Inclusion Criteria:
- - Provision of a voluntarily given, personally signed and dated, written informed
consent document;
- Age≥18 years, male or female;
- The presence of an EGFR activating mutation (exon 19 deletion or the L858R mutation in
exon 21) in tumor specimen determined by the local laboratory.
It is acceptable for
subjects with the presence of the exon 20 T790M mutation together with either EGFR
activating mutation (exon 19 deletion or the L858R mutation in exon 21) to be included
in this study;
- - Evidence of newly diagnosed stage IIIB/IV (based on Union for International Cancer
Control (UICC) staging system version 7) or recurrent (minimum of 12 months disease
free interval between completion of systemic therapy and recurrence of NSCLC required)
NSCLC of adenocarcinoma histo- and/or cytopathology or its pathologically accepted
variants using tumor specimen (assessed according to accepted standards by a local
laboratory).
For this purpose the World Health Organization/International Association
of Study of Lung Cancer Histologic Classification of Lung Cancer Criteria will be used
and the diagnosis of NSCLC NOS (not otherwise specified), squamous or mixed
adeno-squamous lung carcinomas will not be allowed;
- - Have an ECOG PS of 0 or 1;
- No prior treatment with systemic therapy for locally advanced or metastatic NSCLC.
Completed neoadjuvant/adjuvant chemotherapy/immunotherapy and/or combined modality
chemotherapy/radiation therapy permitted only in cases in which there is a minimum of
12 months disease free interval between completion of systemic therapy and recurrence
of NSCLC. Prior treatment with an EGFR-TKI or other TKIs is not allowed;
- - Brain metastases lesions should be more than or equal to 3 metastatic lesions in the
brain .
At least one target lesion's diameter among these lesions should be more than
1 centimeter（ Patients with CNS metastases. whose condition was neurologically stable
were eligible. Any previous definitive treatment or glucocorticoid therapy had to be
completed at least 2 weeks before initiation of the trial treatment.）.
- - Radiologically measurable disease by RECIST v1.1 criteria:
1.
At least one target lesion that has not previously been radiated, and is
measurable according to RECIST v1.1;
2. Acceptable radiologic procedures for disease assessment include contrast enhanced
conventional or spiral computed tomography (CT), or contrast enhanced magnetic
resonance imaging (MRI); Non contrast CT scan is acceptable only for subjects who
are both allergic to intravenous contrast and unable to cooperate with MRI, or
MRI is not available. The following are not allowed as sole documentation of
target lesions: CT component of positron emission tomography (PET)/CT, ultrasound
alone, nuclear scans (including bone or PET scans), chest X-ray or bone
radiographs, and tumor markers;
- - Adequate organ function, including:
1.
Estimated creatinine clearance >30 mL/min (as determined by Cockcroft-Gault
formula or the study site's standard formula);
2. Urinary protein <3+ by urine dipstick. If urine protein by dipstick is ≥3+, then
a urine protein/creatinine ratio (UPC) should be obtained. The subject may enter
only if UPC is <2.0;
3. Absolute neutrophil count (ANC) ≥1500 cells/mm3;
4. Platelets ≥100,000 cells/mm3;
5. Hemoglobin ≥10.0 g/dL；
6. Bilirubin≤1.5 x ULN;
7. AST (also known as SGOT) and ALT (also known as SGPT) <2.5 x ULN (<5.0 x ULN if
hepatic metastases).
- - Female subjects must be postmenopausal (defined as 12 months of amenorrhea following
last menses), or they or their partners must be surgically sterile, or must agree to
use effective contraception while receiving study treatment and for at least 3 months
thereafter.
The definition of effective contraception will be based on the judgment of
the investigator using following criteria:
Acceptable contraception for women include implants, injectables, combined oral
contraceptives, intrauterine devices (IUDs), sexual abstinence, or a partner who has been
surgically sterile (e.g. by vasectomy) for at least 6 months. Acceptable contraception for
a male includes surgical sterility (e.g. by vasectomy) for at least 6 months, sexual
abstinence, or condoms plus spermicide.
- - All female subjects with reproductive potential must have a negative pregnancy test
(serum or urine) prior to starting study treatment;
- Male subjects or their female partners must be surgically sterile or must agree to use
effective contraception while receiving study treatment and for at least 3 months
thereafter.
The definition of effective contraception will be based on the judgment of
the investigator. Or female partners must be postmenopausal (defined as 12 months of
amenorrhea following last menses);
- - Willing and able to comply with study scheduled visits, treatment plans, laboratory
tests, and other study procedures.
Exclusion Criteria:
- - Any evidence of mixed histo- and/or cytology that includes elements of small cell or
carcinoid lung cancer.
Variations of adenocarcinoma are allowed, however no squamous
element can be present;
- - Any other mutation other than exon 19 deletion or L858R in exon 21, with or without
the presence of the exon 20 T790M mutation.
Both mutations (exon 19 deletion and L858R
mutation in exon 21) within a tumor sample;
- - Symptomatic brain or leptomeningeal metastases, who are neurologically unstable or
require increasing doses of steroids to manage CNS symptoms within two weeks prior to
starting dacomitinib;
- Any previous anti-cancer systemic treatment of locally advanced, or metastatic NSCLC
including but not limited to chemotherapy, targeted therapies, small molecules,
EGFR-TKIs and other TKIs, monoclonal antibodies, anti-cancer vaccines, radiotherapy
(other than palliative radiotherapy to lesions that will not be followed for tumor
assessment on this study, i.e., non-target lesions).
Completed neoadjuvant/adjuvant
chemotherapy/immunotherapy and/or combined modality chemotherapy/ radiation therapy
permitted only in cases in which there is a minimum of 12 months disease free interval
between completion of systemic therapy and recurrence of NSCLC. Prior treatment with
an EGFR-TKI or other TKIs is not allowed;
- - Any surgery (not including minor procedures such as lymph node biopsy), palliative
radiotherapy or pleurodesis within 2 weeks of baseline assessments;
- Any clinically significant gastrointestinal abnormalities that may impair intake,
transit or absorption of the study drug, such as the inability to take oral
medication;
- Current enrollment in another therapeutic clinical study;
- Any psychiatric or cognitive disorder that would limit the understanding or rendering
of informed consent and/or compromise compliance with the requirements of this study;
or known drug abuse/alcohol abuse;
- History of, or currently suspected, diffuse non-infectious pneumonitis or interstitial
lung disease including:
1.
Past medical history of interstitial lung disease, drug-induced interstitial
disease, radiation pneumonitis which required steroid treatment or any evidence
of clinically active interstitial lung disease;
2. Pre-existing idiopathic pulmonary fibrosis evidenced by CT scan at baseline;
3. Insufficient lung function as determined by either clinical examination or an
arterial oxygen tension of <70 Torr.
- - Any history of galactose intolerance, Lapp lactase deficiency or glucose-galactose
malabsorption.
- - Clinically important abnormalities in cardiac rhythm, conduction or morphology of
resting ECG (e.g. complete left bundle branch block, second degree heart block, third
degree heart block) OR:
1.
Diagnosed or suspected congenital long QT syndrome;
2. Any history of clinically significant ventricular arrhythmias (such as
ventricular tachycardia, ventricular fibrillation, or Torsades de pointes);
3. Prolonged QTc on ECG; QTc must be less than CTCAE v4.0 Grade 2 (≤480 msec) using
Fridericia's or Bazett's correction formula with a manual reading by the
investigator if required. The ECG may be repeated for evaluation of eligibility
after management of correctable causes for observed QTc prolongation;
4. Any history of second or third degree heart block;
5. Heart rate <45 beats per minute on ECG in the presence of clinical symptoms
(e.g., hypotension, evidence of hypoperfusion);
- - Severely impaired (defined as Child-Pugh Class C) hepatic dysfunction;
- Prior malignancy: Subjects will not be eligible if they have history of, or evidence
of active disease of another concurrent malignancy within the previous five years.
Exception would be effectively treated past history of non melanoma skin cancer or
in-situ cervical cancer with no evidence of active disease;
- - Other severe acute or chronic medical condition that may increase the risk associated
with study participation or investigational drug administration or may interfere with
the interpretation of study results and, in the judgment of the investigator, would
make the subject inappropriate for entry into this study;
- Use of narrow therapeutic index drugs that are CYP2D6 substrates (procainamide,
pimozide, and thioridazine etc.) from screening to randomization.
