Overview

Local Non-salvage Radiotherapy for Synchronous Oligometastatic Non-small-cell Lung Cancer.

Status:
Recruiting
Trial end date:
2021-09-01
Target enrollment:
0
Participant gender:
All
Summary
Aggressive therapy may improve survival in synchronous oligometastatic NSCLC and the goal of this clinical trial is to assess the efficacy and safety of local definitive radiotherapy in this subset of patients.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Southern Medical University, China
Criteria
Inclusion Criteria:

1. Male or female aged 18 to 70 years old;

2. Histologically or cytologically confirmed non-small cell lung cancer;

3. Stage IV patients with measurable primary tumor and distant metastases number ≤5;

4. PS score 0-2;

5. Have never received local or systemic anti-cancer treatment, including surgery (biopsy
is allowed), first line chemotherapy, targeted therapy or immunotherapy;

6. Life expectancy of >3 months;

7. Organ function levels must meet the following requirements:

(1)Bone marrow: White blood cell (WBC)≥4.0G/L;neutrophile granulocyte
(NEU)≥1.5G/L;platelets (PLT)≥100G/L; hemoglobin (HGB)≥9g/L; (2)Liver and kidney: total
bilirubin (TBIL), aspartate aminotransferase (AST), alanine aminotransferase (ALT)≤2.0 ×
the upper limit of normal (ULN);creatinine≤1.5×ULN; 8.Patient must be willing and able to
provide written informed consent.

Exclusion Criteria:

1. The amount of metastatic focus >5;

2. Patient can't tolerate chemotherapy or targeted therapy;

3. Local or systemic anti-cancer treatment had been used for the primary foci and
metastatic lymph nodes, including surgery (biopsy is allowed), first line
chemotherapy, targeted therapy or immunotherapy;

4. Previous or concurrent suffered from other malignancies;

5. Concurrent with other serious disease that can not be controlled;

6. Women who are breast-feeding or pregnant;

7. Have an allergy to pemetrexed, cisplatin, taxanes, targeted medicine and contrast
agent;

8. Patients with poor obedience or researchers think that the patient may not be able to
accomplish the whole trial.