Trabectedin and RAdiotherapy in Soft Tissue Sarcoma (TRASTS): Results of a Phase I Study in Myxoid Liposarcoma from Spanish (GEIS), Italian (ISG), French (FSG) Sarcoma Groups

被引:47
|
作者
Gronchi, Alessandro [1 ]
Hindi, Nadia [2 ,3 ]
Cruz, Josefina [4 ]
Blay, Jean-Yves [5 ]
Lopez-Pousa, Antonio [6 ]
Italiano, Antoine [7 ]
Alvarez, Rosa [8 ]
Gutierrez, Antonio [9 ]
Rincon, Inmaculada [3 ]
Sangalli, Claudia [1 ]
Perez Aguiar, Jose Luis [4 ]
Romero, Jesus [10 ]
Morosi, Carlo [1 ]
Sunyach, Marie Pierre [5 ]
Sanfilippo, Roberta [1 ]
Romagosa, Cleofe [11 ]
Ranchere-Vince, Dominique [5 ]
Dei Tos, Angelo P. [12 ,13 ]
Casali, Paolo G. [1 ,2 ,3 ,4 ,5 ,6 ,7 ,8 ,9 ,10 ,11 ,12 ,13 ,14 ]
Martin-Broto, Javier [2 ,3 ]
机构
[1] Fdn IRCCS Ist Nazl Tumori, Milan, Italy
[2] Biomed Inst Seville IBIS, Seville, Spain
[3] Univ Hosp Virgen del Rocio, Seville, Spain
[4] Univ Hosp Canarias, Tenerife, Spain
[5] Ctr Leon Berard, Lyon, France
[6] Hosp Santa Creu & Sant Pau, Barcelona, Spain
[7] Inst Bergonie Bourdeaux, Bordeaux, France
[8] Univ Hosp Gregorio Maranon, Madrid, Spain
[9] Son Espases Univ Hosp IdISBa, Palma De Mallorca, Illes Baleares, Spain
[10] Puerta de Hierro Univ Hosp, Madrid, Spain
[11] Vall dHebron Univ Hosp, Barcelona, Spain
[12] Treviso Gen Hosp, Treviso, Italy
[13] Univ Padua, Dept Med, Padua, Italy
[14] Univ Milan, Dept Oncol & Hematooncol, Milan, Italy
关键词
Sarcoma; Myxoid Liposarcoma; Trabectedin; Radiotherapy; Chemotherapy; Neoadjuvant; Prognosis; Survival; TUMOR RESPONSE ASSESSMENT; RADIATION-THERAPY; NEOADJUVANT CHEMOTHERAPY; HIGH-RISK; CLINICAL-TRIAL; LOCAL-CONTROL; HIGH-GRADE; EXTREMITY; CELL; ECTEINASCIDIN-743;
D O I
10.1016/j.eclinm.2019.03.007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Myxoid liposarcoma (ML) exhibits a special sensitivity to trabectedin (T) and radiation therapy (RT). Preclinical data suggest a synergistic effect. We aimed to study safety, feasibility and activity of the administration of pre-operative concurrent T and RT in patients affected by localized resectable ML. Methods: Patients received 3 cycles (C) of T in combination with RT (45 Gy) in 25 fractions (1.8 Gy/fraction). Dose Levels for T were:-1 (1.1mg/m2), 0 (1.3mg/m2) and 1 (1.5mg/m2). Primary endpoint was safety; antitumor activity was assessed by RECIST and Choi criteria. This study is registered at ClinicalTrials.gov, number NCT02275286. The phase 1 part of the study is complete and phase 2 is ongoing. Findings: From February 2015 to May 2016, 14 patients (M/F 7/7), median age 36 years (range 24-70) and median tumor size 12.5 cm (range 7-17 cm), were enrolled. One dose limiting toxicity (G3 transaminitis) occurred at Level 0 and one (sepsis due to catheter infection) at Level 1. All patients completed RT. Five patients achieved PR (36%), 8 SD(57%), 1 distant PD (7%) by RECIST, while 12 achieved PR (86%), 1 SD (7%) and 1 distant PD(7%) by Choi criteria. Twelve patients underwent surgery. Median viable residual tumor was 5% (0-60). Interpretation: T in combination with RT showed a favorable safety profile and antitumor activity in localized ML. T dose of 1.5 mg/m2 is the recommended dose for the phase 2 study, which is ongoing. (C) 2019 Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license
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页码:35 / 43
页数:9
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