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Phase II Study of Dasatinib in Previously Treated Patients With Advanced NSCLC (TOP0801)

31. Mai 2016 aktualisiert von: Duke University

Phase II Study of Dasatinib in Previously Treated Patients With Advanced Non-Small Cell Lung Cancer (NSCLC)

On this study patients will receive dasatinib, a targeted therapy, for advanced NSCLC that has progressed after previous therapy. Safety and response to dasatinib will be assessed.

Fresh frozen tumor tissue must be available for genomics analysis prior to initiating dasatinib therapy. A biopsy must be obtained after any prior chemotherapy. If fresh frozen tumor tissue is not available, a biopsy will be required to participate in this trial.

Studienübersicht

Status

Beendet

Intervention / Behandlung

Detaillierte Beschreibung

Lung cancer is the leading cause of cancer death in the United States. Twenty to seventy-five percent of patients initially treated with surgery or radiotherapy recur and become candidates for systemic therapy. Src expression has been identified in a majority of NSCLC cell lines and may be important in hypoxic growth and angiogenesis of NSCLC.

This phase II trial will investigate the activity of the oral Src inhibitor dasatinib in advanced stage NSCLC. We hypothesize that the inhibition of Src pathway with dasatinib will show anti-tumor activity in advanced NSCLC, with a tolerable safety profile.

Fresh frozen tissue is needed for the genomics analysis, thus a biopsy will be required to participate in this trial. The genomic analysis will determine if the tumor is Src-active or Src-inactive and responses to dasatinib compared. In stage I, 40 patients will be treated without prior knowledge of their tumoral Src-activity. If all stage I responses are observed in the Src-active patients, the second stage will only accrue that cohort. If all responses are observed in the Src-inactive cohort, the activity of dasatinib and genomic determination of dasatinib response will be re-evaluated. Otherwise, if during Stage I, responses are observed in both cohorts, they will be accrued separately and evaluated in a two-stage manner.

Dasatinib will be give orally twice daily and continue until progression of disease, intolerable toxicity or patient withdrawal. Imaging studies will be done pre-treatment then every 6 weeks to assess radiologic response to therapy.

Patients will be followed for 30 days after the last dose of dasatinib to assess toxicity.

Studientyp

Interventionell

Einschreibung (Tatsächlich)

37

Phase

  • Phase 2

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

    • North Carolina
      • Durham, North Carolina, Vereinigte Staaten, 27710
        • Duke University Medical Center
      • Durham, North Carolina, Vereinigte Staaten, 27705
        • Durham VA Medical Center
      • Raleigh, North Carolina, Vereinigte Staaten, 27609
        • Duke Raleigh

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

18 Jahre und älter (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

Inclusion Criteria:

  1. Histological/cytological documented non-small cell lung cancer (NSCLC). Documentation of recurrence required if treated with surgical resection and/or external beam radiation therapy (XRT) with curative intent and now have recurrent disease.
  2. Fresh tissue biopsy material for genomics analysis prior to initiating dasatinib. If prior XRT, tissue biopsy must be outside XRT field. Biopsy must be after any prior chemotherapy.
  3. Prior treatment (tx) to include one of the following:

    • At least 1 prior systemic regimen (IV or oral agent) for Stage IV NSCLC or for recurrent disease.
    • Recurrence within 12 months after completion of systemic neoadjuvant/adjuvant chemotherapy for early stage NSCLC.
    • Combined modality platinum-based tx for Stage III NSCLC.
  4. Prior XRT permitted if ≥1 week since completion, XRT must be <25% of bone marrow reserve.
  5. At least one, non-radiated, measurable lesion (per RECIST).
  6. Age ≥18 years.
  7. Eastern Cooperative Oncology Group (ECOG) 0-2.
  8. Adequate Organ Function:

    1. Total bilirubin < Upper limit normal (ULN)
    2. Hepatic enzymes (AST, ALT) ≤2.5x ULN
    3. Serum creatinine <1.5x ULN
    4. Hemoglobin ≥9 gm/dL
    5. Neutrophil count (ANC/AGC) ≥1500 per μL
    6. Platelets ≥100,000 per μL
    7. Prothrombin time (PT)/a Partial thromboplastin time (PTT) ≤1.5x control
  9. No other serious medical or psychiatric illness.
  10. Ability to take oral medication (dasatinib must be swallowed whole).
  11. Women of childbearing potential must have negative serum pregnancy test ≤72 hours and not >7 days prior to starting study drug.
  12. Sexually active males and females of reproductive potential must agree to use adequate method of contraception during tx and for at least 4 weeks after study drug stopped.
  13. Signed, written informed consent including Health Insurance Portability and Accountability Act (HIPAA) according to institutional guidelines.

Exclusion Criteria:

  1. Previous or concomitant malignancy in past 2 years other than curatively treated carcinoma in situ of cervix, or basal cell/squamous cell carcinoma of the skin.
  2. Prior tx with dasatinib or other agents that inhibit Src.
  3. Evidence of symptomatic pleural effusions (grade 2) unless undergo therapeutic thoracentesis as part of non-study care. Successful pleurodesis allowed. Patients who require supplemental oxygen or with oxygen saturation on room air <89% are not eligible. Pericardial effusions of any grade are not eligible.
  4. Untreated documented symptomatic central nervous system (CNS) metastases.
  5. Cardiac Symptoms:

    1. Uncontrolled angina, congestive heart failure(CHF)or myocardial infarction within 6 months
    2. Diagnosed congenital long QT syndrome
    3. Any h/o clinically significant ventricular arrhythmias
    4. Prolonged QT corrected (QTc) interval on pre-entry EKG (>450 msec)
    5. Uncontrolled B/P as defined as >160/90 on B/P therapy
  6. Hypokalemia or hypomagnesaemia if it cannot be corrected.
  7. H/o diagnosed congenital acquired bleeding disorders.
  8. Ongoing or recent (≤3 months) significant (≥grade 3) GI bleeding.
  9. Con Meds:

    1. Drugs having risk of causing Torsades de Pointes (must stop drug 7 days before dasatinib);
    2. Current therapeutic dose unfractionated heparin, low-molecular weight heparin, or coumadin therapy;
    3. St. John's Wort must be stopped while on dasatinib;
    4. IV bisphosphonates stopped 2 weeks pre/6 weeks post dasatinib.
  10. Prisoners/subjects compulsorily detained for tx of psychiatric and/or physical illness.
  11. Pregnant or breastfeeding.
  12. Active or uncontrolled infection requiring IV antibiotics.
  13. Impairment of GI function/disease that may alter absorption of dasatinib (e.g., ulcerative diseases, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome, or small bowel resection).
  14. Received investigational drugs ≤4 weeks prior to starting study drug and/or not recovered from side effects of such therapy. Any other anti-neoplastic and/or molecular therapy must be discontinued 7 days prior to starting dasatinib.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: N / A
  • Interventionsmodell: Einzelgruppenzuweisung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Dasatinib

After a biopsy is done to obtain fresh frozen tumor tissue (Stage I), dasatinib is to be administered as an oral dose of 70 mg twice daily on a continuous basis for 6 weeks. Every 6 weeks radiologic exam will be done to assess response. Treatment will continue until progression of disease, intolerable toxicity or patient withdrawal.

For Stage II, a biopsy to obtain fresh frozen tumor tissue will also be done. Depending on results from Stage I and results of biopsy, treatment with dasatinib will be determined.

70 mg PO twice daily until progression. Re-assess radiographically every 6 weeks.
Andere Namen:
  • Sprycel

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Tumor Response
Zeitfenster: 2 years

Tumor response rate was defined by RECIST criteria:

CR (complete response) = disappearance of all target lesions taking as reference the baseline sum of the longest diameter (LD); PR (partial response) = at least a 30% decrease in the sum of the longest diameter of target lesions; PD (progressive disease) = at least a 20% increase in the sum of the longest diameter of target lesions as reference the smallest sum LD recorded since the treatment started or the appearance of one or more new lesions; SD (stable disease) = Neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD taking as reference the smallest sum LD since the treatment started

2 years

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Overall Survival
Zeitfenster: Progression and survival every 6 months
Overall survival (OS) is the duration from date of consent to date of death from any cause.
Progression and survival every 6 months
Grade 3-5 Toxicity Associated With Dasatinib Treatment
Zeitfenster: Duration of dasatinib treatment plus 30 days
Number of subjects with Grade 3-5 toxicity as assessed using NCI CTCAE criteria with the attribution of possibly, probably, or definitely related to protocol treatment.
Duration of dasatinib treatment plus 30 days
Describe Change in Serum Levels of C-terminal Cross-linked Collagen I Between Pre-treatment and 6 Weeks After Starting Dasatinib.
Zeitfenster: 2 years
2 years
Determine Relationship Between K-ras Gene Mutation and Response to Dasatinib.
Zeitfenster: 2 years
2 years

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Sponsor

Mitarbeiter

Ermittler

  • Hauptermittler: Michael Kelley, MD, Duke University

Publikationen und hilfreiche Links

Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn

1. September 2008

Primärer Abschluss (Tatsächlich)

1. Juni 2013

Studienabschluss (Tatsächlich)

1. Juni 2013

Studienanmeldedaten

Zuerst eingereicht

6. November 2008

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

6. November 2008

Zuerst gepostet (Schätzen)

7. November 2008

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Schätzen)

30. Juni 2016

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

31. Mai 2016

Zuletzt verifiziert

1. Mai 2016

Mehr Informationen

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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