Literature DB >> 31594777

Symptom interval and treatment burden for patients with malignant central nervous system germ cell tumours.

James Hayden1,2, Matthew J Murray3, Ute Bartels4, Thankamma Ajithkumar5, Brinda Muthusamy6, Anthony Penn7,8, Gabriele Calaminus9, James Nicholson10.   

Abstract

OBJECTIVE: Patients with central nervous system germ cell tumours (CNS-GCTs) commonly initially present to primary care or general paediatricians. Prolonged symptom intervals (SI) are frequently seen in CNS-GCTs and have been associated with inferior outcomes in other brain tumours. This study reviewed the clinical presentation of CNS-GCTs and examined the effect of prolonged SI. DESIGN/SETTING/PATIENTS/OUTCOMES: International multicentre 10-year retrospective study (2002-2011 inclusive), across six international paediatric oncology treatment centres. All newly diagnosed patients with CNS-GCT were included. Main outcome measure was time interval from first symptom to diagnosis.
RESULTS: The study cohort included 86 (58 males:28 female) patients (59 'germinoma' and 27 'non-germinomatous' GCTs), with tumours being pineal (n=33), suprasellar (n=25), bifocal (pineal+suprasellar; n=24) and 'other' site (n=4), of which 16 (19%) were metastatic. Median age at diagnosis was 14 years (0-23 years). The time to diagnosis from first symptom (SI) was 0-69 months (median 3 months, mean 9 months). A prolonged SI (>6 months) was observed in 28/86 patients (33%) and significantly associated with metastatic disease (11/28 (39%) vs 5/58 (9%); p=0.002)) at diagnosis, but not overall survival. With prolonged SI, endocrine symptoms, particularly diabetes insipidus, were more common (21/28 (75%) vs 14/58 (24%) patients; p<0.002), but raised intracranial pressure (RICP) was less frequent (4/28 (14%) vs 43/58 (74%) patients; p<0.001)) at first symptom.
CONCLUSIONS: One-third of patients with CNS-GCT have >6 months of symptoms prior to diagnosis. Delayed diagnosis is associated with metastatic disease. Early symptom recognition, particularly related to visual and hormonal disturbances in the absence of RICP, may improve timely diagnosis, reduce metastatic disease frequency and consequently reduce treatment burden and late effects. © Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  Outcomes research; brain tumour; intervention; prolonged symptom interval; symptom interval

Year:  2019        PMID: 31594777     DOI: 10.1136/archdischild-2019-317245

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  3 in total

1.  Hypophyseal Dysfunction and Difficulties in Management of Pediatric Intracranial Germ Cell Tumors.

Authors:  Mehmet İsakoca; Gökmen Kahiloğulları; Zeynep Şıklar; Tuğba Kontbay; Emel Ünal; Nurdan Taçyıldız; Handan Dinçaslan; Merih Berberoğlu
Journal:  Turk Arch Pediatr       Date:  2022-05

2.  Clinical utility of circulating miR-371a-3p for the management of patients with intracranial malignant germ cell tumors.

Authors:  Matthew J Murray; Thankamma Ajithkumar; Fiona Harris; Rachel M Williams; Ibrahim Jalloh; Justin Cross; Milind Ronghe; Dawn Ward; Cinzia G Scarpini; James C Nicholson; Nicholas Coleman
Journal:  Neurooncol Adv       Date:  2020-04-13

3.  Central nervous system germ cell tumor, an archetypal AYA tumor and a model for pediatric and neuro-oncology collaboration, review from the EURACAN domain 10 group.

Authors:  Cecile Faure Conter; Gabriele Calaminus; James Nicholson; Ahmed Idbaih; Khê Hoang Xuan; Alexandre Vasiljevic; Giovanni Morana; Alexandru Szathmari; Thankamma Ajithkumar; Didier Frappaz
Journal:  Front Oncol       Date:  2022-09-29       Impact factor: 5.738

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.