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Clinical outcome of cerebrospinal fluid shunts in patients with leptomeningeal carcinomatosis

Cited 12 time in Web of Science Cited 13 time in Scopus
Authors

Kim, Hye Seon; Park, Jong Bae; Gwak, Ho-Shin; Kwon, Ji-Woong; Shin, Sang-Hoon; Yoo, Heon

Issue Date
2019-03-27
Publisher
BioMed Central
Citation
World Journal of Surgical Oncology, 17(1):59
Keywords
Cerebrospinal fluidComplicationEfficacyLeptomeningeal carcinomatosisShunt
Abstract
Background
Leptomeningeal carcinomatosis (LMC) is frequently associated with hydrocephalus, which quickly devastates the performance of the patient. Cerebrospinal fluid (CSF) shunt is a widely accepted treatment of choice, but the clinical outcomes in patients with LMC are not well studied. This study aimed to examine the efficacy of a CSF shunt in patients with LMC.

Methods
Seventy patients with LMC confirmed by cytology or magnetic resonance imaging (MRI) underwent ventriculoperitoneal (VP) or lumboperitoneal (LP) shunt surgery. We retrospectively analyzed the clinical characteristics of patients, symptom improvement after the shunt, rate of complications associated with the surgery, and overall survival.

Results
Fifty-five patients had systemic cancer as a preceding disease, including lung cancer (45), breast cancer (6), and others (4). Primary brain tumors were mainly glioma (7) and medulloblastoma (5). Fifty-one patients had VP shunt, and 19 had LP shunt. After surgery, preoperative symptoms improved in 35 patients (50%) and were normalized in 24 of those patients (34%). Shunt malfunction occurred in eight patients, and infection occurred in eight patients. Seventeen patients underwent revision due to infection, shunt malfunction, or over-drainage. There were no complications associated with peritoneal seeding during a median follow-up of 3.3 months after surgery. The median overall survival was 8.7months (95% confidence interval, 6.0–11.4) from LMC diagnosis and 4.1 months from shunt surgery.

Conclusion
VP or LP shunt is effective for patients with hydrocephalus from LMC in terms of symptom improvement and prolonging of overall survival with an acceptable rate of procedure-related complications.


Trial registration
This study was approved by the Institutional Review Board (IRB) of the National Cancer Center (retrospectively registered,
NCC2018-0051

).
ISSN
1477-7819
Language
English
URI
https://hdl.handle.net/10371/153120
DOI
https://doi.org/10.1186/s12957-019-1595-7
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