Study of Sorafenib Maintenance in Patients With ED-SCLC After Response to Induction Chemotherapy
- Registration Number
- NCT01159327
- Lead Sponsor
- National Cancer Center, Korea
- Brief Summary
A Phase I trial of weekly topotecan in combination with sorafenib in treatment of relapsed Small cell lung cancer (SCLC) has been commenced. In the present randomized phase 2 study, the investigators will research whether Sorafenib maintenance prolongs progression free survival (PFS) and overall survival (OS) in patients with ED-SCLC who achieved CR or PR after platinum-based induction chemotherapy.
- Detailed Description
Small cell lung cancer (SCLC) comprises 10-15 % of all lung cancer. Despite high responsiveness to initial chemotherapy, its high relapse rate makes the treatment of SCLC is challenging. With platinum plus etoposide or irinotecan, overall response rate is as high as 85%, however, the median duration of response is short (approximately 4 months), and median survival times are 9 to 11 months, with a 2-year survival rate of less than 10% \[J Clin oncology. 2009 Oct 1;27(28):4787-92\]. New and more effective agents are clearly needed against SCLC. Sorafenib is a multikinase inhibitors acting on pathways involved in tumour progression and angiogenesis, and is undergoing investigation for the treatment of SCLC in either the first- or second-line setting. The only data available so far are on sorafenib, which seems to be a promising agent with a median survival of 7 and 5 months in platinum-sensitive and platinum-refractory patients, respectively (2008 J Clin oncology 26. Abstract 8039). This compared favourably with historical controls receiving salvage chemotherapy.
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 13
Not provided
- History of cardiac disease/ HIV infection / chronic hepatitis B or C / of organ allograft
- Active clinically serious infections
- Patients with seizure disorder requiring medication or evidence or history of bleeding diathesis or coagulopathy
- Patients undergoing renal dialysis
- Pulmonary hemorrhage/ bleeding event ≥ CTCAE grade 2 within four weeks
- Any other hemorrhage/ bleeding event ≥ CTCAE grade 3 within four weeks
- Non-healing wound, ulcer or bone fracture
- Thrombotic or embolic venous or arterial events of study drug
- Previous or concurrent cancer that is distinct in histology of primary site, EXCEPT cervical carcinoma in situ, treated basal cell carcinoma, superficial bladder tumors (Ta, Tis, T1). Any cancer curatively treated >3 years prior to entry is permitted.
- Substance abuse, medical, psychological or social conditions that may interfere with the subject's participation in the study or evaluation of the study results
- Known or suspected allergy or any other contraindication for Sorafenib administration
- Pregnant or breast-feeding women.
- Any disease which could affect the evaluation of the study drug
- Any condition that is unstable or could jeopardize the safety of the subject and their compliance in the study
- Any condition which could affect the absorption or pharmacokinetics of the Study drug including any type of gastrointestinal resection or surgery
- Uncontrolled symptomatic brain metastasis
Excluded therapies and medications, previous and concomitant:
- Investigational drug or device therapy including outside of this trial during or within 4 weeks prior to study entry (signing Informed Consent).
- The toxicity effects of previous antitumor chemotherapy or immunotherapy must be resolved to less than CTC Grade 2 level (exception: alopecia).
- Prior treatment with other VEGFR inhibitors (i.e. sunitinib, thalidomide, vandetanib and other experimental agents of this class).
- Major surgery within 4 weeks prior to start of study (Informed Consent signature). Minimal invasive biopsy is allowed.
- Use of biologic response modifiers, such as G-CSF, within 3 weeks prior to study entry. [Therapeutic G-CSF and other hematopoietic growth factors may be used in the management of acute toxicity such as febrile neutropenia when clinically indicated or at the discretion of the investigator, however they may not be substituted for a required dose reduction].
- Any agents which could affect the absorption or pharmacokinetics of the study drug
- Prior exposure to the study drug
- Therapeutic anticoagulation with vitamin K antagonists such as warfarin, or with heparins or heparinoids. Prophylactic low dose warfarin (1 mg po qd) is permitted if the INR (International normalized ratio) is ≤ 1.5. Low-dose aspirin is permitted (80-100 mg daily).
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Arm A Sorafenib Sorafenib maintenance arm
- Primary Outcome Measures
Name Time Method Progression-free survival every 8 weeks Progression-free survival was calculated from the randomization date until evidence of PD or death
- Secondary Outcome Measures
Name Time Method Overall survival the date of registration to the date of death The duration of overall survival is measured from randomization date to the date of death from any cause or the last follow-up examination
Toxicity First drug intake until 30 days after last treatment admisitration For grading of adverse events CTCAE criteria (version 4.0) will be utilized. All adverse events occurring between first drug intake until 30 days after last treatment administration will be reported.
Trial Locations
- Locations (1)
National Cancer Center, Korea
🇰🇷Goyang-si, Gyeonggi-do, Korea, Republic of