Literature DB >> 28833417

Comprehensive evaluation of the revised international staging system in multiple myeloma patients treated with novel agents as a primary therapy.

Hyungwoo Cho1, Dok Hyun Yoon2, Jung Bok Lee3, Sung-Yong Kim4, Joon Ho Moon5, Young Rok Do6, Jae Hoon Lee7, Yong Park8, Ho Sup Lee9, Hyeon Seok Eom10, Ho-Jin Shin11, Chang-Ki Min12, Jin Seok Kim13, Jae-Cheol Jo14, Hye Jin Kang15, Yeung-Chul Mun16, Won Sik Lee17, Je-Jung Lee18, Cheolwon Suh2, Kihyun Kim19.   

Abstract

The revised International Staging System (R-ISS) has recently been developed to improve the risk stratification of multiple myeloma (MM) patients over the ISS. We assessed the R-ISS in MM patients who were treated with novel agents as a primary therapy and evaluated its discriminative power and ability to reclassify patients from the ISS. A total of 514 newly diagnosed MM patients treated with novel agents including thalidomide, bortezomib, and lenalidomide as a primary therapy were included in this retrospective analysis. With a median follow-up duration of 42.3 months (range, 40.5-44.1), the median overall survival (OS) was 61.0 months. There was a significant difference in median OS (not reached, 60.9, and 50.1 months for stages 1, 2, and 3, respectively, P < 0.001) among the three stages of R-ISS. The C-statistic was significantly greater for R-ISS than for ISS (0.769 vs. 0.696, P < 0.001). The event NRI was -0.08 (95% confidence interval [CI], -0.18-0.01) and the non-event NRI was 0.05 (95% CI, -0.03-0.10), resulting in a total NRI of -0.03 (95% CI, -0.14-0.08, P = 0.602). The R-ISS performs well and has significantly better discriminative power than the ISS in MM patients treated with novel agents as a primary therapy. However, it does not better reclassify patients from the ISS, suggesting that there is still room to improve the staging system. Moreover, new statistical measures for assessing and quantifying the risk prediction of new prognostic models are necessary in future studies.
© 2017 Wiley Periodicals, Inc.

Entities:  

Mesh:

Substances:

Year:  2017        PMID: 28833417     DOI: 10.1002/ajh.24891

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  8 in total

1.  18F-FDG PET/CT is useful for determining survival outcomes of patients with multiple myeloma classified as stage II and III with the Revised International Staging System.

Authors:  Sung-Hoon Jung; Seong Young Kwon; Jung-Joon Min; Hee-Seung Bom; Seo-Yeon Ahn; Seung-Yeon Jung; Seung-Shin Lee; Moo-Rim Park; Deok-Hwan Yang; Jae-Sook Ahn; Hyeoung-Joon Kim; Je-Jung Lee
Journal:  Eur J Nucl Med Mol Imaging       Date:  2018-09-05       Impact factor: 9.236

2.  Hypermethylation of the Promoter Region of miR-23 Enhances the Metastasis and Proliferation of Multiple Myeloma Cells via the Aberrant Expression of uPA.

Authors:  Qijie Ran; Dehong Xu; Qi Wang; Dongsheng Wang
Journal:  Front Oncol       Date:  2022-05-30       Impact factor: 5.738

3.  Improved survival outcomes and relative youthfulness of multiple myeloma patients with t(4;14) receiving novel agents are associated with poorer performance of the revised international staging system in a real aging society.

Authors:  Yoshiaki Abe; Kazutaka Sunami; Takeshi Yamashita; Mikio Ueda; Hiroyuki Takamatsu; Kentaro Narita; Hiroki Kobayashi; Akihiro Kitadate; Masami Takeuchi; Kosei Matsue
Journal:  Oncotarget       Date:  2019-01-15

4.  Development of a new risk stratification system for patients with newly diagnosed multiple myeloma using R-ISS and 18F-FDG PET/CT.

Authors:  Je-Jung Lee; Joon Ho Moon; Hee Jeong Cho; Sung-Hoon Jung; Jae-Cheol Jo; Yoo Jin Lee; Sang Eun Yoon; Sung-Soo Park; Do Young Kim; Ho-Jin Shin; Yeung-Chul Mun; Jun Ho Yi; Hyo Jung Kim; Da Jung Kim; Ho Sup Lee; Sung Hwa Bae; Chae Moon Hong; Shin Young Jeong; Jung-Joon Min; Sang Kyun Sohn; Chang-Ki Min; Kihyun Kim
Journal:  Blood Cancer J       Date:  2021-12-01       Impact factor: 11.037

5.  Development and Validation of a Novel Prognostic Model for Overall Survival in Newly Diagnosed Multiple Myeloma Integrating Tumor Burden and Comorbidities.

Authors:  Shuangshuang Jia; Lei Bi; Yuping Chu; Xiao Liu; Juan Feng; Li Xu; Tao Zhang; Hongtao Gu; Lan Yang; Qingxian Bai; Rong Liang; Biao Tian; Yaya Gao; Hailong Tang; Guangxun Gao
Journal:  Front Oncol       Date:  2022-03-17       Impact factor: 6.244

6.  High expression of nucleoporin 133 mRNA in bone marrow CD138+ cells is a poor prognostic factor in multiple myeloma.

Authors:  Soushi Ibata; Masayoshi Kobune; Shohei Kikuchi; Masahiro Yoshida; Shogo Miura; Hiroto Horiguchi; Kazuyuki Murase; Satoshi Iyama; Kohichi Takada; Koji Miyanishi; Junji Kato
Journal:  Oncotarget       Date:  2018-05-18

7.  A simple additive staging system for newly diagnosed multiple myeloma.

Authors:  Nadine H Abdallah; Moritz Binder; S Vincent Rajkumar; Patricia T Greipp; Prashant Kapoor; Angela Dispenzieri; Morie A Gertz; Linda B Baughn; Martha Q Lacy; Suzanne R Hayman; Francis K Buadi; David Dingli; Ronald S Go; Yi L Hwa; Amie L Fonder; Miriam A Hobbs; Yi Lin; Nelson Leung; Taxiarchis Kourelis; Rahma Warsame; Mustaqeem A Siddiqui; Robert A Kyle; P Leif Bergsagel; Rafael Fonseca; Rhett P Ketterling; Shaji K Kumar
Journal:  Blood Cancer J       Date:  2022-01-31       Impact factor: 9.812

8.  Desmoglein-2 expression is an independent predictor of poor prognosis patients with multiple myeloma.

Authors:  Lisa M Ebert; Kate Vandyke; M Zahied Johan; Mark DeNichilo; Lih Y Tan; Kay K Myo Min; Benjamin M Weimann; Brenton W Ebert; Stuart M Pitson; Andrew C W Zannettino; Craig T Wallington-Beddoe; Claudine S Bonder
Journal:  Mol Oncol       Date:  2021-07-24       Impact factor: 6.603

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.