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1.
J Clin Oncol ; 24(4): 612-8, 2006 Feb 01.
Article in English | MEDLINE | ID: mdl-16380410

ABSTRACT

PURPOSE: Patients with natural killer T (NK/T) -cell lymphomas have poor survival outcome, and for this condition there is no optimal therapy. The purpose of this study was to design a prognostic model specifically for extranodal NK/T-cell lymphoma, which can identify high-risk patients who need more aggressive therapy. PATIENTS AND METHODS: This multicenter retrospective study was comprised of 262 patients who were diagnosed with NK/T-cell lymphoma. RESULTS: After a median follow-up duration of 51.2 months, 5-year overall survival rate in 262 patients was 49.5%. Prognostic factors for survival were "B" symptoms (P = .0003; relative risk, 2.202; 95% CI, 1.446 to 3.353), stage (P = .0006; relative risk, 2.366; 95% CI, 1.462 to 3.828), lactate dehydrogenase (LDH) level (P = .0005; relative risk, 2.278; 95% CI, 1.442 to 3.598), and regional lymph nodes (P = .0044; relative risk, 1.546; 95% CI, 1.009 to 2.367). Of 262 patients, 219 had complete information on four parameters. We identified four different risk groups: group 1, no adverse factor; group 2, one factor; group 3, two factors; and group 4, three or four factors. The new model showed a superior prognostic discrimination as compared with the International Prognostic Index (IPI). Notably, the distribution of patients was balanced when a new model was adopted (group 1, 27%; group 2, 31%; group 3, 20%; group 4, 22%), whereas 81% of patients were categorized as low or low-intermediate risks using IPI. CONCLUSION: The newly proposed model for extranodal NK/T-cell lymphoma demonstrated a more balanced distribution of patients into four groups with better prognostic discrimination as compared with the IPI.


Subject(s)
Killer Cells, Natural , Lymphoma, T-Cell/diagnosis , Nose Neoplasms/diagnosis , Aged , Analysis of Variance , Confidence Intervals , Female , Follow-Up Studies , Humans , Lymphatic Metastasis , Lymphoma, T-Cell/pathology , Male , Middle Aged , Models, Statistical , Neoplasm Invasiveness , Nose Neoplasms/pathology , Odds Ratio , Prognosis , Proportional Hazards Models , Retrospective Studies , Risk Assessment , Survival Analysis
2.
J Neurooncol ; 66(1-2): 167-74, 2004 Jan.
Article in English | MEDLINE | ID: mdl-15015782

ABSTRACT

We analyzed 19 cases of cytologically confirmed leptomeningeal carcinomatosis (LMC) treated at our institution over the past 11 years. LMC was the initial manifestation of gastric cancer in 2 patients. With the exception of 1 patient, the primary gastric cancer was Borrmann type III or IV, and 88% had poorly differentiated or signet-ring cell histology. The gastric cancer was progressive or a recurrent disease in most of the patients. The distribution of extraneural metastasis suggested that Batson's venous plexus might be the predominant route to the subarachnoid space. Eighty percent of the patients had multiple neuraxis syndrome, and the combination of brain plus cranial nerve syndrome was the most common manifestation. Computed tomography (CT) findings were abnormal in a minor proportion of the patients, while magnetic resonance imaging (MRI) revealed abnormality in 67% of the patients, which could help the diagnosis. LMC complicating gastric cancer was ultimately fatal. Median survival was very short, 4 weeks. By univariate analysis, good performance status, intrathecal chemotherapy, and low CSF LDH concentration favored survival. Multivariate analysis revealed that the administration of CSF chemotherapy was the independent prognostic factor for survival.


Subject(s)
Carcinoma/pathology , Meningeal Neoplasms/pathology , Neoplasms, Second Primary/pathology , Stomach Neoplasms/pathology , Adolescent , Adult , Aged , Carcinoma/complications , Carcinoma/diagnosis , Carcinoma/mortality , Cranial Nerve Neoplasms/pathology , Disease Progression , Female , Humans , Magnetic Resonance Imaging , Male , Meningeal Neoplasms/complications , Meningeal Neoplasms/diagnosis , Meningeal Neoplasms/mortality , Middle Aged , Multivariate Analysis , Neoplasm Recurrence, Local , Nervous System Diseases/etiology , Retrospective Studies , Survival Analysis , Tomography, X-Ray Computed
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