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Pharmacodynamic Study to Assess the Anti-proliferative Activity of the PARP Inhibitor Olaparib in Patients With HPV Positive and HPV Negative HNSCC

9. januar 2020 oppdatert av: Yale University

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)

This is an open label pilot study evaluating the pharmacodynamics and safety of single agent olaparib administered at 300mg bid (twice a day) for 14 days orally in patients with human papillomavirus (HPV) -positive and human papillomavirus (HPV)-negative head and neck squamous cell carcinoma (HNSCC)

Studieoversikt

Status

Tilbaketrukket

Intervensjon / Behandling

Studietype

Intervensjonell

Fase

  • Fase 1

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

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

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Ikke-randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 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 navn:
  • Lynparza
Eksperimentell: 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 navn:
  • Lynparza

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
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

Resultatmål
Tiltaksbeskrivelse
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

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Sponsor

Etterforskere

  • Hovedetterforsker: Anne Chiang, MD, PhD, Yale University

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Forventet)

1. januar 2018

Primær fullføring (Forventet)

1. januar 2019

Studiet fullført (Forventet)

1. juli 2019

Datoer for studieregistrering

Først innsendt

24. september 2015

Først innsendt som oppfylte QC-kriteriene

18. februar 2016

Først lagt ut (Anslag)

19. februar 2016

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

13. januar 2020

Siste oppdatering sendt inn som oppfylte QC-kriteriene

9. januar 2020

Sist bekreftet

1. januar 2020

Mer informasjon

Begreper knyttet til denne studien

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Ja

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

produkt produsert i og eksportert fra USA

Ja

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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