TY - JOUR
T1 - Application of the international metastatic renal cell carcinoma database consortium and memorial sloan kettering cancer center risk models in patients with metastatic non-clear cell renal cell carcinoma
T2 - A multi-institutional retrospective study using the Korean metastatic renal cell carcinoma registry
AU - Korean Renal Cell Carcinoma Study Group
AU - Kim, Jung Kwon
AU - Kim, Sung Han
AU - Song, Mi Kyung
AU - Joo, Jungnam
AU - Seo, Seong Il
AU - Kwak, Cheol
AU - Jeong, Chang Wook
AU - Song, Cheryn
AU - Hwang, Eu Chang
AU - Seo, Ill Young
AU - Lee, Hakmin
AU - Hong, Sung Hoo
AU - Park, Jae Young
AU - Chung, Jinsoo
N1 - Publisher Copyright:
Copyright © 2019 by the Korean Cancer Association.
PY - 2019
Y1 - 2019
N2 - Purpose The International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) and the Memorial Sloan Kettering Cancer Center (MSKCC) risk models were developed predominantly with clear cell renal cell carcinoma (RCC). Accordingly, whether these two models could be applied to metastatic non-clear cell RCC (mNCCRCC) as well has not been well-known and was investigated herein. Materials and Methods From the Korean metastatic RCC registry, a total of 156 patients (8.1%) with mNCCRCC among the entire cohort of 1,922 patients were analyzed. Both models were applied to predict first-line progression-free survival (PFS), total PFS, and cancer-specific survival (CSS). Results The median first-line PFS, total PFS, and CSS were 5, 6, and 24 months, respectively. The IMDC risk model reliably discriminated three risk groups to predict survival: the median first-line PFS, total PFS, and CSS for the favorable, intermediate, and poor risk groups were 9, 5, and, 2 months (p=0.001); 14, 7, and 2 months (p < 0.001); and 41, 21, and 8 months (p < 0.001), all respectively. The MSKCC risk model also reliably differentiated three risk groups: 9, 5, and, 2 months (p=0.005); 10, 7, and 3 months (p=0.002); and 50, 21, and 8 months (p < 0.001), also all respectively. The concordance indices were 0.632 with the IMDC model and 0.643 with the MSKCC model for first-line PFS: 0.748 and 0.655 for CSS. Conclusion The current IMDC and MSKCC risk models reliably predict first-line PFS, total PFS, and CSS in mNCCRCC.
AB - Purpose The International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) and the Memorial Sloan Kettering Cancer Center (MSKCC) risk models were developed predominantly with clear cell renal cell carcinoma (RCC). Accordingly, whether these two models could be applied to metastatic non-clear cell RCC (mNCCRCC) as well has not been well-known and was investigated herein. Materials and Methods From the Korean metastatic RCC registry, a total of 156 patients (8.1%) with mNCCRCC among the entire cohort of 1,922 patients were analyzed. Both models were applied to predict first-line progression-free survival (PFS), total PFS, and cancer-specific survival (CSS). Results The median first-line PFS, total PFS, and CSS were 5, 6, and 24 months, respectively. The IMDC risk model reliably discriminated three risk groups to predict survival: the median first-line PFS, total PFS, and CSS for the favorable, intermediate, and poor risk groups were 9, 5, and, 2 months (p=0.001); 14, 7, and 2 months (p < 0.001); and 41, 21, and 8 months (p < 0.001), all respectively. The MSKCC risk model also reliably differentiated three risk groups: 9, 5, and, 2 months (p=0.005); 10, 7, and 3 months (p=0.002); and 50, 21, and 8 months (p < 0.001), also all respectively. The concordance indices were 0.632 with the IMDC model and 0.643 with the MSKCC model for first-line PFS: 0.748 and 0.655 for CSS. Conclusion The current IMDC and MSKCC risk models reliably predict first-line PFS, total PFS, and CSS in mNCCRCC.
KW - Criteria
KW - Korean
KW - Metastatic renal cell carcinoma
KW - Non-clear cell
KW - Prognosis
KW - Validation
UR - http://www.scopus.com/inward/record.url?scp=85064495289&partnerID=8YFLogxK
U2 - 10.4143/crt.2018.421
DO - 10.4143/crt.2018.421
M3 - Article
C2 - 30189720
AN - SCOPUS:85064495289
SN - 1598-2998
VL - 51
SP - 758
EP - 768
JO - Cancer Research and Treatment
JF - Cancer Research and Treatment
IS - 2
ER -