Refining M1 stage in medulloblastoma: criteria for cerebrospinal fluid cytology and implications for improved risk stratification from the HIT-2000 trial

• Published in: European journal of cancer (1990) Vol. 164; pp. 30 - 38
• Main Authors: Hagel, Christian, Sloman, Veronika, Mynarek, Martin, Petrasch, Katharina, Obrecht, Denise, Kühl, Joachim, Deinlein, Frank, Schmid, Renate, von Bueren, André O., Friedrich, Carsten, Juhnke, B. Ole, Gerber, Nicolas U., Kwiecien, Robert, Girschick, Hermann, Höller, Alexandra, Zapf, Antonia, von Hoff, Katja, Rutkowski, Stefan
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.03.2022; Elsevier Science Ltd
• Subjects: Brain Neoplasms; Brain tumors; Cerebellar Neoplasms; Cerebrospinal Fluid; Child; Clusters; Criteria; Cytology; Cytospin preparation; Humans; Medical prognosis; Medulloblastoma; Metastases; Patients; Prognosis; Prospective Studies; Quality assurance; Risk; Risk Assessment; Risk factors; Staging; Tumors; Cytospin preparation; Quality assurance; Cerebrospinal fluid; Staging; Medulloblastoma
• ISSN: 0959-8049; 1879-0852
• DOI: 10.1016/j.ejca.2021.12.032

Medulloblastoma is the most common malignant paediatric brain tumour, and cerebrospinal fluid (CSF) dissemination (M1 stage) is a high-risk prognostic factor. Criteria for CSF evaluation and for differentiating M0 from M1 stage are not clearly defined, and the prognostic significance of M1 stage in this context is unknown. CSF investigations from 405 patients with medulloblastoma of the prospective multicenter trial HIT-2000 (HIirnTumor-2000) were reviewed. Data from 213 patients aged ≥4 years were related to 5-year progression-free (5y-PFS) and overall survival. Patients with cytological tumour dissemination only (M1 stage only) aged ≥4 years (n = 18) and patients with radiologically detected metastases (M2/3, n = 85) showed a worse 5y-PFS than M0 patients (n = 110) without signs of metastatic disease (5y-PFS 61.1% and 59.6% vs 80.7%; p < 0.02 and p < 0.01, log rank). Patients with positive samples drawn early after surgery who turned negative within 14 days postoperatively (n = 9) and patients with atypical cells (n = 6) showed a 5y-PFS similar to M0 patients. No tumour cells were detected in samples containing <10 nucleated cells. Analysis of cytological criteria showed a better predictive value for tumour cell clusters than ≥2 individual tumour cells. Based on our results, we suggest that CSF medulloblastoma staging should be performed 14 days postoperatively by lumbar puncture, and specimens should contain at least 10 nucleated cells. Cytological tumour dissemination alone (M1 stage only) appears a high-risk prognostic factor associated with an outcome comparable to M2/M3 stage. Tumour cell clusters seem to have a greater impact on prognosis than single tumour cells. This should be validated further. •Cerebrospinal fluid (CSF) samples of 405 patients with medulloblastoma were assessed by central reference.•Cytospin preparation recommended within 2 h.•CSF preparations should contain ≥10 intact nucleated cells.•Detection of ≥2 tumour cells and/or ≥1 cell cluster corresponds to M1 stage.•Prognosis of M1 and M2/M3 is both significantly poorer than M0.