Characterizing impact of positive lymph node number in endometrial cancer using machine-learning: A better prognostic indicator than FIGO staging?


Journal

Gynecologic oncology
ISSN: 1095-6859
Titre abrégé: Gynecol Oncol
Pays: United States
ID NLM: 0365304

Informations de publication

Date de publication:
01 2022
Historique:
received: 16 07 2021
revised: 02 11 2021
accepted: 08 11 2021
pubmed: 20 11 2021
medline: 23 2 2022
entrez: 19 11 2021
Statut: ppublish

Résumé

Number of involved lymph nodes (LNs) is a crucial stratification factor in staging of numerous disease sites, but has not been incorporated for endometrial cancer. We evaluated whether number of involved LNs provide improved prognostic value. Patients diagnosed with node-positive endometrial adenocarcinoma without distant metastasis were identified in the National Cancer Database. We trained a machine-learning based model of overall survival. Shapley additive explanation values (SHAP) based on the model were used to identify cutoffs of number of LNs involved. Results were validated using a Cox proportional hazards regression model. We identified 11,381 patients with endometrial cancer meeting the inclusion criteria. Using the SHAP values, we selected the following thresholds: 1-3 LNs, 4-5 LNs, and 6+ LNs. The 3-year OS was 82.0% for 1-3 LNs, 74.3% for 4-5 LNs (hazard ratio [HR] 1.38; p < 0.001), and 59.9% for 6+ LNs (HR 2.23; p < 0.001). On univariate Cox regression, PA nodal involvement was a significant predictor of OS (HR 1.20; p < 0.001) but was not significant on multivariate analysis when number of LNs was included (HR 1.05; p = 0.273). Additionally, we identified an interaction between adjuvant therapy and number of involved LNs. Patients with 1-3 involved LNs had 3-year OS of 85.2%, 78.7% and 74.2% with chemoradiation (CRT), chemotherapy, and radiation, respectively. Patients with 6+ involved LNs had 3-yr OS of 67.8%, 49.6%, and 48.9% with CRT, chemotherapy, and radiation, respectively (p < 0.001). Number of involved LNs is a stronger prognostic and predictive factor compared to PA node involvement.

Sections du résumé

BACKGROUND
Number of involved lymph nodes (LNs) is a crucial stratification factor in staging of numerous disease sites, but has not been incorporated for endometrial cancer. We evaluated whether number of involved LNs provide improved prognostic value.
PATIENTS AND METHODS
Patients diagnosed with node-positive endometrial adenocarcinoma without distant metastasis were identified in the National Cancer Database. We trained a machine-learning based model of overall survival. Shapley additive explanation values (SHAP) based on the model were used to identify cutoffs of number of LNs involved. Results were validated using a Cox proportional hazards regression model.
RESULTS
We identified 11,381 patients with endometrial cancer meeting the inclusion criteria. Using the SHAP values, we selected the following thresholds: 1-3 LNs, 4-5 LNs, and 6+ LNs. The 3-year OS was 82.0% for 1-3 LNs, 74.3% for 4-5 LNs (hazard ratio [HR] 1.38; p < 0.001), and 59.9% for 6+ LNs (HR 2.23; p < 0.001). On univariate Cox regression, PA nodal involvement was a significant predictor of OS (HR 1.20; p < 0.001) but was not significant on multivariate analysis when number of LNs was included (HR 1.05; p = 0.273). Additionally, we identified an interaction between adjuvant therapy and number of involved LNs. Patients with 1-3 involved LNs had 3-year OS of 85.2%, 78.7% and 74.2% with chemoradiation (CRT), chemotherapy, and radiation, respectively. Patients with 6+ involved LNs had 3-yr OS of 67.8%, 49.6%, and 48.9% with CRT, chemotherapy, and radiation, respectively (p < 0.001).
CONCLUSION
Number of involved LNs is a stronger prognostic and predictive factor compared to PA node involvement.

Identifiants

pubmed: 34794840
pii: S0090-8258(21)01600-0
doi: 10.1016/j.ygyno.2021.11.007
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

39-45

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Auteurs

Colton Ladbury (C)

Department of Radiation Oncology, City of Hope National Medical Center, Duarte, CA, USA.

Richard Li (R)

Department of Radiation Oncology, City of Hope National Medical Center, Duarte, CA, USA.

Jay Shiao (J)

Department of Radiation Oncology, University of Colorado School of Medicine, Aurora, CO, USA.

Jason Liu (J)

Department of Radiation Oncology, City of Hope National Medical Center, Duarte, CA, USA.

Mihaela Cristea (M)

Department of Medical Oncology, City of Hope National Medical Center, Duarte, CA, USA.

Ernest Han (E)

Department of Gynecologic Oncology, City of Hope National Medical Center, Duarte, CA, USA.

Thanh Dellinger (T)

Department of Gynecologic Oncology, City of Hope National Medical Center, Duarte, CA, USA.

Stephen Lee (S)

Department of Gynecologic Oncology, City of Hope National Medical Center, Duarte, CA, USA.

Edward Wang (E)

Department of Medical Oncology, City of Hope National Medical Center, Duarte, CA, USA.

Christine Fisher (C)

Department of Radiation Oncology, University of Colorado School of Medicine, Aurora, CO, USA.

Yi-Jen Chen (YJ)

Department of Radiation Oncology, City of Hope National Medical Center, Duarte, CA, USA.

Arya Amini (A)

Department of Radiation Oncology, City of Hope National Medical Center, Duarte, CA, USA.

Tyler Robin (T)

Department of Radiation Oncology, University of Colorado School of Medicine, Aurora, CO, USA.

Scott Glaser (S)

Department of Radiation Oncology, City of Hope National Medical Center, Duarte, CA, USA. Electronic address: sglaser@coh.org.

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