This is an Italian, multicentre, single arm, phase II study, with an intra-patient comparison end point. This study aims at confirming the activity of the drug trabectedin as second/further line treatment in retroperitoneal leiomyosarcoma and well differentiated/dedifferentiated liposarcoma expressed in terms of slowing down tumour growth. Another objective is to investigate this peculiar benefit of trabectedin in typical retroperitoneal sarcomas may be exploited to help multidisciplinary clinical decision-making in the management of retroperitoneal sarcomas
Retroperitoneal soft-tissue sarcomas (R-STSs) are rare neoplasms, accounting for 10% to 15% of Soft Tissue Sarcomas (STSs), which represent 1-3% of all cancers. They may show different histological types, but the predominant ones in the retroperitoneal region are: leiomyosarcoma, liposarcoma. The most commonly encountered in the retroperitoneum is the well differentiated/dedifferentiated liposarcoma. First-line chemotherapy usually consists of doxorubicin and/or ifosfamide. These two drugs are the most active agents in adult STSs, with a dose-response relationship and response rates between 20% and 50%. However, the sarcoma community is currently doubtful as to the activity of ifosfamide in the subgroup of leiomyosarcomas. Trabectedin has been found to be mainly active in leiomyosarcoma and liposarcoma and is approved by European Medicines Agency (EMA) as second-line chemotherapy for STSs. Although the response rate observed in pre-registration studies did not exceed 10%, trabectedin provided disease control, with progression arrest rates exceeding 50% and Progression Free Survival (PFS) rates exceeding 20% at 6 months. Since so far no phase II studies tested the activity of trabectedin in retroperitoneal sarcomas, this is the specific aim of this study. Target population: Patients with previously treated, histologically confirmed, retroperitoneal leiomyosarcoma and well differentiated/dedifferentiated liposarcoma. Patients may be either unamenable to surgery or amenable but in whom the addition of medical treatment is considered clinically advisable. Translational studies will be performed, with the aim of characterising the tumour biological features associated with different response patterns to trabectedin. These assessments will be done in 15-20 patients who will undergo surgery after trabectedin, comparing tumour tissue specimens collected before and after treatment.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
105
Trabectedin administered at a dose of 1.5 mg/m2 - 1.3 mg/m2 (at investigator's discretion, with a top-dose of 2.6 total mg per cycle) as a 24-hour continuous infusion via a central venous access until progressive disease, major toxicity, patient's intolerance, unwillingness to continue treatment, or medical decision by the responsible physician
Istituto Tumori Giovanni Paolo II
Bari, BA, Italy
Azienda Ospedaliera Giovanni Paolo XXIII
Bergamo, BG, Italy
Azienda Ospedaliera S. Orsola-Malpighi
Bologna, BO, Italy
A.O. Spedali Civili
Brescia, BS, Italy
Ospedale Oncologico A. Businco
Cagliari, CA, Italy
Azienda Ospedaliera S Croce e Carle
Cuneo, CN, Italy
Azienda Ospedaliera Sant'Anna
Como, CO, Italy
IRST IRCCS Meldola
Meldola, FC, Italy
Fondazione IRCCS Istituto Nazionale dei Tumori
Milan, MI, Italy
Istituto Europeo di Oncologia
Milan, MI, Italy
...and 11 more locations
Growth Modulation Rate
The primary end point of the study will be the proportion of responders to trabectedin, based on the ratio, in each single patient, between PFS under trabectedin (PFS) and time to progression after previous chemotherapy treatment (TTP1).
Time frame: From date of randomization until progressive disease, assessed up to 48 months
Objective response (OR) in the overall sample
Time frame: From date of randomization until progressive disease, assessed up to 48 months
Pathological tumour response in the two eligible histological types, in patients undergoing surgery after treatment
Time frame: From date of randomization until the best tumour dimensional response, assessed up to 48 months
PFS and OR in the two eligible histological types
Time frame: From date of randomization until progressive disease, assessed up to 48 months
PFS in patients who undergo surgery after, or during, medical therapy and those who do not
Time frame: From date of randomization until progressive disease, assessed up to 48 months
Number of patients with grade>=3 adverse drug reactions, number of serious adverse events related to study drug and number of patients who will experience at least one serious adverse event
Time frame: From date of randomization until progressive disease, assessed up to 48 months
Efficacy of trabectedin in reducing cancer related pain
All patients will be administered a standardized questionnaire evaluating cancer related pain and use of antalgic medication.
Time frame: From date of randomization until progressive disease, assessed up to 48 months
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