E.1 Medical condition or disease under investigation |
E.1.1 | Medical condition(s) being investigated |
Stage IB (T ≥ 4 cm), II and IIIA NSCLC |
|
E.1.1.1 | Medical condition in easily understood language |
Early stage non small cell lung cancer after resection |
|
E.1.1.2 | Therapeutic area | Diseases [C] - Cancer [C04] |
MedDRA Classification |
E.1.2 Medical condition or disease under investigation |
E.1.2 | Version | 19.1 |
E.1.2 | Level | PT |
E.1.2 | Classification code | 10061873 |
E.1.2 | Term | Non-small cell lung cancer |
E.1.2 | System Organ Class | 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps) |
|
E.1.3 | Condition being studied is a rare disease | No |
E.2 Objective of the trial |
E.2.1 | Main objective of the trial |
To prospectively investigate whether adjuvant treatment with pembrolizumab after completion of radical surgery (lobectomy/pneumonectomy) with or without standard adjuvant chemotherapy for stage IB (T ≥ 4 cm) -II-IIIA NSCLC patients improves Disease Free Survival (DFS), as assessed locally by the investigator, compared to placebo in the PD-L1 strong positive subgroup and overall population. |
|
E.2.2 | Secondary objectives of the trial |
- To prospectively compare DFS as assessed by the investigator in the PD-L1 positive population; - To prospectively determine and compare OS in the PD-L1 strong positive and overall population; - To prospectively determine and compare OS in the PD-L1 positive population; - To prospectively determine and compare the Lung Cancer Specific Survival (LCSS) in the whole population irrespective of PD-L1 status; - To prospectively assess the safety of pembrolizumab after radical surgery followed by standard adjuvant chemotherapy.
|
|
E.2.3 | Trial contains a sub-study | No |
E.3 | Principal inclusion criteria |
- Pathological diagnosis of NSCLC confirmed at surgery, any histology is eligible; - Confirmed UICC v7 stage IB with T ≥ 4 cm, II-IIIA NSCLC after complete surgical resection (lobectomy, sleeve lobectomy, bi-lobectomy or pneumonectomy) as documented in the pathology report; - Resection margins proved microscopically free (R0); Resection margins should be considered to be the bronchial, venous and arterial stumps, peribronchial soft tissue, any peripheral margin near the tumor or of additionally resected tissue; - A systematic nodal dissection is recommended or at least a lobespecific systematic nodal dissection. However, the intraoperative lymph node evaluation can be accepted if no lymph nodes are found in those area and there is clear documentation in the operative report by the surgeon of exploration of the required lymph node areas. At minimum, the pathology and/or operative report should include the examination of at least two different mediastinal nodal (N2) station with one being subcarinal (level 7); - No extracapsular nodal extension of the tumor; - The highest mediastinal node removed can be positive - Carcinoma in situ can be present at bronchial margin - Availability of tumor sample obtained at surgical resection for PD-L1 Immunohistochemistry (IHC) expression assessment. - At least 18 years; - Written informed consent must be given according to ICH/GCP, and national/local regulations; - Adjuvant chemotherapy is not mandatory but considered for patients with stage IB (T ≥ 4 cm) and strongly recommended for stage II and IIIA, and will be administered according to national and local guidelines. Patients who received more than 4 cycles of adjuvant therapy are not eligible; - ECOG Performance status 0-1; - Adequate organ function performed within 10 days of treatment initiation; - Female patients with childbearing potential must have a negative urine or serum pregnancy test at screening (within 72 hours of first dose of study medication) - If of childbearing potential, female patients must be willing to use two adequate barrier methods throughout the study, starting with the screening visit up to 120 days after last dose of chemotherapeutic and investigational agents as specified in the protocol; - Male patients with a female partner(s) of child-bearing potential must agree to use two adequate barrier methods throughout the trial starting with the screening visit through 120 days after the last dose of study treatment is received. Males with pregnant partners must agree to use a condom; no additional method of contraception is required for the pregnant partner. - Female patients who are breast feeding should discontinue nursing prior to the first dose of study treatment and until 120 days after the last study treatment; - Absence of severe comorbidities that in the opinion of the Investigator might hamper the participation to the study and/or the treatment administration |
|
E.4 | Principal exclusion criteria |
- Evidence of disease at clinical examination and/or baseline radiological assessment on baseline assessment as documented by contrast enhanced chest/upper abdomen CT scan, brain CT/MRI and clinical examination within 8 weeks prior to the randomization date; - Prior or foreseen neoadjuvant or adjuvant radiotherapy and/or neoadjuvant chemotherapy; - Prior treatment with an anti-PD-1, anti-PD-L1/2, anti- CD137, CTLA-4 modulators; patients receiving live vaccine within 30 days prior to the first dose of study treatment are not eligible; - Current participation in a interventional clinical trial or treatment with an investigational agent or use of an investigational device within 4 weeks of the first dose of study treatment; - Known history of Human Immunodeficiency Virus (HIV) (known HIV 1/2 antibodies positive). Known active Hepatitis B or C. Active Hepatitis B is defined as a known positive HBsAg results. Active Hepatitis C is defined by a known positive Hep C Ab result and known quantitative HCV RNA results greater than the lower limits of detection of the assay; - Chronic use of immunosuppressive agents and/or systemic corticosteroids or any use in the last 3 days prior to the first dose of trial treatment; - History of interstitial lung disease (ILD) OR a history of (noninfectious) pneumonitis that required oral or IV steroids (other than COPD exacerbation) or current pneumonitis; - Active autoimmune disease that has required systemic treatment in past 2 years (i.e. with use of disease modifying agents, corticosteroids or immunosuppressive drugs). Any replacement therapy (i.e., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a form of systemic treatment and is allowed. Patients with hyperthyroidism or hypothyroidism but that are stable on hormone replacement are also allowed - History of a hematologic or primary solid tumor malignancy, unless in remission for at least 5 years. A pT1-2 prostatic cancer Gleason score <6, superficial bladder cancer, non melanomatous skin cancer or carcinoma in situ of the cervix is eligible; - Previous allogeneic tissue/solid organ transplant; - Active infection requiring therapy; - Surgery or chemotherapy related toxicity (toxicity resolved to grade 1 (see Appendix D), with the exception of alopecia, fatigue, neuropathy and lack of appetite /nausea) |
|
E.5 End points |
E.5.1 | Primary end point(s) |
1. DFS in the PD-L1 strong positive sub-group; 2. DFS in the overall population (co-primary endpoint).
|
|
E.5.1.1 | Timepoint(s) of evaluation of this end point |
1. Every 12 weeks (± 2 weeks) during the 1st year after randomization, every 6 months for the 2nd and 3rd year, yearly up to the end of the 5th year 2. Every 12 weeks (± 2 weeks) during the 1st year after randomization, every 6 months for the 2nd and 3rd year, yearly up to the end of the 5th year
|
|
E.5.2 | Secondary end point(s) |
1. DFS in the PD-L1 positive population; 2. OS in the overall population; 3. OS in the PD-L1 strong positive subgroup; 4. OS in the PD-L1 positive population; 5. LCSS in the overall population; 6. Toxicity according to CTCAE version 4.0.
|
|
E.5.2.1 | Timepoint(s) of evaluation of this end point |
1. Every 12 weeks (± 2 weeks) during the 1st year after randomization, every 6 months for the 2nd and 3rd year, yearly up to the end of the 5th year 2. OS will be measured from the date of randomization until the date of death. 3. OS will be measured from the date of randomization until the date of death. 4. OS will be measured from the date of randomization until the date of death. 5. LCSS will be measured from the date of randomization until the date of death (due to lung cancer specifically) 6. Every 3 weeks during treatment and at 12 weeks after the last treatment |
|
E.6 and E.7 Scope of the trial |
E.6 | Scope of the trial |
E.6.1 | Diagnosis | No |
E.6.2 | Prophylaxis | No |
E.6.3 | Therapy | No |
E.6.4 | Safety | Yes |
E.6.5 | Efficacy | Yes |
E.6.6 | Pharmacokinetic | Yes |
E.6.7 | Pharmacodynamic | Yes |
E.6.8 | Bioequivalence | No |
E.6.9 | Dose response | No |
E.6.10 | Pharmacogenetic | No |
E.6.11 | Pharmacogenomic | Yes |
E.6.12 | Pharmacoeconomic | Yes |
E.6.13 | Others | No |
E.7 | Trial type and phase |
E.7.1 | Human pharmacology (Phase I) | No |
E.7.1.1 | First administration to humans | No |
E.7.1.2 | Bioequivalence study | No |
E.7.1.3 | Other | No |
E.7.1.3.1 | Other trial type description | |
E.7.2 | Therapeutic exploratory (Phase II) | No |
E.7.3 | Therapeutic confirmatory (Phase III) | Yes |
E.7.4 | Therapeutic use (Phase IV) | No |
E.8 Design of the trial |
E.8.1 | Controlled | Yes |
E.8.1.1 | Randomised | Yes |
E.8.1.2 | Open | No |
E.8.1.3 | Single blind | No |
E.8.1.4 | Double blind | Yes |
E.8.1.5 | Parallel group | Yes |
E.8.1.6 | Cross over | No |
E.8.1.7 | Other | No |
E.8.2 | Comparator of controlled trial |
E.8.2.1 | Other medicinal product(s) | No |
E.8.2.2 | Placebo | Yes |
E.8.2.3 | Other | No |
E.8.2.4 | Number of treatment arms in the trial | 2 |
E.8.3 |
The trial involves single site in the Member State concerned
| No |
E.8.4 | The trial involves multiple sites in the Member State concerned | Yes |
E.8.4.1 | Number of sites anticipated in Member State concerned | 7 |
E.8.5 | The trial involves multiple Member States | Yes |
E.8.5.1 | Number of sites anticipated in the EEA | 100 |
E.8.6 Trial involving sites outside the EEA |
E.8.6.1 | Trial being conducted both within and outside the EEA | Yes |
E.8.6.2 | Trial being conducted completely outside of the EEA | No |
E.8.6.3 | If E.8.6.1 or E.8.6.2 are Yes, specify the regions in which trial sites are planned |
Australia |
Austria |
Belgium |
Canada |
Czech Republic |
Denmark |
Estonia |
France |
Germany |
Greece |
Hungary |
Ireland |
Israel |
Italy |
Japan |
Korea, Republic of |
Latvia |
Netherlands |
Poland |
Portugal |
Russian Federation |
Slovenia |
Spain |
Sweden |
Switzerland |
Turkey |
United Kingdom |
|
E.8.7 | Trial has a data monitoring committee | Yes |
E.8.8 |
Definition of the end of the trial and justification where it is not the last
visit of the last subject undergoing the trial
|
End of study occurs when all of the following criteria have been satisfied: 1. The trial is mature for the analysis of the primary/co-primary endpoints as defined in the protocol 2. The database has been fully cleaned and frozen for this analysis
|
|
E.8.9 Initial estimate of the duration of the trial |
E.8.9.1 | In the Member State concerned years | 7 |
E.8.9.1 | In the Member State concerned months | 1 |
E.8.9.1 | In the Member State concerned days | 15 |
E.8.9.2 | In all countries concerned by the trial years | 8 |
E.8.9.2 | In all countries concerned by the trial months | 4 |
E.8.9.2 | In all countries concerned by the trial days | 0 |