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Increased Metastasis of Malignant Fibrous Histiocytoma in Patients With Chronic Lymphocytic Leukemia and Non-Hodgkin Lymphoma

机译:慢性淋巴细胞白血病和非霍奇金淋巴瘤患者恶性纤维组织细胞瘤的转移增加

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摘要

OBJECTIVE: >To further understand the characteristics and behavior of malignant fibrous histiocytoma (MFH) in the clinical setting of chronic lymphocytic leukemia (CLL) or non-Hodgkin lymphoma (NHL).PATIENTS AND METHODS: >The patient database of MHF diagnosed at our institution from January 1, 1976, to December 31, 2008, was reviewed. For each MFH case with prior NHL or CLL, 3 matched controls from the same cohort without prior CLL or NHL were randomly selected. A retrospective chart review collected patient data, including sex; age; pathologic confirmation of MFH; tumor grade, size, and location; time since MFH diagnosis; history of chemotherapy or irradiation; treatment of MFH; recurrence; metastasis; and death. The Kaplan-Meier method was used to estimate overall survival, survival free of recurrence, and survival free of metastasis. Cox proportional hazards models were fit to evaluate associations between case status and outcomes.RESULTS: >Fifteen MFH cases with prior NHL or CLL were identified. Cases had frequent bone (n=7 [47%]) and cutaneous (n=5 [33%]) involvement. Five cases (33%) had previous irradiation, 6 (40%) had metastases, and 4 (27%) had recurrence. Overall survival and survival free of recurrence were not significantly different between the cases and controls (5-year overall survival, 49.9% and 58.7%; 12-month survival free of recurrence, 79.4% and 90.3%). However, cases were significantly more likely than controls to have metastasis (hazard ratio, 3.79; 95% confidence interval, 1.22-11.79; P=.02). In addition, survival free of metastasis at 12 months was 65.2% and 90.7%, respectively.CONCLUSION: >In the presence of CLL or NHL, MFH seems to behave more aggressively, suggested by the increased likelihood of metastases compared with controls without prior CLL or NHL. However, overall survival does not appear to be worse in cases of MFH and CLL or NHL than in MFH alone.
机译:目的:>在慢性淋巴细胞性白血病(CLL)或非霍奇金淋巴瘤(NHL)的临床环境中进一步了解恶性纤维组织细胞瘤(MFH)的特征和行为。患者和方法:>回顾了我们机构自1976年1月1日至2008年12月31日诊断的MHF患者数据库。对于具有先前NHL或CLL的每个MFH病例,随机选择同一队列中没有先前CLL或NHL的3个匹配对照。回顾性图表审查收集了包括性别在内的患者数据;年龄; MFH的病理证实;肿瘤等级,大小和位置;自MFH诊断以来的时间;化疗或放疗史; MFH的治疗;复发转移;和死亡。 Kaplan-Meier方法用于估计总生存期,无复发生存期和无转移生存期。 Cox比例风险模型适合评估病例状态与结果之间的关联。结果:>确定了15例既往有NHL或CLL的MFH病例。病例有频繁的骨骼受累(n = 7 [47%])和皮肤受累(n = 5 [33%])。 5例(33%)曾接受过放疗,6例(40%)有转移,4例(27%)复发。病例和对照之间的总生存率和无复发生存率无显着差异(5年总生存率分别为49.9%和58.7%; 12个月无复发生存率分别为79.4%和90.3%)。然而,与转移相比,病例更有可能发生转移(危险比,3.79; 95%置信区间,1.22-11.79; P = .02)。此外,在12个月时无转移生存率分别为65.2%和90.7%。结论:>在存在CLL或NHL的情况下,MFH的行为似乎更具攻击性,提示转移的可能性增加与没有先前CLL或NHL的对照进行比较。但是,MFH和CLL或NHL的总生存似乎并不比单独的MFH差。

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