- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT01159327
Study of Sorafenib Maintenance in Patients With ED-SCLC After Response to Induction Chemotherapy
9 novembre 2015 aggiornato da: Ji-youn Han, National Cancer Center, Korea
A Randomized Phase II Study of Sorafenib Maintenance in Patients With Extensive Disease Small Cell Lung Cancer (ED-SCLC) After Response to Induction Chemotherapy
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.
Panoramica dello studio
Stato
Terminato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
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.
Tipo di studio
Interventistico
Iscrizione (Effettivo)
13
Fase
- Fase 2
Contatti e Sedi
Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.
Luoghi di studio
-
-
Gyeonggi-do
-
Goyang-si, Gyeonggi-do, Corea, Repubblica di
- National Cancer Center, Korea
-
-
Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
1 anno e precedenti (Bambino, Adulto, Adulto più anziano)
Accetta volontari sani
No
Sessi ammissibili allo studio
Tutto
Descrizione
Inclusion criteria:
- Histologically or cytologically confirmed ED-SCLC patients who have achieved a complete or partial response after four to six cycles of platinum based induction chemotherapy.
- Extensive stage SCLC is defined as disease not meaning the definition of limited stage disease
- Previous radiotherapy is allowed only if < 30% of marrow bearing bones were irradiated and if radiotherapy was completed at least 2 weeks prior to enrollment and the patient has recovered from all adverse effects of prior radiotherapy.
- Age >18 years.
- Written informed consent that is consistent with ICH-GCP guidelines
- Life expectancy of greater than 3 months.
- ECOG performance status 2 (Karnofsky ≥50%).
- Ability to swallow oral medication
- Women of childbearing potential must have a negative serum pregnancy test performed within 7 days prior to the start of treatment
- Both men and women enrolled in this trial must use adequate barrier birth control measures during the course of the trial and during the first 3 months after the completion of trial
- Adequate bone marrow, liver and renal function
Exclusion Criteria:
- 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).
Piano di studio
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: Arm A
Sorafenib maintenance arm
|
Sorafenib 400mg, bid(800mg/day), daily, PO
Altri nomi:
|
|
Nessun intervento: Arm B
observation arm
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Progression-free survival
Lasso di tempo: every 8 weeks
|
Progression-free survival was calculated from the randomization date until evidence of PD or death
|
every 8 weeks
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Overall survival
Lasso di tempo: 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
|
the date of registration to the date of death
|
|
Toxicity
Lasso di tempo: 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.
|
First drug intake until 30 days after last treatment admisitration
|
Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Sponsor
Collaboratori
Investigatori
- Investigatore principale: JI-YOUN HAN, PhD.MD, National Cancer Center
Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio
1 dicembre 2010
Completamento primario (Effettivo)
1 aprile 2013
Completamento dello studio (Effettivo)
1 giugno 2013
Date di iscrizione allo studio
Primo inviato
8 luglio 2010
Primo inviato che soddisfa i criteri di controllo qualità
8 luglio 2010
Primo Inserito (Stima)
9 luglio 2010
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Stima)
11 novembre 2015
Ultimo aggiornamento inviato che soddisfa i criteri QC
9 novembre 2015
Ultimo verificato
1 novembre 2015
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
- Malattie delle vie respiratorie
- Neoplasie
- Malattie polmonari
- Neoplasie per sede
- Neoplasie delle vie respiratorie
- Neoplasie toraciche
- Carcinoma, broncogeno
- Neoplasie bronchiali
- Neoplasie polmonari
- Carcinoma polmonare a piccole cellule
- Meccanismi molecolari dell'azione farmacologica
- Inibitori enzimatici
- Agenti antineoplastici
- Inibitori della chinasi proteica
- Sorafenib
Altri numeri di identificazione dello studio
- NCCCTS-10-476
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .