Preoperative neurocognitive function as an independent survival prognostic marker in primary glioblastoma

Author:

Liouta Evangelia12ORCID,Koutsarnakis Christos13ORCID,Komaitis Spyridon13ORCID,Kalyvas Aristotelis V13ORCID,Drosos Evangelos13ORCID,García-Gómez Juan M3,Juan-Albarracín Javier3,Katsaros Vasileios4ORCID,Stavrinou Lampis5,Stranjalis George123ORCID

Affiliation:

1. 1st Department of Neurosurgery, National and Kapodistrian University of Athens, Evangelismos Hospital , Athens , Greece

2. Hellenic Center for Neurosurgical Research “Prof. Petros Kokkalis,” Athens , Greece

3. Athens Microneurosurgery Laboratory, Grupo de Informática Biomédica (IBIME), Instituto de Aplicaciones de las Tecnologías de la Información y de las Comunicaciones Avanzadas (ITACA), Universitat Politècnica de València , Valencia , Spain

4. Department of Radiology, General Anti-Cancer and Oncological Hospital of Athens “St. Savvas” , Athens , Greece

5. 2nd Department of Neurosurgery, National and Kapodistrian University of Athens, ATTIKO Hospital , Athens , Greece

Abstract

Abstract Background Aim of the present study is to investigate whether preoperative neurocognitive status is prognostically associated with overall survival (OS) in newly diagnosed glioblastoma (GBM) patients. Methods Ninety patients with dominant-hemisphere IDH-wild-type GBM were assessed by Mini Mental Status Exam (MMSE), Trail Making Test (TMT) A and B parts, and Control Word Association Test (COWAT) phonemic and semantic subtests. Demographics, Karnofsky Performance Scale, tumor parameters, type of surgery, and adjuvant therapy data were available for patients. Results According to Cox proportional hazards model the neurocognitive variables of TMT B (P < .01), COWAT semantic subset (P < .05), and the MMSE (P < .01) were found significantly associated with survival prediction. From all other factors, only tumor volume and operation type (debulking vs biopsy) showed a statistical association (P < .05) with survival prediction. Kaplan Meier Long rank test showed statistical significance (P < .01) between unimpaired and impaired groups for TMT B, with median survival for the unimpaired group 26 months and 10 months for the impaired group, for COWAT semantic (P < .01) with median survival 23 months and 12 months, respectively and for MMSE (P < .01) with medial survival 19 and 12 months respectively. Conclusions Our study demonstrates that neurocognitive status at baseline—prior to treatment—is an independent prognostic factor for OS in wild-type GBM patients, adding another prognostic tool to assist physicians in selecting the best treatment plan.

Publisher

Oxford University Press (OUP)

Subject

Medicine (miscellaneous)

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