Skip to content

Histological Response Rate After Mastectomy and Immediate Breast Reconstruction at the End of Neoadjuvant Chemotherapy and Radiotherapy

Histological Response Rate After Mastectomy and Immediate Breast Reconstruction at the End of Neoadjuvant Chemotherapy and Radiotherapy

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02679040
Acronym
HIST-RIC
Enrollment
101
Registered
2016-02-10
Start date
2016-01-27
Completion date
2025-02-28
Last updated
2023-07-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Brief summary

At present, it is widely admitted not proposing immediate mammary reconstruction when an adjuvant radiotherapy is indicated because of the significant change of the cosmetic result (profit) and it whatever is the technique of reconstruction adopted. This is true all the more as it is about a reconstruction by prosthesis because of the prothetic died risk of hull(shell). Teams proposed immediate mammary reconstructions to expanding (carrier) patients of carcinoma infiltrating, sometimes locally moved forward. For these patients, was not brought back(reported) by increase of the risk of local or remote relapse. Two studies estimated afterward the feasibility of the mastectomy with immediate mammary reconstruction at the close of the chemotherapy and of the radiotherapy. The rate of morbidity is judged as acceptable. The rate of local second offense(recurrence) was similar to the patients benefiting from the classic therapeutic plan. During an other study ( M-RIC), it was shown that the inversion of therapeutic sequence is possible and that by prescribing the chemotherapy and the radiotherapy before immediate mammary reconstruction, the morbidity is acceptable. It is acquired that the chemotherapy néoadjuvant is equivalent to the post-operative chemotherapy as regards the global survival. On the other hand, the rate of histological answer, according to subgroups, is very different. This rate can vary of 9 % for tumors RH +, negative Her2 in 45 % for tumors RH-, Her2 over expression. There are 33 % for the RH +, Her2 + and of 35 % for triple-negative. The purpose of the investigators study is to estimate the rate of histological response during the inversion of therapeutic sequence to make sure of the oncologic safety(security), in particular by molecular subgroups, considering the heterogeneousness of the results(profits) after chemotherapy néoadjuvant only. Sataloff and Chevallier Classifications is the references and will be used here, but the investigators can also use Symmans classification in addition. The rate of local and metastatic second offenses(recurrences) will also be estimated.

Interventions

PROCEDUREImmediate mammary reconstruction

Chemotherapy administration then radiotherapy and then surgery : mastectomy and immediate mammary reconstruction.

DRUGChemotherapy

Chemotherapy treatment

RADIATIONRadiation therapy

Radiation therapy

Sponsors

Institut Paoli-Calmettes
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age \> 18 years, * Infiltrating carcinoma, * Neoadjuvant chemotherapy indication, * Radiotherapy indication, * 0 or 1 score Performance status (WHO), * Signed informed consent, * Affiliation to Social Security System

Exclusion criteria

* Lobular carcinoma, * Luminal A Tumor (RH+ and Her2 negative with grade I, and tumor RH+ Her2 negative with grade II and with Ki67\<20%), * Attempt of first conservative treatment, * Metastatic breast cancer, * Inflammatory carcinoma, * History of homolateral or controlateral mammary carcinoma, * Progression disease (despite neoadjuvant chemotherapy), * Contraindications in an immediate mammary reconstruction by scrap of big dorsal (comorbidity), * Any psychological, familial, sociological or geographical condition-potentially hampering compliance with the study protocol or follow-up schedule, * Patients deprived of liberty or placed under the authority of a tutor.

Design outcomes

Primary

MeasureTime frameDescription
Rate of histological response of an infiltrating tumor within various molecular subgroupsfrom surgery up to 1 monthTumor Histological response (group RH+ Her2+, group RH+ Her2-, group RH- Her2+, and group RH- Her2-)

Secondary

MeasureTime frameDescription
Rate of ganglionar response on the axillary lymph nodes after chemotherapy and radiotherapy néoadjuvantfrom surgery up to 1 monthNumber of lymph nodes collected and number of positive lymph nodes

Other

MeasureTime frameDescription
Rate of local and metastatic relapsefrom surgery up to 5 yearsLocal and metastatic relapse evaluated by radiological exams (Echo-mammography and MRI)
Quality of life in post-operative at 4 months and at 1 year and patient satisfactionBefore surgery, at day 21, at 6 months and at 12 monthsQuality of life evaluated by questionnaire QLQ-C30
Rate of post-operative complicationsfrom surgery up to 1 monthPost operative complications evaluated by clinical exam

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026