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恶性胸膜间皮瘤:一种不受当前治疗手段影响的疾病。

Malignant pleural mesothelioma: a disease unaffected by current therapeutic maneuvers.

作者信息

Alberts A S, Falkson G, Goedhals L, Vorobiof D A, Van der Merwe C A

机构信息

Department of Medical Oncology, University of Pretoria, Republic of South Africa.

出版信息

J Clin Oncol. 1988 Mar;6(3):527-35. doi: 10.1200/JCO.1988.6.3.527.

Abstract

From 1965 to 1985, 262 patients with malignant pleural mesothelioma were treated with cytostatics only; radiotherapy (RT); RT and cytostatics; or decortication plus RT plus cytostatics. The median survival (MS) from diagnosis was 9.6 months. This was similar for all comparable treatment groups. In a univariate analysis, significant favorable prognostic factors were good performance status (PS), duration of symptoms greater than 6 months at the time of diagnosis, early stage of disease, white race, and female sex. In a multivariate analysis, PS, race, duration of symptoms, and stage were of significance for a favorable prognosis. Age, pain as first symptom, histologic subtype, and RT dose were not of prognosis significance in this study. The stepwise addition of treatment modalities did not increase survival, which remained the same as that reported for untreated patients. Therefore, phase II trials of new agents offer the only hope for advance in the treatment of this disease.

摘要

1965年至1985年期间,262例恶性胸膜间皮瘤患者仅接受了细胞抑制剂治疗、放射治疗(RT)、RT联合细胞抑制剂治疗,或行胸膜剥脱术联合RT及细胞抑制剂治疗。自诊断起的中位生存期(MS)为9.6个月。所有可比治疗组的情况均类似。单因素分析中,显著的有利预后因素包括良好的体能状态(PS)、诊断时症状持续时间超过6个月、疾病早期、白种人及女性。多因素分析中,PS、种族、症状持续时间及分期对预后有利具有重要意义。年龄、以疼痛作为首发症状、组织学亚型及RT剂量在本研究中对预后无显著意义。逐步增加治疗方式并未提高生存率,其与未治疗患者报告的生存率相同。因此,新型药物的II期试验是本病治疗取得进展的唯一希望。

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