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采用类白血病疗法治疗间变性大细胞淋巴瘤:意大利儿科血液学和肿瘤学协会(AIEOP)LNH - 92方案报告

Anaplastic large cell lymphoma treated with a leukemia-like therapy: report of the Italian Association of Pediatric Hematology and Oncology (AIEOP) LNH-92 protocol.

作者信息

Rosolen Angelo, Pillon Marta, Garaventa Alberto, Burnelli Roberta, d'Amore Emanuele S, Giuliano Maria, Comis Margherita, Cesaro Simone, Tettoni Katia, Moleti Maria Luisa, Tamaro Paolo, Visintin Gianluca, Zanesco Luigi

机构信息

Clinica di Oncoematologia Pediatrica, Azienda Ospedaliera-Università di Padova, Padova, Italy.

出版信息

Cancer. 2005 Nov 15;104(10):2133-40. doi: 10.1002/cncr.21438.

DOI:10.1002/cncr.21438
PMID:16211546
Abstract

BACKGROUND

Childhood anaplastic large cell lymphoma (ALCL) is a well defined entity with a rather poor prognosis. Different approaches have been adopted in the treatment of ALCL in various cooperative trials, including short high-dose intensive therapy and leukemia-like protocols. In the early 1990s, the Italian Association of Pediatric Hematology and Oncology (AIEOP) initiated a multicenter trial for the treatment of ALCL based on a modified LSA2-L2 protocol.

METHODS

Thirty-four consecutive eligible children with newly diagnosed ALCL were enrolled in the AIEOP LNH-92 protocol. Treatment was comprised of an induction of remission phase, followed by consolidation and maintenance for a total duration of 24 months, independently of disease stage.

RESULTS

Thirty of 34 patients (88%) achieved complete disease remission and 8 patients experienced disease recurrence. With a median follow-up of 8.4 years, the probabilities of survival and event-free survival were 85% (range, 79-91%) and 65% (range, 57-73%), respectively. Therapy was well tolerated and hematologic toxicity was the most frequent toxicity.

CONCLUSIONS

The leukemia-like protocol AIEOP LNH-92 was found to be an effective treatment for childhood ALCL. Its long duration may be beneficial to specific patient subgroups, but optimal treatment duration in ALCL remains to be elucidated.

摘要

背景

儿童间变性大细胞淋巴瘤(ALCL)是一种定义明确但预后较差的疾病。在各种合作试验中,针对ALCL的治疗采用了不同方法,包括短期高剂量强化治疗和类似白血病的方案。20世纪90年代初,意大利儿童血液学和肿瘤学协会(AIEOP)基于改良的LSA2-L2方案启动了一项治疗ALCL的多中心试验。

方法

34例连续入选的新诊断ALCL合格患儿纳入AIEOP LNH-92方案。治疗包括诱导缓解期,随后进行巩固和维持治疗,总疗程24个月,与疾病分期无关。

结果

34例患者中有30例(88%)实现疾病完全缓解,8例患者疾病复发。中位随访8.4年,生存率和无事件生存率分别为85%(范围79%-91%)和65%(范围57%-73%)。治疗耐受性良好,血液学毒性是最常见的毒性。

结论

发现类似白血病的方案AIEOP LNH-92是治疗儿童ALCL的有效方法。其较长疗程可能对特定患者亚组有益,但ALCL的最佳治疗疗程仍有待阐明。

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