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Lapatinib + Vinorelbine in ErbB2 Overexpressing, First or Second Line Metastatic Breast Cancer Subjects

30. juni 2014 oppdatert av: GlaxoSmithKline

A Phase II, Single-Arm, Multi-Center Study Evaluating the Combination of Vinorelbine and Lapatinib in Women With ErbB2 Overexpressing Metastatic Breast Cancer

This is an open-label, single-arm, multi-center, Phase II study to determine the activity of vinorelbine plus lapatinib in either first- or second-line setting in women with ErbB2 overexpressing metastatic breast cancer (MBC). Sixty subjects will be enrolled in the study. Subjects will receive vinorelbine intravenously once weekly for 3 weeks, followed by a rest week in a 4-week cycle) plus lapatinib daily. Subjects will receive treatment until disease progression or withdrawal from the study. The primary objective of this study is to evaluate overall tumor response rate of lapatinib in combination with vinorelbine. Secondary objectives include progression-free survival, overall survival, duration of response, time to response and time to progression and safety. Safety and efficacy assessments will be performed at 4, 8 and 12 week intervals, and at the end of treatment.

Subject: Metastatic Breast Cancer, ErbB2, First-line or Second-line therapy, Lapatinib, Vinorelbine

Studieoversikt

Status

Avsluttet

Intervensjon / Behandling

Studietype

Intervensjonell

Registrering (Faktiske)

44

Fase

  • Fase 2

Kontakter og plasseringer

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

Studiesteder

    • Alabama
      • Muscle Shoals, Alabama, Forente stater, 35661
        • GSK Investigational Site
    • Arizona
      • Tucson, Arizona, Forente stater, 85715
        • GSK Investigational Site
    • California
      • Sacramento, California, Forente stater, 95817
        • GSK Investigational Site
    • Florida
      • Jacksonville, Florida, Forente stater, 32204
        • GSK Investigational Site
      • Plantation, Florida, Forente stater, 33324
        • GSK Investigational Site
    • Georgia
      • Augusta, Georgia, Forente stater, 30901
        • GSK Investigational Site
    • Iowa
      • Cedar Rapids, Iowa, Forente stater, 52402
        • GSK Investigational Site
    • Maryland
      • Baltimore, Maryland, Forente stater, 21237
        • GSK Investigational Site
      • Bethesda, Maryland, Forente stater, 20817
        • GSK Investigational Site
    • Mississippi
      • Jackson, Mississippi, Forente stater, 39202
        • GSK Investigational Site
    • Missouri
      • Kansas City, Missouri, Forente stater, 64118
        • GSK Investigational Site
      • St. Louis, Missouri, Forente stater, 63141
        • GSK Investigational Site
    • Nebraska
      • Omaha, Nebraska, Forente stater, 68114
        • GSK Investigational Site
    • New York
      • New York, New York, Forente stater, 10065
        • GSK Investigational Site
    • North Carolina
      • Greensboro, North Carolina, Forente stater, 27403
        • GSK Investigational Site
    • Ohio
      • Columbus, Ohio, Forente stater, 43219
        • GSK Investigational Site
    • Oklahoma
      • Oklahoma City, Oklahoma, Forente stater, 73120
        • GSK Investigational Site
      • Tulsa, Oklahoma, Forente stater, 74136
        • GSK Investigational Site
    • Oregon
      • Eugene, Oregon, Forente stater, 97401
        • GSK Investigational Site
      • Portland, Oregon, Forente stater, 97239-3098
        • GSK Investigational Site
    • Pennsylvania
      • Philadelphia, Pennsylvania, Forente stater, 19106
        • GSK Investigational Site
    • Tennessee
      • Memphis, Tennessee, Forente stater, 38120
        • GSK Investigational Site

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

Hunn

Beskrivelse

Inclusion Criteria:

A subject will be eligible for inclusion in this study only if all of the following criteria apply:

  1. Signed informed consent prior to registration.
  2. Considered by the Investigator to have a life expectancy of ≥12 weeks.
  3. Subjects must have histologically confirmed invasive breast cancer with Stage IV disease at primary diagnosis or at relapse after curative-intent surgery.

    • Where the disease is restricted to a solitary lesion, the neoplastic nature of the lesion should be confirmed by cytology or histology.

  4. Documented amplification of ErbB2 3+ by immunohistochemistry or a positive score (>2.2) by fluorescence in situ hybridization (FISH) using a local laboratory result (which will be considered sufficient in this study with no further verification by a central laboratory). NOTE: If both IHC and FISH results available, FISH results must be used for eligibility.
  5. Subjects must not have received more than 1 prior chemotherapeutic regimen in the metastatic setting.
  6. All prior chemotherapy, immunotherapy, biologic therapy, or surgery (except for minor surgical procedures) must be discontinued at least 4 weeks prior to first dose of investigational product. Hormonal therapy must be discontinued at least 1 week prior to first dose.
  7. Prior diagnosis of cancer is allowed as long as the subject is free of disease and has been off treatment for prior malignancies for 5 years. Subjects with completely resected basal or squamous cell skin cancer or successfully treated cervical carcinoma in situ will be allowed if it has been 1 year or longer since definitive surgery.
  8. Subjects must have measurable disease, according to Response Evaluation Criteria in Solid Tumors (RECIST) guidelines.
  9. Females aged ≥18 years with any menopausal status:

    • Non-child-bearing potential (i.e., women with functioning ovaries who have a current documented tubal ligation or hysterectomy, or women who are postmenopausal)
    • Child-bearing potential (i.e., women with functioning ovaries and no documented impairment of oviductal or uterine function that would cause sterility): This category includes women with oligomenorrhea (severe), women who are perimenopausal, and young women who have begun to menstruate. These subjects must have a negative serum pregnancy test at screening and agree to one of the following:
    • Complete abstinence from intercourse from 2 weeks prior to administration of the first dose of study medication until 28 days after the final dose of study medication; or
    • Consistent and correct use of one of the following acceptable methods of birth control: male partner who is sterile prior to the female subject's entry into the study and is the sole sexual partner for that female subject; any intrauterine device with a documented failure rate of less than 1% per year; oral contraceptives (either combined or progestogen only) where not contraindicated for this subject population or per local practice.; or barrier methods, including diaphragm or condom with a spermicide.
  10. ECOG performance status (PS) of 0 to 2 [Oken, 1982] (Appendix 1).
  11. Subjects must have normal organ and marrow function as defined in Table 1. Table 1 Baseline Laboratory Values for Adequate Organ Function System Laboratory Value Hematologic Absolute neutrophil count ≥1.5 × 10^9/L Hemoglobin ≥9 g/dL Platelets ≥100 × 10^9/L Hepatic Serum bilirubin ≤1.25 × upper limit of normal (ULN) Aspartate aminotransferase and alanine aminotransferase

    • 3 × ULN without liver metastases
    • 5 × ULN if documented liver metastases Renal Serum creatinine ≤1.5 mg/dL

      • OR - Calculated creatinine clearance ≥40 mL/min
  12. Subjects must have a cardiac ejection fraction of at least 50% (as measured by echocardiogram [ECHO] or multigated acquisition scan [MUGA]) and within the institutional range of normal. Subjects who require cardiac medications (e.g. positive inotropic agents or afterload reducers) for abnormal ejection fraction are ineligible. MUGA scans will be accepted in cases where an ECHO cannot be performed or is inconclusive. The same modality to assess cardiac ejection fraction must be used consistently throughout the study.
  13. Radiotherapy prior to initiation of study medication is allowed to a limited area (e.g., palliative therapy), if it is not the sole site of disease. Subjects must have completed radiation treatment and recovered from all acute radiation treatment-related toxicities (e.g., bone marrow suppression) prior to commencement of combination treatment.
  14. Subjects with stable central nervous system (CNS) metastases. Subjects with stable CNS metastases are defined as follows: subject is asymptomatic with CNS metastases that have been stable for at least 3 months as confirmed by computed tomography (CT)/magnetic resonance imaging (MRI). Subjects with evidence of leptomeningeal/parenchymal involvement are eligible only if they are not taking steroids or enzyme-inducing anticonvulsants within 4 weeks of commencement of the study. Treatment with prophylactic anticonvulsants is permitted, unless listed as a prohibited medication.
  15. Subject must be free of gastrointestinal diseases that impede swallowing and retaining of oral medications.
  16. Able to swallow and retain oral medication (intact pill).
  17. Bisphosphonate therapy for bone metastases is allowed; however, treatment must be initiated prior to the first dose of study medication. Prophylactic use of bisphosphonates in subjects without bone disease, except for the treatment of osteoporosis, is not permitted.
  18. Subjects whose disease is estrogen receptor + and/or progesterone receptor + or unknown status will only be included in the study if they meet the following criteria:

    • They have symptomatic visceral disease that requires chemotherapy.
    • The disease is considered by the Investigator to be progressing rapidly or is life threatening.
    • Subjects who have received endocrine therapy and who are no longer benefiting from this therapy.

Exclusion Criteria:

A subject will not be eligible for inclusion in this study if any of the following criteria apply:

  1. Subjects taking treatment with medications provided in the list of restricted medications and substances in the drug information section for lapatinib are not eligible for the study. This includes human immunodeficiency virus-positive subjects receiving combination anti-retroviral therapy because of possible pharmacokinetic interactions with lapatinib.
  2. Prior therapy with lapatinib.
  3. Prior therapy with vinorelbine for treatment of breast cancer.
  4. More than 1 line of therapy for treatment of MBC.
  5. Concurrent anticancer or concomitant radiotherapy treatment.
  6. History of uncontrolled or symptomatic angina; history of arrhythmias requiring medications; clinically significant myocardial infarction <6 months from study entry; uncontrolled or symptomatic congestive heart failure; ejection fraction below the institutional normal limit; or any other cardiac condition, which in the opinion of the treating physician, would make this protocol unreasonably hazardous for the patient.
  7. Have current active hepatic or biliary disease (with exception of patients with Gilbert's syndrome, asymptomatic gallstones, liver metastases or stable chronic liver disease per investigator assessment)
  8. Use of an investigational drug within 30 days or 5 half-lives, whichever is longer, preceding the first dose of investigational treatment, or, concurrent treatment with an investigational agent or participation in another clinical trial involving investigational agents.
  9. Known immediate or delayed hypersensitivity reaction or idiosyncrasy to drugs chemically related to any of the agents used in this study or their excipients.
  10. Known history of uncontrolled inter-current illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, clinically significant cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
  11. Concurrent disease or condition that would make the woman inappropriate for study participation, or any serious medical disorder that would interfere with the woman's safety.
  12. Pregnant or lactating females at any time during the study (due to the potential teratogenic or abortifacient effects of lapatinib and breastfeeding).
  13. Subjects with diseases affecting gastrointestinal function resulting in an inability to take oral medication, including; malabsorption syndrome, disease significantly affecting gastrointestinal function, or resection of the stomach or small bowel.

    Women with ulcerative colitis are also excluded.

  14. Peripheral neuropathy of Grade 2 or greater.
  15. Unresolved or unstable, serious toxicity from prior administration of another investigational drug and/or of prior cancer treatment.
  16. Dementia, altered mental status, or any psychiatric condition that would prohibit the understanding or rendering of informed consent.

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: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Number of Participants With Overall Response (OR), as Assessed by the Investigator
Tidsramme: From the start of study medication until disease progression, assessed every 8 weeks for up to 2 years
OR is defined as the number of participants achieving either a confirmed complete response (CR: the disappearance of all target lesions [TLs]) or partial response (PR: a >=30% decrease in the sum of the longest diameter [LD] of the TLs, taking as a reference the baseline sum LD) as assessed by the investigator as the best OR. The best OR is the best response recorded from the start of treatment until disease progression (PD: a >=20% increase in the sum of the LD of TLs, taking as a reference the smallest sum LD recorded since treatment started or the appearance of >=1 new lesions)/recurrence.
From the start of study medication until disease progression, assessed every 8 weeks for up to 2 years

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Progression-Free Survival (PFS), as Assessed by the Investigator
Tidsramme: From the start of study medication until disease progression, assessed every 8 weeks for up to 2 years
PFS is defined as the time from the start of treatment until the earliest date of disease progression (PD) or death due to any cause, if sooner. PD is defined as at least a 20% increase in the sum of the LD of target lesions, taking as a reference the smallest sum LD recorded since the treatment started or the appearance of 1 or more new lesions.
From the start of study medication until disease progression, assessed every 8 weeks for up to 2 years
Duration of Response, as Assessed by the Investigator
Tidsramme: From the start of study medication until disease progression, assessed every 8 weeks for up to 2 years
Duration of response, for the subset of participants who had a confirmed CR (the disappearance of all TLs) or PR (a >=30% decrease in the sum of the LD of the TLs, taking as a reference the baseline sum LD), is defined as the time from the first documented evidence of CR or PR until the first documented sign of disease progression (a >=20% increase in the sum of the LD of TLs, taking as a reference the smallest LD recorded since treatment started or the appearance of >=1 new lesions) or death due to any cause, if sooner.
From the start of study medication until disease progression, assessed every 8 weeks for up to 2 years
Time to Response, as Assessed by the Investigator
Tidsramme: From the start of study medication until disease progression, assessed every 8 weeks for up to 2 years
Time to response, for the subset of participants who had a confirmed CR (the disappearance of all TLs) or PR (a >=30% decrease in the sum of the LD of the TLs, taking as a reference the baseline sum LD), is defined as the time from the start of treatment until the first documented evidence of CR or PR (whichever status was recorded first). When tumor response was confirmed at a repeat assessment, the time to response was taken to be the first time that the response was observed.
From the start of study medication until disease progression, assessed every 8 weeks for up to 2 years
Time to Progression (TTP), as Assessed by the Investigator
Tidsramme: From the start of study medication until disease progression, assessed every 8 weeks for up to 2 years
TTP is defined as the time from the start of treatment until the earliest date of disease progression (a >=20% increase in the sum of the LD of TLs, taking as a reference the smallest LD recorded since treatment started or the appearance of >=1 new lesions) or death due to breast cancer, if sooner.
From the start of study medication until disease progression, assessed every 8 weeks for up to 2 years
Number of Participants With the Indicated Adverse Events Occurring in at Least 5 Participants and Related to the Combination of Lapatinib and Vinorelbine
Tidsramme: From the start of study medication until disease progression, assessed every 4 weeks for up to 2 years
Qualitative and quantitative toxicities associated with the combination of lapatinib and vinorelbine during the study are those adverse events (AEs) that are judged to be related to the study treatment by the investigator. Those AEs occuring in more than 5 participants in the ITT Population are listed here.
From the start of study medication until disease progression, assessed every 4 weeks for up to 2 years
Overall Survival
Tidsramme: From the start of study treatment to the date of death, assessed for up to 3 years
OS is defined as the time from the start of study treatment to the date of death. In the absence of confirmation of death, survival time was to be censored at the last date the participant was known to be alive. Overall survival was not assessed because the study was terminated due to low screening and a low enrollment rate after 3 years. There were no-survival follow-up visits required.
From the start of study treatment to the date of death, assessed for up to 3 years

Samarbeidspartnere og etterforskere

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

Sponsor

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. juni 2008

Primær fullføring (Faktiske)

1. mai 2012

Studiet fullført (Faktiske)

1. mai 2012

Datoer for studieregistrering

Først innsendt

2. juli 2008

Først innsendt som oppfylte QC-kriteriene

2. juli 2008

Først lagt ut (Anslag)

3. juli 2008

Oppdateringer av studieposter

Sist oppdatering lagt ut (Anslag)

14. juli 2014

Siste oppdatering sendt inn som oppfylte QC-kriteriene

30. juni 2014

Sist bekreftet

1. juni 2014

Mer informasjon

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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