共 50 条
Efficacy of combination-chemotherapy with pirarubicin, ifosfamide, and etoposide for soft tissue sarcoma: a single-institution retrospective analysis
被引:1
|作者:
Saito, Shiro
[1
]
Aiba, Hisaki
[1
]
Yamada, Satoshi
[1
]
Okamoto, Hideki
[1
]
Hayashi, Katsuhiro
[1
,2
]
Kimura, Hiroaki
[1
,2
]
Miwa, Shinji
[1
,2
]
Otsuka, Takanobu
[1
,3
]
Murakami, Hideki
[1
]
机构:
[1] Nagoya City Univ, Grad Sch Med Sci, Dept Orthoped Surg, Mizuho Ku, 1 Kawasumi,Mizuho Cho, Nagoya, Aichi 4678601, Japan
[2] Kanazawa Univ, Grad Sch Med Sci, Dept Orthoped Surg, 13-1 Takaramachi, Kanazawa, Ishikawa 9208641, Japan
[3] Tokai Gakuen Univ, Dept Educ, Tenpaku Ku, 2-901 Nakadaira, Nagoya, Aichi 4680014, Japan
来源:
关键词:
Chemotherapy;
Pirarubicin;
Ifosfamide;
Etoposide;
Soft tissue sarcoma;
1ST-LINE TREATMENT;
DOXORUBICIN;
OSTEOSARCOMA;
GEMCITABINE;
GUIDELINE;
DOCETAXEL;
TUMORS;
D O I:
10.1186/s12885-020-07378-z
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
BackgroundThe standard chemotherapy regimens for soft tissue sarcoma are doxorubicin-based. This retrospective study aimed to assess the efficacy and safety of pirarubicin, ifosfamide, and etoposide combination therapy for patients with this disease.MethodsBetween 2008 and 2017, 25 patients with soft tissue sarcoma were treated with pirarubicin (30mg/m(2), 2days), ifosfamide (2g/m(2), 5days), and etoposide (100mg/m(2), 3days) every 3weeks. The primary endpoint was overall response, and the secondary endpoint was adverse events of this regimen.ResultsResponses to this regimen according to RECIST criteria were partial response (n=9, 36%), stable disease (n=9, 36%) and progressive disease (n=7, 28%). During the treatment phase, frequent grade 3 or worse adverse events were hematological toxicities including white blood cell decreases (96%), febrile neutropenia (68%), anemia (68%), and platelet count decreases (48%). No long-term adverse events were reported during the study period.ConclusionThis regimen was comparable to previously published doxorubicin-based combination chemotherapy in terms of response rate. Although there were no long-lasting adverse events, based on our results, severe hematological toxicity should be considered.
引用
收藏
页数:6
相关论文