| Eligibility |
Inclusion Criteria:
- Able and willing to give a signed informed consent which includes compliance with the
requirements and restrictions listed in the informed consent form (ICF) and in this
protocol. Written informed consent obtained from the patient prior to performing any
protocol-related procedures, including screening evaluations.
- Age > 18 years.
- Patients must have histologically confirmed diagnosis of advanced (proven advanced
stage) or recurrent NSCLC, (both squamous and non-squamous pathologies are accepted;
patients with a mixed NSCLC and SCLC component are ineligible)
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
- Body weight >35kg
- Patients with evidence of radiological progression after more than 6 weeks of a
registered second or third line PD1 or PD-L1 inhibitor in monotherapy (to include ,
Nivolumab, Pembrolizumab, Atezolizumab) or more than 12 weeks for a first line PD-1 or
PD-L1 inhibitor in combination with platinum-based chemotherapy.Patients who have
received immunotherapy in the maintenance setting can only have had one prior regimen
containing PD-1/L1 inhibitor. No intervening treatment between the immunotherapy and
entry into this study is permitted.
- Patients with known actionable molecular alteration (EGFR activating mutation, ALK
rearrangement, ROS1 rearrangement) should have received a commercially available
specific inhibitor
- Patients must have an available archived tissue from a standard tumor biopsy for PD-L1
assessment, done before PD-1 ICI initiation.
- As of Week 1 Day 1, subjects with central nervous system (CNS) metastases must have
been treated and must be asymptomatic and meet the following:
1. No concurrent treatment, inclusive of but not limited to surgery, radiation,
and/or corticosteroids
2. At least 14 days after CNS treatment, clinically stable with no symptoms of CNS
metastasis or sequelae of radiation and at least 14 days since last dose of
corticosteroids NOTE: Subjects with clinical symptoms or cord compression or with
leptomeningeal disease are excluded from the study
- Adequate organ and bone marrow function as defined below:
1. Haemoglobin =10.0 g/dL (transfusion to achieve this level is not permitted within
2 weeks of first study drug administration)
2. Absolute neutrophil count (ANC) 1.5 x (> 1500 per mm3) (stable off any growth
factor within 4 weeks of first study drug administration)
3. Platelet count =100 x 109/L (>100,000 per mm3) (transfusion to achieve this level
is not permitted within 2 weeks of first study drug administration)
4. Serum bilirubin =1.5 x institutional upper limit of normal (ULN). This will not
apply to patients with confirmed Gilbert's syndrome (no upper limit for those
patients with persistent or recurrent hyperbilirubinemia that is predominantly
unconjugated in the absence of hemolysis or hepatic pathology, =3 x ULN for
patients with liver metastases), who will be allowed only in consultation with
their physician.
5. Normal thyroid function, subclinical hypothyroidism (TSH < 10 mIU/mL) or have
controlled thyroid disorder
6. AST (SGOT)/ALT (SGPT) =2.5 x institutional upper limit of normal unless liver
metastases are present, in which case it must be =5x ULN
7. Measured creatinine clearance (CL) >45 mL/min or Calculated creatinine CL>45
mL/min by the Cockcroft-Gault formula (Cockcroft and Gault 1976) or by 24-hour
urine collection for determination of creatinine clearance.
- Women must not be breastfeeding
Exclusion Criteria:
- Individuals deprived of liberty or placed under the authority of a tutor
- Patient unable to understand, read and/or sign an informed consent
- Absence of a measurable target lesion according to RECIST criteria 1.1
- Any symptomatic or untreated brain metastasis
- Any previous treatment with Docetaxel
- Prior randomisation or treatment with durvalumab AZD6738, Medi9447, Monalizumab
- Concurrent enrolment in another clinical study, unless it is an observational
(non-interventional) clinical study or during the follow-up period of an
interventional study
- Any previous treatment with a PD1 or PD-L1 inhibitor with the following events:
1. Must not have experienced a toxicity that led to permanent discontinuation of
prior immunotherapy.
2. All AEs while receiving prior immunotherapy must have completely resolved or
resolved to baseline prior to screening for this study.
3. Must not have experienced a =Grade 3 immune related AE or an immune related
neurologic or ocular AE of any grade while receiving prior immunotherapy.
4. Must not have required the use of additional immunosuppression other than
corticosteroids for the management of an AE, not have experienced recurrence of
an AE if re-challenged, and not currently require maintenance doses of > 10 mg
prednisone or equivalent per day
5. No systemic intervening treatment between progression on ICI and entry into this
study
- Last dose of immunotherapy =21 days prior to the first dose of study drug.
- The patient 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 5 days
prior to the study treatment.
- Current or prior use of steroids or other immunosuppressive medication within 28 days
before the first dose of durvalumab, with the exceptions of intranasal and inhaled
corticosteroids or systemic corticosteroids at physiological doses, which do not
exceed 10 mg/day of prednisone, or an equivalent corticosteroid. - Any unresolved
toxicity NCI CTCAE Grade =2 from previous anticancer therapy with the exception of
alopecia, vitiligo, and the laboratory values defined in the inclusion criteria
- Palliative radiotherapy (to a non target lesion) must have been completed at least 7
days before Cycle 1 Day 1 (with the exception of patients receiving radiation to more
than 30% of the bone marrow or with a wide field of radiation who must have completed
treatment within 28 days of the first dose of study treatment).
- Major surgical procedure (as defined by the Investigator) within 28 days prior to the
first dose of IMP : patients must have recovered from any effects of any major surgery
Note: Localsurgery and other procedures (radiotherapy) of isolated lesions for
palliative intent is acceptable.
- History of allogenic organ or stem cell transplantation.
- Active or prior documented autoimmune related inflammatory disorders treated with
systemic immunosuppressive drugs within the last 3 months or history of clinically
severe auto-immune disease (including inflammatory bowel disease [e.g., colitis or
Crohn's disease], diverticulitis [with the exception of diverticulosis], systemic
lupus erythematosus, Sarcoidosis syndrome, or Wegener syndrome [granulomatosis with
polyangiitis, Graves' disease, rheumatoid arthritis, hypophysitis, uveitis, etc]).
- Uncontrolled intercurrent illness, including but not limited to, ongoing or active
infection, symptomatic congestive 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 patient to give written
informed consent
- Any other malignancy which has been active or treated within the past three years,with
the exception of :
1. cervical intra-epithelial neoplasia,
2. non-melanoma skin cancer, or lentigo maligna without evidence of disease
3. ductal Carcinoma in Situ (DCIS),
4. stage 1 grade 1 endometrial carcinoma,
5. or other solid tumours curatively treated with no evidence of disease for = 5
years prior to study entry
- History of leptomeningeal carcinomatosis
- Mean QT interval corrected for heart rate using Fridericia's formula (QTcF) =470 ms
calculated from 3 ECGs (within 15 minutes at 5 minutes apart) For durvalumab in
combination with an agent with pro-arrhythmic potential or where effect of the
combination on QT is not known if this criterion should be retained. Patient safety
and the cardiac EKG should be consulted as needed.
- History of active primary immunodeficiency
- 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). Patients
with a past or resolved HBV infection (defined as the presence of hepatitis B core
antibody [anti-HBc] and absence of HBsAg) are eligible. Patients positive for
hepatitis C (HCV) antibody are eligible only if polymerase chain reaction is negative
for HCV RNA.
- Receipt of live attenuated vaccine within 30 days prior to the first dose of
Investigational Medicinal Product (IMP).
Note: Patients, if enrolled, should not receive live vaccine whilst receiving IP and up to
30 days after the last dose of IP.
- Female patients who are pregnant or breastfeeding or male or female patients of
reproductive potential who are not willing to employ effective birth control from
screening to 180 days after the last dose of durvalumab in combination with an other
agent.
- Known allergy or hypersensitivity to any of the study drugs or any of the study drug
excipients.
- Judgment by the investigator that the patient is unsuitable to participate in the
study and the patient is unlikely to comply with study procedures, restrictions and
requirements.
- A diagnosis of ataxia telangiectasia
- Refractory nausea and vomiting, chronic gastrointestinal diseases or previous
significant bowel resection, with clinically significant sequelae
- Patients receiving, 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 5 half-lives( minimum2 weeks), but
3 weeks for St. John's Wort). NOTE these include common azole antifungals, macrolide
antibiotics and other medications.
- Patient has had prescription or non-prescription drugs or other products known to be
CYP3A4 and/or CYP2B6 substrates or CYP3A4 and/or CYP2B6 substrates with a narrow
therapeutic index. Exposure of other drugs metabolised by CYP3A4 and/or CYP2B6 may be
reduced and additional monitoring may be required, see Appendix E.
- The use of herbal supplements or 'folk remedies' (and medications and foods that
significantly modulate CYP3A activity) should be discouraged. If deemed necessary,
such products may be administered with caution and the reason for use documented in
the CRF. Please see Appendix E, for further details.
- Patients with relative hypotension (<90/60 mmHg) or clinically relevant orthostatic
hypotension, including a fall in blood pressure of >20 mmHg at screening.
- Any of the following cardiac criteria currently or within the last 6 months (by New
York Heart Association (NYHA) = Class 2 where applicable)
1. Patients at risk of brain perfusion problems, e.g., medical history of carotid
stenosis or pre-syncopal or syncopal episodes, history of TIAs
2. Uncontrolled hypertension (grade 2 or above) requiring clinical intervention
3. Mean resting corrected QT interval (QTc) >470 msec for females and >450 for
men,obtained from 3 electrocardiograms (ECGs) 5-10 minutes apart using the
Fredericia formula
4. Conduction abnormality not controlled with pacemaker or medication e.g. complete
left bundle branch block, third degree heart block
5. Any factors that increase the risk of QTc prolongation or risk of arrhythmic
events such as hypokalaemia, congenital long QT syndrome, immediate family
history of long QT syndrome or unexplained sudden death under 40 years of age
6. Unstable angina pectoris or acute myocardial infarction
7. Congestive heart failure or known reduced LCEF < 55%
8. INR =1.5 or other evidence of impaired hepatic function.
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