Evidence map›Paper›PMID 37865413›Full record

ArticleBMJ open2023

Nomogram incorporating log odds of positive lymph nodes improves prognostic prediction for ovarian serous carcinoma: a real-world retrospective cohort study.

Shuming Zhang, Xiwen Liu, Qiao Li, Yidan Pan, Ye Tian, Xingbo Gu

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Article in BMJ open, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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6 authors.

Shuming Zhang *Department of Biostatistics, International School of Public Health, Hainan Medical University, Haikou, Hainan, China.
Xiwen Liu *Department of Medical Record, Hainan General Hospital, Haikou, China.
Qiao LiDepartment of Biostatistics, International School of Public Health, Hainan Medical University, Haikou, Hainan, China.
Yidan PanDepartment of Biostatistics, International School of Public Health, Hainan Medical University, Haikou, Hainan, China.
Ye TianDepartment of Biostatistics, International School of Public Health, Hainan Medical University, Haikou, Hainan, China hy0208051@hainmc.edu.cn tianyetongji@163.com.
Xingbo GuDepartment of Biostatistics, International School of Public Health, Hainan Medical University, Haikou, Hainan, China hy0208051@hainmc.edu.cn tianyetongji@163.com.ORCID 0009-0001-3781-3414

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesOvarian serous carcinoma (OSC) is a major cause of gynaecological cancer death, yet there is a lack of reliable prognostic models. To address this, we developed and validated a nomogram based on conventional clinical characteristics and log odds of positive lymph nodes (LODDS) to predict the prognosis of OSC patients.

settingA Real-World Retrospective Cohort Study from the Surveillance, Epidemiology and End Results programme.

participantsWe obtained data on 4192 patients diagnosed with OSC between 2010 and 2015. Eligibility criteria included specific diagnostic codes, OSC being the primary malignant tumour and age at diagnosis over 18 years. Exclusion criteria were missing information on various factors and unknown cause of death or survival time. PRIMARY AND SECONDARY OUTCOME MEASURES: The primary outcome were overall survival (OS) and ovarian cancer-specific survival (OCSS).

resultsFor OS and OCSS outcomes, we selected 7 and 5 variables, respectively, to establish the nomogram. In the training and validation cohorts, the C index for OS or OCSS was 0.716 or 0.718 and 0.731 or 0.733, respectively, with a 3-year time-dependent area under the curve (AUC) of 0.745 or 0.751 and a 5-year time-dependent AUC of 0.742 or 0.751. Calibration curves demonstrated excellent consistency between predicted and observed outcomes. The Net Reclassification Index, integrated discrimination improvement and decision curve analysis curves indicated that our nomogram performed better than the International Federation of Gynaecology and Obstetrics (FIGO) staging system in predicting OS and OCSS for OSC patients in both the training and validation cohorts.

conclusionOur nomogram, which includes LODDS, offers higher accuracy and reliability than the FIGO staging system and can predict overall and OCSS in OSC patients.

Indexed as

NomogramsOvarian NeoplasmsAdolescentCarcinoma, Ovarian EpithelialFemaleHumansLymph NodesNeoplasm StagingPregnancyPrognosisReproducibility of ResultsRetrospective StudiesEpidemiologyPrognosisRisk Factors

Identifiers

PMID37865413
PMCPMC10603516

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