Ph II Intraperitoneal Paclitaxel + System Therapy in GI Ca w/Peritoneal Carcinomatosis (STOPGAP-B)
Phase II Basket Trial of Intraperitoneal Paclitaxel Plus Systemic Therapy in Gastrointestinal Malignancies With Peritoneal Carcinomatosis (STOPGAP - B)
Studienübersicht
Status
Status
Bedingungen
Bedingungen
Intervention / Behandlung
Intervention / Behandlung
Studientyp
Studientyp
Einschreibung (Geschätzt)
Einschreibung
Phase
Phase
- Phase 2
Kontakte und Standorte
Studienkontakt
Studienkontakt
- Name: Chao Family Comprehensive Cancer Center University of California, Irvine
- Telefonnummer: 1-877-827-8839
- E-Mail: ucstudy@uci.edu
Studieren Sie die Kontaktsicherung
- Name: University of California Irvine Medical
Studienorte
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California
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Orange, California, Vereinigte Staaten, 92868
- Rekrutierung
- Chao Family Comprehensive Cancer Center, University of California, Irvine
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Kontakt:
- Maheswari Senthil, MD
- Telefonnummer: 877-827-8839
- E-Mail: ucstudy@uci.edu
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-
Teilnahmekriterien
Zulassungskriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Beschreibung
Inclusion Criteria:
- Cohort A: Patients must have histologically or cytologically confirmed primary gastric or gastroesophageal adenocarcinoma with a clinical diagnosis of metachronous PC with a history of prior gastric cancer resection. Extraperitoneal metastases are allowed.
- Cohort B: Patients must have histologically or cytologically confirmed primary colorectal or appendiceal adenocarcinoma with PC . Extraperitoneal metastases are allowed. Patients with PC amenable to cytoreductive surgery (CRS) without the need for upfront systemic therapy as determined by a peritoneal malignancy surgeon within 4 weeks prior to enrollment are excluded.
- Cohort C: Patients must have adenocarcinomas of the digestive tract with PC not included in Cohorts A and B (including but not limited to carcinomas of the small bowel and hepatobiliary tract).
- Must have peritoneal cytology positive disease or peritoneal carcinomatosis detected by imaging, laparoscopy or laparotomy
- Age ≥ 18
- Performance status: ECOG performance status ≤ 2 (Appendix A) . ECOG 2 allowed if attributed to malignancy (rather than comorbidities)
- Life expectancy of greater than 3 months
- Adequate organ and marrow function as defined below: Leukocytes: ≥ 2,000/mcL; Absolute neutrophil count: ≥ 1,500/mcL (may receive gcsf); Platelets: ≥ 70,000/mcl (may receive TPO); Total bilirubin: within 2x of normal institutional limit; AST(SGOT)/ALT(SPGT): ≤5 X institutional upper limit of normal; Creatinine: < 2 X institutional upper limit of normal; Hemoglobin: Hemoglobin > 8.0 g/dL (may be transfused); Serum albumin: ≥ 2.5 g/dL
- Ability to understand and the willingness to sign a written informed consent
Exclusion Criteria:
- Any evidence of small or large bowel obstruction with the exception of gastric outlet obstruction due to primary malignancy
- Uncontrolled intercurrent illness including, but not limited to, the following conditions: Ongoing or active infection; Symptomatic congestive heart failure; Stroke (including transient ischemic attack [TIA]), myocardial infarction (MI), or other ischemic event,) within 3 months before initiation of treatment; Unstable angina pectoris; Cardiac arrhythmia
- History of another primary cancer within the last 3 years with the exception of non-melanoma skin cancer, early-stage prostate cancer, or curatively treated cervical carcinoma in-situ and not treated with systemic therapy.
- History of prior iterative intraperitonealtherapy administered either as HIPEC, PIPAC or NIPEC. Single exposure to HIPEC at the time of cytreduction is not an exclusion
- Inability to comply with study and follow-up procedures as judged by the Investigator
- Patients must not be pregnant or nursing due to the potential for congenital abnormalities and the potential of this regimen to harm nursing infants.
- Women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry, for the duration of study participation, and for 90 days following completion of therapy. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately.
- Has an active infection requiring systemic therapy.
- Prior surgery that would preclude safe diagnostic laparoscopy and port placement
- Has a known history of active tuberculosis (TB; Bacillus tuberculosis).
- Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the study, interfere with the participant's participation for the full duration of the study, or is not in the best interest of the participant to participate, in the opinion of the treating investigator.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Nicht randomisiert
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Keine (Offenes Etikett)
Anzahl der Arme
Waffen und Interventionen
Teilnehmergruppe / ArmTeilnehmergruppe / Arm |
Intervention / BehandlungIntervention / Behandlung |
|---|---|
|
Experimental: CohtAQ2W: Chort A Gastric/Esophageal Carcinoma (Paclitaxel Q2W)
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Given IP-IV, every 2 weeks
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Experimental: CohtAQ3W: Cohort A Gastric/Esophageal Carcinoma (Paclitaxel Q3W)
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Given IP-IV, every 3 weeks
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Experimental: CohtBQ2W: Cohort B Colorectal/Appendiceal Adenocarcinoma (Paclitaxel Q2W)
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Given IP-IV, every 2 weeks
|
|
Experimental: CohtBQ3W: Cohort B Colorectal/Appendiceal Adenocarcinoma (Paclitaxel Q3W)
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Given IP-IV, every 3 weeks
|
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Experimental: CohtCQ2W: Cohort C Other Malignancies of the Digestive Tract (Paclitaxel Q2W)
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Given IP-IV, every 2 weeks
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Experimental: CohtCQ3W: Cohort C Other Malignancies of the Digestive Tract (Paclitaxel Q3W)
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Given IP-IV, every 3 weeks
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Was misst die Studie?
Primäre Ergebnismessungen
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Protocol Treatment Completion Rate
Zeitfenster: 6 weeks
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Number of patients that complete treatment at 2 cycles
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6 weeks
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Sekundäre Ergebnismessungen
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Overall Survival of Participants
Zeitfenster: 3 years
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To assess the overall survival of participants from the start of systemic treatment to the death from any cause.
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3 years
|
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Participants with Progression Free Survival
Zeitfenster: 3 years
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Progression-free survival is defined as the duration of time from start of systemic treatment to time of progression, death, or clinical deterioration attributed to disease progression as judged by the investigator.
Radiographic progression is defined using the Response Evaluation Criteria in Solid Tumors Criteria (RECIST v1.1) as a 20% increase in the sum of diameters of target lesions and an absolute increase of at least 5 mm and/or appearance of new lesions.
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3 years
|
|
Patient Reported Quality of Life Outcomes
Zeitfenster: 1 year
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To assess the quality of life of participants such as mobility, self-care, daily activities, pain/discomfort and anxiety/depression and a visual analog scale (VAS).
VAS consists of endpoints labeled best imaginable health status at the top and worse imaginable health state at the bottom having numeric values of 100 and 0 respectively.
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1 year
|
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Incidence of Treatment-Emergent Adverse Events [Safety]
Zeitfenster: 1 year
|
To evaluate the safety of IP paclitaxel and IV paclitaxel, 5-FU, and leucovorin in patients with primary gastric/GEJ adenocarinoma with peritoneal carcinomatosis determined by the incidence of treatment-emergent adverse events.
Adverse events are based on the CTCAE (NCI Common Terminology Criteria for Adverse Events) Version 5.0.
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1 year
|
|
Overall Response Rate (ORR) by RECIST v1.1
Zeitfenster: 1 year
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Sum of Complete Response (CR) and Partial Response (PR) by RECIST v1.1.
Per Response Evaluation Criteria in Solid Tumors (RECIST v1.1): Complete Response (CR) is defined as the disappearance of all target lesions; Partial Response (PR) is defined as a 30% decrease in the sum of diameters of target lesions.
ORR = CR + PR
|
1 year
|
Mitarbeiter und Ermittler
Sponsor
Sponsor
Ermittler
Ermittler
- Hauptermittler: Maheswari Senthil, MD, Chao Family Comprehensive Cancer Center
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Studienbeginn
Primärer Abschluss (Geschätzt)
Primärer Abschluss
Studienabschluss (Geschätzt)
Studienabschluss
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Zuerst gepostet
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes Update gepostet
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
- Pathologische Prozesse
- Neubildungen nach Standort
- Neubildungen
- Neubildungen nach histologischem Typ
- Gastrointestinale Neubildungen
- Neoplasmen des Verdauungssystems
- Erkrankungen des Verdauungssystems
- Magen-Darm-Erkrankungen
- Magenerkrankungen
- Kopf-Hals-Neubildungen
- Neubildungen, Drüsen und Epithelien
- Adenokarzinom
- Erkrankungen der Speiseröhre
- Karzinom
- Neubildungen, zystische, schleimige und seröse
- Pathologische Zustände, Anzeichen und Symptome
- Magenneoplasmen
- Ösophagusneoplasmen
- Erkrankung
- Adenokarzinom, muzinös
Andere Studien-ID-Nummern
Andere Studien-ID-Nummern
- STUDY00001075
- UCI 25-190 (Andere Kennung: UCI CFCCC)
Plan für individuelle Teilnehmerdaten (IPD)
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Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
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