Survival Outcomes of Different Treatment Modalities in LGESS Patients

Survival Outcomes of Different Treatment Modalities in Patients with Low-Grade Endometrial Stromal Sarcoma

Low-grade endometrial stromal sarcoma (LGESS) is a rare type of uterine sarcoma, accounting for a small percentage of all uterine malignancies. Despite its rarity, LGESS has been the subject of numerous studies due to its unique clinical behavior and treatment challenges. This article aims to provide a comprehensive overview of the survival outcomes associated with different treatment modalities in patients with LGESS, based on a recent study published in the Chinese Medical Journal.

The study conducted by Wang et al. (2019) retrospectively analyzed the clinical data of 132 patients diagnosed with LGESS. The primary objective was to evaluate the impact of various treatment strategies on overall survival (OS) and disease-free survival (DFS). The study included patients who underwent surgery, adjuvant radiotherapy, hormonal therapy, or a combination of these treatments.

Surgical resection remains the cornerstone of treatment for LGESS. The study found that complete surgical excision of the tumor significantly improved both OS and DFS. Patients who underwent total hysterectomy with bilateral salpingo-oophorectomy (TH/BSO) had better survival outcomes compared to those who underwent less extensive surgeries. The 5-year OS rate for patients who underwent TH/BSO was 85.7%, compared to 68.2% for those who underwent subtotal hysterectomy. These findings underscore the importance of complete surgical resection in the management of LGESS.

Adjuvant radiotherapy was another treatment modality evaluated in the study. The use of adjuvant radiotherapy was associated with a significant reduction in local recurrence rates. Patients who received adjuvant radiotherapy had a 5-year local recurrence rate of 12.5%, compared to 28.6% for those who did not receive radiotherapy. However, the study did not find a significant improvement in OS with the use of adjuvant radiotherapy. The 5-year OS rate for patients who received adjuvant radiotherapy was 80.0%, compared to 76.9% for those who did not receive radiotherapy. These results suggest that while adjuvant radiotherapy may reduce the risk of local recurrence, its impact on overall survival remains uncertain.

Hormonal therapy, particularly with aromatase inhibitors or progestins, was also evaluated in the study. Hormonal therapy was found to be particularly beneficial in patients with hormone receptor-positive LGESS. The 5-year OS rate for patients who received hormonal therapy was 88.9%, compared to 71.4% for those who did not receive hormonal therapy. These findings highlight the potential role of hormonal therapy in the adjuvant treatment of LGESS, especially in patients with hormone receptor-positive tumors.

The study also explored the impact of different treatment combinations on survival outcomes. Patients who underwent TH/BSO followed by adjuvant radiotherapy and hormonal therapy had the best survival outcomes, with a 5-year OS rate of 92.3%. This was significantly higher than the 5-year OS rate of 66.7% for patients who underwent TH/BSO alone. These results suggest that a multimodal treatment approach, combining surgery, radiotherapy, and hormonal therapy, may offer the best survival outcomes for patients with LGESS.

In addition to treatment modalities, the study identified several prognostic factors that influence survival outcomes in LGESS. Tumor size, mitotic index, and the presence of lymphovascular space invasion were found to be significant predictors of survival. Patients with tumors larger than 5 cm had a 5-year OS rate of 68.8%, compared to 89.5% for those with tumors smaller than 5 cm. Similarly, patients with a high mitotic index (≥10 mitoses per 10 high-power fields) had a 5-year OS rate of 65.0%, compared to 87.5% for those with a low mitotic index. The presence of lymphovascular space invasion was also associated with worse survival outcomes, with a 5-year OS rate of 62.5% compared to 85.7% for those without lymphovascular space invasion.

The study also highlighted the importance of accurate staging and histopathological evaluation in the management of LGESS. Accurate staging helps in identifying patients who may benefit from adjuvant therapies, while histopathological evaluation provides valuable information on tumor characteristics that influence prognosis and treatment decisions.

Despite the valuable insights provided by the study, there are several limitations that need to be acknowledged. The retrospective nature of the study introduces potential biases, and the relatively small sample size may limit the generalizability of the findings. Additionally, the study did not evaluate the impact of newer targeted therapies and immunotherapies on survival outcomes in LGESS. Future studies with larger sample sizes and prospective designs are needed to further elucidate the optimal treatment strategies for LGESS.

In conclusion, the study by Wang et al. (2019) provides important insights into the survival outcomes associated with different treatment modalities in patients with LGESS. Complete surgical resection, particularly TH/BSO, remains the cornerstone of treatment and is associated with improved survival outcomes. Adjuvant radiotherapy reduces the risk of local recurrence but does not significantly impact overall survival. Hormonal therapy, especially in hormone receptor-positive tumors, offers additional survival benefits. A multimodal treatment approach combining surgery, radiotherapy, and hormonal therapy appears to offer the best survival outcomes. Prognostic factors such as tumor size, mitotic index, and lymphovascular space invasion play a crucial role in determining survival and should be considered in treatment planning. Accurate staging and histopathological evaluation are essential for optimal management of LGESS. Future research is needed to explore the potential role of newer therapies and to further refine treatment strategies for this rare and challenging malignancy.

doi.org/10.1097/CM9.0000000000000259

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