Denne siden ble automatisk oversatt og nøyaktigheten av oversettelsen er ikke garantert. Vennligst referer til engelsk versjon for en kildetekst.

Fase II-protokoll for protonterapi for delvis brystbestråling i tidlig stadium av brystkreft

25. september 2026 oppdatert av: Proton Collaborative Group

The purpose of this research study is to compare the effects (good and bad) on women and their cancer using proton radiation therapy.

This study is being done to see if proton radiation therapy will prove to be beneficial for women with early stage breast cancer. A clinical study is necessary to compare the results (good or bad) of proton radiation therapy.

Studieoversikt

Status

Rekruttering

Forhold

Intervensjon / Behandling

Detaljert beskrivelse

Current standard of care for early stage breast cancer is mastectomy or breast conserving therapy with whole breast irradiation following lumpectomy. However, studies of breast cancer recurrence have demonstrated the majority of tumors to recur in or adjacent to the original tumor site. The question has thus been raised as to whether radiation to the whole breast is necessary or justified. Limiting radiation to the area of the original tumor may reduce acute and long-term skin and organ toxicities while making radiation therapy more convenient and less expensive. Several clinical trials are underway comparing partial breast irradiation (PBI) to whole breast irradiation. Numerous centers are offering partial breast irradiation outside of clinical trials as well, despite the lack of long-term safety and efficacy data on PBI.

Available PBI methods include brachytherapy, in which catheters or balloons are surgically inserted to deliver radiation therapy to the lumpectomy cavity, and conventional external beam radiation therapy, or EBRT. External beam photon therapy is attractive for its non-invasive nature and ability to deliver a more homogenous dose distribution compared to brachytherapy, however it also delivers a greater radiation dose to surrounding normal breast tissue.Proton therapy has the capacity to provide the same advantages as photon EBRT while minimizing dose to normal surrounding tissue. Clinical data on PBI with protons is minimal, however, leaving many questions unanswered. The impetus behind this protocol is to address these gaps by further investigating the feasibility, safety, and efficacy of proton therapy for partial breast irradiation.

Studietype

Intervensjonell

Registrering (Antatt)

132

Fase

  • Fase 2

Kontakter og plasseringer

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

Studiesteder

  • Forente stater
    • Arizona
      • Scottsdale, Arizona, Forente stater, 85259
        • Rekruttering
        • Mayo Clinic
        • Hovedetterforsker:
          • Carlos Vargas, MD
        • Ta kontakt med:
    • California
      • San Diego, California, Forente stater, 92121
        • Rekruttering
        • California Protons Cancer Therapy Center
        • Ta kontakt med:
        • Hovedetterforsker:
          • James Urbanic, MD
    • Illinois
      • Warrenville, Illinois, Forente stater, 60555
        • Rekruttering
        • Northwestern Medicine Chicago Proton Center
        • Ta kontakt med:
        • Hovedetterforsker:
          • Arpi Thukral, MD
    • Maryland
      • Baltimore, Maryland, Forente stater, 21201
        • Rekruttering
        • Maryland Proton Treatment Center
        • Ta kontakt med:
        • Hovedetterforsker:
          • Elizabeth Nichols, MD
    • Michigan
      • Flint, Michigan, Forente stater, 48532
        • Rekruttering
        • McLaren Proton Therapy Center
        • Ta kontakt med:
        • Hovedetterforsker:
          • Brian Yeh, MD
    • New York
      • New York, New York, Forente stater, 10035
        • Rekruttering
        • New York Proton Center
        • Ta kontakt med:
        • Hovedetterforsker:
          • Isabelle Choi, MD
    • Oklahoma
      • Oklahoma City, Oklahoma, Forente stater, 73142
        • Rekruttering
        • Oklahoma Proton Center
        • Hovedetterforsker:
          • John Chang, MD
        • Ta kontakt med:
    • Virginia
      • Fairfax, Virginia, Forente stater, 22031
        • Rekruttering
        • Inova Schar Cancer Institute
        • Ta kontakt med:
        • Hovedetterforsker:
          • Ashish Chawla, MD
      • Hampton, Virginia, Forente stater, 23666
        • Rekruttering
        • Hampton University Proton Therapy Institute
        • Ta kontakt med:
        • Hovedetterforsker:
          • Christopher Sinesi, MD

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

50 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Hunn

Beskrivelse

Inclusion Criteria:

  • Must sign study-specific, IRB approved informed consent form prior to study entry. Note consent by legally authorized representative is not allowed for this trial.

  • Must be female.

  • Must be > = 50 years of age.

  • Must have a life expectancy of at least 5 years based on age and co-morbidities.

  • Must have pathology proven invasive ductal carcinoma (lobular is not allowed) and/or ductal carcinoma in situ (DCIS).

  • One of the following criteria must be met: (a) Tumors that are microscopically multifocal must be 3.0 cm or less in total aggregate size and encompassed within a single scar (b) Patient does not have microscopically multifocal tumor.

  • For tumors that are invasive, if in the presence of extensive intraductal component (EIC), the entire pathologic tumor size (including both the intraductal and invasive component) must be 3.0 cm or less.

  • Must be Stage 0, I, II (Tis, T1, or T2, N0, M0 per AJCC criteria 7th and/or 8th Ed.). If stage II, the tumor size must be < = 3.0 cm. A patient with invasive histology must have nodal stage pN0 by H&E stains on sentinel node biopsy or axillary lymph node dissection.

  • Must have ER positive disease with ER/PR report available.

  • For tumors that are invasive, HER2 must be performed (positive or negative is acceptable).

  • Must have a lumpectomy performed, with documented negative surgical margins by 0.2 cm or more. If re-excision results in negative surgical margins 0.2 cm or more, patient is eligible.

  • If image guidance with daily cone beam CT with direct physician visual assessment is used for treatment positioning, the presence of markers or clips in the surgical bed is recommended but not required. If cone beam CT imaging will NOT be used for image guidance, then the patient must be prepared to have 2 fiducial markers minimum, 3 preferred, placed prior to treatment (if not previously done).

    • If markers or clips were placed at the time of surgery, patient must be able to start treatment within 12 weeks after lumpectomy or re-excision for adequate margins.
    • If markers were not placed at the time of surgery and are needed, patient must have markers placed within 6 weeks after surgery.
    • If systemic chemotherapy was given, patient must have had clips or markers placed at the time of surgery (if they are needed) and patient must have simulation scans within 6 weeks of the completion of the chemotherapy.

  • Must be able to start treatment within 12 weeks of surgery or 8 weeks of finalization of chemotherapy.

Exclusion Criteria:

  • Previous history of ipsilateral invasive breast cancer or DCIS.
  • Any clinical or radiographically suspicious nodes, unless biopsy proven benign.
  • Non-epithelial malignancies such as sarcoma or lymphoma.
  • Suspicious residual microcalcifications on mammography of either breast, unless negative for malignancy on pathology.
  • Multicentric or bilateral disease unless biopsy of the clinical abnormalities are performed and result is negative.
  • Lymphovascular space invasion (LVSI) on pathology specimen.
  • Any previously treated breast carcinoma or synchronous breast carcinoma in ipsilateral breast.
  • Prior radiation therapy to the ipsilateral breast or thorax.
  • Paget's disease of the nipple.
  • Histologic examination showing invasive lobular histology.
  • Skin involvement.
  • Breasts technically unsatisfactory for radiation treatment upon the discretion of the treating physician.
  • Significant infection or other co-existing medical condition that would preclude protocol therapy such as pregnancy, HIV/AIDS or collagen vascular diseases specifically systemic lupus erythematosus, scleroderma, or dermatomyositis.
  • Known BRCA 1 or BRCA 2 mutation.
  • Pregnant or lactating.

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: Proton Radiotherapy

Proton Radiotherapy 4.0 Gy (RBE) x10 fractions to 40 Gy (RBE) Total Dose
Stråling: Protonstrålebehandling

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
To assess events of freedom from ipsilateral breast recurrence occurrences in patients receiving partial breast proton radiation therapy limited to the region of the tumor.
Tidsramme: At 3 years

Freedom from failure (FFF): The events for FFF will be the first ipsilateral breast cancer recurrence. It is expected that less than 3% of patients will experience an ipsilateral breast cancer recurrence (FFF ≥ 97%). A recurrence rate of ≥ 10% (FFF ≤ 90%) is considered unacceptable. Therefore, the null hypothesis is the FFF of ipsilateral breast cancer recurrence is 90% or lower and the alternative hypothesis is that FFF of ipsilateral breast cancer is 97% or higher.
At 3 years

Sekundære resultatmål

Resultatmål
Tidsramme
Vurder antall og alvorlighetsgrad av akutt og langsiktig toksisitet av delvis brystbestråling ved bruk av protonterapi for behandling av brystkreft i tidlig stadium.
Tidsramme: I gjennomsnitt hver 6. måned livet ut
I gjennomsnitt hver 6. måned livet ut
For å vurdere sammenhengen mellom bryststørrelse og delvis brystdosimetri.
Tidsramme: Gjennomsnittlig hver 6. måned i 3 år
Gjennomsnittlig hver 6. måned i 3 år
Bestem resultater for livskvalitet.
Tidsramme: Gjennomsnittlig hver 6. måned i 3 år
Gjennomsnittlig hver 6. måned i 3 år
For å bestemme total overlevelsesrate for pasienter med brystkreft behandlet med protonstråling.
Tidsramme: Ved 3 år
Ved 3 år
For å bestemme tilbakefallsmønster for pasienter med brystkreft behandlet med protonpartiell brystbestråling.
Tidsramme: Ved 3 år
Ved 3 år

Samarbeidspartnere og etterforskere

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

Sponsor

Proton Collaborative Group

Etterforskere

  • Studiestol: Andrew Chang, MD, Proton Collaborative Group

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. februar 2013

Primær fullføring (Antatt)

1. januar 2027

Studiet fullført (Antatt)

1. januar 2035

Datoer for studieregistrering

Først innsendt

28. desember 2012

Først innsendt som oppfylte QC-kriteriene

9. januar 2013

Først lagt ut (Antatt)

11. januar 2013

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

29. september 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

25. september 2026

Sist bekreftet

1. september 2026

Mer informasjon

Begreper knyttet til denne studien

Nøkkelord

Ytterligere relevante MeSH-vilkår

Andre studie-ID-numre

  • BRE007-12

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. .

Abonnere