Abstract | BACKGROUND: METHODS: Between 2008 and 2017, 25 patients with soft tissue sarcoma were treated with pirarubicin (30 mg/m2, 2 days), ifosfamide (2 g/m2, 5 days), and etoposide (100 mg/m2, 3 days) every 3 weeks. The primary endpoint was overall response, and the secondary endpoint was adverse events of this regimen. RESULTS: Responses 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. CONCLUSION: This 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.
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Authors | Shiro Saito, Hisaki Aiba, Satoshi Yamada, Hideki Okamoto, Katsuhiro Hayashi, Hiroaki Kimura, Shinji Miwa, Takanobu Otsuka, Hideki Murakami |
Journal | BMC cancer
(BMC Cancer)
Vol. 20
Issue 1
Pg. 868
(Sep 09 2020)
ISSN: 1471-2407 [Electronic] England |
PMID | 32907549
(Publication Type: Journal Article)
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Chemical References |
- Etoposide
- Doxorubicin
- pirarubicin
- Ifosfamide
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Topics |
- Adult
- Aged
- Antineoplastic Combined Chemotherapy Protocols
(administration & dosage, adverse effects)
- Disease-Free Survival
- Doxorubicin
(administration & dosage, adverse effects, analogs & derivatives)
- Drug-Related Side Effects and Adverse Reactions
(classification, pathology)
- Etoposide
(administration & dosage, adverse effects)
- Female
- Humans
- Ifosfamide
(administration & dosage, adverse effects)
- Leukopenia
(chemically induced, pathology)
- Male
- Middle Aged
- Sarcoma
(drug therapy, pathology)
- Thrombocytopenia
(chemically induced, pathology)
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