LBH Phase II in Small Cell Lung Cancer (SCLC)

This is an interventional treatment trial for Small Cell Lung Carcinoma focused on measuring LBH581, Panobinostat, Small Cell Lung Carcinoma Read More

Inclusion Criteria:

1. Histological/cytological diagnosis of SCLC, mixed small and non small cell tumours are excluded
2. ≤ 2 prior chemotherapy lines
3. Progression after, and not during, last previous chemotherapy treatment
4. Age ≥ 18 and ≤ 75 years
5. Life expectancy of at least 3 months
6. ECOG Performance Status 0-1
7. At least one measurable lesion according to modified RECIST criteria defined as ≥ 1 lesion with longest diameter ≥ 20 mm by conventional techniques or ≥ 10 mm with spiral CT scan. In case of solitary measurable lesion, histological confirmation is not required.

8. Adequate haematological function:

   • haemoglobin ≥ 9 g/dl
   • platelet count ≥ 100,000/mm3
   • neutrophils count ≥ 1,500/mm3

9. Adequate liver and renal functions:

   • Total serum bilirubin ≤ 1.5 x UNL
   • Serum creatinine ≤ 1.5 x UNL or 24 hours creatinine clearance ≥ 50 mL/min
   • AST and ALT ≤ 2.5 x UNL or ≤ 5.0 x UNL if the transaminase elevation is due to hepatic involvement
   • Albumin ≥ 2.5 g/dl
   • Alkaline phosphatase ≤ 2.5 x UNL
10. Fertile patients must use effective contraception during and for ≥ 6 weeks after completion of study therapy
11. Ability to signed informed consent

Exclusion Criteria:

1. Progression while on previous chemotherapy
2. Other chemotherapy treatment < 4 weeks prior to enrolment
3. Presence of active infection
4. A known history of HIV positivity
5. Participation to any investigational drug study < 4 weeks preceding study enrolment
6. Radiotherapy involving > 30% of the active bone marrow
7. Thoracic and brain radiotherapy < 4 weeks prior to enrolment. Palliative radiotherapy is allowed during study treatment
8. Presence of any serious neurological or psychiatric disorder

9. Impaired cardiac function, including any one of the following:

   • Complete Left Bundle Branch Block or obligate use of a cardiac pacemaker or congenital long QT syndrome or history or presence of atrial or ventricular tachyarrhythmias or clinically significant resting bradycardia (< 50 beats per minute) or QTcF > 480 msec on screening ECG or Right Bundle Branch block + left anterior hemiblock (biphasic block)
   • Acute MI ≤ 3 months prior to starting study drug
   • Other clinically significant heart disease (e.g. congestive heart failure, previous history angina pectoris, uncontrolled hypertension, history of labile hypertension or arrhythmia, or history of poor compliance with an antihypertensive regimen)
   • Any other case of current abnormal cardiac functionality or history of cardiac disease causing LVEF < 45% as determined by ECHO
10. Known hypersensitivity/allergic reaction to the study product
11. Presence of uncontrolled intercurrent illness or any condition which in the judgement of the investigator would place the subject at undue risk or interfere with the results of the study.
12. Previous or current concomitant malignancy at other site, other than basal or squamous cell carcinoma of the skin and carcinoma in situ of the uterine cervix, within 3 years.
13. Symptomatic or progressive brain metastases
14. Patients with an active bleeding diathesis or on anticoagulants Therapeutic doses of sodium warfarin (Coumadin) are not allowed. Low doses of Coumadin (e.g., ≤ 2 mg/day) for line patency are allowed
15. Pregnant or lactating women
16. Concomitant use of CYP3A4/5 inhibitors or inducers, or drug that prolong the QT interval and/or induce torsades ventricular arrythmia, where the treatment can not be discontinued or switched to a different medication prior to starting study drug.
17. Treatment with any hematopoietic colony-stimulating growth factors (e.g., G-CSF, GMCSF) ≤ 2 weeks prior to starting study drug.
18. Unable or unwilling to comply with all study procedures