox regression only age, sex, extent of surgery, access to adjuvant chemotherapy and brain D98% were independently associated with OS. Conclusion Although iatrogenic immunosuppression could be associated with inferior clinical outcomes, our data show that treatment-related lymphopenia does not adversely affect GBM survival. Prospective studies are required to confirm these findings.

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