TY - JOUR
T1 - Efficacy of trabectedin in patients with advanced translocation- related sarcomas
T2 - Pooled analysis of two phase II studies
AU - Takahashi, Mitsuru
AU - Takahashi, Shunji
AU - Araki, Nobuhito
AU - Sugiura, Hideshi
AU - Ueda, Takafumi
AU - Yonemoto, Tsukasa
AU - Morioka, Hideo
AU - Hiraga, Hiroaki
AU - Hiruma, Toru
AU - Kunisada, Toshiyuki
AU - Matsumine, Akihiko
AU - Shimura, Masashi
AU - Kawai, Akira
N1 - Publisher Copyright:
© AlphaMed Press 2017.
PY - 2017/8
Y1 - 2017/8
N2 - Background. Trabectedin is reported as effective, especially against translocation-related sarcomas (TRSs) after failure of or intolerance to standard chemotherapy. We conducted two phase II studies of TRS, confirming high efficacy of 1.2 mg/m2 trabectedin. The updated data of 66 patients in these studies was integrated to evaluate the efficacy of trabectedin against each histological subtype, and analyze final overall survival (OS). Methods. Trabectedin was administered on day one of a 21-day cycle. Efficacy was assessed using progression-free survival (PFS), OS, and best overall response. An analysis of OS and PFS was performed for subgroups divided by baseline lymphocyte count (<1,000/µL,≥µ1,000/lL) or number of previous chemotherapy regimens (0, 1, 2 ≥3 regimens), and a Weibull parametric model was used to estimate the numerical relationship between lymphocyte count and PFS and OS. Results. Median PFS and OS in overall patients were 5.6 (95% confidence interval [CI]: 4.1-7.3) and 17.5 months (95% CI: 12.6-23.6), respectively. PFS in the myxoid and round-cell liposarcoma (MRCL) group (7.4 months [95% CI: 5.6-11.1]) was longer than in the other subtypes. The response rate was also highest in the MRCL group. Median OS was longer in patients with baseline lymphocyte counts ≥1,000/µL than in those with counts of <1,000/µL, but median PFS was not different between the two subgroups. Conclusion. Our updated and pooled data showed that trabectedin exerted prolonged disease control and antitumor effects in patients with advanced TRS, especially in MRCL.We consider that the subgroup analyses also provide important information for trabectedin treatment in patients with TRS.
AB - Background. Trabectedin is reported as effective, especially against translocation-related sarcomas (TRSs) after failure of or intolerance to standard chemotherapy. We conducted two phase II studies of TRS, confirming high efficacy of 1.2 mg/m2 trabectedin. The updated data of 66 patients in these studies was integrated to evaluate the efficacy of trabectedin against each histological subtype, and analyze final overall survival (OS). Methods. Trabectedin was administered on day one of a 21-day cycle. Efficacy was assessed using progression-free survival (PFS), OS, and best overall response. An analysis of OS and PFS was performed for subgroups divided by baseline lymphocyte count (<1,000/µL,≥µ1,000/lL) or number of previous chemotherapy regimens (0, 1, 2 ≥3 regimens), and a Weibull parametric model was used to estimate the numerical relationship between lymphocyte count and PFS and OS. Results. Median PFS and OS in overall patients were 5.6 (95% confidence interval [CI]: 4.1-7.3) and 17.5 months (95% CI: 12.6-23.6), respectively. PFS in the myxoid and round-cell liposarcoma (MRCL) group (7.4 months [95% CI: 5.6-11.1]) was longer than in the other subtypes. The response rate was also highest in the MRCL group. Median OS was longer in patients with baseline lymphocyte counts ≥1,000/µL than in those with counts of <1,000/µL, but median PFS was not different between the two subgroups. Conclusion. Our updated and pooled data showed that trabectedin exerted prolonged disease control and antitumor effects in patients with advanced TRS, especially in MRCL.We consider that the subgroup analyses also provide important information for trabectedin treatment in patients with TRS.
KW - Histological subtype
KW - Lymphocyte count
KW - Number of previous chemotherapy regimen
KW - Trabectedin
KW - Translocation-related sarcoma
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U2 - 10.1634/theoncologist.2016-0064
DO - 10.1634/theoncologist.2016-0064
M3 - Article
C2 - 28526720
AN - SCOPUS:85027304397
SN - 1083-7159
VL - 22
SP - 980
EP - 988
JO - Oncologist
JF - Oncologist
IS - 8
ER -