PD-L1 Imaging in Non Small Cell Lung Cancer' (PINNACLE)

Non Small Cell Lung Cancer Clinical Trial

— PINNACLE  

Official title:

PD-L1 Imaging in Non Small Cell Lung Cancer' (PINNACLE)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03514719
• Other study ID #: MS100070_0167
• Status: Completed
• Phase: Phase 1
• Start date: October 1, 2018
• Est. completion date: December 2, 2021

Study information

• Verified date: January 2022
• Source: Radboud University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

In this feasibility study, a zirconium-89 (89Zr)-avelumab positron emission tomography (PET) scan will be performed in 37 patients prior to treatment with avelumab to: 1. assess the tumor and systemic tissue uptake 89Zr-avelumab 2. assess the potential to predict avelumab treatment response

Description:

The programmed death 1 (PD1)/ programmed death ligand 1 (PD-L1) pathway plays an important role in regulating the T-cell anti tumor response. Blocking this interaction with the anti PD-L1 monoclonal antibody avelumab is effective in patients with non-small cell lung cancer (NSCLC) resulting in durable disease control rates. Currently, PD-L1 expression as determined by immune histochemistry (IHC) is the best available biomarker for treatment response, but standardized scoring criteria are lacking and the risk for sampling errors exists. Molecular imaging using 89Zr-labeled antibodies may overcome these limitations, enabling the visualization of PD-L1 expression in primary and metastatic tumor lesions and providing information on the in vivo accessibility of the PD-L1 target following intravenous administration. This study enables PD-L1 PET-imaging with 89Zr-avelumab in patients with: - early stage NSCLC (stage Ia (≥T1b) -IIIa) followed by 2 cycles of neo-adjuvant avelumab treatment and surgical resection of the tumor. - advanced stage NSCLC (Stage IIIb-IV) followed by avelumab treatment until disease progression or intolerable toxicity.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 24
• Est. completion date: December 2, 2021
• Est. primary completion date: September 15, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Male or female subjects aged = 18 years, and >50 years in patients with resectable stage Ia (=T1b tumor) - IIIa NSCLC)

2. Histological or cytologic proven stage IIIb/IV NSCLC or resectable stage Ia (=T1b tumor) - IIIa NSCLC, where no pathological evaluation of mediastinal lymph nodes by mediastinoscopy is indicated according to the multidisciplinary tumor board

3. ECOG performance score (0-1)

4. At least one lesion with a tumour size = 1 cm

5. Haematologic function: absolute neutrophil count (ANC) = 1.5 × 109/L, platelet count = 100 × 109/L, and haemoglobin = 9 g/dL (may have been transfused)

6. Hepatic function: total bilirubin level = 1.5 × the upper limit of normal (ULN) range and AST and ALT levels = 2.5 × ULN for all subjects or AST and ALT levels = 5 x ULN (for subjects with documented metastatic disease to the liver).

7. Estimated creatinine clearance = 30 mL/min according to the Cockcroft-Gault formula (or local institutional standard method)

8. Highly effective contraception for both male and female subjects throughout the study and for at least after avelumab treatment administration intrinsic factor the risk of conception exists

9. Fit for surgery (for patients with resectable stage Ia-IIIa disease), as assessed by treating thoracic surgeon / anesthesiologists based on sufficient cardiopulmonary status and absence of major contra-indications for surgery according to local guidelines

Exclusion Criteria:

1. Immunosuppressants: "Current use of immunosuppressive medication, EXCEPT for the following: a. intranasal, inhaled, topical steroids, or local steroid injection (eg, intra-articular injection); b. Systemic corticosteroids at physiologic doses = 10 mg/day of prednisone or equivalent; c. Steroids as premedication for hypersensitivity reactions (eg, CT scan premedication)."

2. Active autoimmune disease that might deteriorate when receiving an immunostimulatory agent: Subjects with diabetes type I, vitiligo, psoriasis, hypo- or hyperthyroid disease not requiring immunosuppressive treatment are eligible

3. Prior organ transplantation, including allogeneic stem cell transplantation

4. Infections: active infection requiring systemic therapy

5. HIV/AIDS: known history for testing positive to an HIV test or known acquired immunodeficiency syndrome (AIDS)

6. Hepatitis: hepatitis B virus (HBV) or hepatitis C virus (HCV) infection at screening (positive HBV surface antigen or confirmatory HCV RNA if anti-HCV antibody screening test positive)

7. Vaccination within 4 weeks of the first dose of avelumab and while on trial is prohibited except for administration of inactivated vaccines

8. Hypersensitivity to study drug: "Known prior severe hypersensitivity reactions to investigational product or any component in its formulations, including known severe hypersensitivity reactions to antibodies (Grade = 3 NCI CTCAE v 4.03)

9. Cardiovascular disease: "Clinically significant (i.e., active) cardiovascular disease:

cerebral vascular accident/stroke (< 6 months prior to enrollment), myocardial infarction (< 6 months prior to enrollment), unstable angina, congestive heart failure (= New York Heart Association Classification Class II), or serious cardiac arrhythmia requiring medication."8. Persisting toxicity related to prior therapy of Grade >1 NCI-CTCAE v 4.03; however, alopecia and sensory neuropathy Grade = 2 is acceptable

10. Other persisting toxicities: Persisting toxicity related to prior therapy (NCI CTCAE v. 4.03 > 1); however, alopecia, sensory neuropathy Grade = 2 not constituting a safety risk based on investigator's judgment are acceptable.

11. Other severe acute or chronic medical conditions including colitis, inflammatory bowel disease, pneumonitis, pulmonary fibrosis or psychiatric conditions including recent (within the past year) or active suicidal ideation or behavior; or laboratory abnormalities that may increase the risk associated with study participation or study treatment administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the patient inappropriate for entry into this study.

Related Conditions & MeSH terms

• Carcinoma, Non-Small-Cell Lung
• Lung Neoplasms
• Non Small Cell Lung Cancer

Intervention

Diagnostic Test:
• 89Zr-avelumab PET
89Zr-avelumab injection followed by 89Zr-Avelumab PET scan

Drug:
• Avelumab
Early stage disease (stage Ia (=T1b tumor)-IIIa: neo-adjuvant avelumab treatment (10mg/kg iv q2w) for a maximum duration of 2 cycles after PET-imaging, followed by surgical resection of the tumor with curative intent Stage IIIb-IV disease: systemic treatment with avelumab 10mg/kg iv q2w after PET-imaging

Locations

Country	Name	City	State
Netherlands	Radboud University	Nijmegen

Sponsors (2)

Lead Sponsor	Collaborator
Radboud University	Merck KGaA, Darmstadt, Germany

Country where clinical trial is conducted

Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Tumor uptake of 89Zr-Avelumab	Standardized uptake values (SUV) of 89Zr-Avelumab uptake in tumor lesions will be measured	1 year
Secondary	Correlation 89Zr-Avelumab uptake in tumor lesions and PD-L1 expression as determined by immunohistochemistry		1-2 year
Secondary	Correlation between 89Zr-Avelumab uptake in tumor lesions and response to (neo)-adjuvant avelumab treatment	To assess the potential of PD-L1 PET/CT to image PD-L1 expression in tumor lesions, and predict response to (neo)-adjuvant avelumab treatment in patients with NSCLC	1-2 years
Secondary	The number of treatment delays in surgical resections	In resectable early stage disease (stage Ia (=T1b) - IIIa)	1-2 years
Secondary	Asses post-operative complications	In resectable early stage disease (stage Ia (=T1b) - IIIa)	1-2 years