Rechallenge With Panitumumab Driven by RAS Dynamic of Resistance

Colorectal Cancer Clinical Trial

— CHRONOS  

Official title:

A Phase II Trial of Rechallenge With Panitumumab Driven by RAS Clonal-mediated Dynamic of Resistance

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03227926
• Other study ID #: 013-IRCC-10IIS-16
• Secondary ID: 2016-002597-12
• Status: Completed
• Phase: Phase 2
• Start date: October 11, 2017
• Est. completion date: December 31, 2021

Study information

• Verified date: August 2022
• Source: Fondazione del Piemonte per l'Oncologia
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a hypothesis driven, open label, single-arm, multiple centers, Phase II trial. The trial has been designed to prove or disprove whether a rechallenge with panitumumab can achieve an objective response rate (ORR= CR+PR) of 30% or more in a population of RAS wild type mCRC patients selected on the basis of RAS extended clonal evolution in their plasma.

Description:

Colorectal cancer (CRC) is the third most common cancer in the world and the second leading cause of cancer death in the United States and the European Union. In the last decade, substantial advances in the treatment of the metastatic disease (mCRC) have more than doubled overall survival (OS) from 12 months to 30 months due to the refinement of fluoropirimidine-based chemotherapy and the introduction of antiangiogenics and targeted therapies.

Pharmacologic blockade of the epithelial growth factor receptor (EGFR) with specific monoclonal antibodies, namely, cetuximab and panitumumab, represents the mainstay of tumour targeted therapy for mCRC in patients with tumors not harboring extended RAS pathway mutations (KRAS, NRAS, or BRAF). Such alterations, which constitutively activate typical EGFR downstream transducers, have been shown to trigger substitute survival pathways that bypass therapeutic blockade of EGFR signalling, thus abating the efficacy of anti-EGFR antibodies ("primary resistance"). Even when response to anti-EGFR therapy occurs in the context of appropriate molecular selection, acquired ("secondary") resistance inevitably arises in all cases. Our group has extensively studied this phenomenon and has shown that extended-RAS alterations are the principal culprit of anti EGFR acquired resistance, and that altered RAS clones decay upon anti-EGFR treatment withdrawal, while tumor cells regain sensitivity to anti EGFR treatment. We have also documented that ctDNA profiles of individuals who benefit from multiple challenges with anti-EGFR antibodies, exhibit pulsatile levels of mutant KRAS. Collectively, these results indicate that the CRC genome adapts dynamically to intermittent anti-EGFR drug schedules, and provide a molecular explanation for the efficacy of re-challenge therapies based on EGFR blockade. Our results also give experimental support to the empirical-based clinical benefit observed, following cetuximab or panitumumab rechallenge in two small series of originally KRAS exon 2 wild type mCRC patients.

We propose to assess the efficacy and safety of re-challenging with panitumumab RAS-extend wild type mCRC patients with ctDNA-confirmed secondary resistance to anti EGFR treatment, after progression on second or further lines chemotherapy. As proof-of-concept, patients will be blood monitored throughout their therapeutic itinerary for the presence of extended-RAS alterations and EGFR-ectodomain mutations by ctDNA determination (liquid biopsy). We also include in our ddPCR panel 7 different EGFR extracellular domain (ECD) mutations as they occur in 15-20% of patients who acquired resistance to anti-EGFR drugs.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 32
• Est. completion date: December 31, 2021
• Est. primary completion date: November 6, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria

1. Histologically confirmed diagnosis of metastatic colorectal cancer;

2. Age = 18 years;

3. Written informed consent;

4. Documented WT RAS exons 2, 3 and 4 (KRas and NRas) and WT BRAF V600E for anti-EGFR treatment.

5. Complete or partial response to anti EGFR antibodies in any line either received as monotherapy or in combination with chemotherapy;

6. Imaging documented progression while on therapy with a therapeutic regimen including anti-EGFR mAb;

7. Imaging documented progression at the last treatment regimen that must be anti-EGFR free;

8. Patient must be RAS and EGFR ectodomain wild type in a liquid biopsy performed no longer that 4 weeks after progression to the last anti-EGFR free treatment

9. FFPE sample used for eligibility to anti-EGFR prescription (see criteria 4) must be available for custom gene panel profiling (as described in appendix B). Otherwise if sample is not available, center must have already perfomed a genotyping on this tissue sample according to appendix B.

10. ECOG performance status = 2;

11. At least one measurable tumor lesion as per RECIST v1.1. Lesions in previously irradiated areas or those that have received other loco-regional therapies (i.e. percutaneous ablation) should not be considered measurable unless there is clear documented evidence of progression of the lesion since therapy. Imaging must be performed maximum within 28 days prior to registration;

12. Normal organ functions;

13. Negative serum pregnancy test within 1 week prior to the first study dose in all women of childbearing potential;

14. Subjects and their partners must be willing to avoid pregnancy during the trial. Male subjects with female partners of childbearing potential and female subjects of childbearing potential must, therefore, be willing to use adequate contraception;

15. Absence of 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.

Exclusion Criteria

1. History of severe infusion reactions to monoclonal antibodies cetuximab or panitumumab;

2. Symptomatic or untreated leptomeningeal disease and symptomatic brain metastasis;

3. Clinically significant cardiac disease including:

1. congestive heart failure requiring treatment (NYHA grade = 2), Left ventricular ejection fraction (LVEF) < 45% as determined by Multigated acquisition (MUGA) scan or echocardiogram;

2. history or presence of clinically significant ventricular arrhythmias or atrial fibrillation;

3. clinically significant resting bradycardia;

4. unstable angina pectoris = 3 months prior to starting study drug;

5. acute myocardial infarction = 3 months prior to starting study drug;

6. QTcF > 480 msec;

4. History of thromboembolic or cerebrovascular events within the last 6 months, including transient ischemic attack, cerebrovascular accident, deep vein thrombosis, or pulmonary embolism;

5. Patients with interstitial pneumonitis or pulmonary fibrosis;

6. Abnormal organ or bone marrow functions defined as:

1. Absolute neutrophil count < 1.5 x 10/L;

2. hemoglobin < 9 g/dL;

3. alkaline phosphatase > 2.5 x upper normal limit (ULN), if liver metastases > 5 x ULN;

4. aspartate aminotransferase (AST)/ alanine aminotransferase (ALT) > 2.5 x ULN, if liver metastases > 5 x ULN;

5. bilirubin > 1.5 x ULN, if liver metastases > 2 x ULN;

6. serum creatinine > 1.5 x ULN and/or creatinine clearance = 50 mL/min calculated according to Cockroft-Gault;

7. Patients with platelet count <100 x 10^9/L

7. Previous or concurrent second malignancy. Exceptions: adequately treated basal cell or squamous cell skin cancer; in situ carcinoma of the cervix, treated curatively and without evidence of recurrence for at least 3 years prior to study entry; or other solid tumor treated curatively and without evidence of recurrence for at least 3 years prior to study entry.

8. Patients with positive serology for HIV, HBV, HCV.

9. Patients with a history of severe or life threatening hypersensitivity to the active substance or to any of the excipients.

Related Conditions & MeSH terms

• Colorectal Cancer
• Colorectal Neoplasms

Intervention

Drug:
• Panitumumab 20 MG/ML Intravenous Solution [VECTIBIX]
Panitumumab 6 mg/kg in 100 cc 0.9% NaCl solution on Day 1 every two weeks by IV administration over 1 hour.

Diagnostic Test:
• Molecular Screening
Patients without plasmatic evidence of potentially resistant clones harbouring RAS or EGFR-ectodomain mutations in the RML liquid biopsy, will be molecular eligible for the trial phase

Locations

Country	Name	City	State
Italy	Fondazione del Piemonte per l'Oncologia - IRCCS	Candiolo
Italy	Grande Ospedale Metropolitano Niguarda	Milano
Italy	Istituto Nazionale Tumori - IRCCS	Milano	Via Giacomo Venezian, 1
Italy	Istituto Oncologico Veneto - IRCCS	Padova

Sponsors (1)

Lead Sponsor	Collaborator
Fondazione del Piemonte per l'Oncologia

Country where clinical trial is conducted

Italy, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Overall response rate (ORR) to panitumumab according to RECIST v1.1.	Main objective of the study is the evaluation of objective response rate according to RECIST 1.1 criteria	Tumor assessments every 8 weeks from date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months
Secondary	Progression Free Survival	PFS is defined as the time from first treatment to the time of disease progression	every 2 weeks from date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months
Secondary	Overall Survival	OS is defined as the length of time from the start of treatment to death from any cause	every 2 weeks from date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months
Secondary	Toxicity according to CTCAE version 4.03.	Toxicity will be assessed using the Common Toxicity Criteria for Adverse Events version 4.03 (CTCAE).	every 2 weeks from date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months