Cediranib as Palliative Treatment in Patients With Symptomatic Malignant Ascites or Pleural Effusion

• Status: Terminated
• Trial end date: 1969-12-31
• Target enrollment: 0
• Participant gender: All

Summary

In some patients with cancer there are also cancer cells in the abdominal cavity or between the lung membranes. These cancer cells create too much moisture in the abdominal cavity or between the lung membranes. If there is fluid in the abdominal cavity (ascites fluid) this can bring on abdominal distension, abdominal pain, loss of appetite, fatigue, bloating and sometimes wheezing. Too much fluid between the lung membranes (we call this pleural fluid) gives breathlessness, chest pain and coughing. The use of diuretics may offer a small group of patients symptom reduction. Additionally, the fluid can be drained through a needle puncture or fluid collection (through a biopsy). But usually, the moisture quickly returns.

Previous research done in this hospital with cediranib showed that with some patients with cancer who suffered from fluid in the abdominal cavity or between the lung membranes, this moisture reduces while using this drug. It also reduced the symptoms caused by this excessive moisture.

The current study is conducted to see whether patients with cancer and fluid in the abdominal cavity or fluid between the lung blades benefit from using cediranib. This involves not only whether the amount moisture reduces, but also if the complains decrease. In addition, we will carefully consider the possible side effects of cediranib.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Radboud University
• Treatments: Cediranib

Criteria

Inclusion Criteria:

• Symptomatic malignant ascites and/or pleural effusion (from a histological proven solid malignancy which is refractory to standard anti-tumour therapy of for which no standard therapy exists)

• Karnofsky score ≥ 50 if the low performance score is due to ascites and/or pleural effusion, otherwise ≥ 60

• Age ≥ 18 years

• Written informed consent

Exclusion Criteria:

Contraindications for treatment with cediranib:

• The presence of a pleural or peritoneal tap

• Untreated unstable brain or meningeal metastases.

• Previous treatment with chemotherapeutic agents or tyrosine kinase inhibitors (TKIs) within 14 days prior to the first dose of cediranib, with cetuximab within 30 days prior to the first dose of cediranib, or with bevacizumab within 60 days prior to the first dose of cediranib

• Inadequate bone marrow reserve as demonstrated by an absolute neutrophil count ≤1.5 x 109/L or platelet count ≤100 x 109/L

• Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) ≥ 2,5 x ULN

• Serum creatinine > 1.5 x ULRR or a creatinine clearance of ≤ 50mL/min calculated by Cockcroft-Gault

• Greater than +1 proteinuria on two consecutive dipsticks taken no less than 1 week apart unless urinary protein < 1.5g in a 24 hr period

• Prothrombin time (PT) and activated partial thromboplastin time (APTT) > 2 x ULN History of significant gastrointestinal impairment, as judged by the Investigator, that would significantly affect the absorption of cediranib, including the ability to swallow the tablet whole. Patients with an ileostoma.

• Patients with a history of poorly controlled hypertension with resting blood pressure >150/100 in the presence or absence of a stable regimen of anti-hypertensive therapy. Patients who are currently receiving maximal doses of calcium channel blockers or more than 1 antihypertensive for the treatment of hypertension are also ineligible.

• Any evidence of severe or uncontrolled diseases e.g., unstable or uncompensated respiratory, cardiac, hepatic or renal disease.

• Unresolved toxicity > CTC grade 1 from previous anti-cancer therapy (including radiotherapy) except alopecia (if applicable) or polyneuropathy.

• Mean QTc with Bazetts correction >470msec in screening ECG or history of familial long QT syndrome

• Significant haemorrhage (>30mL bleeding/episode in previous 3 months) or haemoptysis (>5mL fresh blood in previous 4 weeks)

• Recent (<14 days) major surgery prior to entry into the study, or a surgical incision that is not fully healed

• Pregnant or breast-feeding women or women of childbearing potential with a positive pregnancy test prior to receiving study medication

• Known risk of the patient transmitting HIV, hepatitis B or C via infected blood

• Treatment with an investigational (non-registered) drug within 30 days prior to the first dose of cediranib

• Other concomitant anti-cancer therapy (including LHRH agonists) except steroids

• Concomitant use of any medication that may significantly affect hepatic cytochrome P450 drug metabolising activity by way of enzyme induction (e.g., phenytoin) or inhibition (e.g., ketoconazole, ritonavir, erythromycin) within 2 weeks if the first dose of cediranib and throughout the study period

• Patients being treated with anticoagulants (with the exception of low molecular weight heparin).

• Patients previously treated with anthracyclines (total of > 550 mg/m2 doxorubicine) and an ejection fraction on the MUGA scan below 40%