K-SAB Trial - Sotorasib Followed by SBRT to 1-3 Lesions in Advanced NSCLC With KRASG12C Mutation

Trial Title: K-SAB Trial - Sotorasib Followed by SBRT to 1-3 Lesions in Advanced NSCLC With KRASG12C Mutation

NCT ID: NCT06127940

Condition: Non-small Cell Lung Cancer Metastatic

Conditions: Official terms:
Carcinoma, Non-Small-Cell Lung
Sotorasib

Conditions: Keywords:
Stereotactic body radiation therapy
KRAS-G12C mutation
NSCLC

Study type: Interventional

Study phase: Phase 1

Overall status: Recruiting

Study design:

Allocation: N/A

Intervention model: Single Group Assignment

Intervention model description: Single arm phase I study

Primary purpose: Treatment

Masking: None (Open Label)

Intervention:

Intervention type: Radiation
Intervention name: Stereotactic body radiation therapy (SBRT)
Description: SBRT is delivered using institutional standard dosing while sotorasib is withheld during radiation.
Arm group label: Radiotherapy + sotorasib

Other name: Sotorasib

Intervention type: Drug
Intervention name: Temporary Stopping
Description: Temporary stop of sotorasib during SBRT
Arm group label: Radiotherapy + sotorasib

Summary: The goal of this interventional study is to learn about the combination of sotorasib and stereotactic radiation therapy (SBRT) in patients with metastatic non-small cell lung cancer (NSCLC) with KRASG12C mutations. The main question it aims to answer is: • can SBRT be safely delivered in patients treated with sotorasib Participants will be treated with sotorasib for an 8-week-induction period and if the patient has stable disease or partial response, 1-3 of the remaining lesions will be irradiated with SBRT and sotorasib will then be contiuned after irradiation. The patients will then be followed and evaluated for toxicity to identify if grade 3-5 toxicity attributed to SBRT occurs within 6 months post SBRT. Tumour effects measured according to RECIST v1.1 will also be evaluated.

Detailed description: Eligible subjects are those with a diagnosis of advanced KRASG12C mutated NSCLC who have received at least one line of standard medical treatment with immuno(chemo)therapy. The subjects start with sotorasib and in parallel, 2-5 target lesions which are technically feasible to treat with SBRT, are identified. After 8 weeks of induction treatment of with sotorasib, the subjects are radiologically evaluated and subjects with stable disease (SD) or partial response (PR) on sotorasib will receive SBRT to minimum 1 and maximum 3 of the predefined lesions. Sotorasib is withheld during SBRT and then restarted after SBRT. Sotorasib will continue until progression or other discontinuation criteria are met. The patients are followed clinically every month during the first 6 months post SBRT and then every 2-3 months. Radiological evaluation is performed every 2 months during the first year. After the first 10 treated patients, a safety review meeting will be held and a decision whether to include 10 more patients will be performed.

Criteria for eligibility:
Criteria:
Main inclusion criteria: 1. Histological or cytological confirmed advanced NSCLC 2. KRASG12C mutation 3. Previous at least one line of treatment with immune- or/and chemotherapy or contraindications for immune- and/or chemotherapy. 4. Adequate organ function to tolerate sotorasib (see section 6.1 and 6.2 for details) 5. 2-5 lesions technically amenable to SBRT with 15 Gy x 3, 10 Gy x 5, or 7-8 Gy x 5. 6. Adequate organ function to tolerate SBRT: o Fulfilment of dose constraints to adequate organs at risk 7. ECOG performance status (PS) 0-1 8. FEV1 ≥1 litre (only applicable for lung targets) 9. Age ≥ 18 years 10. Measurable lesions according to RECIST Main exclusion criteria: 1. Leptomeningeal carcinosis (on MRI or in cerebrospinal fluid) or metastases in the central nervous system 2. Previous RT for any cancer within the last 3 years possibly interfering with the planned RT within this study 3. Life expectancy of less than 6 months 4. Inability to understand given information or undergo study procedures according to protocol 5. Has evidence or a past medical history of interstitial lung disease or active, non-infectious pneumonitis or known pulmonary fibrosis 6. Woman who is pregnant or breastfeeding or planning to become pregnant or breastfeed during treatment and for an additional 7 days after the last dose of sotorasib 7. Women of childbearing potential (WOCBP) unwilling to use a highly effective method of contraception during treatment and for an additional 7 days after the last dose of sotorasib. WOCBP using hormonal contraceptives should also use a barrier method 8. WOCBP with a positive pregnancy test assessed at screening or day 1 by a serum pregnancy test and/or urine pregnancy test 9. Centrally located pulmonary target (i.e., within 1 cm of the main bronchi or intermedius bronchus) and targets located within 1 cm of the gut, for SBRT 10. Use of known cytochrome P450 (CYP) 3A4 or P-gp sensitive substrates (with a narrow therapeutic window), within 14 days or 5 half-lives of the drug or its major active metabolite, whichever is longer, prior to study day 1 that was not reviewed and approved by the principal investigator 11. Use of strong inducers of CYP3A4 (including herbal supplements such as St. John´s wort) within 14 days or 5 half-lives, whichever is longer, prior to study day 1 that was not reviewed and approved by the principal investigator 12. Use of proton pump inhibitors (PPIs) within 3 days or H2-receptor antagonists within 1 day prior to study intervention 13. Use of warfarin. Use of Direct-Acting Oral Anticoagulants (DOAC) within 14 days or 5 half-lives, whichever is longer, prior to study day 1. Other anticoagulation may be allowed with principal investigator approval.

Gender: All

Minimum age: 18 Years

Maximum age: N/A

Healthy volunteers: No

Locations:

Facility:
Name: Karolinska University Hospital

Address:
City: Stockholm
Zip: 17176
Country: Sweden

Status: Recruiting

Contact:
Last name: Karin Lindberg, MD, PhD

Investigator:
Last name: Karin Lindberg, MD, PhD
Email: Principal Investigator

Start date: October 15, 2023

Completion date: January 1, 2026

Lead sponsor:
Agency: Karolinska University Hospital
Agency class: Other

Collaborator:
Agency: Sahlgrenska University Hospital, Sweden
Agency class: Other

Collaborator:
Agency: Amgen
Agency class: Industry

Source: Karolinska University Hospital

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT06127940