Consolidation Conventional Radiotherapy + Stereotactic Body Radiotherapy at 3 Months After First-line Chemotherapy in Stage IV Oligometastatic Non-small Cell Lung Cancer

Not Applicable

Recruiting

• Conditions: Non-small Cell Lung Cancer

• Registration Number: NCT04758481
• Lead Sponsor: University Hospital Ostrava

Brief Summary

Lung cancer is the main cause of death among cancer diseases, in the Czech Republic, as well as worldwide. Non-small cell lung cancer (NSCLC) is responsible for more than 80% of deaths among cancer patients. Bronchogenic carcinoma is the reason of death of almost 5.500 cases every year in the Czech Republic, the mortality/incidence ration varies around 85%. The main cause for these unfavorable findings is the late detection of the carcinoma in late stages only (III and IV), when a long-term control of the disease is exceptional. Chemotherapy is able to prolong the life of patients with NSCLC by less than one year on average, that is why new treatment approaches are being examined.

Detailed Description

The basic treatment modality of lung cancer is radiotherapy, which has a proven therapeutic benefit in radical and palliative indications in up to 76% of all patients. Stereotactic robotic radiotherapy reaches maximum precision due to the precise definition of the target volume. In some localities, management with images has been solved using modern software instruments, which are able to visualize the tumor and monitor it during the whole course of respiratory cycle. This is directly associated with minimizing radiation of healthy tissues, especially the healthy lung parenchyma. In order to define predictive factors of survival of cancer patients, it is necessary to use molecular markers.

The aim of the study is to verify the feasibility of consolidation SBRT (Stereotactic Body RadioTherapy) - CyberKnife, with subsequent maintenance chemotherapy in patients with stage IV NSCLC, with max. 10 metastatic nidi. The main focus of the study will be on assessment of combination treatment toxicity.

The project is a phase I/II non-randomized clinical trial. Patients with stage IV NSCLC will be treated with 2-4 cycles of chemotherapy - platinum doublet (cisplatinum - cDDP/carboplatinum - CBDCA + Pemetrexed/navelibne - NVB). In cases when disease stabilization (SD)/partial resection (PR) will be achieved, based upon restaging examinations (CT), radiotherapy (RT) of the primary tumour will follow, with lymphadenopathy and SBRT of all metastatic nidi (max. 10 intra- or extracranial metastases). Standard fractionation schemes for RT and SBRT will be used (RT 40-50 Gy/16-20 fractions, SBRT 30 Gy/1 fractionation, 50-60 Gy/3-5 fractionations). At 3-6 weeks after the end of RT, maintenance treatment will be initiated in all patients treated with Peterexed. Regular restaging examinations are planned every 3 months.

Study Timeline

• Study First Submitted: 2021-02-04
• Study First Submitted QC: 2021-02-12
• Study First Posted: 2021-02-17
• Study Start: 2021-05-04
• Status Verified: 2022-12
• Last Update Submitted: 2022-12-06
• Last Update Posted: 2022-12-07
• Primary Completion: 2023-12-31
• Study Completion: 2023-12-31

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

• Patients with previously untreated, non-resectable, stage IV NSCLC verified with histology or cytology (according to American Joint Committee on Cancer Version 8).
• Patients must undergo 2-4 cycles of first-line chemotherapy, with the effect of disease stabilization or partial response.
• Patients over 18 years of age.
• Patients with measureable disease (on CT, PET/CT, MRI).
• Patients with 3-10 extracranial/intracranial lesions confirmed on CT, PET/CT, MRI, max. 4 weeks prior to start of SBRT.
• Max. 10 irradiated volumes (primary tumour + lymphadenopathy in one volume, if technically feasible).
• Performance status (PS) 0-2 according to ECOG. Assessment of PS max. 7 days prior to start of treatment.
• AST, ALT & ALP ≤ 2.5x norm. Total bilirubin must be within the normal range. 9. Normal function of bone marrow - Adiponectin ≥ 1.5, Haemoglobin ≥ 100, thrombo ≥ 100.
• Serum creatinine ≤1.5x norm.
• The entry laboratory tests must not be older than 14 days prior to start of treatment.
• Negative pregnancy test and use of contraception in women of childbearing age.
• Patients undergoing SBRT for pulmonary nidi must undergo entry spirometry with the value FEV1 (forced expiratory volume in 1 second) ≥ 1L.
• Patients must sign informed consent.

Exclusion Criteria

• Patients with small-cell lung cancer or with mixed aetiology with SCLC.
• Serious ongoing infections.
• Patients with a history of haematopoiesis disorders.
• Weight loss exceeding 10% within the last 3 months.
• Patients with skin metastases of NSCLC.
• Patients treated for other malignity within the last 5 years
• Patients with more than 10 extracranial/intracranial metastases.
• Malignant fluidothorax > 1 cm prior to start of treatment.
• Patients treated with targeted treatment for EGFR mutation or EML-4-ALK translocation in the 1st-line (Erlotinib, Gefitinib, Afatinib, Crizotinib, ...).
• Patients treated with immunotherapy (anti-PD-1, anti-PD-L1 or anti-PD-L2, anti CTLA-4, ...).
• Participation in another clinical trial within the last month before the start of NSCLC treatment.
• Inability to cooperate or comply with the study protocol.
• Decision of the patient to discontinue participation in the study.
• Pregnant women.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Acute and late toxicity	every 3 months, throughout the study duration, up to 32 months in total	Acute and late toxicity of the combination therapy will be observed (according to Common Terminology for Clinical Adverse Event (CTCAE, version 5)
Progression-free survival	every 3 months	Progression-free survival will be observed

Secondary Outcome Measures

Name	Time	Method
Overall survival	every 3 months, throughout the study duration, up to 32 months in total	Overall survival will be observed
Share of nidi under local control	every 3 months, throughout the study duration, up to 32 months in total	The share of nidi under local control will be observed (in per cent/total number of nidi)
Time to new nidus formation	every 3 months, throughout the study duration, up to 32 months in total	The time to new nidus formation will be observed
Duration of maintenance chemotherapy	every 3 months, throughout the study duration, up to 32 months in total	The duration of maintenance chemotherapy will be observed.

Trial Locations

Locations (1)

University Hospital Ostrava; 🇨🇿 Ostrava, Moravian-Silesian Region, Czechia