- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02788058
A Study of Hypofractionated Radiotherapy for Limited Metastatic NSCLC Harboring Sensitizing EGFR Mutations After First Line TKI Therapy
A Phase II Trial of Hypofractionated Radiotherapy for Limited Metastatic NSCLC Harboring Sensitizing EGFR Mutations After First Line TKI Therapy
Studieoversigt
Status
Intervention / Behandling
Detaljeret beskrivelse
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.
Undersøgelsestype
Tilmelding (Forventet)
Fase
- Fase 2
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Newly diagnosed metastatic lung adenocarcinoma harboring sensitizing EGFR mutations (L858R, exon 19 deletion), and became oligometastatic disease after 3 months TKI, evaluated by PET/CT scan, brain MRI, and abdomen ultrasound (≤6 discrete lesions of disease, exclusive of the brain metastases, ≤3 lesions in the liver, ≤3 lesions in the lung);
- All sites of disease must be amenable to definitive RT;
- An intrathoracic lymph nodal station is considered 1 discrete lesion, according to IASLC lymph nodal station map;
- Age 18 years or older;
- ECOG Performance Status 0-2;
- Adequate bone marrow, liver and renal function, as specified below: Absolute Neutrophil Count (ANC) ≥ 1.5 x 109/L; Hemoglobin ≥ 8 g/dL; Platelets ≥ 100 x 109/L; Serum total bilirubin ≤ 1.5 x upper limit of normal (ULN) ; AST and ALT ≤ 2.5 x ULN or ≤ 5 x ULN if liver metastases are present; Serum creatinine ≤ 1.5 x upper limit of normal or creatinine clearance ≥ 60ml/min for patients with creatinine levels above institutional normal;
- For women of child-bearing potential, negative pregnancy test within 14 days prior to starting treatment;
- Men and women of childbearing age must be willing to use effective contraception while on treatment and for at least 3 months thereafter;
- Patients and their family signed the informed consents;
Exclusion Criteria:
- Received chemotherapy before TKI therapy;
- Brain parenchyma or leptomeningeal disease;
- Any site of disease that is not amenable to definitive RT;
- Concurrent malignancies other than non-melanoma skin cancer that require active ongoing treatment;
- Any medical co-morbidities that would preclude radiation therapy.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: EGFR-TKI
Patients take EGFR-TKI alone till tumor progression
|
Gefitinib 250mg po qd or Erlotinib 150mg po qd or Icotinib 125mg po tid
Andre navne:
|
|
Aktiv komparator: EGFR-TKI+hypofractionated radiotherapy
After 3 mos TKI, patients with limited metastatic take EGFR-TKI concurrent with hypofractionated radiotherapy till tumor progression.
|
40-45 Gy/5-15f
Gefitinib 250mg po qd or Erlotinib 150mg po qd or Icotinib 125mg po tid
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Progressionsfri overlevelse
Tidsramme: 3 år
|
3 år
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
At vurdere den kortsigtede livskvalitet (QOL)
Tidsramme: 4 måneder
|
FACT-E score ved 4 måneder efter docetaxel konsolideringsterapi
|
4 måneder
|
|
Frequency of T790M mutation before treatment detected by ctDNA
Tidsramme: 1 months
|
1 months
|
|
|
Abundance of T790M mutation before treatment detected by ctDNA
Tidsramme: 1 months
|
1 months
|
|
|
Frequency of T790M mutation after radiotherapy detected by ctDNA
Tidsramme: 3 months
|
3 months
|
|
|
Abundance of T790M mutation after radiotherapy detected by ctDNA
Tidsramme: 3 months
|
3 months
|
|
|
Frequency of T790M mutation after 1 year detected by ctDNA
Tidsramme: 1 year
|
1 year
|
|
|
Abundance of T790M mutation after 1 year detected by ctDNA
Tidsramme: 1 year
|
1 year
|
|
|
Rate of CTCAE grade 2 or higher radiation pneumonitis
Tidsramme: 1 years
|
We will assess the rate of symptomatic radiation pneumonitis in patients who received the radiation therapy.
|
1 years
|
Samarbejdspartnere og efterforskere
Datoer for undersøgelser
Studer store datoer
Studiestart
Primær færdiggørelse (Forventet)
Studieafslutning (Forventet)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
- Neoplasmer efter histologisk type
- Neoplasmer
- Neoplasmer efter sted
- Karcinom
- Neoplasmer, kirtel og epitel
- Neoplasmer i luftvejene
- Thoracale neoplasmer
- Lungeneoplasmer
- Adenocarcinom
- Adenocarcinom i lunge
- Molekylære mekanismer for farmakologisk virkning
- Enzymhæmmere
- Antineoplastiske midler
- Proteinkinasehæmmere
- Gefitinib
Andre undersøgelses-id-numre
- HZCH-2016-08
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