Advanced Non-small Cell Lung Cancer Clinical Trial
Official title:
A Randomized Ⅲ Phase Trial of Efficacy of Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor Combined With Early Stereotactic Body Radiation Therapy to the Primary Tumor in Advanced Non-small Cell Lung Cancer Patients Harboring Epidermal Growth Factor Receptor Mutation
Non-small cell lung cancer (NSCLC) is a prevalent disease with high mortality and morbidity,
particularly of adenocarcinoma in Asians. Fortunately, with the development of epidermal
growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI), treatment of lung cancer usher
in a new era, resulting in a hit of precise therapy and molecule sequencing. However, it is
inevitable for patients to gain acquired resistance of EGFR TKI. Several studies have been
demonstrated that there were approximately 30% heterogeneous cells in primary tumors. And
emerging studies illuminated that main pattern of treatment failure was the recurrence of
primary site. Moreover, it was proved that despite of the drug-resistance cells in
progressive site, continual prescription of EGFR TKI in oligometastasis lung cancer could
make a difference for patients in progression free survival (PFS) and overall survival (OS),
owing to the residual responsive cells in another sites. Therefore, to explore an unique
method to control heterogeneous cells in primary site so as to delay or prevent acquired
resistance when taking EGFR TKI orally may be of great benefit and therapy.
It is known to all that stereotactic body radiation therapy (SBRT), with the advantage of
hypofractionation and rapid release, succeed in several cancers, such as early lung cancer,
prostatic, liver cancer and so on, for local control. Numerous reports explained SBRT played
an irreplaceable role in progressive NSCLC patients after oral targeted medicine, regardless
of EGFR or anaplastic lymphoma kinase (ALK) mutation. And the radiosensitivity of EGFR TKI in
vitro and vivo may account for these inspiring results. What's more, it has reported that
SBRT could induce inflammatory cell death, activate dendritic cell as well as accelerate
antigen presentation in the draining lymph node, leading to antigen-specific adaptive immune
response. Nevertheless, although the potential effects of SBRT on advanced NSCLC are
obviously, few studies explore the preventive benefits of early SBRT combined with oral EGFR
TKI on advanced lung cancer by eliminating the heterogeneous cells in primary site. In
addition, the investigators' previous phase II study of SBRT combined with oral EGFR TKI had
revealed its safety and potentially improvement of PFS for 6 months.
In this trial, the investigators put sight into assessing the efficacy of early application
of SBRT to primary site in the advanced NSCLC patients and provide a hypothesis that early
SBRT could strengthen the anti-tumor effect of EGFR TKI through eradicating the heterogenity
of initial tumor cells.
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