A Study of Olaparib With Concomitant Radiotherapy in Locally Advanced/Unresectable Soft-tissue Sarcoma

Inclusion Criteria

• Histology: patients with soft-tissue sarcoma histologically confirmed by central review (Pr Coindre team), except if the diagnosis was already confirmed by the RRePS Network,
• Upper/Lower limb or trunk wall soft-tissue sarcoma,
• Age ≥ 18 years,
• Locally advanced or locally recurrent primitive tumor, outside any previously irradiated field. Patients presenting operable locally Advanced or lacally recurrent tumor can be included. Patients with metastases can be included.
• Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2,
• Life expectancy ≥ 6 months,
• At least one lesion, not previously irradiated, that can be accurately measured at baseline as ≥ 10 mm in the longest diameter (except lymph nodes which must have short axis ≥ 15 mm) with magnetic resonance imaging (MRI) and which is suitable for accurate repeated measurements,
• Adequate hematological, renal, metabolic and hepatic function:
• Haemoglobin ≥ 9 g/dL and no blood transfusions in the 14 days prior to study entry
• Absolute neutrophil count (ANc) ≥ 1.5 x 109/L
• Platelets ≥ 100 x 109/L
• Total bilirubin ≤ 1.5 x upper limit of normality (ULN),
• Alanine aminotransferase (ALAT) or aspartate aminotransferase (ASAT) ≤ 2.5 x ULN,
• Serum creatinine ≤ 150 μmol/L or creatinine clearance ≥ 50 mL/min (according to local institution) in case of serum creatinine > 150 μmol/L,
• TP, INR ≤ 1.5 x ULN
• Women of childbearing potential must have a negative serum pregnancy test within 28 days of study treatment, confirmed prior to treatment on day 1. Female patients of child bearing potential and their partners, who are sexually active, must agree to the use of two highly effective forms of contraception in combination throughout the period of taking study treatment and for at least 1 month after last dose of study drug. Males patients, who are sexually active, must agree to the use of two highly effective forms of contraception in combination throughout the period of taking study treatment and for at least 3 month after last dose of study drug. Acceptable birth control methods are described in appendix 10.

Subjects of non-childbearing potential are those who have:

• Amenorrheic for 1 year or more following cessation of exogenous hormonal treatments,
• LH and FSH levels in the post menopausal range for women under 50,
• radiation-induced oophorectomy with last menses >1 year ago,
• chemotherapy-induced menopause with >1 year interval since last menses,
• or surgical sterilisation (bilateral oophorectomy or hysterectomy).
• Patient is willing and able to comply with the protocol for the duration of the study including undergoing treatment and scheduled visits and examinations including follow up,
• Voluntary signed and dated written informed consent prior to any specific procedure,
• Patients with a social security in compliance with the Law.

Exclusion Criteria

• Any previous treatment with a PARP inhibitor, including Olaparib,
• Patients unable to swallow orally administered medication and patients with gastrointestinal disorders likely to interfere with absorption of the study medication,
• Immunocompromised patients, e.g., patients who are known to be serologically positive for human immunodeficiency virus (HIV) and are receiving antiviral therapy,
• Patients with known active hepatic disease (i.e., Hepatitis B or C) due to risk of transmitting the infection through blood or other body fluids,
• Patients considered a poor medical risk due to a serious, uncontrolled medical disorder, non-malignant systemic disease or active, uncontrolled infection. Examples include, but are not limited to, uncontrolled ventricular arrhythmia, recent (within 3 months) myocardial infarction, unstable spinal cord compression (untreated and unstable for at least 28 days prior to study entry), superior vena cava syndrome, extensive bilateral lung disease on HRCT scan or any psychiatric disorder that prohibits obtaining informed consent,

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