| Eligibility |
Inclusion Criteria:
- For inclusion in the study, patients should fulfill the following criteria
- Histological diagnosis of NSCLC; for non-squamous NSCLC: no known sensitizing
EGFR-mutation, no known EML4-ALK translocation. When a patient with non-squamous
NSCLC has a KRAS mutation, further testing for EGFR and EML4-ALK is not
necessary. For squamous NSCLC, EGFR and EML4-ALK testing is not necessary.
- Availability of adequate in quality and quantity archived tumor material for IHC
PD-L1 testing; (Preferably 15 but 8 mandatory slides or block of tumor tissue
will be collected);
- Stage IIIB or IIIC not eligible for radical treatment or stage IV according to
TNM8 (Ref. 6);
- Brain metastases should be treated with local therapy (stereotactic radiotherapy
or whole brain radiotherapy), and patients should be asymptomatic, without
treatment with steroids for four weeks before enrollment. Before enrollment, new
brain imaging (contrast-CT or gadolinium-MRI) is needed to demonstrate that there
is no progression in the brain when the last brain imaging is more than four
weeks earlier. Screening for brain metastases is not necessary in patients that
were previously not diagnosed with brain metastases and that are without signs
indicative of brain metastases.
- = 18 years of age at time of study entry;
- WHO performance status 0 or 1; at enrollment
- Body weight > 30 kg at enrollment
- Evaluable disease with CT or MRI according to RECIST 1.1 (except for patients
with a CR after 4 cycles of platinum-based doublet chemotherapy, these patients
are also eligible);
- Stable disease or response by RECIST criteria response after 4 cycles of
platinum-based doublet chemotherapy;
- Adequate normal organ and marrow function:
- Absolute neutrophil count (ANC) = 1.5 x 109/L (> 1500 per mm3)
- Platelet count = 100 x 109/L (>100,000 per mm3)
- Serum bilirubin = 1.5 x institutional upper limit of normal (ULN). This will not
apply to subjects with confirmed Gilbert's syndrome (persistent or recurrent
hyperbilirubinemia that is predominantly unconjugated in the absence of hemolysis
or hepatic pathology)AST (SGOT)/ALT (SGPT) = 2.5 x institutional upper limit of
normal; for patients with liver metastases = 5 x institutional upper limit of
normal
- Measured or calculated creatinine clearance =45 mL/min by the Cockcroft-Gault
formula (Appendix E)
- Haemoglobin = 9.0 g/dL
- Patient with following autoimmune or inflammatory disorders are eligible:
- Vitiligo or alopecia
- Hypothyroidism (eg, following Hashimoto syndrome) stable on hormone replacement
- Any chronic skin condition that does not require systemic therapy
- Active disease in the last 5 years may be included but only after consultation
with the study investigator
- Celiac disease controlled by diet alone
- Patient with history of another primary malignancy are eligible in the following
cases:
- Malignancy treated with curative intent and with no known active disease =5 years
before the first dose of IP and of low potential risk for recurrence
- Adequately treated non-melanoma skin cancer or lentigo maligna without evidence
of disease
- Adequately treated carcinoma in situ without evidence of disease
- Women of child bearing potential (WOCBP) must have a negative serum pregnancy
test within 72 hours prior to the first dose of study treatment.
Note: women of childbearing potential are defined as premenopausal females capable of
becoming pregnant (i.e. females who have had any evidence of menses in the past 12 months,
with the exception of those who had prior hysterectomy). However, women who have been
amenorrheic for 12 or more months are still considered to be of childbearing potential if
the amenorrhea is possibly due to prior chemotherapy, antiestrogens, low body weight,
ovarian suppression or other reasons.
- Patients of childbearing / reproductive potential should use adequate birth control
measures, as defined by the investigator, during the study treatment period and from
screening to 90 days after the last dose of durvalumab monotherapy or 180 days after
the last dose of durvalumab + tremelimumab combination. A highly effective method of
birth control is defined as a method which results in a low failure rate (i.e. less
than 1% per year) when used consistently and correctly. Such methods include:
- Combined (estrogen and progestogen containing) hormonal contraception associated with
inhibition of ovulation (oral, intravaginal, transdermal)
- Progestogen-only hormonal contraception associated with inhibition of ovulation (oral,
injectable, implantable)
- Intrauterine device (IUD)
- Intrauterine hormone-releasing system (IUS)
- Bilateral tubal occlusion
- Vasectomized partner
- Sexual abstinence (the reliability of sexual abstinence needs to be evaluated in
relation to the duration of the clinical trial and the preferred and usual lifestyle
of the patient)
- Female subjects who are breast feeding should discontinue nursing prior to the first
dose of study treatment, from screening to 90 days after the last dose of durvalumab
monotherapy or 180 days after the last dose of durvalumab + tremelimumab combination
therapy or pemetrexed.
- Subject is willing and able to comply with the protocol for the duration of the study
including undergoing treatment and scheduled visits and examinations including follow
up;
- Before patient registration, written informed consent must be given according to
ICH/GCP, and national/local regulations.
Exclusion Criteria:
- Patients should not enter the study if any of the following exclusion criteria is
fulfilled
- Concurrent enrollment in another clinical study, unless it is an observational
(non-interventional) clinical study or the follow-up period of an interventional
study
- Mixed small-cell lung cancer and NSCLC histology, sarcomatoid variant or large
cell neuro-endocrine variant
- Patients with known history of leptomeningeal carcinomatosis
- 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
- Patients with Grade =2 neuropathy will be evaluated on a case-by-case basis after
consultation with the study investigator
- Patients with irreversible toxicity not reasonably expected to be exacerbated by
treatment with durvalumab or tremelimumab may be included only after consultation
with the study investigator
- Any previous treatment with a PD1 or PD-L1 inhibitor, including durvalumab, a
CTLA-4 including tremelimumab or other checkpoint inhibitors or other immune
therapy during the last 12 months
- Current or prior use of immunosuppressive medication within 14 days before the
first dose of durvalumab and tremelimumab, with the exceptions of intranasal and
inhaled corticosteroids or systemic corticosteroids at physiological doses, which
are not to exceed 10 mg/day of prednisone, or an equivalent corticosteroid, or
steroids as premedication for hypersensitivity reactions (eg, CT scan
premedication)
- Radiotherapy treatment to more than 30% of the bone marrow or with a wide field
of radiation within 4 weeks of the first dose of study drug. Note: Local
treatment of isolated lesions, excluding target lesions, for palliative intent is
acceptable when it is not within 7 days of the first dose of study drug.
- Major surgical procedure (as defined by the study investigator) within 28 days
prior to the first dose of IP. Note: Local surgery of isolated lesions for
palliative intent is acceptable
- History of allogenic organ transplantation
- Receipt of live attenuated vaccination within 30 days prior to enrollement
- Active or prior documented autoimmune or inflammatory disorders (including
inflammatory bowel disease [eg, colitis or Crohn's disease], diverticulitis [with
the exception of diverticulosis], systemic lupus erythematosus, Sarcoidosis
syndrome, or Wegener syndrome [granulomatosis with polyangitis, Graves' disease,
rheumatoid arthritis, hypophysitis, uveitis, etc]).
- History of hypersensitivity to durvalumab, tremelimumab or any excipient
- Uncontrolled intercurrent illness including, but not limited to:
- 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.
- Symptomatic congestive heart failure, uncontrolled hypertension (defined as blood
pressure above 160/90 mm Hg despite medication), unstable angina pectoris,
cardiac arrhythmia
- Active peptic ulcer disease or gastritis
- Liver cirrhosis CHILD B+, C (Appendix J)
- Active bleeding diatheses
- History of primary immunodeficiency
- Mean QT interval corrected for heart rate (QTc) =470 ms calculated from 3
electrocardiograms (ECGs) using Frediricia's Correction
- Female patients who are pregnant or male or female patients of reproductive
potential who are not willing to employ effective birth control from screening to
90 days after the last dose of durvalumab monotherapy or 180 days after the last
dose of durvalumab + tremelimumab combination therapy or pemetrexed.
- Any psychological, familial, sociological or geographical condition potentially
hampering compliance with the study protocol and follow-up schedule; those
conditions should be discussed with the patient before registration in the trial
- History of another primary malignancy
- For non-squamous: unable to interrupt aspirin or other nonsteroidal
anti-inflammatory agents, other than an aspirin dose <1.3 grams per day, for a
5-day period (8-day period for long-acting agents, such as piroxicam). Unable or
unwilling to take folic acid, vitamin B12 supplementation.
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