Life sciences · Journal article
Frontiers in Oncology · September 22, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Journal article.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
The source did not state who this applies to in practice.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
This record has not been graded across any dimension yet. Treat the label above as provisional and read the source.
What is missing. This record has no bottom line, key findings, reported figures, evidence dimensions. That is a gap in the analysis, not a judgement about the study.
Background Giant ulcerative breast cancers (>2,000 cc) with active hemorrhage present a critical therapeutic challenge, as conventional radiotherapy carries a high risk of severe toxicity to surrounding organs. Lattice radiotherapy (LRT) delivers spatially fractionated high-dose vertices within a low-dose background, offering the potential to overcome dose constraints. However, rapid tumor regression induced by LRT may render fixed plans unsafe, necessitating adaptive replanning. Case presentation A 46-year-old female with stage IV triple-negative breast cancer (TNBC; BRCA1 germline mutation) presented with a 2,772.2-cc ulcerative left breast and axillary masses complicated by persistent hemorrhage, recurrent infection, and Eastern Cooperative Oncology Group (ECOG 3). After failure of systemic therapies including fluzoparib, image-guided adaptive LRT was initiated (gross tumor volume [GTV]: 12 Gy/4 fractions; lattice vertices: 60 Gy/4 fractions). Before fractions 2–4, the GTV was re-contoured on daily fan-beam computed tomography (FBCT), lattice vertices were redistributed away from the skin surface, and plans were recalculated. LRT was followed by conventionally fractionated VMAT (40 Gy/20 fractions). Hemorrhage ceased within 2 weeks and persistent fever subsided, becoming intermittent and progressively less frequent. Tumor volume progressively decreased by 21.2% during LRT (before fraction 4), 81.5% post-VMAT, and 96.1% (108.3 cc residual) at 2-month follow-up. Cumulative organ-at-risk (OAR) doses, estimated by rigid-registration dose accumulation, remained within tolerance, with only Grade 2 dermatitis and no ≥Grade 3 toxicity. Conclusion This case demonstrates the technical feasibility of image-guided adaptive lattice replanning in a rapidly changing, ultra-large fungating breast tumor. Adaptive replanning may reduce geometric displacement of high-dose vertices; however, its dosimetric and clinical benefits require confirmation in further patients and with longer follow-up.