OlaReDo - Olaratumab and Rechallenge With Doxorubicin in Soft Tissue Sarcoma Patients

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追踪信息

首次提交日期 ^ICMJE

October 1, 2018

首次发布日期e ^ICMJE

October 5, 2018

最后更新发布日期

October 5, 2018

预计研究开始日期 ^ICMJE

October 4, 2018

预计主要完成日期

December 31, 2019 (主要结果测量的最终数据收集日期)

目前主要观察指标 ^ICMJE

Progression-free survival rate after 3 months (PFSR3), assessed by applying RECIST 1.1[ Time Frame: After 3 months treatment ]

number of patients proven progression-free and alive after 3 months divided through the total number of patients in the all-treated-subjects population

原始主要观察测量 ^ICMJE

与当前相同

目前的二级观察 ^ICMJE

Progression free survival (PFS)[ Time Frame: 6 months of Follow Up ]
Time from the first dosing date of any study medication to the date of the first Objectively documented tumor progression, as determined by investigators (per RECIST v1.1), or death due to any cause.
Objective response rate (ORR) (i.e. CR or PR)[ Time Frame: 6 months of Follow Up ]
Number and percentage of participants with a best overall response (BOR) of complete response (CR) or partial response (PR)
Disease control rate (DCR) (i.e. CR, PR or SD)[ Time Frame: 6 months of Follow Up ]
Number and percentage of participants with complete response (CR) or partial response (PR) or stable disease (SD)
Overall survival (OS)[ Time Frame: 6 months of Follow Up ]
Time from date of the first dosing date of any study medication to the date of death (due to any cause)
Assessment of adverse events[ Time Frame: During study conduct up to a maximum of 18 months (EOT) ]
Type, incidence and severity of AEs, SAEs
Study therapy discontinuation rate due to cardiac toxicity[ Time Frame: After treatment discontinuation up to a maximum of 18 months (EOS) ]
Number of patients proven study therapy discontinuation due to cardiac toxicity (i.e. due to LVEF reduction by more than 20% or LVEF <45%) divided through the total number of patients in the all-treated-subjects population

描述性信息

简略标题 ^ICMJE

OlaReDo - Olaratumab and Rechallenge With Doxorubicin in Soft Tissue Sarcoma Patients

正式标题 ^ICMJE

Efficacy of Olaratumab and Rechallenge With Doxorubicin in Anthracycline Pretreated, Advanced Soft Tissue Sarcoma Patients. An Exploratory Phase-II Study

简要概况

This is an exploratory, prospective, open label, single arm, phase II-study for the evaluation of efficacy and feasibility (as determined by safety and tolerability) of olaratumab and doxorubicin rechallenge in anthracycline pretreated locally advanced (unresectable) or metastatic soft tissue sarcoma patients.

详细说明

Until now, rechallenge with anthracyclines in patients with metastatic STS which had a benefit from prior anthracycline containing therapy was never investigated in a prospective study. Due to the very promising effect of olaratumab and doxorubicin in anthracycline-naïve patients and further taking into consideration the results of the retrospective anthracycline rechallenge study, there is a clear rationale to evaluate the effects of olaratumab and doxorubicin also in anthracycline pretreated patients by conducting a prospective clinical trial.

研究类型 ^ICMJE

Interventional

研究阶段

Phase 2

研究设计 ^ICMJE

分配:
干预模型: Single Group Assignment
干预模型描述: Olaratumab and doxorubicin rechallenge in anthracycline pretreated, advanced soft tissue sarcoma patients
盲法: Interventional
盲法描述:
主要目的: Treatment

适用条件 ^ICMJE

干预项目 ^ICMJE

Drug: Olaratumab
iv infusion
Drug: Dexrazoxane
iv infusion
Drug: Doxorubicin
iv infusion

研究工具

Experimental: Study treatment
Olaratumab 20 mg/kg IV on day 1 and day 8 of cycle 1 and 15 mg/kg olaratumab IV on day 1 and day 8 of cycles 2-8. Plus dexrazoxane at a dose equal to 10 times the doxorubicin dose (mg/m2) IV on day 1 of each 21 day cycle for 8 cycles Plus doxorubicin 75 mg/m2 IV on day 1 of each 21 day cycle for 8 cycles Beginning with cycle 9, olaratumab maintenance monotherapy at 15 mg/kg IV on day 1 and day 8 of each subsequent 21 day cycle

招募信息

招募状态 ^ICMJE

Not yet recruiting

预计入组 ^ICMJE

原始预计入组 ^ICMJE

与当前相同

预计研究完成日期

December 31, 2019

预计主要完成日期

December 31, 2019 (主要结果测量的最终数据收集日期)

合格标准 ^ICMJE

Inclusion Criteria: 1. Patients must have histologically confirmed soft tissue sarcoma (STS) Note: Evidence of disease progression at study entry is required. 2. Treated in any order (neoadjuvant, adjuvant or for metastatic disease) with an anthracycline containing chemotherapy (The participant may have had any number of prior systemic cytotoxic therapies for advanced/metastatic disease. All previous anticancer treatments must be completed ≥ 3 weeks (21 days) prior to first dose of study drug.) 3. No progression on prior therapy with anthracyclines or within three months after stopping this therapy 4. Signed written informed consent 5. Men and women aged ≥ 18 years 6. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 7. Locally advanced (unresectable) or metastatic disease 8. Presence of measurable or non-measurable but evaluable disease as defined by the Response Evaluation Criteria in Solid Tumors (RECIST 1.1, Eisenhauer et al. 2009) 9. Adequate haematologic, organ, and coagulation function within 2 weeks (14 days) prior to enrollment: - Absolute neutrophil count (ANC) ≥ 1,500/mm3; G-CSF is not permitted within 2 weeks (14 days) prior to enrollment - Platelet count ≥ 100,000/mm3 - Creatinine clearance ≥ 45 mL/min (calculated by using the Cockcroft-Gault formula (refer to study protocol Appendix 4) - Total bilirubin ≤ upper limit of normal (ULN). In patients with Gilbert's Syndrome, total bilirubin should be < 3 mg/dL - AST/ALT ≤ 3.0 x upper limit of normal (ULN); in case of liver involvement, AST/ALT ≤ 5.0 x are acceptable - Haemoglobin ≥ 9 g/dl. If haemoglobin <9 g/dl, blood transfusion is permitted. If haemoglobin cannot be enhanced to ≥ 9 g/dl, patient cannot be included into the study - International Normalized Ration (INR) ≤ 1.5 or prothrombin time (PT) ≤ 1.5 x ULN - Partial thromboplastin time (PTT or aPTT) ≤ 1.5 x ULN if not on anticoagulant therapy. For patients receiving anticoagulants, coagulation parameters within the intended or expected range for their therapeutic use are allowed. Patients must have no history of active bleeding (defined as within 14 days of first dose of study drug) or pathological condition that carries a high risk of bleeding (for example, tumor involving major vessels or known esophageal varices) - If routine urinalysis ≥2+ proteinuria, patient must have ≤1000 mg protein on a 24-hour urine, or urine protein/creatinine ratio ≤1 on spot urine 10. Left ventricular ejection fraction (LVEF) ≥50% assessed within 28 days prior to enrollment 11. Females of child-bearing potential must have a negative serum pregnancy test within 7 days prior to enrollment (refer to study protocol Appendix 3) 12. Females of child-bearing potential and males and must agree to use highly effective contraceptive precautions during the trial and up to 6 months following the last dose of study drug (refer to study protocol Appendix 3) 13. The participant has, in the opinion of the investigator, a life expectancy of at least 3 months Exclusion Criteria: 1. Diagnosis of GIST or Kaposi sarcoma 2. Active central nervous system (CNS) or leptomeningeal metastasis (brain metastasis) at the time of enrollment. Participants with a history of a CNS metastasis previously treated with curative intent (for example, stereotactic radiation or surgery) that have not progressed on follow-up imaging, have been asymptomatic for at least 60 days and are not receiving systemic corticosteroids and/or anticonvulsants, are eligible. Participants with signs or symptoms of neurological compromise should have appropriate radiographic imaging performed before enrollment to rule out brain metastasis 3. Prior radiotherapy of the mediastinal/pericardial area or whole pelvis radiation 4. The participant has symptomatic congestive heart failure (CHF), or severe cardiac arrhythmia 5. The participant has unstable angina pectoris, angioplasty, cardiac stenting, or myocardial infarction within 6 months of enrollment 6. The participant has a QTcB interval calculated using Bazett's formula interval of >450 milliseconds (msec) for males and >470 msec for females on screening electrocardiogram (ECG) 7. Females who are pregnant or breastfeeding 8. Known allergy to any of the treatment components including a history of allergic reactions attributed to compounds of chemical or biological composition similar to olaratumab, dexrazoxane or doxorubicin 9. The participant has a known active fungal, bacterial, or viral infection including human immunodeficiency virus (HIV) or viral (A, B, or C) hepatitis (screening is not required) 10. Known history of active bleeding (defined as within 14 days of first dose of study drug) or pathological condition that carries a high risk of bleeding (for example, tumor involving major vessels or known esophageal varices) 11. History of another primary cancer, with the exception of i) curatively treated non-melanomatous skin cancer or ii) curatively treated cervical carcinoma in situ or iii) other primary non-haematologic malignancies or solid tumor treated with curative intent, no known active disease and no treatment administered during the last 3 years prior to enrollment 12. Electively planned or required major surgery during the course of the clinical trial 13. Any condition that, in the opinion of the investigator, would compromise the well-being of the participant or the study or prevent the participant from meeting or performing study requirements 14. On-treatment participation in another clinical study in the period 30 days prior to start of study treatment and during the study 15. Legal incapacity or limited legal capacity 16. Any condition that requires concomitant vaccination with yellow fever vaccine

性别

参与研究的性别:

All

年龄

最小年龄：18 Years ，最大年龄：N/A

接受健康的志愿者

没有

可入组国家 ^ICMJE

Germany

管理信息

数据检测委员会

Yes

研究涉及美国FDA监管的产品

研究美国FDA监管的药品: No
研究涉及美国FDA监管的设备产品: No

IPD 共享声明

计划分享 IPD:

责任方

，

研究赞助商 ^ICMJE

IKF Klinische Krebsforschung GmbH at Krankenhaus Nordwest

合作者 ^ICMJE

研究员 ^ICMJE

Principal Investigator: Daniel Pink, MD Helios Klinikum Bad Saarow

PRS 账户

验证日期

October 2018

^ICMJE 国际医学期刊编辑委员会和世界卫生组织 ICTRP 要求的元素

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