Literature DB >> 29576383

Ifosfamide and doxorubicin in the treatment of advanced leiomyosarcoma.

Serkan Akin1, Omer Dizdar2, Yusuf Karakas3, Alev Turker3, Ayse Kars3.   

Abstract

Leiomyosarcomas (LMS) are rare tumors with poor prognosis owing to the high rate of recurrent and metastatic disease. The combination of doxorubicin (Adriamycin) plus ifosfamide and mesna (AIM) results in moderate response rates of 10%-30%. The aim of this study was to assess the efficacy of the AIM regimen along with multimodality treatment including surgery and radiotherapy in patients with LMS. The clinicopathologic characteristics and outcomes of 51 patients with recurrent or metastatic LMS diagnosed between 2000 and 2014 who received the AIM regimen were analyzed retrospectively. Treatment consisted of ifosfamide 2500mg/m² on days 1-3 (with mesna 2500mg/m² days 1-3, 4-hour i.v. infusion), and doxorubicin 60mg/m² on day 1 (2-hour i.v. infusion), which was repeated every 21 days. The mean age of the patients at diagnosis was 48.9 ± 11.2 years. A total of 42 patients were females (82.4%). The primary tumor site was the uterus in 30 (58.8%) patients. The most common metastatic sites were lung and liver. The median follow-up was 27.9 months (min: 4.3 max: 164.8). The median progression-free survival was 6.7 months (95% CI: 4.1-9.2). The median overall survival (OS) was 24.6 months (95% CI: 16.2-33.0). The overall response rate was 12% (6/51 pts). Response rates were higher in patients with uterine LMS (17%) compared with those with nonuterine LMS (5%); however, the OS times were similar. Surgical intervention for local or distant recurrence was associated with improved median OS (41 vs 16.6 months, P < 0.001). Myelosuppression was the major toxicity of this combination. In our study, the AIM regimen was effective in patients with LMS. Resection of local or distant recurrence was found to improve survival in our study.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  AIM; Doxorubicin; Ifosfamide; Leiomyosarcoma

Mesh:

Substances:

Year:  2018        PMID: 29576383     DOI: 10.1016/j.currproblcancer.2018.01.011

Source DB:  PubMed          Journal:  Curr Probl Cancer        ISSN: 0147-0272            Impact factor:   3.187


  3 in total

1.  A case of pulmonary leiomyosarcoma achieving long-term survival after multiple metastasectomies.

Authors:  Yuki Azumi; Tomoyuki Wakahara; Kiyonori Kanemitsu; Shinobu Tsuchida; Mitsuru Sasako; Kyoko Otani; Takeshi Iwasaki
Journal:  Int Cancer Conf J       Date:  2022-02-14

2.  Metastases of soft tissue sarcoma to the liver: A Historical Cohort Study from a Hospital-based Cancer Registry.

Authors:  Masanori Okamoto; Masatake Matsuoka; Tamotsu Soma; Ryuta Arai; Hidenori Kato; Toru Harabayashi; Hirohumi Adachi; Toshiki Shinohara; Tamotsu Sagawa; Noriaki Nishiyama; Toshikazu Nambu; Wataru Sakai; Hiroaki Suzuki; Hiroyuki Kato; Hiroaki Hiraga
Journal:  Cancer Med       Date:  2020-07-10       Impact factor: 4.452

3.  The systemic treatment of uterine leiomyosarcomas: A systematic review. No news is good news?

Authors:  Anastasios Kyriazoglou; Michalis Liontos; Ioannis Ntanasis-Stathopoulos; Maria Gavriatopoulou
Journal:  Medicine (Baltimore)       Date:  2021-04-02       Impact factor: 1.817

  3 in total

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