Clinical Study of Concurrent Pazopanib and Radiotherapy for Non-metastatic Sarcoma Patients

Sarcoma Clinical Trial

— PASART-2  

Official title:

Phase II Clinical Study of Concurrent Pazopanib for Non-metastatic Sarcoma Patients to be Treated With Radiotherapy, Localized in the Extremities, Trunk and Chest Wall or the Head and Neck Region (PASART-2)

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02575066
• Other study ID #: M15PAS
• Secondary ID: DSSG02
• Status: Terminated
• Phase: Phase 2
• Start date: March 17, 2016
• Est. completion date: March 20, 2019

Study information

• Verified date: June 2019
• Source: The Netherlands Cancer Institute
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Radiotherapy (RT) alone is able to induce a clinically significant effect with a variable pathologic response (a pathological complete remission, pCR, defined as ≥ 95%, or ≤ 5% remaining visible tumour cells) in only about 10% of cases. A prior phase I study (PASART-1; NCT01985295) suggested that 25 x 2 Gy preoperative RT in combination with once daily 800mg oral pazopanib is feasible, while inducing tissue replacing tumor that can consist of fibrosis and necrosis in 40% of thus treated patients.

During this study, the interim analysis showed that the combination treatment of preoperative radiation with orally pazopanib is more effective than was anticipated. For this reason, the pazopanib dose of 800 mg once daily is maintained but the RT dose is reduced to 18x2Gy instead of 25x2Gy. Predominant aim of this RT dose reduction is lowering the wound complication risk after preoperative radiotherapy.

Description:

Patients of the first part of the study received radiotherapy (25x2Gy) and pazopanib (QD 800 mg).

Patients of the second part of the study received/ will receive radiotherapy (18x2Gy) and pazopanib (QD 800 mg).

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 25
• Est. completion date: March 20, 2019
• Est. primary completion date: March 20, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Histologically confirmed newly diagnosed intermediate to high grade soft tissue sarcoma localized to the extremities, trunk and chest wall or the head and neck area, for which the standard treatment is a combination of and radiotherapy and surgery(deep seated and/or > 5cm according to the RECIST 1.1 criteria and/or an anticipated close resection margin and/or grade II/III according to the WHO definition)

• Age = 18 years

• WHO performance status of = 1

• Able and willing to undergo blood sampling for PK and PD analysis

• Able to swallow and retain oral medication

• Able and willing to undergo MRI scanning

• Able and willing to undergo tumor biopsies

• Adequate organ functions as described by the laboratory findings in the table 1. For thyroid function, the T4 and TSH values must be within normal values of the range of the participating centers

• Written informed consent prior to performance of study-specific procedures or assessments and must be willing to comply with treatment and follow up.

Exclusion Criteria

• Prior malignancies; except another malignancy and disease-free for = 5 years, or completely resected non-melanomatous skin carcinoma or successfully treated in situ carcinoma.

• Patients with recurrent sarcomas (even without prior radiotherapy)

• Ewing sarcoma and other PNET family tumors, rhabdomyosarcomas (both pediatric and adult), osteosarcomas

• Clinically significant gastrointestinal abnormalities which might interfere with oral dosing diagnosed

• Poorly controlled hypertension [defined as systolic blood pressure (SBP) of =140 mmHg or diastolic blood pressure (DBP) of = 90mmHg]

• Unstable or serious concurrent condition (e.g., active infection requiring systemic therapy)

• Prolongation of corrected QT interval (QTc) > 480 msecs on ECG

• History of any of more of the following cardiovascular conditions within the past 6 months:

• Cardiac angioplasty or stenting

• Myocardial infarction

• Unstable angina

• Symptomatic peripheral vascular disease

• Coronary artery by-pass graft surgery

• Class II, III or IV congestive heart failure as defined by the New York Heart Association (NYHA)

• History of cerebrovascular accident, pulmonary embolism or untreated deep venous thrombosis (DVT) within the past 6 months

• Macroscopic hematuria

• Hemoptysis that is clinically relevant within 4 weeks of first dose of pazopanib

• Evidence of active bleeding or bleeding diathesis

• Prior major surgery or trauma within 28 days prior to first dose of study medication and/or presence of any non-healing wound, fracture, or ulcer

• Chemotherapy or radiation therapy within 2 weeks prior to the first dose of study medication

• Biological therapy or treatment with an investigational agent within 28 days or five half-lives, whichever is longer prior to the first dose of study medication

• Prohibited medications listed in the protocol for 14 days or five half-lives of a drug (whichever is longer) prior to visit 1 and for the duration of the study

• Known immediate or delayed hypersensitivity reaction or idiosyncrasy to drugs chemically related to pazopanib

• Any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the trial

• Female patients who are pregnant, breast-feeding or male or female patients of reproductive potential who are not employing an effective method of birth control

Related Conditions & MeSH terms

• Sarcoma
• Soft Tissue Sarcomas

Intervention

Radiation:
• external beam radiotherapy
external beam radiotherapy 25 x 2 Gy / 18 x 2 Gy

Drug:
• pazopanib
pazopanib QD 800 mg

Locations

Country	Name	City	State
Netherlands	Antoni van Leeuwenhoek	Amsterdam
Netherlands	Leids Universitair Medisch Centrum	Leiden
United Kingdom	Royal Marsden Hospital	London

Sponsors (2)

Lead Sponsor	Collaborator
The Netherlands Cancer Institute	Royal Marsden NHS Foundation Trust

Countries where clinical trial is conducted

Netherlands,  United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	pathological near complete remission of the resected specimen which has been treated with radiotherapy	Proportion of patients with resection specimens demonstrating induction of a pathological (near) complete remission (= 95% tumor regression). Pathological (near) complete remission is defined as = 95% replacement of tumor with other tissue, usually fibrosis and) in the resection specimen post combined pazopanib and radiotherapy treatment	6 weeks post treatment
Secondary	Incidence toxicities measured by NCI-CTCAE v4.0 (radiotherapy alone, pazopanib alone or both) measured from start of treatment until 6 weeks post-treatment		during treatment and up to 6 weeks post treatment
Secondary	Rate of response as measured by RECIST v 1.1 at 4 weeks after completing radiotherapy		4 weeks post treatment
Secondary	Incidence of acute post-operative wound complications up to 3 weeks (+/- 1 week) after surgery as defined in section 6.1.3 and reference 29 (see also appendix XII)		up to 3 weeks post surgery