Pharmacodynamic Study to Assess the Anti-proliferative Activity of the PARP Inhibitor Olaparib in Patients With HPV Positive and HPV Negative HNSCC
A Pilot Pharmacodynamic Study to Assess the Anti-proliferative Activity a of the Poly ADP Ribose Polymerase (PARP) Inhibitor Olaparib in Patients With Human Papilloma Virus (HPV) Positive and Human Papilloma Virus (HPV) Negative Head and Neck Squamous Cell Carcinoma (HNSCC)
Studieoversigt
Status
Status
Betingelser
Betingelser
Intervention / Behandling
Intervention / Behandling
Undersøgelsestype
Undersøgelsestype
Fase
Fase
- Fase 1
Deltagelseskriterier
Berettigelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Histologically confirmed HNSCC with surgically resectable disease
- No prior chemotherapy or radiation therapy as treatment for the observed HNSCC
- Patients must provide written informed consent
- Age >=18 years of age
- Eastern Cooperative Oncology Group (ECOG) Performance Status score of <2
- Normal organ and bone marrow function measured within 28 days prior to administration of study treatment as defined below:
- Hemoglobin >= 10 g/dL and no blood transfusions in the 28 days prior to entry/randomization
- Absolute neutrophil count >=1.5 x 10^9/L
- No features suggesting of MDS/AML on peripheral blood smear
- White blood cells > 3 x 10^9/L
- Platelet count >= 100 x 10^9/L
- Total bilirubin <= 1.5 x institutional upper limit of normal (ULN)
- AST (SGOT)/ALT (SGPT) < 2.5 x institutional upper limit of normal unless liver metastases are present in which case it must be < 5x ULN
- Serum creatinine <= 1.5 x institutional ULN OR creatinine clearance >= 50 mL/min/1.73 m^2 for patients with creatinine levels above institutional normal
- Women of child-bearing potential must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of the study participation and must have negative serum or urine pregnancy test within 1 week prior to beginning treatment on this trial
- Must be abler to understand and sign a written informed consent document
Exclusion Criteria:
- Patients with known brain metastases. Patients may have received WBRT within 14 days or focal radiation within 1 week of cycle 1, day 1. The patient can receive a stable dose of corticosteroids before and during the study as long as these were started at least 28 days prior to treatment
- Women must not be pregnant or breastfeeding
- Patients with known hypersensitivity to olaparib or any of the excipients of the product
- Patients receiving any other investigational agents within 4 weeks of starting the study
- Involvement in the planning and/or conduct of the study
- Any previous treatment with a PARP inhibitor, including olaparib
- Concomitant use of known CYP3A4 inhibitors such as ketoconazole, itraconazole, ritonavir, indinavir, saquinavir, telithromycin, clarithromycin, and nelfinavir
- Persistent toxicities (>=CTCAE grade 2)
- Resting ECG with QTC >470msec on 2 or more time points within a 24 hour period or family history of long QT syndrome
- Blood transfusions within 1 month prior to study start
- Patients with myelodysplastic syndrome/acute myeloid leukemia
- Major surgery within 14 days of starting study treatment and patients must have recovered from any effects of any major surgery
- Patients considered a poor medical risk due to a serious, uncontrolled medical disorder, non-malignant systemic disease or active, uncontrolled infection.
- Unable to swallow oral medication
- Immunocompromised patients, e.g., patients who are known to be serologically positive for HIV and are receiving antiviral therapy
- Known active hepatic disease
- Uncontrolled seizures
- Previous cancer, except: adequately treated non-melanoma skin cancer, curatively treated in-situ cancer of the cervix, or other solid tumors curatively treated with no evidence of disease for 5 years
- Currently on warfarin(subcutaneous heparin is permitted)
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Ikke-randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Antal våben
Våben og indgreb
Deltagergruppe / ArmDeltagergruppe / Arm |
Intervention / BehandlingIntervention / Behandling |
|---|---|
|
Eksperimentel: HPV negative tumors
10 patients with HPV negative tumors: Non-oropharyngeal tumors or p16 negative and HPV negative oropharyngeal tumors
|
Patients will receive olaparib administered at 300 mg bid x 14 days orally
Andre navne:
|
|
Eksperimentel: HPV positive tumors
10 patients with HPV positive tumors: p16 positive and HPV positive tumors
|
Patients will receive olaparib administered at 300 mg bid x 14 days orally
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Change in Level of IHC-Ki-67 expression
Tidsramme: Baseline and 14 days
|
Tissue biopsy sections will be analyzed for proliferation (IHC-Ki-67) Ki-67 is a nuclear non-histone protein that is present at low levels in quiescent cells but is increased in proliferating cells.
Thus, Ki-67 reactivity, defined as percent tumor cells staining positive as measured by immunohistochemical (IHC) staining, is a specific nuclear marker for cell proliferation.
|
Baseline and 14 days
|
Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Change in Tissue apoptosis
Tidsramme: Baseline and 14 days
|
Tissue biopsy sections will be analyzed for apoptosis.
For example using the IHC-cleaved caspase-3 assay.
|
Baseline and 14 days
|
|
Change in DNA repair pathways
Tidsramme: Baseline and 14 days
|
Tissue biopsy sections will be analyzed to determine effect on DNA repair pathways (PARP activity).
Specifically Poly(ADP-ribose) immunohistochemical staining of tissue biopsies will be performed and PAR intensity scored as 0 (no signal), 1 (weak), 2 (strong intensity in >50% of tumor cells).
|
Baseline and 14 days
|
Samarbejdspartnere og efterforskere
Sponsor
Sponsor
Efterforskere
Efterforskere
- Ledende efterforsker: Anne Chiang, MD, PhD, Yale University
Datoer for undersøgelser
Studer store datoer
Studiestart (Forventet)
Studiestart
Primær færdiggørelse (Forventet)
Primær færdiggørelse
Studieafslutning (Forventet)
Studieafslutning
Datoer for studieregistrering
Først indsendt
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Først opslået
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering sendt
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
- Neoplasmer efter histologisk type
- Neoplasmer
- Neoplasmer efter sted
- Neoplasmer, kirtel og epitel
- Neoplasmer i hoved og hals
- Neoplasmer, pladecelle
- Karcinom
- Karcinom, pladecelle
- Planocellulært karcinom i hoved og hals
- Molekylære mekanismer for farmakologisk virkning
- Enzymhæmmere
- Antineoplastiske midler
- Poly(ADP-ribose) polymerasehæmmere
- Olaparib
Andre undersøgelses-id-numre
Andre undersøgelses-id-numre
- 1409014536
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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