the Effect of Therapeutic Mammoplasty on the Start of Adjuvant Chemotherapy

Sponsor
Assiut University (Other)
Overall Status
Completed
CT.gov ID
NCT05920070
Collaborator
(none)
50
97

Study Details

Study Description

Brief Summary

the purpose of this study was to examine the impact of therapeutic mammoplasty on the delivery of adjuvant chemotherapy

Condition or Disease Intervention/Treatment Phase
  • Procedure: therapeutic mammoplasty

Detailed Description

One out of every eight women will be diagnosed with breast cancer in her lifetime, making it the most common cancer in women. Over the last decades the survival rate has increased slowly, which is currently estimated to be 85 % in developed countries. However, with an estimated annual number of breast cancer deaths of 537,000 worldwide, breast cancer still is the most important cause of death by cancer among women. Despite advances in different treatment modalities, about 45 % of all breast cancer patients still undergoes a mastectomy for adequate local control. The resulting loss of a breast may have a negative effect on body image, sexuality, and sense of femininity. (8) Oncoplastic breast techniques are being increasingly employed to allow breast conservation whilst maintaining a quality aesthetic outcome. Therapeutic mammoplasty (TM) describes multiple breast-conserving techniques1 which remove the breast tumour in combination with adjuvant radiotherapy (1). TM is available to women with early stage breast cancer with larger or ptotic breasts who would benefit from a reduction mammoplasty technique in addition to tumour removal. The use of TM is increasing worldwide, with the potential to deliver benefits both oncologically, in terms of increased tumour free margin width, and with an associated superior long-term aesthetic outcome. Despite increasing enthusiasm for the techniques there is limited data on long-term oncological safety or effects upon delivery of adjuvant treatments.TM techniques can enable a larger volume of tissue to be resected with the tumour6 enabling patients to have breast-conserving surgery for larger tumours. Just as the role of TM is expanding, adjuvant chemotherapy is increasingly being used in women with early stage breast cancer and if delivered in a timely fashion after the primary resection, decreases recurrence and improves overall survival (3). However, TM is associated with higher complication rates than traditional breast-conserving methods and one barrier to TM is the concern that post-operative complications may lead to a delay in initiation of chemotherapy or even omission. There is increasing evidence that immediate breast reconstruction has an effect on adjuvant chemotherapy delivery. Three recent series involving over 4000 patients suggest that immediate breast reconstruction does lead to a significant delay in the delivery of adjuvant chemotherapy (2). However, the clinical significance of this delay has not been established. On the contrary, a recent study performed by Doughty et al. compared 95 patients undergoing immediate breast reconstruction following mastectomy with cohorts having breast-conserving surgery and simple mastectomy with no reconstruction, in which no delay to commencement of adjuvant chemotherapy was noted. The majority of case series on TM do not comment on the timing of adjuvant treatments. When they are reported, studies vary between no delays to adjuvant treatment through to five studies reporting delays in between 1.9%9 and 6% of patients (8).

Study Design

Study Type:
Observational
Actual Enrollment :
50 participants
Observational Model:
Other
Time Perspective:
Retrospective
Official Title:
Therapeutic Mammoplasty Doesn't Delay Adjuvant Therapy for Breast Cancer Patients
Actual Study Start Date :
Mar 1, 2015
Actual Primary Completion Date :
Mar 1, 2023
Actual Study Completion Date :
Apr 1, 2023

Outcome Measures

Primary Outcome Measures

  1. assesing the complocation of therapeutic mammoplasty and whether it delays the start of adjuvant chemotherapy or not [about two months]

    noting the date of the operation and whether or not it delays the start of adjuvant chemotherapy due to any complications

Eligibility Criteria

Criteria

Ages Eligible for Study:
25 Years to 65 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Oncoplastic procedures were proposed for patients in whom breast conservative treatment is possible on oncologic grounds but in whose cases a standard resection without reconstruction would result in poor cosmesis with the following criteria:
  1. Female patients with ages ranging from 25 to 65 years

  2. Patients with early surgically treatable breast cancer (Stage I, II and IIIa)

  3. Patients whose management was by surgery followed by adjuvant chemotherapy.

  4. Patients with tumors in any quadrant of the breast

  5. Patients with large/ptotic breasts (especially with brassiere size C, D or DD).

  6. patients underwent therapeutic mammoplasty as primary ttt for breast cancer.

Exclusion Criteria:
    1. Patients with a contraindication to breast conservative surgery. 2) Patients with small sized breasts, which are not suitable for reduction (with brassiere size A or B).
  1. Patients who are not compliant; Non-compliant patients included those demanding mastectomy for fear of local recurrence, patients not consenting to the proposed procedure after adequate counseling, those refusing post-operative adjuvant Radiotherapy, refusal of a reduction mammoplasty of the contralateral breast as a symmetrizing procedure and patients who are not able to consent such as mentally challenged patients.

  2. patients who have received neoadjuvant chemotherapy. 5) patients underwent conventional breast conservative surgery . 6) patient underwent immediate reconstruction surgery.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Assiut University

Investigators

  • Study Director: abdelradi amdelsalam, proffessor, Assiut University
  • Study Director: mostapha thabet, professor, Assiut University
  • Study Director: negmeldeen abulnaga, assistant lecturer, Assiut University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Mariam Nabil Anwer, resident at general surgery department, Assiut University
ClinicalTrials.gov Identifier:
NCT05920070
Other Study ID Numbers:
  • tmp and adjuvant chemotherapy
First Posted:
Jun 27, 2023
Last Update Posted:
Jun 27, 2023
Last Verified:
Jun 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Jun 27, 2023