| Eligibility |
INCLUSION CRITERIA
1. Historologically diagnosed ENKTL: The standards of WHO Classification 2016 for
diagnosis of ENKTL satisfied.
2. Became relapsed or refractory after at least one kind of treatment after initial
diagnosis.
3. If there is at least one measurable lesion.
4. In case full-body activity (ECOG PS) is levels 0-2.
5. In case of written consent to participation in clinical study: Must sign the subject
consent form that states the sampling done at the time of diagnosis or relapse (must
provide sample): 10 4um (at least 5) and biomarker (3~5 ml peripheral blood drawn
during screening period, must provide sample) and that the subject has comprehended
the purpose and the necessary procedures of clinical study with intention to
participate in the clinical study (or signed by the subject's representative).
6. If older than 19 years of age.
7. If the following hematological results are satisfied:
- Absolute neutrophil count is 1500/mm3 or greater regardless of growth factor
supply.
- Platelet count is 100,000/mm3 or greater regardless of blood supply. (However, in
cases of disease involvement, for example, platelet decrease due to bone marrow
involvement or spleen enlargement, patients with a platelet count greater than
50000/mm3 may participate in this study.)
- Hemoglobin is 9.0 g/dL or greater.
8. If the following biochemical results are satisfied:
- Alanine transaminase (ALT) and Aspartate transaminase (AST) = 2.5 x upper limit
(ULN): If liver blood enzyme count is increasing due to a disease, such as the
lymphoma's hepatic intrusion, may register up to = 5 x ULN at investigator's
discretion.
- If bilirubin is increasing due to the Gilbert Syndrome, total bilirubin = 1.5 x
ULN unless non-hepatic.
- Serum creatinine = 2 x ULN or glomerular filtration rate (Cockroft Gault) = 30
mL/min/1.73m2.
9. Highly efficient birth control that meets the local regulations must be adopted for
birth control of subjects that participate in the clinical study during or after the
clinical study for women in fertility or sexually active men (in case of women in
fertility, effective birth control must be used during the administration of study
drug and for 1 month after that and men must use it during the administration of
studyt drug and for 3 months after that).
10. Women in fertility must show negative results at platelet (beta-chorionic
gonadotropin) or pregnancy test by urine at screening.
EXCLUSION CRITERIA
1. If there is history of carcinomatous meningitis, symptomatic leptomeningeal diseases
or evidence of secondary intrusion on the central nervous system based on CT or MRI
scanning.
2. In case there are other carcinomas besides the target disease or in case of anamnesis
of other malicious tumers during the past 3 years from the start of clinical study:
Excluding basal cell carcinoma and cervical intraepithelial neoplasia that are
appropriately treated.
3. If any toxicity from the previous chemotherapy has not recovered to grade 1 or lower
at the time of screening; however hair loss and bone marrow inhibition are excluded
and peripheral polyneuropathy may be registered at researcher's discretion if there is
no risk of safety at Grade= 2.
4. In case of major operation within 4 weeks from registration for the clinical study or
failure to recover from a major complication of such operation.
5. If using immunosuppressant drugs at the time of registration for the clinical study:
Excluding local steroid injections such as nasal or inhalated steroid, steroid
ointment, and injections in articular cavities. In case of full-body steroid
administration, 10 mg or smaller prednisolonum a day is permissible (If adrenal
insufficiency is necessary to maintain a dose of prednisolone 10 mg or more, it is
acceptable according to the investigator's judgment) and steroid injections used for
pre-treatment before CT or other examination are also permitted.
6. In case of uncontrolled or symptomatic arrhythmia, congestive heart failure,
myocardial infarction, cerebral infarction, or other clinically significant
cardiovascular diseases or Class 3 (Moderate) or Class 4 (Severe) cardiac diseases
functionally classified by New York Heart Association within 6 months of screening.
7. In case of history of serious hypersensitivity against the study drug used for this
study or its substances including serious hypersensitivity against monoclonal antibody
(NCI CTCAE v4.03 Grade = 3).
8. In case of known history of human immunodeficiency virus (HIV), active type C
hepatitis virus, or active type B hepatitis virus (However, in the case of healthy
carriers who did not require asymptomatic treatment, if the antiviral drug can be
taken, it can be registered by the judgment of the investigator. In this case, the HBV
DNA test should be monitored periodically through division of gastroenterology) or
uncontrolled active full-body infection that requires intravenous (IV) antibiotics.
9. In case of life-threatening diseases, medical conditions, or respiratory failure that
may threaten the safety of subjects or put the results of clinical study in danger.
10. In case of homogeneous hematopoietic stem cell transplant.
11. In case of active autoimmune disease that may affect the administration of study drug;
excluding type 1diabetes, psoriasis, vitiligo, hyperthyroidism, or hypothyroidism that
does not require immunosuppressant.
12. If the candidate cannot comprehend the clinical study or comply with the rules of
clinical study including an active attempt to commit suicide or hurt oneself recently
or in the past and other severe acute or chronic diseases such as immunocolitis,
ulcerative colitis, immunopneumonia, pulmonary fibrosis, or mental conditions; or if
determined by investigator that participation in the study is inappropriate due to any
risk of participation or treatment in the study that may increase due to adverse
effects or the interpretation of study results that may be hindered.
13. If candidate is pregnant or breast-feeding at the time of screening.
14. In case of a major operation or live attenuated vaccine within 4 weeks of registration
for the clinical study.
15. In case of the following hepatic diseases:
- Chronic hepatitis or liver cirrhosis related to type B or type C hepatitis.
- Positive reaction for surface antigen of type B hepatitis without symptoms.
(However, in the case of healthy carriers who did not require asymptomatic
treatment, if the antiviral drug can be taken, it can be registered by the
judgment of the investigator. In this case, the HBV DNA test should be monitored
periodically through division of gastroenterology): Positive reaction to RNA of
type C hepatitis without symptoms.
16. Previously exposed to PD-1 / PD-L1 inhibitor
17. Use of other anticancer treatment or other study drugs within 4 weeks of registration
for the clinical study.
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