Not provided
Not provided
Not provided
| ID | Type | Description | Link |
|---|---|---|---|
| 2013-A01846-39 | Other Identifier | ANSM |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Adjuvant radiotherapy after lumpectomy allows a local long-term control of the order 85 to 95% with a survival rate equivalent to that of the totally mastectomy. The diminution of the local recurrence rate after irradiation post- lumpectomy is also associated to a best global survival than only the surgery. The adjuvant radiotherapy after partially or totally mastectomy for the progressive tumors is a therapeutic standard (Early Breast Cancer Trialists' Collaborative Group 2011). The aim of our trial of routine care is to record our practices under this breast adjuvant radiotherapy.
Patients responding criteria for selection and not objecting to participate in this trial will address the quality of life questionnaires at baseline and during their standard follow-up (1, 6, 12 and 24 months after the end of radiotherapy). The data of toxicity and disease-free survival will be collected from data on medical record of the patient.
The therapeutic support and monitoring are standard.
Not provided
Not provided
Not provided
Not provided
| Measure | Description | Time Frame |
|---|---|---|
| acute and tardive toxicity according to NCI-CTCAE v4.0 | according to NCI-CTCAE v4.0 | up to 5 years |
| Measure | Description | Time Frame |
|---|---|---|
| Quality of life according to QLQC-30 | Quality of life according to QLQC-30 | up to 24 months |
| Quality of life according to BR-23 module | Quality of life according to BR-23 module |
Not provided
Inclusion Criteria:
1-Patient with breast cancer proved by histology and treated surgically 2. Relevant of adjuvant radiotherapy after partial or total mastectomy with or without lymph node irradiation 3- Age ≥ 18 years 4- Information and no opposition to the patient
Exclusion Criteria:
Not provided
Not provided
Not provided
prospective study of routine care done on women with breast cancer treated by adjuvant radiotherapy with intensity modulated
Not provided
| Name | Affiliation | Role |
|---|---|---|
| David PASQUIER, MD | Centre Oscar Lambret | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Centre Léonard de Vinci | Douai | 59500 | France | |||
| Centre Oscar Lambret |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 33574446 | Derived | Pasquier D, Bataille B, Le Tinier F, Bennadji R, Langin H, Escande A, Tresch E, Darloy F, Carlier D, Crop F, Lartigau E. Correlation between toxicity and dosimetric parameters for adjuvant intensity modulated radiation therapy of breast cancer: a prospective study. Sci Rep. 2021 Feb 11;11(1):3626. doi: 10.1038/s41598-021-83159-3. |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D001943 | Breast Neoplasms |
| ID | Term |
|---|---|
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
| D001941 | Breast Diseases |
| D012871 | Skin Diseases |
Not provided
Not provided
Not provided
Not provided
Not provided
| up to 24 months |
| Disease free survival | according to RECIST 1.1 | up to 5 years |
| esthetic results | by physician and patient according to a scale (good, excellent, moderate and poor) | up to 5 years |
| Lille |
| 59020 |
| France |
| D017437 |
| Skin and Connective Tissue Diseases |