ArticleNeuro-oncology2017
Primary intramedullary spinal cord lymphoma: a population-based study.
Article in Neuro-oncology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.
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Who cites it
16 citing papers in PubMed, 33 citations in OpenAlex.
- Successful treatment of primary intramedullary spinal cord lymphoma based on the molecular diagnosis of a MYD88 mutation in the cerebrospinal fluid: a case report.International cancer conference journal · 2025Article
- Spinal subdural empyema: A two-dimensional illustrative operative video.Surgical neurology international · 2025Article
- Incidence and Survival of Patients With Malignant Primary Spinal Cord Tumors: A Population-Based Analysis.Neurospine · 2024Article
- Primary intracranial lymphomas-incidence and survival: a population-based study.Neurosurgical review · 2023Article
- Primary intramedullary spinal cord lymphoma misdiagnosed as longitudinally extensive transverse myelitis: a case report and literature review.BMC neurology · 2023Review
- Effect of race, sex, and socioeconomic factors on overall survival following the resection of intramedullary spinal cord tumors.Journal of neuro-oncology · 2023Article
- Impact of Racial Disparities on All-Cause Mortality in Patients With Tumors of the Spinal Cord or Spinal Meninges: A Propensity-Score Analysis.Global spine journal · 2023Article
- B-Cell Lymphoma Intramedullary Tumor: Case Report and Systematic Review.Asian journal of neurosurgery · 2023Review
- Primary central nervous system lymphoma presenting as an isolated intramedullary spinal cord lesion: a case report.AME case reports · 2023Article
- An Atypical Presentation of Non-Hodgkin's Lymphoma.Cureus · 2022Article
- Primary intradural extramedullary spinal Burkitt's lymphoma mimicking a nerve sheath tumor: a case report.Spinal cord series and cases · 2022Article
- Primary Brainstem Lymphoma: A Population-Based Study.Frontiers in surgery · 2022Article
- Primary Intradural Extramedullary Spinal Burkitt's Lymphoma: A Case Report.International medical case reports journal · 2020Article
- Nomograms Predict Survival Outcome of Primary Intramedullary Spinal Cord Lymphoma Patients.Medical science monitor : international medical journal of experimental and clinical research · 2019Article
- Clinicopathological Characteristics and Survival of Small Cell Carcinoma of the Salivary Gland: a Population-Based Study.Cancer management and research · 2019Article
- Primary Peripheral Gamma Delta T-Cell Lymphoma of the Central Nervous System: Report of a Case Involving the Intramedullary Spinal Cord and Presenting with Myelopathy.Journal of pathology and translational medicine · 2019Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors at 5 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Primary intramedullary spinal cord lymphoma (PISCL) is a rare diagnosis with poorly understood disease progression. Clarification of the factors associated with survival in PISCL patients is warranted. Methods: We conducted a population-based cohort study utilizing prospectively collected data from the Surveillance, Epidemiology, and End Results (SEER) database. Patients with histological diagnosis of primary lymphoma in spinal cord (C72.0) from 1973 to 2012 in the SEER database were included. Multivariable survival analysis between patient, lesion characteristics, and PISCL-related death was performed to adjust for confounding factors. Results: We included 346 PISCL patients in our study. Average age was 56.5 ± 17.8 years, with 62.7% being male. Racial distribution of these patients was white (87.6%), black (8.0%), and other (4.3%). More than half (55.8%) of patients were married. The most prevalent histology of PISCL was diffuse B-cell (46.2%), and the majority (55.2%) were low stage (Ann Arbor stage I/II). Most patients (67.9%) received radiation therapy. Average survival interval of patients with PISCL-related death (n=135, 39.0%) was 27.8 months. General cumulative survival probability at 1 year, 2 years, and 5 years was 73.8%, 67.9%, and 63.1%, respectively. Multivariable accelerated failure time (AFT) regression showed follicular lymphoma (HR:0.25, P=.008) and more recent diagnosis (HR:0.96, P<.001) was positively associated with PISCL-related survival. Conversely, nonwhite race (HR:1.69, P=.046), older age (HR:1.02, P<.001), unmarried status (HR:2.14, P<.001), and higher stage (HR:1.54, P=.022) were negatively associated with survival. Conclusions: Age, race, marital status, tumor histology, tumor stage, and year of diagnosis were associated with survival of PISCL. While most PISCL-related deaths occur within a 1-year period, subsequent slow progression was observed after the first year of survival.
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