Acute and Long-Term Toxicity after Planned Intraoperative Boost and Whole Breast Irradiation in High-Risk Patients with Breast Cancer-Results from the Targeted Intraoperative Radiotherapy Boost Quality Registry (TARGIT BQR).

IORT boost breast cancer fibrosis high risk intraoperative radiotherapy toxicity whole breast irradiation

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
30 May 2024
Historique:
received: 30 04 2024
revised: 22 05 2024
accepted: 24 05 2024
medline: 19 6 2024
pubmed: 19 6 2024
entrez: 19 6 2024
Statut: epublish

Résumé

In the context of breast cancer treatment optimization, this study prospectively examines the feasibility and outcomes of utilizing intraoperative radiotherapy (IORT) as a boost in combination with standard external beam radiotherapy (EBRT) for high-risk patients. Different guidelines recommend such a tumor bed boost in addition to whole breast irradiation with EBRT for patients with risk factors for local breast cancer recurrence. The TARGIT BQR (NCT01440010) is a prospective, multicenter registry study aimed at ensuring the quality of clinical outcomes. It provides, for the first time, data from a large cohort with a detailed assessment of acute and long-term toxicity following an IORT boost using low-energy X-rays. Inclusion criteria encompassed tumors up to 3.5 cm in size and preoperative indications for a boost. The IORT boost, administered immediately after tumor resection, delivered a single dose of 20 Gy. EBRT and systemic therapy adhered to local tumor board recommendations. Follow-up for toxicity assessment (LENT SOMA criteria: fibrosis, teleangiectasia, retraction, pain, breast edema, lymphedema, hyperpigmentation, ulceration) took place before surgery, 6 weeks to 90 days after EBRT, 6 months after IORT, and then annually using standardized case report forms (CRFs). Between 2011 and 2020, 1133 patients from 10 centers were preoperatively enrolled. The planned IORT boost was conducted in 90%, and EBRT in 97% of cases. Median follow-up was 32 months (range 1-120, 20.4% dropped out), with a median age of 61 years (range 30-90). No acute grade 3 or 4 toxicities were observed. Acute side effects included erythema grade 1 or 2 in 4.4%, palpable seroma in 9.1%, punctured seroma in 0.3%, and wound healing disorders in 2.1%. Overall, chronic teleangiectasia of any grade occurred in 16.2%, fibrosis grade ≥ 2 in 14.3%, pain grade ≥ 2 in 3.4%, and hyperpigmentation in 1.1%. In conclusion, a tumor bed boost through IORT using low-energy X-rays is a swift and feasible method that demonstrates low rates in terms of acute or long-term toxicity profiles in combination with whole breast irradiation.

Identifiants

pubmed: 38893184
pii: cancers16112067
doi: 10.3390/cancers16112067
pii:
doi:

Types de publication

Journal Article

Langues

eng

Auteurs

Lukas Goerdt (L)

Department of Gynecology and Obstetrics, University Medical Center Mannheim, Medical Faculty Mannheim, Heidelberg University, 68167 Mannheim, Germany.

Robert Schnaubelt (R)

Radiation Oncology, MVZ Rheinland Klinikum Neuss, 41462 Neuss, Germany.

Uta Kraus-Tiefenbacher (U)

Department of Radiation Oncology, Krankenhaus Nordwest, 60488 Frankfurt am Main, Germany.

Viktoria Brück (V)

Breast Center, Asklepios Klinik Barmbek, 22307 Hamburg, Germany.

Lelia Bauer (L)

Breast Center, GRN Klinik Weinheim, 69469 Weinheim, Germany.

Stefan Dinges (S)

Department of Radiation Oncology, Städtisches Klinikum Lüneburg, 21339 Lüneburg, Germany.

Albert von der Assen (A)

Breast Center, Department of Senology, Franziskus Hospital Harderberg-Niels Stensen Kliniken, 49124 Georgsmarienhütte, Germany.

Heidrun Meye (H)

Department of Radiation Oncology, MVZ Gesundheit Nordhessen, 34125 Kassel, Germany.

Christina Kaiser (C)

University Medical Center Bonn, Medical Faculty Bonn, Bonn University, 53113 Bonn, Germany.

Christel Weiss (C)

Department of Medical Biometry, University Medical Center Mannheim, Medical Faculty Mannheim, Heidelberg University, 68167 Mannheim, Germany.

Sven Clausen (S)

Department of Radiation Oncology, University Medical Center Mannheim, Medical Faculty Mannheim, Heidelberg University, 68167 Mannheim, Germany.

Frank Schneider (F)

Department of Radiation Oncology, University Medical Center Mannheim, Medical Faculty Mannheim, Heidelberg University, 68167 Mannheim, Germany.

Yasser Abo-Madyan (Y)

Department of Radiation Oncology, University Medical Center Mannheim, Medical Faculty Mannheim, Heidelberg University, 68167 Mannheim, Germany.

Katharina Fleckenstein (K)

Department of Radiation Oncology, University Medical Center Mannheim, Medical Faculty Mannheim, Heidelberg University, 68167 Mannheim, Germany.

Sebastian Berlit (S)

Department of Gynecology and Obstetrics, University Medical Center Mannheim, Medical Faculty Mannheim, Heidelberg University, 68167 Mannheim, Germany.

Benjamin Tuschy (B)

Department of Gynecology and Obstetrics, University Medical Center Mannheim, Medical Faculty Mannheim, Heidelberg University, 68167 Mannheim, Germany.

Marc Sütterlin (M)

Department of Gynecology and Obstetrics, University Medical Center Mannheim, Medical Faculty Mannheim, Heidelberg University, 68167 Mannheim, Germany.

Frederik Wenz (F)

University Hospital Freiburg, 79106 Freiburg, Germany.

Elena Sperk (E)

Department of Radiation Oncology, University Medical Center Mannheim, Medical Faculty Mannheim, Heidelberg University, 68167 Mannheim, Germany.
Mannheim Cancer Center, University Medical Center Mannheim, Medical Faculty Mannheim, Heidelberg University, 68167 Mannheim, Germany.

Classifications MeSH