Your browser doesn't support javascript.
loading
Enhanced clinical outcomes with radiotherapy in diagnostically challenging intracranial plasmacytomas: Analysis of 190 cases.
Feng, Yuan; Zhang, Zongpu; Qiu, Fufang; Yang, Zixiao; Xiong, Ji; Zhu, Wei; Wan, Fangzhu; Chen, Bobin; Wang, Jiguang; Zhang, Yi; Hua, Wei.
Afiliação
  • Feng Y; Department of Neurosurgery, Huashan Hospital, Fudan University, Shanghai, China.
  • Zhang Z; National Center for Neurological Disorders, Shanghai, China.
  • Qiu F; Shanghai Key Laboratory of Brain Function Restoration and Neural Regeneration, Shanghai, China.
  • Yang Z; Neurosurgical Institute of Fudan University, Shanghai, China.
  • Xiong J; Shanghai Clinical Medical Center of Neurosurgery, Shanghai, China.
  • Zhu W; Department of Neurosurgery, Huashan Hospital, Fudan University, Shanghai, China.
  • Wan F; National Center for Neurological Disorders, Shanghai, China.
  • Chen B; Shanghai Key Laboratory of Brain Function Restoration and Neural Regeneration, Shanghai, China.
  • Wang J; Neurosurgical Institute of Fudan University, Shanghai, China.
  • Zhang Y; Shanghai Clinical Medical Center of Neurosurgery, Shanghai, China.
  • Hua W; Department of Neurosurgery, Huashan Hospital, Fudan University, Shanghai, China.
Cancer Med ; 13(4): e7017, 2024 Feb.
Article em En | MEDLINE | ID: mdl-38457205
ABSTRACT

BACKGROUND:

Intracranial plasmacytomas are rare tumors arising from plasma cells with approximately half of the cases progressing to multiple myeloma (MM). However, there is a lack of comprehensive clinical cohort analysis on the clinical and pathological features, progression, and outcomes of intracranial plasmacytomas.

METHODS:

A retrospective analysis of 190 cases was conducted, combining data from 38 cases in a single institution and 152 cases from the literature. Patient demographics, clinical presentations, tumor locations, imaging features, surgical treatments, and follow-up outcomes were collected and analyzed. Survival analysis and Cox regression analysis were performed to identify prognostic factors.

RESULTS:

A total of 190 intracranial plasmacytoma patients with an average age of 55.4 years were included in the study. The preoperative misdiagnosis ratio was high at 55.3%, and 59.7% of the tumors affected the calvaria convexity, compared to 40.3% located at the skull base. Resection and biopsy were achieved in 72.4% and 27.6% patients, respectively. Among them, 34.2% (65/190) of patients were initially diagnosed with MM with intracranial plasmacytoma as their first presentation (MM-IPFP), while 63.2% (120/190) of patients were diagnosed with solitary intracranial plasmacytoma (SIP), including 61 extramedullary plasmacytomas and 59 solitary bone plasmacytomas. In the SIP group, 22.4% (24/107) of patients experienced disease progression leading to the development of MM during a median follow-up time of 42.6 months (range 1-230 months). Multivariate analysis unveiled that radiotherapy (HR, 0.05; 95% CI, 0.00-0.87; p = 0.04), not surgery, was a protective prognostic factor for overall survival in MM-IPFP patients. Comparison between the SIP progression group and non-progression group revealed a significant difference of Ki-67 index (non-progression vs. SIP progression, 8.82% ± 7.03 vs. 16.5% ± 10.5, p < 0.05). AUC analysis determined that a cutoff value of 9.0% was the best predictor of SIP progression, with an area under the curve of 0.712.

CONCLUSIONS:

This retrospective clinical analysis highlights the potential role of radiotherapy, rather than surgical resection, in improving the outcomes of intracranial plasmacytoma. Additionally, the Ki-67 index is identified as a valuable marker for predicting disease progression. This would provide some evidence for the paradigm of diagnosis and treatment modalities for intracranial plasmacytomas from the large cohort.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Plasmocitoma / Neoplasias Ósseas / Mieloma Múltiplo Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Plasmocitoma / Neoplasias Ósseas / Mieloma Múltiplo Idioma: En Ano de publicação: 2024 Tipo de documento: Article