Clinical and pathological analysis of small renal cell carcinoma

  • Xiao-peng ZHANG ,
  • Zi-xiong HUANG ,
  • Lu-ping YU ,
  • Xiao-wei ZHANG ,
  • Qing LI ,
  • Shi-jun LIU ,
  • Tao XU
Expand
  • Department of Urology, Peking University People’s Hospital, Beijing 100044, China

Received date: 2019-03-18

  Online published: 2019-09-03

Abstract

Objective: To analyze the clinical and pathological features of small renal cell carcinoma (RCC), especially of those with diameter less than 4 cm and to understand the characteristics and factors related to recurrence and progression.Methods: A total of 200 patients with RCC were stratifiedly selected for retrospective analysis. Their baseline demographic features, tumor-specific clinical features, pathological features of renal lesions, especially microscopic features were collected. The patients were divided according to the largest diameter of renal tumor lesions. Univariate analysis was used to compare the differences between tumor staging and microscopic pathological features between the groups. Binary multivariate Logistic regression was used to investigate factors related to tumor progression and prognosis in the patients with small RCC.Results: The tumor diameters of 127 RCC patients were less than 4 cm and most of them had clear cell renal cell carcinoma (ccRCC). The increase in tumor diameter resulted in significantly higher T stage (P<0.01), higher WHO/International Society of Urological Pathology (ISUP) grade (P<0.05) and increasing chance of lymph node metastasis (P<0.01). Even when the tumor diameter was less than 4 cm, the patients might still have perirenal fat invasion, renal sinus invasion and greater elevated tumor grade (greater than grade 3) and synchronous lung metastasis. The incidences of intravascular thrombus (9.3% vs. 0) and tumor necrosis (27.8% vs. 5.5%) in the patients with RCC between 4-7 cm were significantly higher than those with RCC less than 4 cm (P<0.01). Sub-group analysis of small RCC (less than 4 cm) indicated that the patients with RCC between 2-4 cm were more likely to have intratumoral hemorrhage (44.7% vs. 23%, P<0.05) and necrosis than those with RCC less than 2 cm (8.2% vs. 0, P=0.095). Logistic regression analysis of small RCC showed that the incidence of tumor invasion to renal capsule was higher in ccRCC (OR=5.15, 95%CI: 1.36-19.52). Necrosis was closely related to the formation of peritumor pseudocapsule in small RCC (OR=14.90, 95%CI: 1.41-157.50). Increase in the tumor diameter was related to higher tumor grade (greater than grade 3) (OR=3.49, 95%CI: 1.11-10.93).Conclusion: The tumor stage and grade of small RCC (less than 4 cm) are low, but extra-renal invasion and synchronous distant metastasis may occur. Internal hemorrhage and necrosis in tumor, ccRCC subtype, along with microscopic features, such as the renal capsule invasion and perirenal pseudocapsule formation are relevant factors of malignant behavior of small RCC and could be considered in prognosis evaluation.

Cite this article

Xiao-peng ZHANG , Zi-xiong HUANG , Lu-ping YU , Xiao-wei ZHANG , Qing LI , Shi-jun LIU , Tao XU . Clinical and pathological analysis of small renal cell carcinoma[J]. Journal of Peking University(Health Sciences), 2019 , 51(4) : 623 -627 . DOI: 10.19723/j.issn.1671-167X.2019.04.004

References

[1] Kim SP, Thompson RH, Boorjian SA , et al. Comparative effectiveness for survival and renal function of partial and radical nephrectomy for localized renal tumors: A systematic review and meta-analysis[J]. J Urol, 2012,188(1):51-57.
[2] Van Poppel H, Pozzo LF, Albrecht W , et al. A prospective, randomised EORTC intergroup phase 3 study comparing the oncologic outcome of elective nephron-sparing surgery and radical nephrectomy for low-stage renal cell carcinoma[J]. Eur Urol, 2007,59(4):543-552.
[3] Long CJ, Canter D, Kutikov A , et al. Partial nephrectomy for renal masses ≥ 7 cm: technical, oncological and functional outcomes[J]. BJU Int, 2012,109(10):1450-1456.
[4] Ljungberg B . Nephron-sparing surgery strategy: the current stan-dard for the treatment of localised renal cell carcinoma[J]. Eur Urol Suppl, 2011,10(3):e49-e51.
[5] Thompson RH, Blute ML, Krambeck AE , et al. Patients with pT1 renal cell carcinoma who die from disease after nephrectomy may have unrecognized renal sinus fat invasion[J]. Am J Surg Pathol, 2007,31(7):1089-1093.
[6] Feifer A, Savage C, Rayala H , et al. Prognostic impact of muscular venous branch invasion in localized renal cell carcinoma cases[J]. J Urol, 2011,185(1):37-42.
[7] Huang Z, Du Y, Zhang X , et al. Clear cell renal cell carcinoma bone metastasis: What should be considered in prognostic evaluation[J]. Eur J Surg Oncol, 2019,45(7):1246-1252.
[8] Forbes CM, Rendon RA, Finelli A , et al. Disease progression and kidney function after partial vs. radical nephrectomy for T1 renal cancer [J]. Urol Oncol, 2016, 34(11): 486. e17- 486. e23.
[9] Moch H, Cubilla AL, Humphrey PA , et al. The 2016 WHO classification of tumours of the urinary system and male genital organs—Part A: renal, penile, and testicular tumours[J]. Eur Urol, 2016,70(1):93-105.
[10] European Association of Urology. EAU guidelines [R]. EAU Annual Congress Copenhagen, 2018.
[11] Dash A, Vickers AJ, Schachter LR , et al. Comparison of outcomes in elective partial vs radical nephrectomy for clear cell renal cell carcinoma of 4-7 cm[J]. BJU Int, 2006,97(5):939-945.
[12] Crepel M, Jeldres C, Perrotte P , et al. Nephron-sparing surgery is equally effective to radical nephrectomy for T1BN0M0 renal cell carcinoma: A population-based assessment[J]. Urology, 2010,75(2):271-275.
[13] Lughezzani G, Jeldres C, Isbarn H , et al. Tumor size is a determinant of the rate of stage T1 renal cell cancer synchronous metastasis[J]. J Urol, 2009,182(4):1287-1293.
[14] Syed JS, Nawaf CB, Rosoff J , et al. Adverse pathologic characte-ristics in the small renal mass: implications for active surveillance[J]. Can J Urol, 2017,24(2):8759-8764.
[15] Sun M, Shariat SF, Cheng C , et al. Prognostic factors and predictive models in renal cell carcinoma: A contemporary review[J]. Eur Urol, 2011,60(4):644-661.
[16] Jeong IG, Jeong CW, Hong SK , et al. Prognostic implication of capsular invasion without perinephric fat infiltration in localized renal cell carcinoma[J]. Urology, 2006,67(4):709-712.
[17] Pickhardt PJ, Lonergan GJ, Davis CJ Jr , et al. From the archives of the AFIP. Infiltrative renal lesions: radiologicpathologic correlation. Armed Forces Institute of Pathology[J]. Radiographics, 2000,20:215-243.
[18] Cho S, Lee JH, Jeon SH , et al. A prospective, multicenter analysis of pseudocapsule characteristics: Do all stages of renal cell carcinoma have complete pseudocapsules?[J]. Urol Oncol, 2017,35(6):370-378.
[19] Capitanio U, Cloutier V, Zini L , et al. A critical assessment of the prognostic value of clear cell, papillary and chromophobe histological subtypes in renal cell carcinoma: a population-based study[J]. BJU Int, 2009,103(11):1496-1500.
[20] Keegan KA, Schupp CW, Chamie K , et al. Histopathology of surgically treated renal cell carcinoma: Survival differences by subtype and stage[J]. J Urol, 2012,188(2):391-397.
[21] Kryvenko ON . Tumor necrosis adds prognostically significant information to grade in clear cell renal cell carcinoma: A study of 842 consecutive cases from a single institution[J]. Urol Oncol, 2017,35(6):454-455.
[22] Collins J, Epstein JI . Prognostic significance of extensive necrosis in renal cell carcinoma[J]. Hum Pathol, 2017,66:108-114.
Outlines

/