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Advanced Non-small Cell Lung CancerPhase 3NCT03727867

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

A Phase 3 study testing Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor and Stereotactic Body Radiation Therapy in people with Advanced Non-small Cell Lung Cancer, run by Haihua Yang at 1 site in China.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

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… Read more about this study

Who is it for?
Ages 18 to 85 years
Conditions the study is for
Advanced Non-small Cell Lung Cancer
What is being tested?
Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor and Stereotactic Body Radiation Therapy
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
300 participants
Where
1 siteChina
Study dates
1 Jun 2019to 1 Jun 2022
Phase
Phase 3
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 85 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Patients must sign a study specific informed consent form prior to clinical trial;
  • World Healthy Organization (WHO)/Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 to 2 and kamofsky performance status (KPS) >60 at enrollment;
  • Patients must have tumors that were proven histopathologically or cytologically as advanced non-small cell lung cancer and that harbored sensitizing EGFR mutation (e.g. exon 19 deletion or exon 21 L858R);
  • Estimated life expectancy >8 weeks;
  • Patients should have adequate bone marrow function defined as absolute peripheral granulocyte count (AGC) of >/= 1500 cells/mm3, platelet count of >/= 100000 cells/mm3; adequate hepatic function with bilirubin </= 1.5 mg/dl, creatinine clearance >/= 50 ml/min and international normalized ration (INR) 0.8-1.2; adequate lung function: forced expiratory ration in 1 second >80%;
  • The number of oligometastasis plus primary lesion should be less that 5, and the maximum diameter of the primary lesion in lung should be under 5 cm, without tracheal and thoracic vessels invasion.

Who cannot join

  • Patients must be withdrawn with prior radiotherapy, chemotherapy, immunotherapy and surgery of chest;
  • Uncontrolled intercurrent illness including but not limited to, ongoing or active infection, failure in bone marrow, liver, kidney, heart and lung, or psychiatric illness/social situations that would limit compliance with study requirements;
  • Patients who suffered from symptomatic intracranial metastasis or other malignant tumors, such as cervical cancer,skin cancer and so on;
  • Patients who participated other clinical drug trial.

Trial locations and contacts

1 site in 1 country.

Dongqing Lv, MD contact

13867622009

lvdq@enzemed.com

Haihua Yang, MD contact

13819639006

yhh93181@hotmail.com

China1 site
  • Taizhou Hospital, Wenzhou Medical University

    Taizhou, Zhejiang, 317000

    Dongqing Lv, MD, 13867622009, lvdq@enzemed.com

    Haihua Yang, MD, 13819639006, yhh93181@hotmail.com

Other trials in China

About this study

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.

Being tested
Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor, Stereotactic Body Radiation Therapy

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Epidermal Growth Factor Receptor Tyrosine Kinase InhibitorDrug

    Also called EGFR TKI

    Oral EGFR TKI begins on day 1 and continues until disease progresses.

  • Stereotactic Body Radiation TherapyDevice

    Also called SBRT, stereotactic ablative radiotherapy (SABR)

    Participants were given Stereotactic Body Radiation Therapy in a dose of 60 Gy/8 fraction for the central tumor or 50 Gy/5 fraction for the peripheral lung cancer, respectively.

Study groups in NCT03727867
Study groupRoleWhat they receive
Drug groupPlacebo comparatorParticipants were under prescription of Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor (EGFR TKI) at the beginning and continued until disease progressed.
Receives: Drug: Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor
Drug plus SBRT groupExperimentalAfter the first month of EGFR TKI orally, participants were given Stereotactic Body Radiation Therapy (SBRT) in dose of 50 Gy/5 F or 60 Gy/8 F for peripheral and central primary tumor, respectively, combined with oral EGFR TKI continually until the primary end point.
Receives: Drug: Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor; Device: Stereotactic Body Radiation Therapy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Progression free survival

    Evaluate the effect of EGFR TKI with or without SBRT on progression free survival.

    Measured: Duration of time from the start of EGFR TKI therapy to the time of disease progression, assessed up to 3 years.

Secondary outcomes (3)
  1. Local control rate (LCR)

    To describe the rate of local control and out-of-field disease progression, irrespectively.

    Measured: Up to 3 years.

  2. Overall survival

    To evaluate overall survival in EGFR TKI therapy with SBRT in comparison to EGFR TKI therapy alone.

    Measured: Duration of time from the start of EGFR TKI therapy to 3 years or until time of death, whichever occurs first.

  3. Adverse events

    The acute and chronic profile associated with the study regimen using CTCAE v5.0.

    Measured: Up to 3 years.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted1 Nov 2018
  2. Study start1 Jun 2019 (estimated)
  3. Primary completion1 Jun 2021 (estimated)
  4. Study completion1 Jun 2022 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
300 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03727867
Sponsor's protocol ID
Target-SBRT
Status last verified
Jan 2019
First submitted
27 Oct 2018
Last updated
30 Jan 2019
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor and Stereotactic Body Radiation Therapy in people with Advanced Non-small Cell Lung Cancer, run by Haihua Yang at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 30 Jan 2019. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Dongqing Lv, MD (13867622009, lvdq@enzemed.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Progression free survival (time frame: Duration of time from the start of EGFR TKI therapy to the time of disease progression, assessed up to 3 years.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Jan 2019.

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