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Background

No well‐performing nomogram has been developed specifically to predict individual‐patient cancer‐specific survival (CSS) and overall survival (OS) among patients with resectable colorectal liver metastasis (CRLM) who undergo simultaneous resection of primary and hepatic lesions without neoadjuvant chemotherapy (NAC). We aim to investigate the prognosis of patients with resectable CRLM undergoing simultaneous resection of primary and hepatic lesions without NAC.

Methods

Data of patients with CRLM in the Surveillance, Epidemiology and End Results Program (cohort, n = 225) were collected as the training set, and data of patients with CRLM treated at the National Cancer Center (cohort, n = 180) were collected as the validation set. The prognostic value of the clinicopathological parameters in the training cohort was assessed using Kaplan‒Meier curves and univariate and multivariate Cox proportional hazards models, and OS and CSS nomograms integrated with the prognostic variables were constructed. Calibration analyses, receiver operating characteristic (ROC) curves, and decision curve analyses (DCAs) were then performed to evaluate the performance of the nomograms.

Results

There was no collinearity among the collected variables. Three factors were associated with OS and CSS: the pretreatment carcinoembryonic antigen (CEA) concentration, pathologic N (pN) stage, and adjuvant chemotherapy (each p < 0.05). OS and CSS nomograms were constructed using these three parameters. The calibration plots revealed favorable agreement between the predicted and observed outcomes. The areas under the ROC curves were approximately 0.7. The DCA plots revealed that both nomograms had satisfactory clinical benefits. The ROC curves and DCAs also confirmed that the nomogram surpassed the tumor, node, and metastasis staging system.

Conclusion

The herein‐described nomograms containing the pretreatment CEA concentration, pN stage, and adjuvant chemotherapy may be effective models for predicting postoperative survival in patients with CRLM.


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Survival nomograms for simultaneous resection of primary and hepatic lesions without neoadjuvant chemotherapy in patients with resectable colorectal liver metastasis

Show Author's information Yu‐Juan Jiang1Si‐Cheng Zhou1Zi‐Xing Zhu1Jing‐Hua Chen2Jian‐Wei Liang1, ( )
Department of Colorectal Surgery, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China
Department of Hepatobiliary Surgery, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China

This study has been reported in accordance with the guidelines of the STROBE Statement.

Abstract

Background

No well‐performing nomogram has been developed specifically to predict individual‐patient cancer‐specific survival (CSS) and overall survival (OS) among patients with resectable colorectal liver metastasis (CRLM) who undergo simultaneous resection of primary and hepatic lesions without neoadjuvant chemotherapy (NAC). We aim to investigate the prognosis of patients with resectable CRLM undergoing simultaneous resection of primary and hepatic lesions without NAC.

Methods

Data of patients with CRLM in the Surveillance, Epidemiology and End Results Program (cohort, n = 225) were collected as the training set, and data of patients with CRLM treated at the National Cancer Center (cohort, n = 180) were collected as the validation set. The prognostic value of the clinicopathological parameters in the training cohort was assessed using Kaplan‒Meier curves and univariate and multivariate Cox proportional hazards models, and OS and CSS nomograms integrated with the prognostic variables were constructed. Calibration analyses, receiver operating characteristic (ROC) curves, and decision curve analyses (DCAs) were then performed to evaluate the performance of the nomograms.

Results

There was no collinearity among the collected variables. Three factors were associated with OS and CSS: the pretreatment carcinoembryonic antigen (CEA) concentration, pathologic N (pN) stage, and adjuvant chemotherapy (each p < 0.05). OS and CSS nomograms were constructed using these three parameters. The calibration plots revealed favorable agreement between the predicted and observed outcomes. The areas under the ROC curves were approximately 0.7. The DCA plots revealed that both nomograms had satisfactory clinical benefits. The ROC curves and DCAs also confirmed that the nomogram surpassed the tumor, node, and metastasis staging system.

Conclusion

The herein‐described nomograms containing the pretreatment CEA concentration, pN stage, and adjuvant chemotherapy may be effective models for predicting postoperative survival in patients with CRLM.

Keywords: colorectal liver metastasis, nomogram, overall survival, SEER, cancer‐specific survival

References(23)

1

Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Jemal A, et al. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2021;71(3):209–49. https://doi.org/10.3322/caac.21660

2

Mantke R, Schmidt U, Wolff S, Kube R, Lippert H. Incidence of synchronous liver metastases in patients with colorectal cancer in relationship to clinico‐pathologic characteristics. Results of a German prospective multicentre observational study. Eur J Surg Oncol. 2012;38(3):259–65. https://doi.org/10.1016/j.ejso.2011.12.013

3

Kim YI, Park IJ, Kim JE, Kim SY, Park J‐H, Lee JH, et al. Hepatic resection after neoadjuvant chemotherapy for patients with liver metastases from colorectal cancer: need for cautious planning. Ann Surg Treat Res. 2019;97(5):245–53. https://doi.org/10.4174/astr.2019.97.5.245

4

Guo M, Jin N, Pawlik T, Cloyd JM. Neoadjuvant chemotherapy for colorectal liver metastases: a contemporary review of the literature. World J Gastrointest Oncol. 2021;13(9):1043–61. https://doi.org/10.4251/wjgo.v13.i9.1043

5

Hirokawa F, Ueno M, Nakai T, Kaibori M, Nomi T, Iida H, et al. Neoadjuvant chemotherapy versus upfront surgery for resectable liver metastases from colorectal cancer: a multicenter, propensity score‐matched cohort study. J Gastrointest Surg. 2022;26(4):772–81. https://doi.org/10.1007/s11605-021-05175-y

6

Ono K, Abe T, Oshita A, Sumi Y, Yano T, Okuda H, et al. Efficacy of upfront hepatectomy without neoadjuvant chemotherapy for resectable colorectal liver metastasis. World J Surg Oncol. 2021;19(1):97. https://doi.org/10.1186/s12957-021-02210-9

7

Yoshino T, Arnold D, Taniguchi H, Pentheroudakis G, Yamazaki K, Xu R‐H, et al. Pan‐Asian adapted ESMO consensus guidelines for the management of patients with metastatic colorectal cancer: a JSMO‐ESMO initiative endorsed by CSCO, KACO, MOS, SSO and TOS. Ann Oncol. 2018;29(1):44–70. https://doi.org/10.1093/annonc/mdx738

8

Dennosuke J. General rules for clinical and pathological studies on cancer of the colon, rectum and anus: part. I. Clinical classification. Jpn J Surg. 1983;13: 557–73. https://doi.org/10.1007/BF02469505

9
Guo X, Liu Y, Liu L‐J, Li J, Zhao L, Jin X‐R, et al. Development and validation of survival nomograms in colorectal cancer patients with synchronous liver metastases underwent simultaneous surgical treatment of primary and metastatic lesions. Am J Cancer Res. 2021;11(6):2654–69. https://europepmc.org/article/PMC/8263634
10

Mandrekar JN. Receiver operating characteristic curve in diagnostic test assessment. J Thorac Oncol. 2010;5(9):1315–6. https://doi.org/10.1097/JTO.0b013e3181ec173d

11

Deng GC, Lv Y, Yan H, Sun DC, Qu TT, Pan YT, et al. Nomogram to predict survival of patients with advanced and metastatic pancreatic cancer. BMC Cancer. 2021;21(1):1227. https://doi.org/10.1186/s12885-021-08943-w

12

Vickers AJ, Elkin EB. Decision curve analysis: a novel method for evaluating prediction models. Med Decis Making. 2006;26(6):565–74. https://doi.org/10.1177/0272989X06295361

13

Liu C, Hu C, Huang J, Xiang K, Li Z, Qu J, et al. A prognostic nomogram of colon cancer with liver metastasis: a study of the US SEER database and a Chinese cohort. Front Oncol. 2021;11:591009. https://doi.org/10.3389/fonc.2021.591009

14

Cheng X, Li Y, Chen D, Xu X, Liu F, Zhao F. Nomogram predicting the survival of young‐onset patients with colorectal cancer liver metastases. Diagnostics. 2022;12(6):1395. https://doi.org/10.3390/diagnostics12061395

15

Becerra AZ, Probst CP, Tejani MA, Aquina CT, González MG, Hensley BJ, et al. Evaluating the prognostic role of elevated preoperative carcinoembryonic antigen levels in colon cancer patients: results from the National cancer database. Ann Surg Oncol. 2016;23(5):1554–61. https://doi.org/10.1245/s10434-015-5014-1

16

Spindler BA, Bergquist JR, Thiels CA, Habermann EB, Kelley SR, Larson DW, et al. Incorporation of CEA improves risk stratification in stage II colon cancer. J Gastrointest Surg. 2017;21(5):770–7. https://doi.org/10.1007/s11605-017-3391-4

17

Duffy MJ, van Dalen A, Haglund C, Hansson L, Holinski‐Feder E, Klapdor R, et al. Tumour markers in colorectal cancer: European Group on Tumour Markers (EGTM) guidelines for clinical use. Eur J Cancer. 2007;43(9):1348–60. https://doi.org/10.1016/j.ejca.2007.03.021

18

Locker GY, Hamilton S, Harris J, Jessup JM, Kemeny N, Macdonald JS, et al. ASCO 2006 update of recommendations for the use of tumor markers in gastrointestinal cancer. J Clin Oncol. 2006;24(33):5313–27. https://doi.org/10.1200/JCO.2006.08.2644

19

Derwinger K, Gustavsson B. A study of lymph node ratio in stage IV colorectal cancer. World J Surg Oncol. 2008;6:127. https://doi.org/10.1186/1477-7819-6-127

20

Portier G, Elias D, Bouche O, Rougier P, Bosset J‐F, Saric J, et al. Multicenter randomized trial of adjuvant fluorouracil and folinic acid compared with surgery alone after resection of colorectal liver metastases: FFCD ACHBTH AURC 9002 trial. J Clin Oncol. 2006;24(31):4976–82. https://doi.org/10.1200/JCO.2006.06.8353

21

Benson AB, Venook AP, Al‐Hawary MM, Arain MA, Chen Y‐J, Ciombor KK, et al. NCCN guidelines insights: rectal cancer, version 6.2020. J Natl Compr Cancer Netw. 2020;18(7):806–15. https://doi.org/10.6004/jnccn.2020.0032

22

Wu Q, Wang W, Huang Y, Fang S, Guan Y. Nomograms for estimating survival in patients with liver‐only colorectal metastases: a retrospective study. Int J Surg. 2018;60:1–8. https://doi.org/10.1016/j.ijsu.2018.10.032

23

Liang J, Lin H, Liu J, Wang D, Yuan Y, Li B, et al. A novel prognostic nomogram for colorectal cancer liver metastasis patients with recurrence after hepatectomy. Cancer Med. 2021;10(5):1535–44. https://doi.org/10.1002/cam4.3697

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Received: 11 October 2022
Accepted: 30 November 2022
Published: 17 January 2023
Issue date: August 2023

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© 2022 The Authors. Tsinghua University Press.

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