Suppr超能文献

一项关于II-III期恶性胸膜间皮瘤的胸膜内免疫化疗、胸膜切除术/纤维板剥脱术、放射治疗、全身化疗及长期皮下注射白细胞介素-2的II期研究。

A phase II study of intrapleural immuno-chemotherapy, pleurectomy/decortication, radiotherapy, systemic chemotherapy and long-term sub-cutaneous IL-2 in stage II-III malignant pleural mesothelioma.

作者信息

Lucchi Marco, Chella Antonio, Melfi Franca, Dini Paolo, Ambrogi Marcello, Fino Leonardo, Fontanini Gabriella, Mussi Alfredo

机构信息

Division of Thoracic Surgery, Cardiac and Thoracic Department, University of Pisa, Pisa, Italy.

出版信息

Eur J Cardiothorac Surg. 2007 Mar;31(3):529-33; discussion 533-4. doi: 10.1016/j.ejcts.2006.11.046. Epub 2006 Dec 26.

Abstract

OBJECTIVE

From therapeutic nihilism to extremely aggressive management, there is a wide range of possibilities in the treatment of malignant pleural mesothelioma (MPM). Unfortunately, there is little evidence as regards the best treatment to offer to the MPM patients. In 1999, we started a phase II study based on the multimodality treatment of stage II-III MPM, the results of which have been analysed and reported.

METHODS

From 1999 to 2004, 49 patients with IMIG stage II-III MPM underwent a multimodality treatment including: intrapleural pre-operative interleukin 2 (IL-2, 18x10(6) UI/day per 3 days), pleurectomy/decortication, intrapleural post-operative epidoxorubicin (25mg/m2 per 3 days), IL-2 (18x10(6) UI/day per 3 days), adjuvant radiotherapy (30Gy), systemic chemotherapy (cisplatin 80 mg/m2 day 1, gemcitabine 1250 mg/m2 day 1 and 8 up to 6 courses) and long-term sub-cutaneous IL-2 (3x10(6) UI/day 3 days per week).

RESULTS

There were 41 males and 8 females with a median age of 61 years (range 41-77). All the patients had a diagnosis of MPM by thoracoscopy before inclusion. We did not experience any post-operative mortality. The histology was: 39 epitheliomorf, 6 bifasic and 4 sarcomatous. According to the IMIG the post-operative staging was III in 40 cases and II in 9 cases. With a median follow-up of 59 months (range 14-81) 13 patients are still alive and the median actuarial survival is 26 months (31 and 21 months for stage II and III, respectively). Only the Performance Status at the diagnosis affected survival significantly.

CONCLUSIONS

The multimodality treatment we adopted for stage II-III MPM was feasible, well tolerated by most of the patients and produced a favourable outcome. New targeted therapies are awaited for further improvements in the treatment of this disease.

摘要

目的

从治疗虚无主义到极为积极的治疗手段,恶性胸膜间皮瘤(MPM)的治疗存在广泛的可能性。不幸的是,关于为MPM患者提供最佳治疗方案的证据很少。1999年,我们启动了一项基于II - III期MPM多模式治疗的II期研究,其结果已进行分析并报告。

方法

1999年至2004年,49例IMIG II - III期MPM患者接受了多模式治疗,包括:胸腔内术前白细胞介素2(IL - 2,每3天18×10⁶单位/天)、胸膜切除术/去皮质术、胸腔内术后表柔比星(每3天25mg/m²)、IL - 2(每3天18×10⁶单位/天)、辅助放疗(30Gy)、全身化疗(顺铂80mg/m²第1天,吉西他滨1250mg/m²第1天和第8天,共6个疗程)以及长期皮下注射IL - 2(每周3天,每天3×10⁶单位)。

结果

41例男性和8例女性,中位年龄61岁(范围41 - 77岁)。所有患者在纳入前均通过胸腔镜诊断为MPM。我们未经历任何术后死亡。组织学类型为:39例上皮型,6例双向型,4例肉瘤型。根据IMIG标准,术后分期为III期40例,II期9例。中位随访59个月(范围14 - 81个月),13例患者仍存活,中位精算生存期为26个月(II期和III期分别为31个月和21个月)。仅诊断时的体能状态对生存有显著影响。

结论

我们采用的II - III期MPM多模式治疗是可行的,大多数患者耐受性良好,并产生了良好的结果。期待新的靶向治疗方法进一步改善该疾病的治疗。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验