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首页> 外文期刊>Leukemia and lymphoma >Primary non-Hodgkin's lymphoma of the nasopharynx: prognostic factors and outcome of 113 Indian patients.
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Primary non-Hodgkin's lymphoma of the nasopharynx: prognostic factors and outcome of 113 Indian patients.

机译:鼻咽原发性非霍奇金淋巴瘤:113例印度患者的预后因素和预后。

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摘要

This single institutional study evaluated the prognostic factors and treatment outcome of 113 Indian patients with primary nasopharyngeal non-Hodgkin's lymphoma. At presentation, 28% had stage I and 62% had stage II disease. Treatment comprised of a combination of chemotherapy (CTh) and radiotherapy (RT) in the majority of the patients (76%). After a median follow-up of 56 months, the 5-year disease-free survival (DFS) and overall survival (OS) for the whole group were 55.8% and 57.9%, respectively. Multivariate analysis showed that; age > 30 years [hazard ratio (HR) = 6.59, 95% confidence interval (CI) = 2.59 - 16.7, P < 0.0001], WHO performance score > or = 2 (HR = 2.34, 95% CI = 1.01 - 5.46, P = 0.050), T-cell lymphomas (HR = 2.81, 95% CI = 1.14 - 6.96, P < 0.001) and the presence of B symptoms (HR = 3.65, 95% CI = 1.77 - 7.53, P = 0.025), had a negative influence on survival. Patients treated with a combination of CTh and RT had a significantly better outcome than those treated with CTh alone (OS: 69%vs. 31%, P < 0.00001). HR for death in the CTh alone group was 3.73 (95% CI = 1.95 - 7.13). The CR (P = 0.01), DFS (P = 0.01) and OS (P = 0.03) rates were significantly better for patients receiving a RT dose of > or =4500 cGy. HR in the subgroup that received a RT dose of <4500 cGy was 2.51 (95% CI = 1.04 - 6.06). These results suggest that combined modality treatment, comprising of CTh and RT (with an RT dose of > or =4500 cGy), results in satisfactory outcome in patients with this rare neoplasm.
机译:这项单一的机构研究评估了113例印度原发性鼻咽非霍奇金淋巴瘤患者的预后因素和治疗结果。在介绍时,28%患有I期,62%患有II期疾病。大多数患者(76%)采用化学疗法(CTh)和放射疗法(RT)的组合治疗。中位随访56个月后,整个组的5年无病生存率(DFS)和总生存率(OS)分别为55.8%和57.9%。多变量分析表明:年龄> 30岁[危险比(HR)= 6.59,95%置信区间(CI)= 2.59-16.7,P <0.0001],WHO绩效得分>或= 2(HR = 2.34,95%CI = 1.01-5.46, P = 0.050),T细胞淋巴瘤(HR = 2.81,95%CI = 1.14-6.96,P <0.001)和存在B症状(HR = 3.65,95%CI = 1.77-7.53,P = 0.025),对生存产生负面影响。联合使用CTh和RT治疗的患者的结局明显优于单独使用CTh的患者(OS:69%比31%,P <0.00001)。仅CTh组的死亡HR为3.73(95%CI = 1.95-7.13)。对于RT剂量≥4500 cGy的患者,CR(P = 0.01),DFS(P = 0.01)和OS(P = 0.03)的发生率明显更高。接受<4500 cGy的RT剂量的亚组中的HR为2.51(95%CI = 1.04-6.06)。这些结果表明,由CTh和RT(RT剂量≥4500 cGy)组成的联合模态治疗在患有这种罕见肿瘤的患者中获得令人满意的结果。

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