BIOmarker Driven Trial of VEGFR2 Inhibitor in Advanced Sarcoma

Sarcoma Clinical Trial

— BIOVAS  

Official title:

A Biomarker Driven, Open Label, Phase II Study of VEGFR2 Inhibitor Apatinib in Patients With Recurrent or Refractory Advanced Bone and Soft Tissue Sarcoma

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04072042
• Other study ID #: 2019LLS167
• Status: Recruiting
• Phase: Phase 2
• Start date: August 31, 2019
• Est. completion date: May 25, 2024

Study information

• Verified date: October 2023
• Source: Ruijin Hospital
• Contact: Weibin Zhang, PhD, MD
• Phone: +8613501824630
• Email: zhangweibin10368[@]163.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The aim of this study is to evaluate the efficacy and safety of Apatinib monotherapy for relapsed or refractory advanced bone and soft tissue sarcoma with VEGFR-2 (KDR) 604A>G polymorphism as predictive biomarker

Description:

After standard chemotherapy and surgery for the localized disease, pulmonary metastases of bone and soft tissue sarcoma occurs in up to 40% of cases and still remain challenging without satisfactory regimen. Apatinib has been reported as a novel oral kinase inhibitor of receptor tyrosine (TKI) targeting VEGFR2 as an angiogenesis inhibitor. Previous studies indicated that Apatinib, as well as other novel VEGFR inhibitor (such as Regorafenib, Cabozantinib, Pazopanib ), showed a promising anti-sarcoma activity with a 4 month progression free rate (PFR) ranging from 40 to 60% in advanced bone and soft tissue sarcoma after multi-line chemotherapy failure. However, the significant inter-individual variability of the agents suggests a lack of predictive biomarker for its clinical use. Furthermore, up to 10~30% of patients may encounter pneumothorax, a potentially life-threatening consequence. Other common debilitating adverse effects (AEs) include surgical wound complication, hand foot skin reaction, etc.

Our preliminary data (Presented in ESMO poster session and ESMO Asia oral session in 2019) suggests that rs2071559_VEGFR2 604A>G polymorphism is associated pulmonary tumor cavitation (predisposes one to pneumothorax), hair depigmentation, superior anti-tumor efficacy. Therefore, the investigators aim to explore the clinical signficance of pneumothorax incidence as well as the efficacy of Apatinib monotherapy for advanced bone and soft tissue sarcoma in association with VEGFR-2 (KDR) 604 genotype. We aim to further conduct our clinical study in two cohorts: the observational study cohort and the prospective clinical trial cohort.

In the observational cohort, we recruited patients with anti-angiogenic TKIs who encounter pneumothorax during the course of the treatment from nation-wide as a real world study. We review the radiological features of their tumor (such as cavitation, location, etc.) and the medical history of the pre-treatment. We then prospectively follow up the oncological outcomes and the respiratory outcomes given that all pneumothoraces are treated with multidisciplinary approaches to minimize the adverse effect of pneumothoax and maximize the duration of response to anti-angiogenic TKIs. We expect that the patients with pneumothorax (an efficacy related toxicity), if managed actively, will have a durable progression-free survival compared to historical control. Blood samples will also be collected for genotyping VEGFR2 604A>G polymorphism status as a validation to our preliminary findings.

In the prospective clinical trial cohort, we formally designed a prospective single-arm, open-label, biomarker-driven phase II clinical trial to explore the efficacy of Apatinib, a novel anti-angiogenic oral inhibitor, in biomarker-based selective patients as follows: With all comers(biomarker positive and negative) allowed to be enrolled, only VEGFR-2 (KDR) 604A>G polymorphism positive will be measured for the primary endpoint of the study according to our sample size estimation . The primary objective is to hypothesize that the progression-free rate (PFR) of Apatinib in this population is ≥ 70% at 4 months (tremendous higher than non-biomarker driven historical control), against the null hypothesis of PFR ≤ 50% as in the general sarcoma patients. Using Simon's two stage design, we are going to recruit 9 biomarker-positive patients in the first stage. If the primary objective was reached in >3 patients, study continue to recruit a total of 28 biomarker-positive patients. The primary endpoint will be considered met if 18 or more patients achieve PFR at 4 months. Considering the potential lost to follow-up, a total of 30 patients with biomarker positive is needed in this trial. Biomarker-negative patients will be analyzed as a non-comparative control without pre-specified sample size, which is expected to be similar to the historical control of advanced bone and soft tissue sarcoma.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 30
• Est. completion date: May 25, 2024
• Est. primary completion date: February 25, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 8 Years to 65 Years

Eligibility

Inclusion Criteria:

1. age between 8 and 65 years;

2. diagnosis of histologically confirmed advanced bone and soft tissue sarcoma excluding adipocytic tumor;

3. identification of pulmonary lesion is mandatory;

4. refractory to prior treatment consisted of standard National Comprehensive Cancer Network (NCCN) guideline recommended first-line chemotherapy;

5. Eastern Cooperative Oncology Group(ECOG) performance status 0-2 with a life expectancy >3 months;

6. adequate renal, hepatic, and hemopoietic function;normal or controlled blood pressure;

7. advanced stage that complete surgical resection of all lesions are infeasible;

8. no serious thoracic comorbidities with adequate pulmonary function for daily living;

9. previously treated with tyrosine kinase inhibitors (TKIs) for less than 8 weeks but off treatment due to manageable complications such as wound complications or pneumothorax without adequate interventions. The complications is resolved and disappeared at enrollment.

Exclusion Criteria:

1. have had other kinds of malignant tumors at the same time;

2. cardiac insufficiency or arrhythmia;

3. uncontrolled complications, such as diabetes mellitus and so on;

4. coagulation disorders or Hemorrhagic diseases ;

5. pleural or peritoneal effusion that needs to be handled by surgical treatment;

6. combined with other infections or wound complications;

7. wound dystrophy, poor soft-tissue around implantation risky of non-healing given angiogenesis inhibitor at baseline;

8. previously treated with VEGFR TKIs for more than 8 weeks

9. previous treated with VEGFR TKIs but off treatment due to oncological assessment or dose-limiting complications given adequate interventions.

Related Conditions & MeSH terms

• Sarcoma

Intervention

Drug:
• Apatinib monotherapy
patients will receive Apatinib 250mg tablet by mouth, bid.

Locations

Country	Name	City	State
China	Ruijin Hospital Shanghai Jiao Tong University School of Medicine	Shanghai	Shanghai

Sponsors (1)

Lead Sponsor	Collaborator
Ruijin Hospital

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Exploratory outcome: Subgroup analysis of progression-free survival(PFS)	The PFS for each subgroups in terms of clinicopathological characteristics (age, gender, histological type, solitary or multiple metastases, unilateral or bilateral metastases, early or late metastases, calcifying or non-calcifying lesions, with or without lesion cavitation, with or without AEs [especially pneumothorax, hand-foot skin reactions, hair depigmentation], etc	Baseline until disease progression or death, whichever occurs first, assessed for an average of 8 months
Other	Exploratory outcome: the molecular analysis of tumor sample	To explore the molecular basis underlying the difference of biomarker positive and negative sub-cohorts using next generation sequencing	through study completion, an average of 8 months
Other	Exploratory outcome: the pattern of disease progression between the sub-cohorts	to compare the growth pattern/ distribution of pulmonary versus extrapulmonary lesion at baseline and at disease progression between the two sub-cohorts	Baseline until disease progression or death, whichever occurs first, assessed for an average of 8 months
Other	Exploratory outcome: 1.0-mm CT scan for pulmonary assessment	to compare the diagnostic value of the 1.0 mm versus 5.0 mm CT scan for the radiological evaluation of small lung nodule as tumor recurrence	Baseline until disease progression or death, whichever occurs first, assessed for an average of 8 months
Primary	progression free rate (PFR)	The proportion of patients that are progression-free according to Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1)	4 months from recruitment
Secondary	progression free rate (PFR) in biomarker negative sub-cohort	The proportion of patients with negative biomarker that are progression-free according to RECIST 1.1	4 months from recruitment
Secondary	progression free survival(PFS) between biomarker positive and negative sub-cohorts	The difference of PFS between biomarker positive and biomarker negative sub-cohorts with log-rank test	Baseline until disease progression or death, whichever occurs first, assessed for an average of 8 months
Secondary	Correlation of KDR polymorphism with pulmonary lesion cavitation/pneumothorax	Correlation of KDR 604 AA,AG,GG genotype with the incidence of pulmonary lesion cavitation or pneumothorax among all comers	4 months from recruitment
Secondary	Correlation of KDR polymorphism with hair depigmentation	Correlation of KDR 604 AA,AG,GG genotype with the incidence of hair depigmentation among all comers	4 months from recruitment
Secondary	Correlation of KDR polymorphism with progression-free survival(PFS)	Correlation of KDR 604 AA,AG,GG genotype with progression free survival according to RECIST 1.1 among all comers	Baseline until disease progression or death, whichever occurs first, assessed for an average of 8 months
Secondary	Incidence of Treatment-Emergent Adverse Events	The occurrence of each adverse events(AEs), severe AEs(SAEs) and death according the CTCAE_5.0	through study completion, an average of 8 months
Secondary	Correlation of CSF1R polymorphism (rs10079250) with wound complication	Correlation of CSF1R (rs10079250) genotype with the incidence of wound complications among all comers	through study completion, an average of 8 months
Secondary	Correlation of PDGFRa polymorphism (rs35597368) with hand foot skin reaction	Correlation of PDGFRa (rs35597368) genotype with the incidence of hand foot skin reaction among all comers	through study completion, an average of 8 months
Secondary	Early identification of AEs as predictive biomarker	to correlate the incidence of targeted therapy related AEs (pulmonary lesion cavitation, pneumothorax, hair depigmentation) with the PFS	Baseline until disease progression or death, whichever occurs first, assessed for an average of 8 months