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Updated: Sep 19, 2025

Orthotopic Implantation and Peripheral Immune Cell Monitoring in the II-45 Syngeneic Rat Mesothelioma Model
Published on: October 2, 2015
A short-term prognostic model based on urinary IgG, CO2CP and TP for newly diagnosed multiple myeloma
Jiaxiang He1,2,3,4, Wei Xiao1, Qian Zhao1,5
1The Affiliated Guangdong Second Provincial General Hospital of Jinan University Guangzhou, Guangdong, China.
Abstract:
This study aimed to establish a short-term risk assessment model for patients with newly diagnosed multiple myeloma (NDMM), to augment the current prognosis assessments of MM patients. This model serves as a reference for evaluating the short-term remission of patients. Between January 2013 and March 2023, a total of 232 NDMM patients were enrolled in the Hematology department. The cohort between January 2013 and October 2020 was selected as the training set (n=165) and the cohort between November 2020 and March 2023 was used as the internal validation set (n=67). Using univariate and multivariate forward stepwise Cox analysis, the determined prognostic factors were urinary immunoglobulin G (IgG), carbon dioxide combining power (CO2CP), and total protein (TP). A 3-prognostic factor Nomogram model was established based on Cox regression. The area under the curve (AUC) of the Nomogram in 4-, 5- and 6-month complete remission (CR) was 0.777, 0.722, and 0.708, and the C index was 0.691 (0.661-0.721). Kaplan-Meier curve analysis indicated that the CR rate of the high-risk group was lower than the low-risk group (training set P<0.001, internal validation set P=0.018), which exhibited a better stratification of patients than the International Staging System (ISS, training set P=0.850, internal validation set P=0.900), Revised International Staging System (R-ISS, training set P=0.740, internal validation set P=0.720) and the Second Revision of the ISS (R2-ISS, training set P=0.480, internal validation set P=0.590). This study effectively constructed a Nomogram for short-term risk assessment of NDMM patients based on three widely used clinical markers, thereby enriching factors related to NDMM prognosis and aiding in the evaluation of the short-term complete remission.

