| Literature DB >> 34914005 |
S Acciuffi1, F Meyer1, A Bauschke2, R Croner1, U Settmacher2, A Altendorf-Hofmann3.
Abstract
The following is an overview of the treatment strategies and the prognostic factors to consider in the therapeutic choice of patients characterized by solitary colorectal liver metastasis. Liver resection is the only potential curative option; nevertheless, only 25% of the patients are considered to be eligible for surgery. To expand the potentially resectable pool of patients, surgeons developed multidisciplinary techniques like portal vein embolization, two-stage hepatectomy or associating liver partition and portal vein ligation for staged hepatectomy. Moreover, mini-invasive surgery is gaining support, since it offers lower post-operative complication rates and shorter hospital stay with no differences in long-term outcomes. In case of unresectable disease, various techniques of local ablation have been developed. Radiofrequency ablation is the most commonly used form of thermal ablation: it is widely used for unresectable patients and is trying to find its role in patients with small resectable metastasis. The identification of prognostic factors is crucial in the choice of the treatment strategy. Previous works that focused on patients with solitary colorectal liver metastasis obtained trustable negative predictive factors such as presence of lymph-node metastasis in the primary tumour, synchronous metastasis, R status, right-sided primary colon tumor, and additional presence of extrahepatic tumour lesion. Even the time factor could turn into a predictor of tumour biology as well as further clinical course, and could be helpful to discern patients with worse prognosis.Entities:
Keywords: Liver surgery; Local ablation; Solitary colorectal liver metastasis
Mesh:
Year: 2021 PMID: 34914005 PMCID: PMC8881245 DOI: 10.1007/s00432-021-03880-4
Source DB: PubMed Journal: J Cancer Res Clin Oncol ISSN: 0171-5216 Impact factor: 4.553
Resection versus RFA: OS, DFS, and local recurrence rate after treatment of SLM
| References | Patients no | 3 year OS (%) | 5 year OS (%) | 3 year DFS (%) | 5 year DFS (%) | Local recurrence (%) | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Oshowo et al. ( | RFA | 25 | 52.6 | n.s | – | – | – | – | – | – | – | – |
| Resection | 20 | 55.4 | – | – | – | – | ||||||
| Aloia et al. ( | RFA | 30 | 57 | 27 | 0 | 37 | ||||||
| Resection | 150 | 79 | 71 | 50 | 5 | |||||||
| Lee et al. ( | RFA | 37 | – | – | 48.5 | n.s | 32.2 | n.s | 25.7 | n.s | 29.7 | |
| Resection | 116 | – | 65.7 | 34.5 | 30.1 | 6.9 | ||||||
| Hur et al. ( | RFA | 25 | 60 | 25.5 | – | – | – | – | 28 | n.s | ||
| Resection | 42 | 70 | 50.1 | – | – | 9.5 | ||||||
| Kim et al. ( | RFA | 177 | – | – | 51.1 | n.s | – | – | 33.6 | n.s | – | – |
| Resection | 278 | – | 51.2 | – | 31.6 | – | ||||||
| Aliyev et al. ( | RFA | 44 | 81 | n.s | 57 | n.s | 32 | n.s | – | – | 18 | |
| Resection | 60 | 81 | 47 | 36 | – | 4 |
Bold figures show statistically significant diffenences p< 0.05