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To evaluate the efficacy and toxicity of patients treated with hypofractionated radiotherapy for limited metastatic NSCLC harboring sensitizing EGFR mutations after first line TKI therapy. An exploratory biomarker analysis in blood and tumor samples is also planned.
Rational:
After inductive TKI therapy in NSCLC with sensitizing EGFR mutations, the residual lesion might be the source of subsequent disease progression, defined as acquired resistance to TKI. Two reasons can be used to explain the formation of the residual lesion:1)there is a subgroup of cancer cells that are not sensitive to TKI therapy because of tumor heterogeneity, like de novo T790M mutation; 2)some cancer cells can keep static state during the beginning treatment, and then develops acquired resistance to TKI therapy under the long-term drug pressure and continue to re-proliferation. From this point of view, elimination of residual lesion provides the chance to reduce or slow the possibility of developing resistance to TKI.
Objective:
To evaluate the efficacy and toxicity of patients treated with hypofractionated radiotherapy for limited metastatic NSCLC harboring sensitizing EGFR mutations after first line TKI therapy. An exploratory biomarker analysis in blood and tumor samples is also planned.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| EGFR-TKI | Experimental | Patients take EGFR-TKI alone till tumor progression |
|
| EGFR-TKI+hypofractionated radiotherapy | Active Comparator | After 3 mos TKI, patients with limited metastatic take EGFR-TKI concurrent with hypofractionated radiotherapy till tumor progression. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| EGFR-TKI | Drug | Gefitinib 250mg po qd or Erlotinib 150mg po qd or Icotinib 125mg po tid |
|
| Measure | Description | Time Frame |
|---|---|---|
| Progression free survival | 3 years |
| Measure | Description | Time Frame |
|---|---|---|
| Frequency of T790M mutation before treatment detected by ctDNA | 1 months | |
| Abundance of T790M mutation before treatment detected by ctDNA | 1 months | |
| Frequency of T790M mutation after radiotherapy detected by ctDNA |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Shenglin Ma, MD | Contact | 0571-56007908 | 086 | mashenglin@medmail.com.cn |
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| Thoracic Hypofractionated Radiotherapy | Radiation | 40-45 Gy/5-15f |
|
| 3 months |
| Abundance of T790M mutation after radiotherapy detected by ctDNA | 3 months |
| Frequency of T790M mutation after 1 year detected by ctDNA | 1 year |
| Abundance of T790M mutation after 1 year detected by ctDNA | 1 year |
| Rate of CTCAE grade 2 or higher radiation pneumonitis | We will assess the rate of symptomatic radiation pneumonitis in patients who received the radiation therapy. | 1 years |
| To assess the short-term quality of life (QOL) | FACT-E score at the 4 months after docetaxel consolidation therapy | 4 months |
| ID | Term |
|---|---|
| D000077192 | Adenocarcinoma of Lung |
| ID | Term |
|---|---|
| D000230 | Adenocarcinoma |
| D002277 | Carcinoma |
| D009375 | Neoplasms, Glandular and Epithelial |
| D009370 | Neoplasms by Histologic Type |
| D009369 | Neoplasms |
| D008175 | Lung Neoplasms |
| D012142 | Respiratory Tract Neoplasms |
| D013899 | Thoracic Neoplasms |
| D009371 | Neoplasms by Site |
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| ID | Term |
|---|---|
| D000077156 | Gefitinib |
| ID | Term |
|---|---|
| D011799 | Quinazolines |
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
| D006571 | Heterocyclic Compounds |
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