Literature DB >> 28198567

Sirolimus for Vincristine-Resistant Kasabach-Merritt Phenomenon: Report of Eight Patients.

Huaijie Wang1, Yitao Duan1, Ya Gao1, Xinkui Guo1.   

Abstract

BACKGROUND: The use of sirolimus for patients with multidrug-resistant Kasabach-Merritt phenomenon (KMP) has been reported in recent years. We present the experience of a single center in treating vincristine-resistant KMP using sirolimus alone.
METHODS: Children with vincristine-resistant KMP who were treated with oral sirolimus alone were eligible for inclusion in the study. We evaluated responses according to graded response criteria and acute toxicities according to the National Cancer Institute Common Toxicity Criteria.
RESULTS: Between March 2012 and October 2014, eight patients underwent sirolimus treatment. The response rate of hematologic parameters was 100% (8/8). Three tumors shrank enough to allow excision. The tumors were resected after hematologic parameters normalized. Of the five patients with unresectable vascular lesions, three had complete response, and two had partial response of their tumors at the completion of long-term (39.7 ± 24.4 wks) sirolimus treatment. Grade 3 or 4 adverse events were not documented during treatment or follow-up. No recurrence or progression of the disease was observed during follow-up.
CONCLUSION: In this small case series, we found sirolimus to be highly effective, with minimal side effects, for vincristine-resistant KMP. A larger study to compare sirolimus and vincristine for KMP is warranted.
© 2017 Wiley Periodicals, Inc.

Entities:  

Mesh:

Substances:

Year:  2017        PMID: 28198567     DOI: 10.1111/pde.13077

Source DB:  PubMed          Journal:  Pediatr Dermatol        ISSN: 0736-8046            Impact factor:   1.588


  6 in total

1.  The use of rapamycin to treat vascular tumours and malformations: A single-centre experience.

Authors:  Soumitra Tole; Michelle Fantauzzi; Diana Cottingham; Joao G Amaral; Philip R John; Irene Lara-Corrales; Elena Pope; Manuel D Carcao
Journal:  Paediatr Child Health       Date:  2019-08-20       Impact factor: 2.253

2.  Indications and Limitations of Sirolimus in the Treatment of Vascular Anomalies-Insights From a Retrospective Case Series.

Authors:  Anna Karastaneva; Paolo Gasparella; Sebastian Tschauner; Roman Crazzolara; Gabriele Kropshofer; Manfred Modl; Andreas Pfleger; Ante Burmas; Mirjam Pocivalnik; Raphael Ulreich; Werner Zenz; Wolfgang Schwinger; Besiana P Beqo; Christian Urban; Emir Q Haxhija; Herwig Lackner; Martin Benesch
Journal:  Front Pediatr       Date:  2022-05-23       Impact factor: 3.569

3.  Effective surgical treatment of life-threatening huge vascular anomalies associated with thrombocytopenia and coagulopathy in infants unresponsive to drug therapy.

Authors:  Yaohao Wu; Ronglin Qiu; Lexiang Zeng; Liyang Liang; Jie Zhang; Jiajia Zhou; Wenli Jiang; Jianhang Su; Xiaogeng Deng
Journal:  BMC Pediatr       Date:  2020-04-27       Impact factor: 2.125

Review 4.  Kaposiform hemangioendothelioma: current knowledge and future perspectives.

Authors:  Yi Ji; Siyuan Chen; Kaiying Yang; Chunchao Xia; Li Li
Journal:  Orphanet J Rare Dis       Date:  2020-02-03       Impact factor: 4.123

5.  Cocktail therapy with prednisolone, vincristine and sirolimus for Kasabach‑Merritt phenomenon in 10 infants.

Authors:  Qianlong Liu; Na Xiong; Xinyuan Gong; Haochongyang Tong; Xuanfeng Tan; Xinkui Guo
Journal:  Exp Ther Med       Date:  2022-08-09       Impact factor: 2.751

6.  Effective low-dose sirolimus regimen for kaposiform haemangioendothelioma with Kasabach-Merritt phenomenon in young infants.

Authors:  Veroniek E M Harbers; Nathalie van der Salm; Sjoert A H Pegge; Carine J M van der Vleuten; Bas H Verhoeven; Sabine L A G Vrancken; Leo J Schultze Kool; Joris Fuijkschot; D Maroeska M W M Te Loo
Journal:  Br J Clin Pharmacol       Date:  2022-01-18       Impact factor: 3.716

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.