- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07603375
Upfront Chemotherapy With Radiation Therapy (CRT) Followed by Chemotherapy in Localized Esophageal Adenocarcinoma (TNT Esophagus)
26. august 2026 oppdatert av: Duke University
A Single-arm Study of Upfront Chemotherapy With Radiation Therapy (CRT) Followed by Chemotherapy in Localized Esophageal Adenocarcinoma
The goal of this trial is to learn if adding consolidative chemotherapy to routine chemoradiation can better control both local recurrence and metastasis and reduce the need for surgical intervention.
Studieoversikt
Status
Har ikke rekruttert ennå
Forhold
Intervensjon / Behandling
Studietype
Intervensjonell
Registrering (Antatt)
60
Fase
- Fase 2
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiekontakt
- Navn: Clinical Trials Office
- Telefonnummer: (919) 668-3726
- E-post: RadOnc-Clinical_Trials@dm.duke.edu
Studiesteder
-
-
North Carolina
-
Durham, North Carolina, Forente stater, 27710
- Duke University Medical Center
-
Hovedetterforsker:
- Manisha Palta, MD
-
Ta kontakt med:
- Kaitlin Bailey, RN BSN OCN
- Telefonnummer: (919) 668-3726
- E-post: RadOnc-Clinical_Trials@dm.duke.edu
-
-
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
- Voksen
- Eldre voksen
Tar imot friske frivillige
Nei
Beskrivelse
Inclusion Criteria:
- Subject must be able to provide study specific informed consent prior to study entry
- Must be newly diagnosed, histologically proven diagnosis of adenocarcinoma of the thoracic esophagus or gastroesophageal junction (Siewert I-II);
- Stage II-IVA, excluding T4b, according to the American Joint Committee on Cancer (AJCC) 8th edition;
- Complete history and physical examination within 21 days of signing consent;
- Staging whole-body FDG-PET/CT (fluorodeoxyglucose-positron emission tomography/computed tomography) scan with or without contrast (preferred) or chest/abdominal (CT with contrast) confirming there is no evidence of metastatic disease must be obtained within 45 days of study enrollment
- ECOG (Eastern Cooperative Oncology Group) performance status of 0-2
- Subjects must be appropriate candidates for planned chemoradiation (concurrent carboplatin/paclitaxel) and chemotherapy (FLOT, m-FOLFOX-6) as determined by the treating radiation oncologist, medical oncologist, and surgical oncologist.
- Adequate hematologic, renal, and hepatic function within 14 days of initiation of therapy
Exclusion Criteria:
- Cervical esophageal cancers arising 15-18 cm from the incisors.
- Esophageal squamous cell carcinoma.
- Patients with T4b disease according to the AJCC 8th Edition.
- Definitive clinical or radiologic evidence of metastatic disease.
- Has had prior systemic therapy or radiation therapy for the current diagnosis.
- Prior thoracic radiotherapy for any reason that would result in overlap of radiation therapy fields; all patients with prior radiotherapy must be reviewed by the PI to determine if patient is eligible.
- Has a known additional malignancy that is progressing or requires active treatment. Exceptions include basal cell carcinoma of the skin or squamous cell carcinoma of the skin that has undergone potentially curative therapy or in situ cervical cancer
Severe, active co-morbidity defined as follows:
- Active uncontrolled infection requiring IV antibiotics;
- Pregnant and/or nursing subjects;
- HIV positive with CD4 count < 200 cells/microliter. Note that subjects who are HIV positive are eligible, provided they are under treatment with highly active antiretroviral therapy (HAART) and have a CD4 count ≥ 200 cells/microliter within 30 days prior to registration. Note also that HIV testing is not required for eligibility for this protocol. This exclusion criterion is necessary because the treatments involved in this protocol may be significantly immunosuppressive.
- Has a history or current evidence of physical or physiological contraindication to participation in this study, at the discretion of the treating investigator.
- Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial.
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: N/A
- Intervensjonsmodell: Enkeltgruppeoppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Chemoradiation with consolidative chemotherapy
Participants will receive a standard course of chemoradiation followed by consolidative chemotherapy (FOLFOX regimen at the treating physician's discretion).
|
Modified-FOLFOX-6 or FLOT (Fluorouracil, Leucovorin, Oxaliplatin, Docetaxel)
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Number of participants with Clinical complete response (cCR)
Tidsramme: approximately 36 weeks
|
cCR defined as absence of malignancy on endoscopic biopsies obtained at the time of reassessment following neoadjuvant therapy
|
approximately 36 weeks
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Number of participants with pathologic complete response (pCR)
Tidsramme: approximately 36 weeks
|
Pathologic complete response (pCR) is defined as absence of detectable tumor of esophagectomy tissues.
|
approximately 36 weeks
|
|
Number of participants who complete both chemoradiation and chemotherapy
Tidsramme: approximately 36 weeks
|
approximately 36 weeks
|
|
|
Number of participants with local control
Tidsramme: up to 5 years
|
Local control in participants achieving clinical complete remission (cCR) estimated using the Kaplan-Meier method.
cCR is defined as the disappearance of all detectable signs and symptoms of a disease, such as cancer, have completely disappeared.
|
up to 5 years
|
|
Number of participants with Disease free survival
Tidsramme: up to 5 years
|
Disease free survival in participants achieving cCR estimated using the Kaplan-Meier method.
cCR is defined as the disappearance of all detectable signs and symptoms of a disease, such as cancer, have completely disappeared.
|
up to 5 years
|
|
Time to distant metastasis
Tidsramme: up to 5 years
|
Time to distant metastasis in participants achieving cCR estimated using the Kaplan-Meier method.
cCR is defined as the disappearance of all detectable signs and symptoms of a disease, such as cancer, have completely disappeared.
|
up to 5 years
|
|
Overall survival
Tidsramme: up to 5 years
|
Measured in participants achieving cCR and estimated using the Kaplan-Meier method.
cCR is defined as the disappearance of all detectable signs and symptoms of a disease, such as cancer, have completely disappeared.
|
up to 5 years
|
|
Number of participants with Local control
Tidsramme: up to 5 years
|
Measured in participants achieving pCR and estimated using the Kaplan-Meier method.
pCR is defined as absence of detectable tumor of esophagectomy tissues.
|
up to 5 years
|
|
Disease free survival
Tidsramme: up to 5 years
|
Disease free survival in participants achieving pCR.
pCR is defined as absence of detectable tumor of esophagectomy tissues.
|
up to 5 years
|
|
Time to distant metastasis
Tidsramme: up to 5 years
|
Time to distant metastasis in participants achieving pCR estimated using the Kaplan-Meier method.
pCR is defined as absence of detectable tumor of esophagectomy tissues.
|
up to 5 years
|
|
Overall survival
Tidsramme: up to 5 years
|
Measured in participants achieving pCR and estimated using the Kaplan-Meier method.
pCR is defined as absence of detectable tumor of esophagectomy tissues.
|
up to 5 years
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Etterforskere
- Hovedetterforsker: Manisha Palta, MD, Duke Health
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 (Antatt)
1. september 2026
Primær fullføring (Antatt)
1. august 2029
Studiet fullført (Antatt)
1. februar 2034
Datoer for studieregistrering
Først innsendt
18. mai 2026
Først innsendt som oppfylte QC-kriteriene
18. mai 2026
Først lagt ut (Faktiske)
22. mai 2026
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
28. august 2026
Siste oppdatering sendt inn som oppfylte QC-kriteriene
26. august 2026
Sist bekreftet
1. august 2026
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
- Neoplasmer etter nettsted
- Neoplasmer
- Gastrointestinale neoplasmer
- Neoplasmer i fordøyelsessystemet
- Sykdommer i fordøyelsessystemet
- Gastrointestinale sykdommer
- Neoplasmer i hode og nakke
- Esophageal sykdommer
- Neoplasmer i spiserøret
- Adenokarsinom i spiserøret
- Organiske kjemikalier
- Heterocykliske forbindelser, 1-ring
- Heterocykliske forbindelser
- Heterocykliske forbindelser, 2-ring
- Heterocykliske forbindelser, smeltet ringen
- Enzymer og koenzymer
- Koordinasjonskomplekser
- Pyrimidiner
- Formyltetrahydrofolater
- Tetrahydrofolater
- Folsyre
- Pteriner
- Pteridiner
- Uracil
- Pyrimidinoner
- Koenzymer
- Oksaliplatin
- Fluorouracil
- Leucovorin
- FOLFOX -protokoll
Andre studie-ID-numre
- Pro00120182
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
NEI
IPD-planbeskrivelse
Data may be shared 6 months after publication or as required by the journal
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Ja
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
produkt produsert i og eksportert fra USA
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. .