- ICH GCP
- Registr klinických studií v USA
- Klinická studie NCT01732640
A Phase I/II Study Afatinib/Carboplatin/Paclitaxel Induction Chemotherapy In HPV-Negative HNSCC.
A Phase I/II Study Afatinib/Carboplatin/Paclitaxel Induction Chemotherapy Followed By Standard Chemoradiation In HPV-Negative or High-risk HPV-Positive Locally Advanced Stage III/IVa/IVb HNSCC
Trial Objectives:
The objective is to investigate the efficacy and safety of afatinib with induction chemotherapy in primary unresected patients with locally advanced, HPV-negative, stage III or IVa/b HNSCC including oral cavity, oropharynx, hypopharynx, or larynx.
Primary Objective Phase I The primary objective of the phase I portion of the trial is to determine the maximum tolerated dose (MTD) or the recommended phase II dose of daily oral afatinib that is safe in combination with carboplatin AUC 6 and paclitaxel 175mg/m2 q 21 days as an induction regimen.
Primary Objective Phase 2 The primary objective of the phase 2 portion of the trial is to estimate the objective tumor response rate and toxicity with induction therapy in patients treated on the afatinib dose determined in Phase I.
Secondary Objectives The secondary objective of phase II is to estimate: 1) the overall response to entire treatment after completion of CRT, 2) progression-free survival (PFS) rate at 2 years, and 3) overall survival (OS) at 2 years.
Přehled studie
Postavení
Podmínky
Detailní popis
This is a phase I/phase II prospective multicenter trial to investigate the efficacy and safety of afatinib with induction chemotherapy in primary unresected patients with HPV-negative locally advanced SCC stage III or IVa/b of oral cavity, oropharynx, hypopharynx, or larynx. The primary endpoint is overall response rate after the completion of induction chemotherapy.
Eligible patients will begin with a 14 day lead-in period with afatinib alone. This will be followed immediately by 2 cycles of induction chemotherapy with carboplatin AUC 6 IV, paclitaxel 175mg/m2 day 1, and afatinib as a continuous daily dosing. Each cycle is repeated every 21 days. All patients will receive concurrent chemoradiotherapy beginning 2-3 weeks after the completion of the second cycle of induction chemotherapy (Refer to Study Schema in page 8 of the protocol).
During the period of induction chemotherapy, a complete history and physical (including weight) and tumor assessment by physical examination on Day 1 of each cycle will be performed and documented. Complete blood count with differential and a comprehensive metabolic profile will be performed weekly. After completion of induction chemotherapy, reassessment with blood work, physical exam, CT/MRI of neck and nasopharyngolaryngoscopy will be performed. After the completion of CRT, the patient will have a MRI, CT, or FDG PET approximately 12 weeks after CRT. Follow-up will be standard of care from this point onwards.
Physical exam, blood work and AE assessments will also be frequently performed during entire treatment.
Typ studie
Zápis (Aktuální)
Fáze
- Fáze 2
- Fáze 1
Kontakty a umístění
Studijní místa
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Maryland
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Baltimore, Maryland, Spojené státy, 21287
- Johns Hopkins Sidney Kimmel Comprehensive Cancer Center
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Tennessee
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Nashville, Tennessee, Spojené státy, 37232
- Vanderbilt Ingram Cancer Center
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Kritéria účasti
Kritéria způsobilosti
Věk způsobilý ke studiu
Přijímá zdravé dobrovolníky
Pohlaví způsobilá ke studiu
Popis
Inclusion Criteria:
- Patients must have a histologically confirmed diagnosis of squamous cell carcinoma, operable or inoperable tumors, stage III (T3N0-1) and IVA-B (T1-4 N2-3M0 or T4N0-1M0) of oral cavity, oropharynx, hypopharynx and larynx. For patients with oropharynx primary, either HPV negative or HPV positive with a > 10 pack year tobacco history or current smokers are eligible. HPV status should be determined before the enrollment in only non-smokers with oropharynx primary by HPV in-situ hybridization and/or p16 immunostain.
- Patients must have measurable disease of primary, nodes or both by clinical and radiographic methods per RECIST v1.1..
- No prior therapy, including surgery with curative intent, chemotherapy, radiation therapy, immunotherapy, EGFR targeted therapies, or any other investigational agents.
- Age >= 18 years.
- ECOG performance status 0-1.
Patients must have normal hepatic, renal and bone marrow function.
- Absolute neutrophil count >=1,000/ mm3 Count
- Platelets >= 100,000/mm3 Count
- Total serum bilirubin =< 1.5mg/dL Level:
- AST and ALT =< 2.5 X ULN
- Alkaline Phosphatase =< 2.5 X ULN
- Total calculated creatinine clearance >= 60 mL/min
- Patients with a history of a curatively treated malignancy must be disease-free for at least two years except for carcinoma in situ of cervix and/or non-melanomatous skin cancer.
Patients with the following within the last 6 months prior to pre-registration must be evaluated by a cardiologist and/or neurologist prior to entry into the study.
- Congestive heart failure > NYHA Class II
- CVA/TIA
- Unstable angina
- Myocardial infarction (with or without ST elevation)
- Ability to understand and the willingness to sign a written informed consent document.
Exclusion Criteria:
- Any prior radiation above the clavicles.
- Any prior invasive malignancy (unless non-melanomatous resectable skin or the DFS is 2 years or more).
- History of allergic reactions attributed to compounds of similar chemical or biological composition to afatinib, or other agents used in study.
- Cardiac left ventricular dysfunction with resting ejection fraction of less than institutional lower limit of normal ( if no lower limit of normal is defined in the institution, the lower limit is 50%)
- Gastrointestinal tract disease resulting in an inability to take or absorb oral or enteral medication.
- Baseline significant gastrointestinal symptoms with diarrhoea as a major symptom or a CTCAE Grade >1 diarrhoea of any etiology.
- Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
- Women of childbearing potential and sexually active males are strongly advised to use an accepted and effective method of contraception.
- Known pre-existing interstitial lung disease (ILD)
- Pregnant women are excluded.
Studijní plán
Jak je studie koncipována?
Detaily designu
- Primární účel: Léčba
- Přidělení: N/A
- Intervenční model: Přiřazení jedné skupiny
- Maskování: Žádné (otevřený štítek)
Zbraně a zásahy
Skupina účastníků / Arm |
Intervence / Léčba |
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Experimentální: Study Arm
Eligible patients will begin with a 14-day lead-in period with afatinib alone.
This will be followed immediately by 2 cycles of induction chemotherapy (IC) with carboplatin AUC 6 IV Day 1, paclitaxel 175mg/m2 IV Day 1, and oral afatinib as a continuous daily dosing.
Each cycle is repeated every 21 days.
After completion of 2 cycles of IC, patients will be assessed for response by CT/MRI and clinical exam.
After the induction, all patients will receive Intensity Modulated Radiation Therapy (IMRT) with weekly cisplatin 40mg/m2 IV.
Chemoradiotherapy (CRT) will begin 2-3 weeks after the completion of the second cycle of IC.
The patients will be evaluated with a MRI or CT, and FDG PET approximately 12 weeks after completion of CRT.
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Afatinib will be supplied as film-coated tablets.
Available dosage strengths will be 20, 30, or 40 mg.
Tablets will be supplied in HDPE, child-resistant, tamper-evident bottles.
Ostatní jména:
Induction chemotherapy: 175 mg/m2 day 1 every 21 days for 2 cycles (IV infusion as per institutional standard).
Ostatní jména:
Carboplatin is available as a sterile lyophilized powder in single-dose vials containing 50 mg, 150 mg, or 450 mg of carboplatin.
Each vial contains equal parts by weight of carboplatin and mannitol.
Commercial supplies of carboplatin will be used in this trial.
Ostatní jména:
Concurrent chemotherapy: 40 mg/m2 once weekly for 7 cycles (IV infusion as per institutional standard).
Ostatní jména:
Standard Fractionation 70 Gy /35 fractions at 2 Gy/day for 5 days per week.
Ostatní jména:
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Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
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Maximum Tolerated Dose (MTD) of Afatinib
Časové okno: 1 Year (Average)
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The maximally tolerated dose (MTD) was defined as the dose of afatinib in which <2 of 6 patients experience a DLT with the next higher dose having at least 2 of up to 6 patients experiencing a DLT.
No dose escalations or de-escalations are permitted within each subject's treatment.
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1 Year (Average)
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Objective Tumor Response
Časové okno: After completion of 2 cycles of induction chemotherapy (at least 8 weeks)
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Patients were accessed for response by CT/MRI and clinical exam.
Partial response was defined as a greater than 30 % reduction in tumor size.
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After completion of 2 cycles of induction chemotherapy (at least 8 weeks)
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Number of Participants With Dose Limiting Toxicities
Časové okno: 1 year (average)
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Grade 3 or 4 neutropenia (ie.
absolute neutrophil count <1000 cells/mm^3) that was associated with a fever>38.5
degrees C or lasting longer than 5 days, grade 3 thrombocytopenia with bleeding or grade 4 thrombocytopenia, and any grade 3 or 4 non-hematologic toxicity per CTCAE criteria which were probably or definitely related to study therapy.
During the chemoradiation, an event of stomatitis, pharyngitis, mucositis, or dermatitis was not considered to be a dose limiting toxicity unless it was a grade 4 that did resolve to <grade 2 with a radiation treatment break (not to exceed 10 days) or with withholding chemotherapy (not to exceed 2 weekly doses).
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1 year (average)
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Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
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Overall Response After Chemoradiation
Časové okno: 5 Years
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To estimate the overall response rate after completion of chemoradiation.
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5 Years
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2 Year Progression Free Survival (PFS)
Časové okno: 2 Years
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To estimate the 2 year progression free survival.
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2 Years
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Median Overall Survival at 2 Years
Časové okno: 2 Years
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To estimate the median overall survival.
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2 Years
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Biological Marker Activity of Afatinib
Časové okno: 5 Years
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To estimate the biological marker activity of afatinib by serial sampling of tumor and blood samples from patients, and correlate with clinical and pathological response and outcomes.
On- and off-target effects of afatinib will be assessed for the biological marker activity.
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5 Years
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Activity of Afatinib Based on Serial FLT-PET/CT and DW-MRI
Časové okno: 5 Years
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To estimate the activity of afatinib by obtaining serial FLT-PET/CT and DW-MRI, And compare to standard of care CT images (which will be acquired at baseline and at the completion of treatment, and categorized per RECIST criteria) and correlated with response.
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5 Years
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Correlate Standard Imaging Pre and Post Treatment
Časové okno: 5 Years
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To correlate the response with standard imaging CT/MRI and FDG PET pre and post treatment.
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5 Years
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Overall Response After Chemoradiation
Časové okno: 5 years
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To estimate the overall response rate after completion of chemoradiation
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5 years
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Spolupracovníci a vyšetřovatelé
Vyšetřovatelé
- Vrchní vyšetřovatel: Christine Chung, MD, Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Publikace a užitečné odkazy
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia
Primární dokončení (Aktuální)
Dokončení studie (Aktuální)
Termíny zápisu do studia
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Odhad)
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Více informací
Termíny související s touto studií
Klíčová slova
Další relevantní podmínky MeSH
- Novotvary podle histologického typu
- Novotvary
- Novotvary podle místa
- Karcinom
- Novotvary, žlázové a epiteliální
- Novotvary hlavy a krku
- Novotvary, dlaždicové buňky
- Karcinom, skvamózní buňky
- Spinocelulární karcinom hlavy a krku
- Molekulární mechanismy farmakologického působení
- Inhibitory enzymů
- Antineoplastická činidla
- Tubulinové modulátory
- Antimitotické látky
- Modulátory mitózy
- Antineoplastické látky, fytogenní
- Inhibitory proteinkinázy
- Karboplatina
- Paklitaxel
- Cisplatina
- Afatinib
Další identifikační čísla studie
- J1266
- NA_00074085 (Jiný identifikátor: JHMIRB)
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