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Phase 2 Study of Nivolumab in Solid Tumors Induced by Prior Radiation Exposure

The purpose of this study is to determine whether Nivolumab is effective in the treatment of radiation-induced solid tumors.

Studieoversikt

Status

Avsluttet

Intervensjon / Behandling

Studietype

Intervensjonell

Registrering (Faktiske)

6

Fase

  • Fase 2

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Maryland
      • Baltimore, Maryland, Forente stater, 21231
        • Sidney Kimmel Cancer Center @ Johns Hopkins

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 metastatic or unresectable solid tumor which standard curative or palliative measures do not exist or are no longer effective. The primary site of the metastatic or unresectable tumor must have arisen within a previously irradiated site and be considered a radiation-induced tumor.
  • Pre-treatment tumor specimen available. Patients with no available archived specimen must be willing to undergo a pre-treatment tumor biopsy.
  • Measurable disease.
  • Progressive disease on study entry.
  • Received adjuvant or neoadjuvant chemotherapy and developed recurrent or metastatic disease within 6 months of completing therapy.
  • Age >18 years.
  • Eastern Cooperative Oncology Group (ECOG) performance status <2.
  • Life expectancy of greater than 3 months.
  • Adequate organ and marrow function as defined below:
  • White Blood Cell >2,000/per microliter
  • Absolute neutrophil count >1,500/per microliter
  • Platelets >100,000/per microliter
  • Hemoglobin ≥9.0 g/dL
  • Total bilirubin ≤1.5 times the institutional upper limit of normal (ULN) (except subjects with Gilbert Syndrome, who can have total bilirubin < 3.0 mg/dL)
  • Aspartate Aminotransferase(SGOT)/Alanine Aminotransferase (SGPT) <3 X institutional ULN
  • Creatinine ≤1.5 X institutional ULN OR
  • Creatinine clearance >40 mL/min for patients with creatinine Levels above institutional normal (calculated using the Cockcroft-Gault formula below)
  • Female Creatinine Clearance = (140 - age in years) x weight in kg x 0.85 72 x serum creatinine in mg/dL
  • Male Creatinine Clearance = (140 - age in years) x weight in kg x 1.00 72 x serum creatinine in mg/dL
  • Women of childbearing potential (WOCBP) and men must agree to use adequate contraception prior to study entry and for the duration of study participation and up to 31 weeks after the last dose of nivolumab.
  • Women of childbearing potential (WOCBP) must have a negative serum or urine pregnancy test within 24 hours prior to the start of nivolumab.
  • Ability to understand and the willingness to sign a written informed consent document.
  • Biopsiable disease at the time of enrollment as biopsies after progression are required for participation.

Exclusion Criteria:

  • Any active, known or suspected autoimmune disease.
  • Requiring continuous supplemental oxygen.
  • Chemotherapy or radiotherapy within 2 weeks (6 weeks for nitrosoureas or mitomycin C) prior to entering the study or unresolved toxicity due to agents administered more than 2 weeks earlier.
  • Uncontrolled brain metastases.
  • History of allergic reactions attributed to compounds of similar chemical or biologic composition to nivolumab.
  • Uncontrolled inter-current illness.
  • Pregnant or currently breastfeeding.
  • Receiving any other anticancer therapy.
  • Prior therapy with anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CD137, anti-CTLA- 4 antibody therapies, any other antibody or drug specifically targeting T-cell costimulation or checkpoint pathways.
  • History of Human Immunodeficiency Virus (HIV) (HIV 1/2 antibodies).
  • Positive test for hepatitis B virus surface antigen (HBV sAg) or hepatitis C virus ribonucleic acid (HCV antibody) indicating ongoing acute or chronic infection.
  • Requiring systemic treatment with either corticosteroids (> 10 mg daily prednisone equivalent) or other immunosuppressive medications within 14 days of study drug administration.

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: Radiation-Induced Metastatic Sarcoma
a flat dose of Nivolumab 240 mg will be administered intravenously every 2 weeks until disease progression.
Andre navn:
  • BMS-936558
  • MDX-1106
Eksperimentell: Radiation-Induced Non-Sarcoma Metastatic Solid Tumors
a flat dose of Nivolumab 240 mg will be administered intravenously every 2 weeks until disease progression.
Andre navn:
  • BMS-936558
  • MDX-1106

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Best Objective Response Rate
Tidsramme: Up to 24 weeks
Number of participants with response. Response will be assessed at baseline (within 4 weeks prior to starting nivolumab) and then every 8 weeks while on Nivolumab, up to 24 weeks. The best objective response will be assessed at 24 weeks. Response will be defined based on RECIST 1.1 criteria where complete response (CR)= disappearance of all target lesions, partial response (PR) is =>30% decrease in sum of diameters of target lesions, progressive disease (PD) is >20% increase in sum of diameters of target lesions, stable disease (SD) is <30% decrease or <20% increase in sum of diameters of target lesions.
Up to 24 weeks

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Percentage of Patients Progression-free at 24 Weeks From the Time of Enrollment
Tidsramme: 24 weeks
Disease status at 24 weeks will be compared to disease status at the time of enrollment, and response coded based on RECIST 1.1 criteria.
24 weeks
Progression-free Survival
Tidsramme: Up to 22 months
Number of participants alive without progression.
Up to 22 months
Duration of Response
Tidsramme: Up to 22 months
The duration of overall response is measured from the time measurement criteria are met for Complete Response or Partial Response (whichever is first recorded) until the first date that recurrent or progressive disease is objectively documented, accessed up to 3 years.
Up to 22 months
Number of Participants With Treatment-related Adverse Events
Tidsramme: up to 100 days post-intervention
Number of participants with treatment-related adverse events as defined by CTCAE 4.0 criteria.
up to 100 days post-intervention
Overall Survival
Tidsramme: Up to 22 months
Overall survival was planned to be measured at 5 years post-intervention as the time from enrollment until death. Instead, due to early termination for low accrual, the number of participants alive at the time of study termination is reported.
Up to 22 months

Samarbeidspartnere og etterforskere

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

Samarbeidspartnere

Etterforskere

  • Hovedetterforsker: Patrick Forde, MB, BCH, Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

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

1. desember 2016

Primær fullføring (Faktiske)

1. august 2018

Studiet fullført (Faktiske)

1. september 2018

Datoer for studieregistrering

Først innsendt

2. august 2016

Først innsendt som oppfylte QC-kriteriene

9. august 2016

Først lagt ut (Anslag)

12. august 2016

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

28. august 2019

Siste oppdatering sendt inn som oppfylte QC-kriteriene

9. august 2019

Sist bekreftet

1. august 2019

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

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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