Study of Immune Response Modifier in the Treatment of Breast, Ovarian, Endometrial and Cervical Cancers
Phase II Study of 852A Administered Subcutaneously in Patients With Metastatic Refractory Breast, Ovarian, Endometrial and Cervical Cancers
Přehled studie
Postavení
Postavení
Podmínky
Podmínky
Intervence / Léčba
Intervence / Léčba
Detailní popis
Typ studie
Typ studie
Zápis (Aktuální)
Zápis
Fáze
Fáze
- Fáze 2
Kontakty a umístění
Studijní místa
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Minnesota
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Minneapolis, Minnesota, Spojené státy, 55455
- Masonic Cancer Center, University of Minnesota
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Kritéria účasti
Kritéria způsobilosti
Kritéria způsobilosti
Věk způsobilý ke studiu
Přijímá zdravé dobrovolníky
Pohlaví způsobilá ke studiu
Popis
Inclusion Criteria:
Adequate performance status:
- Breast - Karnofsky score > 50;
- Ovarian, endometrial or cervical - Gynecologic Oncology Group (GOG) performance score ≤2
- If female and of childbearing potential, are willing to use adequate contraception (hormonal, barrier method, abstinence) prior to study entry and for the duration of study participation.
- Normal organ function within 14 days of study entry
Diagnosis of one of the following malignancies:
- Metastatic breast cancer (BR)
- Metastatic ovarian cancer (OV)
- Metastatic endometrial cancer (EM)
- Metastatic cervical cancer (CX)
Breast Cancer Inclusion Criteria:
- Measurable metastatic disease (>1cm) in at least one site other than bone-only
- Progression on or failure to respond to at least one previous chemotherapy regimen for metastatic disease
- Progression on prior therapy with a hormonal agent if estrogen receptor or progesterone receptor positive, and/or with trastuzumab if HER2-neu positive. If patient has progressed through hormone or trastuzumab therapy only, must have received one chemotherapy regimen.
Ovarian Cancer Inclusion Criteria:
- Measurable metastatic disease as defined by Response Evaluation Criteria in Solid Tumors (RECIST)
- Primary tumor must have been diagnosed histologically as either epithelial ovarian cancer, fallopian tube cancer, or primary peritoneal cancer (not borderline or low malignant potential epithelial carcinoma).
- Subjects must have failed at least two previous chemotherapy regimens. Paclitaxel must have been a component of one or both regimens and cisplatin or carboplatin must have been a component of one or both regimens.
Endometrial Cancer Inclusion Criteria:
- Measurable metastatic disease
- Histologically proven recurrent or persistent endometrial cancer that is not amenable to curative treatment with surgery and/or radiation therapy AND has failed 2 previous treatment regimens
Cervical Cancer Inclusion Criteria:
- Measurable metastatic disease
- Histologically proven recurrent or persistent squamous cell carcinoma, adenosquamous carcinoma, or adenocarcinoma of the cervix that is not amenable to curative treatment with surgery and/or radiation therapy AND has failed 2 previous treatment regimens.
Exclusion Criteria:
Had/have the following prior/concurrent therapy:
- Systemic corticosteroids (oral or injectable) within 7 days of first dose of 852A (topical or inhaled steroids are allowed)
- Investigational drugs/agents within 14 days of first dose of 852A
- Immunosuppressive therapy, including cytotoxic agents within 14 days of first dose of 852A (nitrosoureas within 30 days of first dose)
- Drugs known to induce QT interval prolongation and/or induce Torsades de pointes unless best available drug required to treat life-threatening conditions
- Radiotherapy within 3 weeks of the first dose of 852A
- Hematopoietic cell transplantation within 4 weeks of first dose of 852A
- Evidence of active infection within 3 days of first dose of 852A
- Active fungal infection or pulmonary infiltrates (prior treated disease stable for 2 weeks is allowable)
- Cardiac ischemia, cardiac arrhythmias or congestive heart failure uncontrolled by medication
- History of, or clinical evidence of, a condition which, in the opinion of the investigator, could confound the results of the study or put the subject at undue risk
- Uncontrolled intercurrent or chronic illness
- Active autoimmune disease requiring immunosuppressive therapy within 30 days
- Active coagulation disorder not controlled with medication
- Pregnant or lactating
- Concurrent malignancy (if in remission, at least 5 years disease free) except for localized (in-situ) disease, basal carcinomas and cutaneous squamous cell carcinomas that have been adequately treated
- Any history of brain metastases or any other active central nervous system (CNS) disease
Studijní plán
Jak je studie koncipována?
Detaily designu
- Primární účel: Léčba
- Přidělení: Nerandomizované
- Intervenční model: Přiřazení jedné skupiny
- Maskování: Žádné (otevřený štítek)
Počet zbraní
Zbraně a zásahy
Skupina účastníků / ArmSkupina účastníků / Arm |
Intervence / LéčbaIntervence / Léčba |
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Experimentální: Intent-To-Treat
Patients treated with at least one dose - 852A subcutaneous injection.
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0.2% 852a subcutaneous injection, 2 times per week for 12 weeks (24 doses) starting at 0.6 mg/m2; subsequent dose escalation for additional courses may be increased by 0.2 mg/m2 not to exceed 1.2 mg/m2.
Ostatní jména:
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Experimentální: Evaluable Cohort
Patients who received all 24 doses of 852A per protocol.
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0.2% 852a subcutaneous injection, 2 times per week for 12 weeks (24 doses) starting at 0.6 mg/m2; subsequent dose escalation for additional courses may be increased by 0.2 mg/m2 not to exceed 1.2 mg/m2.
Ostatní jména:
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Co je měření studie?
Primární výstupní opatření
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
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Patients With Tumor Response (Response Evaluation Criteria in Solid Tumors) Who Received All 24 Doses of 852A.
Časové okno: after 12 weeks (24 doses of 852A)
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Assessment of anti-tumor activity of 852A using Response Evaluation Criteria in Solid Tumors (RECIST) criteria to evaluate tumor response after 24 doses.
Complete Response (CR)= disappearance of all target lesions, Partial Response (PR) = at least 30% decrease in sum of longest diameter of target lesions, Progressive Disease (PD) = at least 25% increase in sum of longest diameter of target lesions, Stable Disease = neither PR or PD.
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after 12 weeks (24 doses of 852A)
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Sekundární výstupní opatření
Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
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Mean Difference Values for Interleukin 1 Receptor Antagonist (IKL1ra)
Časové okno: Prior to Dose 1 and 6 hours after Dose 1
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Measures the difference of IL1ra (cytokine) values as a means of immune activation pre-treatment and 6 hours post-treatment in patients that received at least one dose of study treatment with 852A.
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Prior to Dose 1 and 6 hours after Dose 1
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Mean Difference Values for 10 kDa Interferon-gamma-induced Protein (IP-10)
Časové okno: Prior to Dose 1 and 6 Hours Post-Dose
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Measures differences in IP-10 (cytokine) values as a means of immune activation pre-treatment and 6 hours post-treatment in patients that received at least one dose of study treatment with 852A.
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Prior to Dose 1 and 6 Hours Post-Dose
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Mean Difference Values for Macrophage Inflammatory Protein-1 Alpha (MIP-1a)
Časové okno: Prior to Dose 1 and 6 Hours Post-Dose
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Measures difference in MIP-1a (cytokine) values as a means of immune activation pre-treatment and 6 hours post-treatment in patients that received at least one dose of study treatment with 852A.
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Prior to Dose 1 and 6 Hours Post-Dose
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Mean Difference Values for Macrophage Inflammatory Protein-1 Beta (MIP-1b)
Časové okno: Prior to Dose 1 and 6 Hours Post-Dose
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Measures difference in Macrophage Inflammatory Protein-1 Beta (cytokine) values as a means of immune activation pre-treatment and 6 hours post-treatment in patients that received at least one dose of study treatment with 852A.
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Prior to Dose 1 and 6 Hours Post-Dose
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Mean Difference Values for Soluble CD40 Ligand (sCD40L)
Časové okno: Prior to Dose 1 and 6 Hours Post-Dose
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Measures difference in Soluble CD40 ligand (cytokine) values as a means of immune activation pre-treatment and 6 hours post-treatment in patients that received at least one dose of study treatment with 852A.
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Prior to Dose 1 and 6 Hours Post-Dose
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Mean Difference Values for Tumor Necrosis Factor-alpha (TNF-a)
Časové okno: Prior to Dose 1 and 6 Hours Post-Dose
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Measures difference in Tumor necrosis factor-alpha (cytokine) values as a means of immune activation pre-treatment and 6 hours post-treatment in patients that received at least one dose of study treatment with 852A.
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Prior to Dose 1 and 6 Hours Post-Dose
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Spolupracovníci a vyšetřovatelé
Sponzor
Sponzor
Spolupracovníci
Spolupracovníci
Vyšetřovatelé
Vyšetřovatelé
- Vrchní vyšetřovatel: Sarah Cooley, MD, Masonic Cancer Center, University of Minnesota
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia
Začátek studia
Primární dokončení (Aktuální)
Primární dokončení
Dokončení studie (Aktuální)
Dokončení studie
Termíny zápisu do studia
První předloženo
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Odhad)
První zveřejněno
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
Poslední zveřejněná aktualizace
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Naposledy ověřeno
Více informací
Termíny související s touto studií
Klíčová slova
Další relevantní podmínky MeSH
- Novotvary
- Urogenitální novotvary
- Novotvary podle místa
- Novotvary dělohy
- Genitální novotvary, ženy
- Onemocnění děložního čípku
- Onemocnění dělohy
- Onemocnění endokrinního systému
- Onemocnění vaječníků
- Adnexální onemocnění
- Gonadální poruchy
- Novotvary endokrinních žláz
- Novotvary děložního čípku
- Novotvary vaječníků
- Novotvary endometria
Další identifikační čísla studie
Další identifikační čísla studie
- 06US03IMP-852A
- MT2006-02 (Jiný identifikátor: Blood and Bone Marrow Transplantation Program)
- 2006LS005 (Jiný identifikátor: Masonic Cancer Center, University of Minnesota)
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