Final results of a multicenter trial addressing role of CSF flow cytometric analysis in NHL patients at high risk for CNS dissemination

Author:

Benevolo Giulia1,Stacchini Alessandra2,Spina Michele3,Ferreri Andrés J. M.4,Arras Marcella5,Bellio Laura6,Botto Barbara1,Bulian Pietro3,Cantonetti Maria7,Depaoli Lorella8,Di Renzo Nicola9,Di Rocco Alice10,Evangelista Andrea11,Franceschetti Silvia12,Godio Laura2,Mannelli Francesco13,Pavone Vincenzo14,Pioltelli Pietro15,Vitolo Umberto1,Pogliani Enrico M.15

Affiliation:

1. Haematology 2 Azienda Ospedaliera Città della Salute e della Scienza, Turin, Italy;

2. Pathology Institute University, Turin, Italy;

3. Division of Medical Oncology A, National Cancer Institute, Aviano, Italy;

4. Unit of Lymphoid Malignancies, Department of Onco-Haematology, San Raffaele Scientific Institute, Milan, Italy;

5. Haematology Division, Cagliari, Italy;

6. Service of Medicine, Transfusion and Hematology, San Raffaele Scientific Institute, Milan, Italy;

7. Haematology Institute University Tor Vergata, Rome, Italy;

8. Haematology Division, Alessandria, Italy;

9. Haematology Division, Lecce, Italy;

10. Haematology Institute University Sapienza, Rome, Italy;

11. Azienda Ospedaliera Città della Salute e della Scienza, Centro Prevenzione Oncologica Piemonte, Turin, Italy;

12. Division of Haematology, Amedeo Avogadro University, Novara, Italy;

13. Haematology Institute University, Florence, Italy;

14. Haematology Division, Tricase, Italy; and

15. Haematology Institute University, Monza, Italy

Abstract

AbstractThis prospective study compared diagnostic and prognostic value of conventional cytologic (CC) examination and flow cytometry (FCM) of baseline samples of cerebrospinal fluid (CSF) in 174 patients with newly diagnosed aggressive non-Hodgkin lymphoma (NHL). FCM detected a neoplastic population in the CSF of 18 of 174 patients (10%), CC only in 7 (4%; P < .001); 11 patients (14%) were discordant (FCM+/CC−). At a median follow-up of 46 months, there were 64 systemic progressions and 10 CNS relapses, including 2 patients with both systemic and CNS relapses. Two-year progression-free and overall survival were significantly higher in patients with FCM− CSF (62% and 72%) compared with those FCM+ CSF (39% and 50%, respectively), with a 2-year CNS relapse cumulative incidence of 3% (95% confidence interval [CI], 0-7) versus 17% (95% CI, 0-34; P = .004), respectively. The risk of CNS progression was significantly higher in FMC+/CC− versus FCM−/CC− patients (hazard ratio = 8.16, 95% CI, 1.45-46). In conclusion, FCM positivity in the CSF of patients with high-risk NHL is associated with a significantly higher CNS relapse risk and poorer outcome. The combination of IV drugs with a higher CNS bioavailability and intrathecal chemotherapy is advisable to prevent CNS relapses in FCM+ patients.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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