# SCART sequential lattice spatial fractionated radiotherapy combined with chemotherapy for recurrent ovarian cancer with bulky bone metastasis: a case report

**Authors:** Yuan Li, Liangfu Han, Weisi Yan, Jun Yang

PMC · DOI: 10.3389/fonc.2026.1761101 · Frontiers in Oncology · 2026-02-04

## TL;DR

A patient with recurrent ovarian cancer and large bone metastasis showed significant tumor shrinkage after a novel radiotherapy and chemotherapy combination.

## Contribution

The study demonstrates the feasibility and effectiveness of combining SCART and Lattice radiotherapy with chemotherapy for bulky, drug-resistant ovarian cancer metastases.

## Key findings

- Sequential SCART and Lattice radiotherapy achieved substantial local tumor regression with minimal toxicity.
- The combination therapy led to a 30.1% reduction in tumor volume at 6-month follow-up.
- The approach safely escalates intratumoral doses while protecting normal tissue and potentially enhancing immunogenic responses.

## Abstract

Bone metastasis from ovarian cancer is relatively rare, and the treatment of giant bone metastatic lesions poses significant clinical challenges. SCART (Stereotactic Centralized Ablative Radiation Therapy) and Lattice technique, as emerging spatial fractionated precision radiotherapy technologies, have shown unique advantages in treating bulky tumor lesions. This case report explores the potential immunomodulatory effects of spatial fractionated radiotherapy in enhancing tumor antigenicity and chemotherapy sensitivity in recurrent, drug-resistant, multi-line treated cancer patients.

We report a 56-year-old female patient with ovarian cancer recurrence and multiple metastases 7 years post-surgery. CT examination revealed a big right iliac bone metastatic lesion (89×78×58mm) with surrounding soft tissue invasion. After limited response to chemotherapy and bevacizumab, the patient underwent sequential SCART, SBRT, and Lattice radiotherapy for her right iliac and surrounding invasive soft tissue metastases. Substantial local tumor regression was achieved without severe acute toxicity.

The initial radiotherapy consisted of SCART followed by SBRT: STV 54 Gy/3 fractions, PGTV 15 Gy/3 fractions, then SBRT PGTV 25 Gy/5 fractions. Stage II treatment used Lattice radiotherapy: VTV 45 Gy/3 fractions and PGTV 9 Gy/3 fractions.

The patient’s pain symptoms were significantly relieved, with good tolerance during treatment and no severe adverse reactions. According to RECIST 1.1 evaluation criteria, the baseline GTV was 399.0cc, decreased to 308.0cc after SCART +SBRT, and further reduced to 136.1cc at 6-month follow-up MRI after Lattice radiotherapy. The diameter decreased by approximately 30.1% compared to baseline, achieving partial response.

The combination of SCART and Lattice techniques offers a promising strategy for managing bulky tumor, particularly suitable for cases with less-responsive to conventional therapy. This technique ensures safe dose at target margins while increasing dose to “cold tumor” areas, offering new clinical options. This approach safely escalates intratumoral dose while protecting normal tissue and may enhance immunogenic and cytotoxic responses. Sequential spatial fractionation techniques appear feasible, with controllable short-term safety and favorable tolerance.

## Linked entities

- **Diseases:** ovarian cancer (MONDO:0005140)

## Full-text entities

- **Genes:** CMPK1 (cytidine/uridine monophosphate kinase 1) [NCBI Gene 51727] {aka CK, CMK, CMPK, UMK, UMP-CMPK, UMPK}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, PAX8 (paired box 8) [NCBI Gene 7849] {aka PAX-8}, MUC16 (mucin 16, cell surface associated) [NCBI Gene 94025] {aka CA125}, KRT7 (keratin 7) [NCBI Gene 3855] {aka CK7, K2C7, K7, SCL}
- **Diseases:** SCART (MESH:D011832), clear cell carcinoma (MESH:D002292), lymph node metastasis (MESH:D008207), pelvic (MESH:D034161), Ovarian cancer (MESH:D010051), gynecological malignancies (MESH:D005833), bone destruction (MESH:D001847), toxicity (MESH:D064420), Bone metastasis (MESH:D009362), lesion (MESH:D009059), diarrhea (MESH:D003967), Cancer (MESH:D009369), metastatic lesion (MESH:D000092182), iliac lesion (MESH:D017543), Pain (MESH:D010146)
- **Chemicals:** SCART (-), carboplatin (MESH:D016190), bevacizumab (MESH:D000068258), paclitaxel (MESH:D017239)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12913186/full.md

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12913186/full.md

## References

17 references — full list in the complete paper: https://tomesphere.com/paper/PMC12913186/full.md

---
Source: https://tomesphere.com/paper/PMC12913186