TY - JOUR
T1 - Prognostic and therapeutic factors influencing the clinical outcome of metastatic Ewing sarcoma family of tumors
T2 - A retrospective report from the Japan Ewing Sarcoma Study Group
AU - Japan Ewing Sarcoma Study Group
AU - Umeda, Katsutsugu
AU - Miyamura, Takako
AU - Yamada, Kenji
AU - Sano, Hideki
AU - Hosono, Ako
AU - Sumi, Minako
AU - Okita, Hajime
AU - Kamio, Takuya
AU - Maeda, Naoko
AU - Fujisaki, Hiroyuki
AU - Jyoko, Ryoji
AU - Watanabe, Atsuko
AU - Hosoya, Yosuke
AU - Hasegawa, Daiichiro
AU - Takenaka, Satoshi
AU - Nakagawa, Shunsuke
AU - Chin, Motoaki
AU - Ozaki, Toshifumi
N1 - Publisher Copyright:
© 2020 Wiley Periodicals LLC
PY - 2021/3
Y1 - 2021/3
N2 - Background: The prognosis of patients with metastatic Ewing sarcoma family of tumors (ESFT) remains poor. Procedure: We retrospectively analyzed 57 patients diagnosed with metastatic ESFT between 2000 and 2018 to identify prognostic and therapeutic factors affecting the clinical outcome. Results: The 3-year overall survival (OS) rate of the entire cohort was 46.8% (95% confidence interval [CI], 33.0-59.4%). Treatment-related death was not observed. Multivariate analysis identified stem cell transplantation (SCT), response to first-line chemotherapy, and bone metastasis as independent risk factors for OS. Objective response rate to first-line chemotherapy was 65.1% in the 43 evaluable patients. There was no significant difference in the response to different types of first-line chemotherapy. Among patients with lung metastasis alone, the 3-year OS rate was higher in 13 patients who received local treatment than in four who did not, although the difference was not significant. Conclusions: One possible reason for the high OS rates was the absence of treatment-related mortality even in patients receiving SCT, which could be attributed to advances in the management of post-SCT complications. Novel first-line chemotherapy strategies need to be established to improve the disease status prior to SCT in a higher proportion of patients.
AB - Background: The prognosis of patients with metastatic Ewing sarcoma family of tumors (ESFT) remains poor. Procedure: We retrospectively analyzed 57 patients diagnosed with metastatic ESFT between 2000 and 2018 to identify prognostic and therapeutic factors affecting the clinical outcome. Results: The 3-year overall survival (OS) rate of the entire cohort was 46.8% (95% confidence interval [CI], 33.0-59.4%). Treatment-related death was not observed. Multivariate analysis identified stem cell transplantation (SCT), response to first-line chemotherapy, and bone metastasis as independent risk factors for OS. Objective response rate to first-line chemotherapy was 65.1% in the 43 evaluable patients. There was no significant difference in the response to different types of first-line chemotherapy. Among patients with lung metastasis alone, the 3-year OS rate was higher in 13 patients who received local treatment than in four who did not, although the difference was not significant. Conclusions: One possible reason for the high OS rates was the absence of treatment-related mortality even in patients receiving SCT, which could be attributed to advances in the management of post-SCT complications. Novel first-line chemotherapy strategies need to be established to improve the disease status prior to SCT in a higher proportion of patients.
KW - Ewing sarcoma family of tumors
KW - chemotherapy
KW - metastatic
KW - stem cell transplantation
UR - http://www.scopus.com/inward/record.url?scp=85097759444&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85097759444&partnerID=8YFLogxK
U2 - 10.1002/pbc.28844
DO - 10.1002/pbc.28844
M3 - Article
C2 - 33340261
AN - SCOPUS:85097759444
SN - 1545-5009
VL - 68
JO - Medical and Pediatric Oncology
JF - Medical and Pediatric Oncology
IS - 3
M1 - e28844
ER -