Phase II Study of Intra-Operative Electron Irradiation and External Beam Irradiation After Lumpectomy in Patients With T1N0M0 and T2N0M0 Breast Cancer
2 april 2014 uppdaterad av: Mayo Clinic
The study is being done to determine the tolerance to single fraction intra-operative electron irradiation (IOERT) and external beam photon irradiation (EBRT) following lumpectomy for T1/T2N0M0 breast cancer.
IOERT is used in lieu of the 5-8 days of electron beam boost irradiation that is usually given after EBRT.
Data from two centers as well as preliminary data from a randomized trial in Europe suggest that IOERT boost is well tolerated and efficacious.
In our study, patients will undergo standard lumpectomy and sentinel lymph node sampling or axillary dissection.
After the lumpectomy, IOERT of 10 Gy will be delivered in a single fraction to the tumor bed by a mobile electron machine in the operating room.
EBRT to the whole breast will be administered once the surgical wound has healed adequately.
The primary objective is to determine the feasibility and acute patient tolerance to IOERT and EBRT after lumpectomy.
Secondary objectives include assessment of local control and distant control of disease, as well as evaluation of long-term side effects and cosmetic outcome of the treatment.
Studieöversikt
Status
Avslutad
Betingelser
Intervention / Behandling
Studietyp
Interventionell
Inskrivning (Faktisk)
65
Fas
- Fas 2
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
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Arizona
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Scottsdale, Arizona, Förenta staterna
- Mayo Clinic
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Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
18 år och äldre (Vuxen, Äldre vuxen)
Tar emot friska volontärer
Nej
Kön som är behöriga för studier
Kvinna
Beskrivning
Eligibility:
- Histologically proven primary invasive breast carcinoma.
- Tumor pathologically determined <= 5cm in diameter.
- Single, discrete, well-defined primary tumor.
- Any micro-calcifications must be focal. A specimen radiograph is required after lumpectomy to assure removal of all malignant appearing calcifications.
- Pathologically negative surgical margins.
- Axillary lymph node status can be determined by level I and II lymph node dissection or sentinel lymph node sampling.
- ECOG performance status 0-2.
Contraindications:
- Multicentric disease and/or diffuse malignant appearing microcalcifications.
- Evidence of metastatic breast cancer.
- Axillary lymph node involvement.
- Pre-existing collagen vascular disease except rheumatoid arthritis that does not require immunosuppressive therapy.
- Prior irradiation to the ara of planned radiation field.
- Pregnant or lactating women.
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Icke-randomiserad
- Interventionsmodell: Enskild gruppuppgift
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
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Experimentell: Single arm study
Patients with stage T1/T2No breast cancer receiving breast conserving treatment
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IOERT is given to the tumor bed.
Applicator selection should allow treatment of the tumor bed plus 1-2 cm margin.
The surgical incision may need to be enlarged slightly to allow the placement of the appropriate applicator.
The use of more than 1 treatment field is discouraged.
In order to encompass the entire tumor bed in 1 treatment field, it may be necessary to suture the mammary parenchyma loosely so that the lateral margins of the tumor bed are brought into apposition.
Electron energy used for the treatment.
If the tumor bed can be flattened and encompassed by an applicator, 6 MeV electron is recommended.
Use of bolus material may be considered to increase the surface dose.
If the mammary parenchyma has been brought into apposition by sutures, a higher electron energy may be necessary to allow adequate dose coverage to a depth of 1.0-2.0
cm into the tumor bed.
The dose of IOERT is 1000 cGy, prescribed to the 90% isodose line.
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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Determine the feasibility and acute patient tolerance of IOERT and EBRT after lumpectomy for patients with stage T1/T2N0M0 breast cancer.
Tidsram: weekly evaluation during 5 weeks of radiation
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To determine the acute skin reaction, breast edema, pnemonitis, cardiac side effects during radiation using RTOG acute toxicity scale
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weekly evaluation during 5 weeks of radiation
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Determine the local tumor control and distant tumor control rates for patients with stage T1/T2N0M0 breast cancer.
Tidsram: every 6 months follow-up for 5 years, then yearly to end in 04/2013
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every 6 months follow-up for 5 years, then yearly to end in 04/2013
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Determine long-term side effects and cosmetic outcome of IOERT to tumor bed and EBRT after lumpectomy for patients with stage T1/T2N0Mo breast cancer.
Tidsram: every 6 months follow-up for 5 years, then yearly to end in 04/2013
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To determine the late skin reaction, breast edema, pneumonitis, cardiac side effects during radiation using RTOG late toxicity scale
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every 6 months follow-up for 5 years, then yearly to end in 04/2013
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Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Sponsor
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart
1 januari 2003
Primärt slutförande (Faktisk)
1 januari 2005
Avslutad studie (Faktisk)
1 januari 2013
Studieregistreringsdatum
Först inskickad
7 augusti 2009
Först inskickad som uppfyllde QC-kriterierna
4 oktober 2010
Första postat (Uppskatta)
6 oktober 2010
Uppdateringar av studier
Senaste uppdatering publicerad (Uppskatta)
3 april 2014
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
2 april 2014
Senast verifierad
1 april 2014
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- 1681-02 (Mayo Clinic IRB)
- MCS066 (Mayo Clinic Cancer Center)
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