Study of Nintedanib Plus Bevacizumab in Advanced Solid Tumors

Inclusion Criteria:

Age >18
Histologically proven advanced or metastatic solid cancer for which Bevacizumab has an indication: renal cell carcinoma, colorectal adenocarcinoma, non-squamous non-small cell lung cancer, platinum- refractory ovarian carcinoma, cervical carcinoma.
Life expectancy at least 3 months
ECOG performance status score 0-1
Progression after at least first-line systemic therapy for metastatic disease
At least one measurable lesion according to RECIST criteria or any other baseline prerequisite for the assessment of the principal judgement criteria.
Signed and dated written informed consent prior to admission to the study
Resolution of all acute adverse events resulting from prior cancer therapies to NCI CTCAE grade less than/equal to 1 or baseline (except alopecia)

Adequate organ function as defined by the following criteria

AST/ALT ≤ 2.5x upper limit of normal (ULN) in the case of liver metastases or AST/ALT ≤ 1.5 x ULN in patients without liver metastases
total serum bilirubin within normal limits regardless of liver metastases
absolute neutrophil count (ANC) > 1500
Platelets > 100k without transfusion support in the past 28 days
Hemoglobin > 9.0 without transfusion support in the past 28 days
Serum creatinine < 1.5x ULN
Prothrombin time/INR and partial thromboplastin time within normal limits
Urinalysis ≤ 1+ protein
Willingness and ability to comply with scheduled visits, treatment plan, laboratory tests, and other study procedures

Exclusion Criteria:

Previous therapy with Bevacizumab is allowed, but patient who experienced serious dose-limiting toxicities while on prior Bevacizumab therapy are excluded
Prior treatment with Nintedanib (BIBF1120). Known hypersensitivity to Nintedanib, peanut or soya or any other trial drug, their excipients or to contrast media
Chemo-, hormone-, radio-(except for brain and extremities) or immunotherapy or therapy with monoclonal antibodies or small tyrosine kinase inhibitors within the past 4 weeks prior to treatment with the trial drug.
Radiotherapy to the target lesion within the past 3 months prior to baseline imaging
Persistence of clinically relevant therapy related toxicity from previous chemo and/or radiotherapy
History of brain involvement with cancer, spinal cord compression, carcinomatous meningitis, or new evidence of brain or leptomeningeal disease. Patients with irradiated or resected brain lesions are permitted provided the lesions are fully treated and inactive, patients are asymptomatic, and no steroids have been used for at least 28 days.
Leptomeningeal disease
Centrally located tumours with radiographic evidence of local invasion of major blood vessels
Treatment with other investigational drugs or treatment in another clinical trial within the past 4 weeks before start of therapy or concomitantly with the trial
Therapeutic anticoagulation (except low-dose heparin and/or heparin flush as needed for maintenance of an in-dwelling intravenous devise) or anti-platelet therapy (except for low-dose therapy with acetylsalicylic acid <325mg per day.
Major injuries and/or surgery within the past 4 weeks prior to start of study treatment with incomplete wound healing and/or planned surgery during the on-treatment study period.
History of clinically significant hemorrhagic or thromboembolic event in the past 6 months.
Known inherited predisposition to bleeding or thrombosis
Significant cardiovascular diseases (i.e. uncontrolled hypertension, unstable angina, history of infarction within the past 6 months prior to start of study treatment, congestive heart failure >New York Heart Association II, serious cardiac arrhythmia, pericardial effusion)
Proteinuria CTCAE grade 2 or greater
Creatinine >1.5 ULN or GFR <45 ml/min
Hepatic function: total bilirubin outside of normal limits; ALT or AST >2.5 ULN in pts without liver metastasis. For patients with liver metastasis: total bilirubin outside of normal limits, ALT or AST >5 x ULN
Coagulation parameters: International normalized ratio (INR) >2, prothrombin time (PT) and partial thromboplastin time (PTT) >50% of deviation of institutional ULN
Absolute neutrophil count (ANC) <1500/ml, platelets <100,000/ml, Hemoglobin <9.0 g/dl
Other malignancies within the past 5 years other than basal cell skin cancer or carcinoma in situ of the cervix
Active serious infections in particular if requiring systemic antibiotic or antimicrobial therapy
Active or chronic hepatitis C and/or B infection
Gastrointestinal disorders or abnormalities that would interfere with absorption of the study drug
Serious illness or concomitant non-oncological disease such as neurologic, psychiatric, infectious disease or active ulcers (gastro-intestinal tract, skin) or laboratory abnormality that may increase the risk associated with study participation or study drug administration and in the judgment of the investigator would make the patient inappropriate for entry into the study.
Patients who are sexually active and unwilling to use a medically acceptable method of contraception (e.g. such as implants, injectables, combined oral contraceptives, some intrauterine devices or vasectomized partner for participating females, condoms for participating males) during the trial and for at least three months after end of active therapy.
Pregnancy or breast feeding. Female patients must have a negative pregnancy test (β-HCG test in urine or serum) prior to commencing study treatment and must agree with the use of effective contraception during the study and for three months following last dose of Nintedanib.
Psychological, familial, sociological or geographical factors potentially hampering compliance with the study protocol and follow-up schedule
Active alcohol or drug abuse
Minor surgical procedures such as Mediport placement or core biopsies within 7 days of study treatment
Stroke, transient ischemic attack, arterial embolism, percutaneous transluminal coronary angioplasty (PTCA), or coronary artery bypass grafting (CABG) within the past 6 months
History of pulmonary hemorrhage or hemoptysis within 6 months of starting study treatment
Open wounds or unhealed fractures within 28 days of starting study treatment
Known HIV or AIDS related illness