Prognostic factors of metastatic myxoid liposarcoma.


Journal

BMC cancer
ISSN: 1471-2407
Titre abrégé: BMC Cancer
Pays: England
ID NLM: 100967800

Informations de publication

Date de publication:
14 Sep 2020
Historique:
received: 18 02 2020
accepted: 07 09 2020
entrez: 15 9 2020
pubmed: 16 9 2020
medline: 21 4 2021
Statut: epublish

Résumé

Myxoid liposarcoma (MLS) has the tendency to metastasize extrapulmonary. Although prognostic factors at the initial diagnosis of MLS have been reported, those at diagnosis of metastasis remain unclear. The purpose of this study was to investigate the prognostic factors for disease-specific survival at the initial diagnosis of metastasis. This retrospective observational study was conducted at three cancer centers and two university hospitals in Japan. Of 274 MLS patients pathologically diagnosed between 2001 and 2015, 48 metastatic patients were examined. Lung metastases were detected in nine patients (18.8%) and extrapulmonary metastases in 45 (93.8%). Interval from primary diagnosis to the first metastasis was significantly shorter in patients with lung metastases than without (p = 0.007). Median disease-specific survival after diagnosis of metastases was 52.5 months in all patients. In multivariable analysis, liver metastasis (hazard ratio (HR), 2.71 [95% confidence interval (CI), 1.00-7.09]) and no evidence of disease (NED) achieved by radical treatment (resection with or without radiation therapy, or radiation therapy ≥60 Gy) or semi-radical (radiation therapy ≥40 Gy) treatment were significantly related to survival (HR, 0.36; 95%CI [0.13-0.95]). The number of metastases (odds ratio (OR), 0.44; 95%CI [0.25-0.78]) and abdominal/retroperitoneal metastases (OR, 0.09; 95%CI [0.008-0.95]) were the significant inhibitory factors of achieving NED. This is the first study to statistically demonstrate the importance of achieving NED with surgical resection or radiation therapy for longer survival in metastatic MLS patients. As number of metastases was a significant factor for achieving NED, early detection of metastases might be important.

Sections du résumé

BACKGROUND BACKGROUND
Myxoid liposarcoma (MLS) has the tendency to metastasize extrapulmonary. Although prognostic factors at the initial diagnosis of MLS have been reported, those at diagnosis of metastasis remain unclear. The purpose of this study was to investigate the prognostic factors for disease-specific survival at the initial diagnosis of metastasis.
METHODS METHODS
This retrospective observational study was conducted at three cancer centers and two university hospitals in Japan. Of 274 MLS patients pathologically diagnosed between 2001 and 2015, 48 metastatic patients were examined.
RESULTS RESULTS
Lung metastases were detected in nine patients (18.8%) and extrapulmonary metastases in 45 (93.8%). Interval from primary diagnosis to the first metastasis was significantly shorter in patients with lung metastases than without (p = 0.007). Median disease-specific survival after diagnosis of metastases was 52.5 months in all patients. In multivariable analysis, liver metastasis (hazard ratio (HR), 2.71 [95% confidence interval (CI), 1.00-7.09]) and no evidence of disease (NED) achieved by radical treatment (resection with or without radiation therapy, or radiation therapy ≥60 Gy) or semi-radical (radiation therapy ≥40 Gy) treatment were significantly related to survival (HR, 0.36; 95%CI [0.13-0.95]). The number of metastases (odds ratio (OR), 0.44; 95%CI [0.25-0.78]) and abdominal/retroperitoneal metastases (OR, 0.09; 95%CI [0.008-0.95]) were the significant inhibitory factors of achieving NED.
CONCLUSIONS CONCLUSIONS
This is the first study to statistically demonstrate the importance of achieving NED with surgical resection or radiation therapy for longer survival in metastatic MLS patients. As number of metastases was a significant factor for achieving NED, early detection of metastases might be important.

Identifiants

pubmed: 32928160
doi: 10.1186/s12885-020-07384-1
pii: 10.1186/s12885-020-07384-1
pmc: PMC7491192
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

883

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Auteurs

Yusuke Shinoda (Y)

Department of Rehabilitation Medicine, The University of Tokyo Hospital, Tokyo, Japan.
Department of Orthopaedic Surgery, Faculty of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan.

Eisuke Kobayashi (E)

Division of Musculoskeletal Oncology, National Cancer Center Hospital, Tokyo, Japan.
Department of Orthopaedic Surgery, Keio University School of Medicine, Tokyo, Japan.

Hiroshi Kobayashi (H)

Department of Orthopaedic Surgery, Faculty of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan. hkobayashi-tky@umin.ac.jp.

Tomoaki Mori (T)

Division of Musculoskeletal Oncology, National Cancer Center Hospital, Tokyo, Japan.
Department of Orthopaedic Surgery, Keio University School of Medicine, Tokyo, Japan.

Naofumi Asano (N)

Department of Orthopaedic Surgery, Keio University School of Medicine, Tokyo, Japan.

Robert Nakayama (R)

Department of Orthopaedic Surgery, Keio University School of Medicine, Tokyo, Japan.

Hideo Morioka (H)

Department of Orthopaedic Surgery, Keio University School of Medicine, Tokyo, Japan.

Shintaro Iwata (S)

Division of Musculoskeletal Oncology, National Cancer Center Hospital, Tokyo, Japan.
Division of Orthopaedic Surgery, Chiba Cancer Center, Chiba, Japan.

Tsukasa Yonemoto (T)

Division of Orthopaedic Surgery, Chiba Cancer Center, Chiba, Japan.

Takeshi Ishii (T)

Division of Orthopaedic Surgery, Chiba Cancer Center, Chiba, Japan.

Tohru Hiruma (T)

Division of Musculoskeletal Tumor Surgery, Kanagawa Cancer Center, Yokohama, Kanagawa, Japan.

Akira Kawai (A)

Division of Musculoskeletal Oncology, National Cancer Center Hospital, Tokyo, Japan.

Hirotaka Kawano (H)

Department of Orthopaedic Surgery, Teikyo University School of Medicine, Tokyo, Japan.

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Classifications MeSH