Inclusion Criteria:
1. Age 20 or more than 20 years-old. 2. Histologically confirmed, "locally advanced and unresectable NSCLC not amenable to
treatment with curative intent (surgery or chemoradiotherapy) or recurrent or de
novo-metastatic non-squamous NSCLC (according to Version 8 of the IASLC Staging Manual
in Thoracic Oncology) locally advanced or metastatic non-squamous NSCLC (Participants
with mixed histology are eligible if adenocarcinoma is the predominant histology).
3. Activating HER2-mutation documented by NGS in tissue or plasma (include activating
HER2 mutation in exon 19 or 20, i.e. , Exon 20: A775_G776insYVMA
insertion/duplication; point mutations, L755S and G776C; transmembrane and the
juxtamembrane domains G660D, R678Q, E693K and Q709Ldocumented mutation) regardless of
HER2 expression.
HER2 expression on tissue based on IHC (IHC 1+, 2+, or 3+)
4. Asymptomatic brain metastases at baseline without local therapy for brain metastasis
or stable brain metastasis after local therapy (WBRTx, SRS, GKS etc), which is defined
as patients who are not requiring therapy with corticosteroids or anticonvulsants to
control associated symptoms.
5. Prior failure on any systemic chemotherapy platinum-based chemotherapy. 6. Measurable disease according to RECIST version 1.1Response Assessment in
Neuro-Oncology Criteria (RANO)
7. LVEF ≥ 50% within 28 days before randomization/enrollmentfirst dose .
8. Eastern Cooperative Oncology Group performance status (ECOG PS) 0-1.
9. Adequate organ and bone marrow function within 14 days before randomization/enrolment
first dose as described in Table 1 below. All parameters must meet the inclusion
criteria on the same day, and must be the most recent results available.
Table 1 Parameters for Adequate Organ and Bone Marrow Function Adequate bone marrow
function Platelet Count ≥ 100000/mm3. Haemoglobin ≥ 9.0 g/dL Absolute neutrophil count
≥ 1500/mm3 Adequate hepatic function Alanine aminotransferase (ALT) and aspartate
aminotransferase (AST) ≤ 3×ULN (< 5×ULN in participants with liver metastases) Total
Bilirubin ≤ 1.5×ULN if no liver metastases or < 3×ULN in the presence of documented
Gilbert's syndrome (unconjugated hyperbilirubinemia) or liver metastases at baseline
Serum albumin ≥ 2.5 g/dL Adequate renal function CrCL ≥ 30 mL/min as determined by
Cockcroft Gault (using actual body weight).
Males:
CLcr (mL/min) = "[140
- - age (years)] × weight (kg)" /"72 × serum creatinine (mg/dL)"
Females:
(CLcr (mL/min) = "[140 - age (years)] × weight (kg)" /"72 × serum creatinine (mg/dL)"
× 0.85 Adequate blood clotting function International normalised ratio or Prothrombin
time and either partial thromboplastin or activated partial thromboplastin time ≤ 1.5
× ULN.
*CrCL = calculated creatinine clearance; ULN = upper limit of normal. 10. Adequate treatment washout period before enrollment, defined in Table 2 below:
Table 2 Adequate treatment washout periods Treatment / Minimum Washout Period Major
Surgery ≥ 4 weeks Radiation Therapy including palliative stereotactic radiation
therapy to chest ≥ 4 weeks Palliative stereotactic radiation therapy to other anatomic
areas including whole brain radiation, bone radiation and GKS ≥ 2 weeks Anti-Cancer
chemotherapy [Immunotherapy (non-antibody based therapy)] ≥ 43 weeks Antibody based
anti-cancer therapy ≥ 4 weeks Targeted agents and small molecules ≥ 242 weeks or 5
half-lives, whichever is longer TKIs approved for treatment of NSCLC ≥ 1 week.
- - baseline CT scan must be completed after discontinuation of TKI.
11. Evidence of post-menopausal status or negative serum pregnancy test for females of
childbearing potential who are sexually active with a non-sterilized male partner. For
women of childbearing potential, a negative result for serum pregnancy test (test must
have a sensitivity of at least 25 mIU/mL) must be available at the screening visit and
urine beta-human chorionic gonadotropin (β-HCG) pregnancy test . prior to each
administration of IMP.
12. Women of childbearing potential are defined as those who are not surgically sterile
(i.e. underwent bilateral salpingectomy, bilateral oophorectomy, or complete
hysterectomy) or post-menopausal(Over 60 years old ). Women will be considered
post-menopausal if they have been amenorrheic for 12 months without an alternative
medical cause.
13. Female patients of childbearing potential who are sexually active with a
non-sterilized male partner must use at least one highly effective method of
contraception, presented in Table 3. from the time of screening and must agree to
continue using such precautions for 7 months after the last dose of IMP. Not all
methods of contraception are highly effective. Female patients must refrain from
breastfeeding while on study and for 7 months after the last dose of IMP. Complete
heterosexual abstinence for the duration of the study and drug washout period is an
acceptable contraceptive method if it is line with the patient's usual lifestyle
(consideration must be made to the duration of the clinical trial); however, periodic
or occasional abstinence, the rhythm method, and the withdrawal method are not
acceptable.
14. Non-sterilized male patients who are sexually active with a female partner of
childbearing potential must use a condom with spermicide from screening to 4 months
after the final dose of IMP. Complete heterosexual abstinence for the duration of the
study and drug washout period is an acceptable contraceptive method if it is in line
with the patient's usual lifestyle (consideration must be made to the duration of the
clinical trial); however, periodic or occasional abstinence, the rhythm method, and
the withdrawal method are not acceptable. It is strongly recommended for the female
partners of a male patient to also use at least one highly effective method of
contraception throughout this period, as described in Table 3. In addition, male
patients should refrain from fathering a child, or freezing or donating sperm from the
time of randomisation/enrolment, throughout the study and for 4 months after the last
dose of IMP. Preservation of sperm should be considered prior to enrollment in this
study.
15. Female subjects must not donate, or retrieve for their own use, ova from the time of
randomization/enrolment and throughout the study treatment period, and for at least 7
months after the final study drug administration. They should refrain from
breastfeeding throughout this time. Preservation of ova may be considered prior to
enrollment in this study.
Exclusion Criteria:
1. Active brain metastases that require intervention. 2. Leptomeningeal metastases. 3. Systemic antitumor therapy within 28 days(Targeted therapy, ≥ 2 weeks or 5 half-lives)
before initiation of T-DXd. 4. Radiation therapy(excluding palliative stereotactic radiation therapy to chest) or
gamma-knife surgery within 2weeks before initiation of T-DXd. 5. Has substance abuse or any other medical conditions such as clinically significant
cardiac or psychological conditions, that may, in the opinion of the investigator,
interfere with the subject's participation in the clinical study or evaluation of the
clinical study results.
6. Has spinal cord compression or clinically active central nervous system metastases,
defined as untreated and symptomatic, or requiring therapy with corticosteroids or
anticonvulsants to control associated symptoms. Subjects with untreated but clinically
inactive brain metastases may be included in the study. Subjects with treated brain
metastases that are no longer symptomatic and who require no treatment with
corticosteroids or anticonvulsants may be included in the study if they have recovered
from the acute toxic effect of radiotherapy. A minimum of 2 weeks must have elapsed
between the end of whole brain radiotherapy and study enrollment/randomization.
7. Unresolved toxicities from previous anticancer therapy, defined as toxicities (other
than alopecia) not yet resolved to Grade ≤ 2 or baseline. 8. Patients with a medical history of myocardial infarction (MI) within 6 months before
enrolment, symptomatic congestive heart failure (CHF) (New York Heart Association
Class II to IV),
9. History of (non-infectious) ILD / pneumonitis that required steroids, has current
ILD/pneumonitis, or where suspected ILD/pneumonitis cannot be ruled out by imaging at
screening.
10. Uncontrolled infection requiring IV antibiotics, antivirals, or antifungals.(Using for
prophylactic antibiotics is allowed.)
11. Active primary immunodeficiency, known uncontrolled active HIV infection or active
hepatitis B or C infection, such as those with serologic evidence of viral infection
within 28 days of Cycle 1 Day 1. Subjects with past or resolved hepatitis B virus
(HBV) infection who are anti-HBc positive (+) are eligible only if they are HBsAg
negative (-).
12. Patients positive for hepatitis C (HCV) antibody are eligible only if polymerase chain
reaction is negative for HCV RNA. Subjects should be tested for HIV prior to
randomization/enrollment if required by local regulations or institutional review
board (IRB)/ethics committee (EC).
13. Receipt of live, attenuated vaccine within 30 days prior to the first dose of
trastuzumab deruxtecan. Receipt of live, attenuated vaccine (mRNA and replication
deficient adenoviral vaccines are not considered attenuated live vaccines) within 30
days prior to the first dose of trastuzumab deruxtecan. Note: Participants, if
enrolled, should not receive live vaccine during the study and up to 30 days after the
last dose of study intervention.
14. Clinically significant pleural effusion, ascites or pericardial effusion that requires
drainage.(Stable. 15. Lung-specific intercurrent clinically significant illnesses including, but not limited
to, any underlying pulmonary disorder (e.g. pulmonary emboli within three months of
the study enrollment, severe asthma, severe COPD, restrictive lung disease, pleural
effusion etc.)
16. Any autoimmune, connective tissue or inflammatory disorders (e.g. Rheumatoid
arthritis, Sjogren's, sarcoidosis etc.) where there is documented, or a suspicion of
pulmonary involvement at the time of screening. Full details of the disorder should be
recorded in the eCRF for patients who are included in the study.
17. Prior complete pneumonectomy. 18. Known allergy or hypersensitivity to study treatment or any of the study drug
excipients.
19. History of severe hypersensitivity reactions to other monoclonal antibodies.
20. Pregnant or breastfeeding female patients, or patients who are planning to become
pregnant.
21. Multiple primary malignancies within 3 years, with the exception of.
- - adequately resected non-melanoma skin cancer.
- - curatively treated in-situ disease.
- - other solid tumors curatively treated Procedures for withdrawal of incorrectly
enrolled subjects see Section 3.4.
22. Prior use of targeted HER2 treatments, except for TKIs.
