Subjects will receive durvalumab and AZD6738 combination therapy. The arm is composed of 45
subjects.
Durvalumab 1500mg via IV administered for every 4weeks(fixed dosing for subjects > 30 kg body
weight) in Day 1 of each cycle and AZD 6738 240mg bid per os administered in each cycle days
15 and 28. One cycle is consisted of 28 days.
Tumour evaluation using CT or MRI, RECIST 1.1, CEA, NSE and LDH will be conducted at
screening (within 28days prior to first dose of Cycle1 Day1) and every 8weeks(±1week) for the
first 56weeks relative to the start of combination therapy(Cycle1 Day1), and thereafter every
12weeks(±1week) until objective disease progression.
Study treatment will be continued until objective disease progression (unless other criteria
for treatment discontinuation are met). Subjects may continue durvalumab and AZD6738 beyond
progression(according to RECIST 1.1), at the discretion of the investigator if they are
clinically benefiting from the treatment and they do not meet any other discontinuation
criteria.
If a subjects discontinues study treatment prior to disease progression, they should continue
to be assessed using RECIST 1.1 until disease progression and then followed up for survival.
Assessments for survival should be made every 3months following objective disease
progression. The details of first and subsequent therapies for cancer, after discontinuation
of durvalumab and AZD6738 treatment, will be collected.
The imaging modalities used for RECIST 1.1 assessment will be CT or MRI scans of chest,
abdomen and pelvis. And CEA, NSE and LDH tests are also used for the evaluation. RECIST 1.1
scans will be analysed by the investigator on site.
Subjects may also be requested to provide tumour samples from the primary or metastatic
tumours on progression to understand resistance mechanisms. Sample provision is optional and
depend on the subject's will.
Inclusion Criteria:
1. Provision of fully informed consent prior to any study specific procedures.
2. Subjects must be ≥ 18years of age.
3. Body weight > 30kg
4. Small cell lung cancer that has progressed during or after first-line therapy.
1. The 1st line regimen must have contained platinum based regimen and must have
documented radiological and/or clinical progression on treatment. The subjects
must not exposed to the prior immunotherapy which could have been received
separately, in combination, or in sequence with platinum-doublet chemotherapy.
2. Refractory to first-line chemotherapy or relapse within 6months since the last
dose of first-line chemotherapy
3. If the subject correspond to sensitive relapse(relapse more than 6months since
the last dose of first-line chemotherapy), (s)he should get second-line treatment
prior to study entry.
5. Subjects are willing and able to comply with the protocol for the duration of the
study including undergoing treatment and scheduled visits and examinations.
6. ECOG performance status 0-1
7. Subjects must have a life expectancy ≥ 3months from proposed first dose date.
8. Subjects must have normal organ and bone marrow function measured within 28 days prior
to administration of study treatment as defined below:
1. Haemoglobin ≥ 9.0g/dL
2. White blood cells(WBC) ≥ 3 x 109/L
3. Platelet count ≥ 100 x 109/L
4. Absolute neutrophil count (ANC) ≥ 1.5 x 109/L
5. Total bilirubin ≤ 1.5 x institutional upper limit of normal (ULN)
6. Aspartate aminotransferase(AST) (Serum Glutamic Oxaloacetic Transaminase (SGOT))
/ Alanine aminotransferase(ALT) (Serum Glutamic Pyruvate Transaminase(SGPT)) ≤
2.5 x institutional upper limit of normal unless liver metastases are present in
which case they must be ≤ 5x ULN
7. Subjects must have serum creatinine (CR)≤1.5 times the normal upper limit of the
study institution or creatinine clearance estimated using the Cockcroft-Gault
equation of ≥ 45 mL/min
9. At least one measurable lesion that can be accurately assessed at baseline by imaging
or physical examination at baseline and is suitable for repeated assessment.
10. Postmenopausal or evidence of non-childbearing status for women of childbearing
potential: negative urine or serum pregnancy test test at screening and confirmed
prior to treatment on Day 1 of every cycle Postmenopausal is defined as:
1. Amenorrheic for 1 year or more following cessation of exogenous hormonal
treatments
2. Luteinizing hormone(LH) and Follicle stimulating hormone(FSH) levels in the post
menopausal range for women under 50
3. Radiation-induced oophorectomy with last menses >1 year ago
4. Chemotherapy-induced menopause with >1 year interval since last menses surgical
sterilisation(bilateral oophorectomy or hysterectomy
11. Male Subjects and their partners, who are sexually active and of childbearing
potential, must agree to the use of two highly effective forms of contraception in
combination for acceptable methods, throughout the period of taking study treatment
and for 6months after last dose of investigational product(s) to prevent pregnancy in
a partner.
12. Provision of informed consent for genetic research. If a subject declines to
participate in the genetic research, there will be no penalty or loss of benefit to
the subject.
Exclusion Criteria:
1. Previous enrolment in the present study.
2. More than two prior chemotherapy regimen for the treatment of small cell lung
cancer(However, immunotherapy is not counted the prior chemotherapy regimen.)
3. Subjects with second primary cancer, except: adequately treated non-melanoma skin
cancer, curatively treated in-situ cancer of the cervix, or other solid tumours
curatively treated with no evidence of disease for > 2years.
4. Treatment with any investigational product during the last 14days before the
enrollment (or a longer period depending on the defined characteristics of the agents
used).
5. Subjects receiving any systemic chemotherapy or radiotherapy (except for palliative
reasons) within 3weeks from the last dose prior to study treatment (or a longer period
depending on the defined characteristics of the agents used). The subject can receive
a stable dose of bisphosphonates or denosumab for bone metastases, before and during
the study as long as these were started at least 4weeks prior to treatment.
6. Rceiving, or having received, concomitant medications, herbal supplements and/or foods
that significantly modulate cytochrome P450 3A4(CYP3A4) or P-glycoprotein(P-gp)
activity(washout periods of 2weeks, but 3weeks for St. John's Wort). Note these
include common azole antifungals, macrolide antibiotics and other medications.
7. Prior exposure to an ATR inhibitor.
8. Refractory nausea and vomiting, chronic gastrointestinal diseases or previous
significant bowel resection, with clinically significant sequelae that would preclude
adequate absorption of AZD6738
9. Current or prior use of immunosuppressive medication within 14days before the first
dose of durvalumab. The following are exceptions to this criterion:
1. Intranasal, inhaled, topical steroids, or local steroid injections(eg,
intra-articular injection)
2. Systemic corticosteroids at physiologic doses not to exceed 10mg/day of
prednisone or its equivalent
3. Steroids as premedication for hypersensitivity reactions(eg, CT scan
premedication)
10. Receipt of live attenuated vaccine within 30days prior to the first dose of
investigational product. Note: Subjects, if enrolled, should not receive live vaccine
whilst receiving investigational product and up to 180days after the last dose of
investigational product.
11. Any unresolved toxicity NCI CTCAE grade≥2 from previous anticancer therapy with the
exception of alopecia, vitilgo, and the laboratory values defined in the inclusion
criteria(CTCAE 5.0)
1. Subjects with Grade ≥2 neuropathy will be evaluated on a case-by-case basis after
consultation with the Study Physician.
2. Subjects with irreversible toxicity not reasonably expected tobe exacerabated by
treatment with durvalumab may be included only after consultation with with the
Study Physician.
12. Intestinal obstruction or CTCAE 5.0 grade 3 or grade 4 upper GI bleeding within 4weeks
before the enrollment.
13. Haematuria: +++ on microscopy or dipstick
14. INR ≥ 1.5 or other evidence of impaired hepatic synthesis function
15. Subject has any of the following cardiac criteria:
1. Mean QT interval corrected for heart rate(QTc) ≥ 470ms calculated from 3
electrocardiograms(ECGs) using Fridericia's correction.
2. Any clinically important abnormalities in rhythm, conduction or morphology of
resting ECG eg, complete left bundle branch block, third degree heart block,
second degree heart heart block, first degree heart block.
3. Any factors that increase the risk of QTc prolongation or risk of arrhythmic
events such as heart failure, hypokalaemia, congenital long QT syndrome, family
history of long QT syndrome or unexplained sudden death under 40years of age or
any concomitant medication known to prolong the QT interval.
4. Uncontrolled hypertension-blood pressure (BP) ≥ 150/95mmHg despite medical
therapy.
5. Unstable atrial fibrillation or unstable cardiac arrhythmia with a ventricular
rate > 100bpm on an ECG at rest.
6. Symptomatic heart failure - New York Heart Association Grade II to Grade IV.
7. Prior or current cardiomyopathy.
8. Severe valvular heart disease.
9. Uncontrolled angina (Canadian Cardiovascular Society Grade II to Grade IV despite
medical therapy) or acute coronary syndrome within 6months prior to screening.
10. Subjects at risk of brain perfusion problems (e.g., carotid stenosis hypotension,
including a fall in blood pressure of > 20mm Hg)
16. Female subjects who are pregnant or breast-feeding or child-bearing or male or female
subjects of of reproductive potential who are not willing to employ effective birth
control from screening to 90 days after the last dose of durvalumab monotherapy.
17. Any evidence of severe or uncontrolled intercurrent illness, including but limited to,
ongoing or active infection, symptomatic conjestive heart failure, uncontrolled
hypertension, unstable angina pectoris, cardiac arrhythmia, interstitial lung disease,
serious chronic gastrointestinal conditions associated with diarrhea, or psychiatric
illness/social situations that would limit compliance with study requirement,
substantially increase risk of incurring AEs or compromise the ability of the subject
to give written informed consent.
18. History of allogenic organ transplantation.
19. Active infection including tuberculosis (clinical evaluation that includes clinical
history, physical examination and radiographic findings, and TB testing in line with
local practice), hepatitis B(known positive HBV surface antigen(HBsAg) result),
Hepatitis C, or human immunodeficiency virus(positive HIV 1/2 antibodies). Subjects
with a past or resolved HBV infection (defined as the antibody[anti-HBc] and absence
of HBsAg) are eligible. Subjects positive for hepatitis C(HCV) antibody are eligible
only if polymerage chain reaction is negative for HCV RNA.
20. Known hypersensitivity to any of study drug or any of the study drug excipients.
21. Known central nervous system(CNS) disease other than neurologically stable,treated
brain metastases - defined as metastasis having no evidence of progression or
haemorrhage for at least 2weeks after treatment.
22. Major surgical procedures ≤ 28days of beginning study treatment, or minor surgical
procedures≤ 7days
23. History of active or prior documented autoimmune or inflammatory disorders (including
inflammatory bowel disease, diverticulitis [with the exception of diverticulosis],
systemic lupus erythematosis, Sarcoidosis syndrome, or Wegener syndrome
[granulomatosis with polyangiitis, Graves' disease, rheumatoid arthritis,
hypophysitis, uveitis, etc]).
The following are exceptions to this criterion:
1. Subjects with vitiligo or alopecia
2. Subjects with hypothyroidism(e.g., following Hashimoto syndrome) stable on hormone
replacement
3. Any chronic skin condition that dose not require systemic therapy
4. Subjects without active disease in the last 5 years may be included but only after
consultation with the study physician
5. Subjects with cardiac disease controlled by diet alone
