# The Use of Radiotherapy in Leptomeningeal Carcinomatosis: A Systematic Review and Random-Effects Proportions Meta-Analysis

**Authors:** Pamela Ochoa-Lantigua, Mauricio Moreno-Bejarano, Cayetana Guarderas-Arias, José Bueno-Miño, Jose E. Leon-Rojas

PMC · DOI: 10.3390/cancers18040547 · Cancers · 2026-02-07

## TL;DR

This study reviews how radiotherapy is used to manage leptomeningeal carcinomatosis, finding it helps with symptoms but does not significantly improve survival.

## Contribution

A systematic review and meta-analysis quantifying radiotherapy's role in symptom control and toxicity in leptomeningeal carcinomatosis.

## Key findings

- Radiotherapy is commonly used for symptom control in leptomeningeal carcinomatosis but does not significantly extend survival.
- Toxicity from radiotherapy is common, with fatigue and nausea being the most frequently reported side effects.
- Patients with lung and breast cancers are most commonly affected by leptomeningeal carcinomatosis.

## Abstract

Leptomeningeal carcinomatosis is a serious complication of advanced cancer in which cancer cells spread to the membranes surrounding the brain and spinal cord, often causing rapid neurological decline and very limited survival. Radiotherapy is frequently used to relieve symptoms, but its real benefits and side effects have not been clearly defined. In this study, we systematically reviewed the published research to better understand how radiotherapy is used in this condition, how long patients survive after treatment, and what side effects may occur. By analyzing data from more than 2800 patients, we found that radiotherapy remains important for symptom control, although it does not clearly extend survival, and that different radiotherapy approaches carry different risks of side effects. These findings help clarify the role of radiotherapy in leptomeningeal carcinomatosis and may guide clinicians and researchers toward more informed, patient-centered treatment decisions.

Objective: Leptomeningeal carcinomatosis (LMC) is a rare but devastating complication of advanced cancer, particularly in patients with breast and lung malignancies. This systematic review provides a descriptive synthesis of radiotherapy approaches used in patients with leptomeningeal metastases, with a quantitative proportions meta-analysis focused on treatment-related toxicity. Materials and methods: A systematic search was conducted in PubMed, Scopus, and the virtual health library (BVS) databases following PRISMA 2020 guidelines. Studies including patients diagnosed with LMC and treated with RT were selected. Outcomes included overall survival (OS), adverse events (toxicities), and functional response. Results: A total of 39 studies comprising 2822 patients were included; the most frequent primary tumors were lung (n = 1337) and breast (n = 990) cancers. The mean time from cancer diagnosis to LMC was 22.4 months. Radiotherapy regimens included whole-brain radiotherapy (WBRT, n = 1054), craniospinal irradiation (CSI, n = 148), and focal RT (n = 27); RT was administered alone or in combination with systemic treatments. Toxicity was reported in 462 patients, primarily fatigue (n = 115), nausea/vomiting (n = 72), and hematological events (notably in CSI). The pooled toxicity prevalence was 50.8% (95% CI, 26.1–75.4; I2 = 96.1; p < 0.0001) for all RT modalities, and 31.6% (95%CI, 15.0–50.8; I2 = 90.7; p < 0.0001) for WBRT. CSI toxicity estimates were based on a limited number of studies and did not reach statistical significance, and should therefore be interpreted as exploratory. Mean OS from LMC diagnosis was 18.2 weeks; OS by treatment was 21.5 weeks and 20.3 weeks, for RT by itself and combined, respectively. Conclusions: LMC predominantly affects patients with advanced-stage lung and breast cancers and presents with variable clinical timelines and functional impairment. Radiotherapy represents a frequently utilized and clinically important component of the palliative management of leptomeningeal disease, particularly for symptom control and neurological stabilization, rather than a treatment associated with superior survival outcomes. Prognosis is more closely linked to patient-specific factors than to treatment type. Radiotherapy toxicity is prevalent; however, most are categorized as type 1 toxicities with insignificant to little damaging effects on patients.

## Linked entities

- **Diseases:** leptomeningeal carcinomatosis (MONDO:0700219), lung cancer (MONDO:0005138), breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** TXK (TXK tyrosine kinase) [NCBI Gene 7294] {aka BTKL, PSCTK5, PTK4, RLK, TKL}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, GYPA (glycophorin A (MNS blood group)) [NCBI Gene 2993] {aka CD235a, GPA, GPErik, GPSAT, HGpMiV, HGpMiXI}
- **Diseases:** head and neck tumors (MESH:D006258), carcinomatosis (MESH:D002277), neurotoxicity (MESH:D020258), lung cancer (MESH:D008175), Tumor (MESH:D009369), lung (MESH:D008171), lymphopenia (MESH:D008231), pain (MESH:D010146), skin erythema (MESH:D012871), LMD (MESH:C537267), headache (MESH:D006261), disease (MESH:D004194), injury to (MESH:D014947), melanoma (MESH:D008545), vomiting (MESH:D014839), cranial neuropathies (MESH:D003389), Cutaneous toxicity (MESH:D013262), seizures (MESH:D012640), neurological decline (MESH:D009461), LMC (MESH:D055756), hematopoietic tumors (MESH:D019337), germ cell tumor (MESH:D009373), fatigue (MESH:D005221), Leptomeningeal disease (MESH:D008577), leukopenia (MESH:D007970), leukoencephalopathy (MESH:D056784), PNS), thyroidal, testicular, gall bladder, leukemia (MESH:D005706), gastric cancer (MESH:D013274), nausea (MESH:D009325), central nervous system tumors (MESH:D016543), Toxicity (MESH:D064420), Primary (MESH:D010538), gastrointestinal disturbance (MESH:D005767), thrombocytopenia (MESH:D013921), breast (MESH:D061325), death (MESH:D003643), cytopenias (MESH:D006402), OS (MESH:D011475), anemia (MESH:D000740), radiation dermatitis (MESH:D011855), metastases (MESH:D009362), cognitive impairment (MESH:D003072), prostatic (MESH:D011472), WBRT (MESH:C531766), peripheral nervous system (MESH:D010523), interstitial lung disease (MESH:D017563), gastrointestinal cancers (MESH:D005770), nausea/vomiting (MESH:D020250), thymic tumors (MESH:D013953), intracranial pressure symptoms (MESH:D019586), breast and lung malignancies (MESH:D001943)
- **Chemicals:** Trastuzumab (MESH:D000068878), osimertinib (MESH:C000596361), CSI (MESH:C040050), aumolertinib (MESH:C000718108), methotrexate (MESH:D008727), WBRT (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

49 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938613/full.md

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Source: https://tomesphere.com/paper/PMC12938613