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

Advanced Soft Tissue Sarcoma Clinical Trial

Official title:

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

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT03698227
• Other study ID #: OlaReDo_GISG-17
• Status: Terminated
• Phase: Phase 2
• Start date: November 12, 2018
• Est. completion date: June 25, 2020

Study information

• Verified date: July 2020
• Source: Institut für Klinische Krebsforschung IKF GmbH at Krankenhaus Nordwest
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Description:

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.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 2
• Est. completion date: June 25, 2020
• Est. primary completion date: June 25, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Advanced Soft Tissue Sarcoma
• Sarcoma

Intervention

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

Locations

Country	Name	City	State
Germany	Helios Klinikum Bad Saarow	Bad Saarow
Germany	Charité Universitätsmedizin Berlin Medizinische Klinik m. S. Hämatologie, Onkologie und Tumorimmunologie Campus Virchow Kliniken	Berlin
Germany	Helios Klinikum Berlin-Buch Klinik für Onkologie und Palliativmedizin	Berlin
Germany	Medizinische Fakultät Carl Gustav Carus Medizinische Klinik I Internistische Onkologie	Dresden

Sponsors (1)

Lead Sponsor	Collaborator
Institut für Klinische Krebsforschung IKF GmbH at Krankenhaus Nordwest

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Progression-free survival rate after 3 months (PFSR3), assessed by applying RECIST 1.1	number of patients proven progression-free and alive after 3 months divided through the total number of patients in the all-treated-subjects population	After 3 months treatment
Secondary	Progression free survival (PFS)	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.	6 months of Follow Up
Secondary	Objective response rate (ORR) (i.e. CR or PR)	Number and percentage of participants with a best overall response (BOR) of complete response (CR) or partial response (PR)	6 months of Follow Up
Secondary	Disease control rate (DCR) (i.e. CR, PR or SD)	Number and percentage of participants with complete response (CR) or partial response (PR) or stable disease (SD)	6 months of Follow Up
Secondary	Overall survival (OS)	Time from date of the first dosing date of any study medication to the date of death (due to any cause)	6 months of Follow Up
Secondary	Assessment of adverse events	Type, incidence and severity of AEs, SAEs	During study conduct up to a maximum of 18 months (EOT)
Secondary	Study therapy discontinuation rate due to cardiac toxicity	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	After treatment discontinuation up to a maximum of 18 months (EOS)