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Published in: Annals of Surgical Oncology 1/2021

01-01-2021 | Pancreatic Tumors

Grading Solid Pseudopapillary Tumors of the Pancreas: the Fudan Prognostic Index

Authors: Feng Yang, MD, PhD, Wenchuan Wu, MD, PhD, Xiaoyi Wang, MD, Qiongyan Zhang, MD, Yun Bao, MD, Zhongwen Zhou, MD, PhD, Chen Jin, MD, PhD, Yuan Ji, MD, PhD, John A. Windsor, MD, FRACS, Wenhui Lou, MD, PhD, Deliang Fu, MD, PhD

Published in: Annals of Surgical Oncology | Issue 1/2021

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Abstract

Background

Ki-67 has been shown to predict outcome of patients with solid pseudopapillary tumor of the pancreas (SPTP) but has not been incorporated into a formal classification system to predict recurrence-free survival (RFS).

Methods

This is a retrospective cohort study of patients with histologically confirmed diagnosis of SPTP who had at least 1 year of follow-up at two tertiary academic centers. Survival data were assessed by Kaplan–Meier method and multivariable Cox regression model. Prognostic performance was compared among various systems.

Results

A total of 193 consecutive patients were included, ranging in age from 12 to 70 years (median 33 years). Seven patients (3.6%) developed tumor recurrence. The 3-, 5-, and 10-year RFS rates were estimated at 96.9%, 96.1%, and 94.8%, respectively. For the AJCC staging system, patients with stage I had similar prognosis to those with stage II. For the ENETS staging system, patients with stage I to III had similar prognosis. Grade based on Ki-67 was superior to both the AJCC and ENETS systems for predicting survival. Multivariate analysis revealed that large tumor size [> 10 cm; hazard ratio (HR), 6.177 95% confidence interval (CI), 1.289–29.603; P = 0.023] and Ki-67 (HR, 17.199 95% CI, 4.001–73.930; P < 0.001) were independent predictors for RFS. The Fudan Prognostic Index based on the combination of Ki-67 and tumor size showed excellent discrimination for RFS and was more accurate and informative than other grading/staging systems.

Conclusion

The Fudan Prognostic Index better predicts RFS compared with either Ki-67 alone or the current AJCC and ENETS TNM-based staging systems.
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Literature
1.
go back to reference Yang F, Fu DL, Jin C, et al. Clinical experiences of solid pseudopapillary tumors of the pancreas in China. J Gastroenterol Hepatol. 2008;23(12):1847–51.CrossRef Yang F, Fu DL, Jin C, et al. Clinical experiences of solid pseudopapillary tumors of the pancreas in China. J Gastroenterol Hepatol. 2008;23(12):1847–51.CrossRef
2.
go back to reference You L, Yang F, Fu DL. Prediction of malignancy and adverse outcome of solid pseudopapillary tumor of the pancreas. World J Gastrointest Oncol. 2018;10(7):184–193.CrossRef You L, Yang F, Fu DL. Prediction of malignancy and adverse outcome of solid pseudopapillary tumor of the pancreas. World J Gastrointest Oncol. 2018;10(7):184–193.CrossRef
3.
go back to reference Yang F, Yu X, Bao Y, Du Z, Jin C, Fu D. Prognostic value of Ki-67 in solid pseudopapillary tumor of the pancreas: Huashan experience and systematic review of the literature. Surgery. 2016;159(4):1023–31.CrossRef Yang F, Yu X, Bao Y, Du Z, Jin C, Fu D. Prognostic value of Ki-67 in solid pseudopapillary tumor of the pancreas: Huashan experience and systematic review of the literature. Surgery. 2016;159(4):1023–31.CrossRef
4.
go back to reference Yang F, Jin C, Fu D. Evolution of liver metastasis from solid pseudopapillary tumor of the pancreas. Surgery. 2017;161(6):1739–40.CrossRef Yang F, Jin C, Fu D. Evolution of liver metastasis from solid pseudopapillary tumor of the pancreas. Surgery. 2017;161(6):1739–40.CrossRef
5.
go back to reference Jutric Z, Rozenfeld Y, Grendar J, et al. Analysis of 340 patients with solid pseudopapillary tumors of the pancreas: a closer look at patients with metastatic disease. Ann Surg Oncol. 2017;24(7):2015–22.CrossRef Jutric Z, Rozenfeld Y, Grendar J, et al. Analysis of 340 patients with solid pseudopapillary tumors of the pancreas: a closer look at patients with metastatic disease. Ann Surg Oncol. 2017;24(7):2015–22.CrossRef
6.
go back to reference Edge SB, Byrd DR, Compton CC, et al. AJCC cancer staging manual. 7th ed. New York, NY: Springer; 2010. Edge SB, Byrd DR, Compton CC, et al. AJCC cancer staging manual. 7th ed. New York, NY: Springer; 2010.
7.
go back to reference Kakar S, Pawlik TM, Allen PJ, et al. Exocrine pancreas. Pancreatic adenocarcinoma. In: Amin MB, ed. AJCC cancer staging manual. 8th ed. New York, NY: Springer; 2016. Kakar S, Pawlik TM, Allen PJ, et al. Exocrine pancreas. Pancreatic adenocarcinoma. In: Amin MB, ed. AJCC cancer staging manual. 8th ed. New York, NY: Springer; 2016.
8.
go back to reference Estrella JS, Li L, Rashid A, et al. Solid pseudopapillary neoplasm of the pancreas: clinicopathologic and survival analyses of 64 cases from a single institution. Am J Surg Pathol. 2014;38(2):147–57.CrossRef Estrella JS, Li L, Rashid A, et al. Solid pseudopapillary neoplasm of the pancreas: clinicopathologic and survival analyses of 64 cases from a single institution. Am J Surg Pathol. 2014;38(2):147–57.CrossRef
9.
go back to reference Lawlor RT, Daprà V, Girolami I, et al. CD200 expression is a feature of solid pseudopapillary neoplasms of the pancreas. Virchows Arch. 2019;474(1):105–9.CrossRef Lawlor RT, Daprà V, Girolami I, et al. CD200 expression is a feature of solid pseudopapillary neoplasms of the pancreas. Virchows Arch. 2019;474(1):105–9.CrossRef
10.
go back to reference Jiang Y, Xie J, Wang B, Mu Y, Liu P. TFE3 is a diagnostic marker for solid pseudopapillary neoplasms of the pancreas. Hum Pathol. 2018;81:166–75.CrossRef Jiang Y, Xie J, Wang B, Mu Y, Liu P. TFE3 is a diagnostic marker for solid pseudopapillary neoplasms of the pancreas. Hum Pathol. 2018;81:166–75.CrossRef
11.
go back to reference Inzani F, Petrone G, Rindi G. The new World Health Organization classification for pancreatic neuroendocrine neoplasia. Endocrinol Metab Clin North Am. 2018;47(3):463–70.CrossRef Inzani F, Petrone G, Rindi G. The new World Health Organization classification for pancreatic neuroendocrine neoplasia. Endocrinol Metab Clin North Am. 2018;47(3):463–70.CrossRef
12.
go back to reference Yang F, Jin C, Long J, et al. Solid pseudopapillary tumor of the pancreas: a case series of 26 consecutive patients. Am J Surg. 2009;198(2):210–5.CrossRef Yang F, Jin C, Long J, et al. Solid pseudopapillary tumor of the pancreas: a case series of 26 consecutive patients. Am J Surg. 2009;198(2):210–5.CrossRef
13.
go back to reference Kim EK, Jang M, Park M, Kim H. LEF1, TFE3, and AR are putative diagnostic markers of solid pseudopapillary neoplasms. Oncotarget. 2017;8(55):93404–13.CrossRef Kim EK, Jang M, Park M, Kim H. LEF1, TFE3, and AR are putative diagnostic markers of solid pseudopapillary neoplasms. Oncotarget. 2017;8(55):93404–13.CrossRef
14.
go back to reference Zou C, Yang F, Fu D. Meta-analysis of Ki-67 expression for recurrence in patients with solid pseudopapillary tumor of the pancreas. HPB (Oxford). 2020;22(4):631–2.CrossRef Zou C, Yang F, Fu D. Meta-analysis of Ki-67 expression for recurrence in patients with solid pseudopapillary tumor of the pancreas. HPB (Oxford). 2020;22(4):631–2.CrossRef
15.
go back to reference Reid MD, Bagci P, Ohike N, et al. Calculation of the Ki67 index in pancreatic neuroendocrine tumors: a comparative analysis of four counting methodologies. Mod Pathol. 2015;28(5):686–94.CrossRef Reid MD, Bagci P, Ohike N, et al. Calculation of the Ki67 index in pancreatic neuroendocrine tumors: a comparative analysis of four counting methodologies. Mod Pathol. 2015;28(5):686–94.CrossRef
16.
go back to reference Rindi G, Klöppel G, Alhman H, et al. TNM staging of foregut (neuro)endocrine tumors: a consensus proposal including a grading system. Virchows Arch. 2006;449(4):395–401.CrossRef Rindi G, Klöppel G, Alhman H, et al. TNM staging of foregut (neuro)endocrine tumors: a consensus proposal including a grading system. Virchows Arch. 2006;449(4):395–401.CrossRef
17.
go back to reference Yang F, Bao Y, Zhou Z, Jin C, Fu D. Preoperative neutrophil-to-lymphocyte ratio predicts malignancy and recurrence-free survival of solid pseudopapillary tumor of the pancreas. J Surg Oncol. 2019;120(2):241–8.PubMed Yang F, Bao Y, Zhou Z, Jin C, Fu D. Preoperative neutrophil-to-lymphocyte ratio predicts malignancy and recurrence-free survival of solid pseudopapillary tumor of the pancreas. J Surg Oncol. 2019;120(2):241–8.PubMed
18.
go back to reference Teo R, Goh BKP, Tai DWM, et al. Validation and comparison between current prognostication systems for pancreatic neuroendocrine neoplasms: A single-institution experience with 176 patients. Surgery. 2017;161(5):1235–45.CrossRef Teo R, Goh BKP, Tai DWM, et al. Validation and comparison between current prognostication systems for pancreatic neuroendocrine neoplasms: A single-institution experience with 176 patients. Surgery. 2017;161(5):1235–45.CrossRef
19.
go back to reference Hanada K, Kurihara K, Itoi T, et al. Clinical and pathological features of solid pseudopapillary neoplasms of the pancreas: a nationwide multicenter study in Japan. Pancreas. 2018;47(8):1019–26.CrossRef Hanada K, Kurihara K, Itoi T, et al. Clinical and pathological features of solid pseudopapillary neoplasms of the pancreas: a nationwide multicenter study in Japan. Pancreas. 2018;47(8):1019–26.CrossRef
20.
go back to reference Watanabe Y, Okamoto K, Okada K, Aikawa M, Koyama I, Yamaguchi H. A case of aggressive solid pseudopapillary neoplasm: comparison of clinical and pathologic features with non-aggressive cases. Pathol Int. 2017;67(4):202–7.CrossRef Watanabe Y, Okamoto K, Okada K, Aikawa M, Koyama I, Yamaguchi H. A case of aggressive solid pseudopapillary neoplasm: comparison of clinical and pathologic features with non-aggressive cases. Pathol Int. 2017;67(4):202–7.CrossRef
21.
go back to reference Tang LH, Aydin H, Brennan MF, Klimstra DS. Clinically aggressive solid pseudopapillary tumors of the pancreas: a report of two cases with components of undifferentiated carcinoma and a comparative clinicopathologic analysis of 34 conventional cases. Am J Surg Pathol. 2005;29(4):512–9.CrossRef Tang LH, Aydin H, Brennan MF, Klimstra DS. Clinically aggressive solid pseudopapillary tumors of the pancreas: a report of two cases with components of undifferentiated carcinoma and a comparative clinicopathologic analysis of 34 conventional cases. Am J Surg Pathol. 2005;29(4):512–9.CrossRef
22.
go back to reference Wu JH, Tian XY, Liu BN, Li CP, Zhao M, Hao CY. Clinicopathological features and prognostic factors of solid pseudopapillary neoplasms of pancreas. Pak J Pharm Sci. 2019;32(1(Special)):459–64.PubMed Wu JH, Tian XY, Liu BN, Li CP, Zhao M, Hao CY. Clinicopathological features and prognostic factors of solid pseudopapillary neoplasms of pancreas. Pak J Pharm Sci. 2019;32(1(Special)):459–64.PubMed
23.
go back to reference Rindi G, Klersy C, Albarello L, et al. Competitive testing of the WHO 2010 versus the WHO 2017 grading of pancreatic neuroendocrine neoplasms: data from a large international cohort study. Neuroendocrinology. 2018;107(4):375–86.CrossRef Rindi G, Klersy C, Albarello L, et al. Competitive testing of the WHO 2010 versus the WHO 2017 grading of pancreatic neuroendocrine neoplasms: data from a large international cohort study. Neuroendocrinology. 2018;107(4):375–86.CrossRef
24.
go back to reference Harimoto N, Hoshino K, Muranushi R, et al. Significance of lymph node metastasis in resectable well-differentiated pancreatic neuroendocrine tumor. Pancreas. 2019;48(7):943–7.CrossRef Harimoto N, Hoshino K, Muranushi R, et al. Significance of lymph node metastasis in resectable well-differentiated pancreatic neuroendocrine tumor. Pancreas. 2019;48(7):943–7.CrossRef
25.
go back to reference Escobar MA Jr, McClellan JM, Thomas W. Solid pseudopapillary tumour (Frantz’s tumour) of the pancreas in childhood: successful management of late liver metastases with sunitinib and chemoembolisation. BMJ Case Rep. 2017;2017. Escobar MA Jr, McClellan JM, Thomas W. Solid pseudopapillary tumour (Frantz’s tumour) of the pancreas in childhood: successful management of late liver metastases with sunitinib and chemoembolisation. BMJ Case Rep. 2017;2017.
26.
go back to reference Tajima H, Takamura H, Kitagawa H, et al. Multiple liver metastases of pancreatic solid pseudopapillary tumor treated with resection following chemotherapy and transcatheter arterial embolization: a case report. Oncol Lett. 2015;9(4):1733–8.CrossRef Tajima H, Takamura H, Kitagawa H, et al. Multiple liver metastases of pancreatic solid pseudopapillary tumor treated with resection following chemotherapy and transcatheter arterial embolization: a case report. Oncol Lett. 2015;9(4):1733–8.CrossRef
27.
go back to reference Hofmann H, von Haken R, Werner J, et al. Unresectable isolated hepatic metastases from solid pseudopapillary neoplasm of the pancreas: a case report of chemosaturation with high-dose melphalan. Pancreatology. 2014;14(6):546–9.CrossRef Hofmann H, von Haken R, Werner J, et al. Unresectable isolated hepatic metastases from solid pseudopapillary neoplasm of the pancreas: a case report of chemosaturation with high-dose melphalan. Pancreatology. 2014;14(6):546–9.CrossRef
28.
go back to reference Khan MS, Luong TV, Watkins J, Toumpanakis C, Caplin ME, Meyer T. A comparison of Ki-67 and mitotic count as prognostic markers for metastatic pancreatic and midgut neuroendocrine neoplasms. Br J Cancer. 2013;108(9):1838–45.CrossRef Khan MS, Luong TV, Watkins J, Toumpanakis C, Caplin ME, Meyer T. A comparison of Ki-67 and mitotic count as prognostic markers for metastatic pancreatic and midgut neuroendocrine neoplasms. Br J Cancer. 2013;108(9):1838–45.CrossRef
29.
go back to reference Kang CM, Choi SH, Kim SC, et al. Predicting recurrence of pancreatic solid pseudopapillary tumors after surgical resection: a multicenter analysis in Korea. Ann Surg. 2014;260(2):348–55.CrossRef Kang CM, Choi SH, Kim SC, et al. Predicting recurrence of pancreatic solid pseudopapillary tumors after surgical resection: a multicenter analysis in Korea. Ann Surg. 2014;260(2):348–55.CrossRef
30.
go back to reference Ricci C, Casadei R, Taffurelli G, et al. Validation of the 2010 WHO classification and a new prognostic proposal: A single centre retrospective study of well-differentiated pancreatic neuroendocrine tumours. Pancreatology. 2016;16(3):403–10.CrossRef Ricci C, Casadei R, Taffurelli G, et al. Validation of the 2010 WHO classification and a new prognostic proposal: A single centre retrospective study of well-differentiated pancreatic neuroendocrine tumours. Pancreatology. 2016;16(3):403–10.CrossRef
Metadata
Title
Grading Solid Pseudopapillary Tumors of the Pancreas: the Fudan Prognostic Index
Authors
Feng Yang, MD, PhD
Wenchuan Wu, MD, PhD
Xiaoyi Wang, MD
Qiongyan Zhang, MD
Yun Bao, MD
Zhongwen Zhou, MD, PhD
Chen Jin, MD, PhD
Yuan Ji, MD, PhD
John A. Windsor, MD, FRACS
Wenhui Lou, MD, PhD
Deliang Fu, MD, PhD
Publication date
01-01-2021
Publisher
Springer International Publishing
Published in
Annals of Surgical Oncology / Issue 1/2021
Print ISSN: 1068-9265
Electronic ISSN: 1534-4681
DOI
https://doi.org/10.1245/s10434-020-08626-z

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