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Published in: BMC Urology 1/2022

Open Access 01-12-2022 | Metastasis | Research

♣Evaluation of clinicopathological profiles and development of a risk model in renal epithelioid angiomyolipoma patients: a large-scale retrospective cohort study

Authors: Aihetaimujiang Anwaier, Wen-Hao Xu, Xi Tian, Tao Ding, Jia-Qi Su, Yue Wang, Yuan-Yuan Qu, Hai-Liang Zhang, Ding-Wei Ye

Published in: BMC Urology | Issue 1/2022

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Abstract

Background

To identify the malignant potential and prognostic indicators of renal epithelioid angiomyolipoma (eAML), clinicopathological and molecular features as well as the drug efficacy of 67 eAML cases were analyzed.

Materials and methods

Sixty-seven renal eAML patients were enrolled and the immunohistochemical features of these patients were examined. FFPE slides of all patients were re-examined. 21 patients with metastasis received Everolimus 10 mg orally once daily. Responses were evaluated with RECIST criteria by three authors. A risk stratification model was constructed using the following factors: pT3 and pT4, presence of necrosis, mitotic count ≥ 2; the presence of atypical mitoses; severe nuclear atypia, SMA negative, Ki-67 ≥ 10%.

Results

The average percentage of the epithelioid component was 85.6% (range 80–95%). Immunohistochemically, Ki-67 ≥ 10% and negative SMA staining were significantly correlated with malignant characteristics (Ki-67: p < 0.001; SMA: p = 0.001). Survival analysis suggested that pT3-pT4 stage, presence of necrosis, severe nuclear atypia, presence of atypical mitoses, mitotic count ≥ 2, Ki-67 ≥ 10% and negative SMA expression were significantly associated with poorer PFS and OS (p < 0.05). The risk model sufficiently discriminated recurrence/metastasis (AUC = 0.897) and cancer-specific mortality (AUC = 0.932) of renal eAML patients in different risk groups. 21 patients had received Everolimus targeted therapy after recurrence/metastasis. The best response for Everolimus treatment was 8/21 (38.1%) partial responses (PR), 9/21 (42.9%) stable disease (SD) and 4/21 (19.0%) progressive disease (PD).

Conclusion

The risk stratification model could well distinguish eAML patients at high risk of recurrence/metastasis. Everolimus targeted treatment showed good efficacy in patients with recurrence/metastasis.
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Literature
1.
go back to reference Jinzaki M, Silverman SG, Akita H, et al. Diagnosis of renal angiomyolipomas: classic, fat-poor, and epithelioid types. Semin Ultrasound CT MR. 2017;38(1):37–46.CrossRef Jinzaki M, Silverman SG, Akita H, et al. Diagnosis of renal angiomyolipomas: classic, fat-poor, and epithelioid types. Semin Ultrasound CT MR. 2017;38(1):37–46.CrossRef
2.
go back to reference Lopez-Beltran A, Scarpelli M, Montironi R, et al. 2004 WHO classification of the renal tumors of the adults. Eur Urol. 2006;49(5):798–805.CrossRef Lopez-Beltran A, Scarpelli M, Montironi R, et al. 2004 WHO classification of the renal tumors of the adults. Eur Urol. 2006;49(5):798–805.CrossRef
3.
go back to reference Faraji H, Nguyen BN, Mai KT. Renal epithelioid angiomyolipoma: a study of six cases and a meta-analytic study: development of criteria for screening the entity with prognostic significance. Histopathology. 2009;55(5):525–34.CrossRef Faraji H, Nguyen BN, Mai KT. Renal epithelioid angiomyolipoma: a study of six cases and a meta-analytic study: development of criteria for screening the entity with prognostic significance. Histopathology. 2009;55(5):525–34.CrossRef
4.
go back to reference Aydin H, Magi-Galluzzi C, Lane BR, et al. Renal angiomyolipoma: clinicopathologic study of 194 cases with emphasis on the epithelioid histology and tuberous sclerosis association. Am J Surg Pathol. 2009;33(2):289–97.CrossRef Aydin H, Magi-Galluzzi C, Lane BR, et al. Renal angiomyolipoma: clinicopathologic study of 194 cases with emphasis on the epithelioid histology and tuberous sclerosis association. Am J Surg Pathol. 2009;33(2):289–97.CrossRef
5.
go back to reference 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. Eur Urol. 2016;70(1):93–105.CrossRef 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. Eur Urol. 2016;70(1):93–105.CrossRef
6.
go back to reference Mete O, van der Kwast TH. Epithelioid angiomyolipoma: a morphologically distinct variant that mimics a variety of intra-abdominal neoplasms. Arch Pathol Lab Med. 2011;135(5):665–70.CrossRef Mete O, van der Kwast TH. Epithelioid angiomyolipoma: a morphologically distinct variant that mimics a variety of intra-abdominal neoplasms. Arch Pathol Lab Med. 2011;135(5):665–70.CrossRef
7.
go back to reference Armah HB, Parwani AV. Perivascular epithelioid cell tumor. Arch Pathol Lab Med. 2009;133(4):648–54.CrossRef Armah HB, Parwani AV. Perivascular epithelioid cell tumor. Arch Pathol Lab Med. 2009;133(4):648–54.CrossRef
8.
go back to reference He W, Cheville JC, Sadow PM, et al. Epithelioid angiomyolipoma of the kidney: pathological features and clinical outcome in a series of consecutively resected tumors. Modern Pathol Off J USA Can Acad Pathol. 2013;26(10):1355–64. He W, Cheville JC, Sadow PM, et al. Epithelioid angiomyolipoma of the kidney: pathological features and clinical outcome in a series of consecutively resected tumors. Modern Pathol Off J USA Can Acad Pathol. 2013;26(10):1355–64.
9.
go back to reference Pea M, Bonetti F, Martignoni G, et al. Apparent renal cell carcinomas in tuberous sclerosis are heterogeneous: the identification of malignant epithelioid angiomyolipoma. Am J Surg Pathol. 1998;22(2):180–7.CrossRef Pea M, Bonetti F, Martignoni G, et al. Apparent renal cell carcinomas in tuberous sclerosis are heterogeneous: the identification of malignant epithelioid angiomyolipoma. Am J Surg Pathol. 1998;22(2):180–7.CrossRef
10.
go back to reference Martignoni G, Pea M, Rigaud G, et al. Renal angiomyolipoma with epithelioid sarcomatous transformation and metastases: demonstration of the same genetic defects in the primary and metastatic lesions. Am J Surg Pathol. 2000;24(6):889–94.CrossRef Martignoni G, Pea M, Rigaud G, et al. Renal angiomyolipoma with epithelioid sarcomatous transformation and metastases: demonstration of the same genetic defects in the primary and metastatic lesions. Am J Surg Pathol. 2000;24(6):889–94.CrossRef
11.
go back to reference Svec A, Velenská Z. Renal epithelioid angiomyolipoma—a close mimic of renal cell carcinoma: report of a case and review of the literature. Pathol Res Pract. 2005;200:851–6.CrossRef Svec A, Velenská Z. Renal epithelioid angiomyolipoma—a close mimic of renal cell carcinoma: report of a case and review of the literature. Pathol Res Pract. 2005;200:851–6.CrossRef
12.
go back to reference Lei JH, Liu LR, Wei Q, et al. A four-year follow-up study of renal epithelioid angiomyolipoma: a multi-center experience and literature review. Sci Rep. 2015;5:10030.CrossRef Lei JH, Liu LR, Wei Q, et al. A four-year follow-up study of renal epithelioid angiomyolipoma: a multi-center experience and literature review. Sci Rep. 2015;5:10030.CrossRef
13.
go back to reference Gamé X, Soulié M, Moussouni S, et al. Renal angiomyolipoma associated with rapid enlargement [correction of enlargment] and inferior vena caval tumor thrombus. J Urol. 2003;170(3):918–9.CrossRef Gamé X, Soulié M, Moussouni S, et al. Renal angiomyolipoma associated with rapid enlargement [correction of enlargment] and inferior vena caval tumor thrombus. J Urol. 2003;170(3):918–9.CrossRef
14.
go back to reference Yamamoto T, Ito K, Suzuki K, et al. Rapidly progressive malignant epithelioid angiomyolipoma of the kidney. J Urol. 2002;168(1):190–1.CrossRef Yamamoto T, Ito K, Suzuki K, et al. Rapidly progressive malignant epithelioid angiomyolipoma of the kidney. J Urol. 2002;168(1):190–1.CrossRef
15.
go back to reference Inoue C, Saito R, Nakanishi W, et al. Renal epithelioid angiomyolipoma undergoing aggressive clinical outcome: the MDM2 expression in tumor cells of two cases. Tohoku J Exp Med. 2019;247(2):119–27.CrossRef Inoue C, Saito R, Nakanishi W, et al. Renal epithelioid angiomyolipoma undergoing aggressive clinical outcome: the MDM2 expression in tumor cells of two cases. Tohoku J Exp Med. 2019;247(2):119–27.CrossRef
16.
go back to reference Brimo F, Robinson B, Guo C, et al. Renal epithelioid angiomyolipoma with atypia: a series of 40 cases with emphasis on clinicopathologic prognostic indicators of malignancy. Am J Surg Pathol. 2010;34(5):715–22.CrossRef Brimo F, Robinson B, Guo C, et al. Renal epithelioid angiomyolipoma with atypia: a series of 40 cases with emphasis on clinicopathologic prognostic indicators of malignancy. Am J Surg Pathol. 2010;34(5):715–22.CrossRef
17.
go back to reference Nese N, Martignoni G, Fletcher CD, et al. Pure epithelioid PEComas (so-called epithelioid angiomyolipoma) of the kidney: A clinicopathologic study of 41 cases: detailed assessment of morphology and risk stratification. Am J Surg Pathol. 2011;35(2):161–76.CrossRef Nese N, Martignoni G, Fletcher CD, et al. Pure epithelioid PEComas (so-called epithelioid angiomyolipoma) of the kidney: A clinicopathologic study of 41 cases: detailed assessment of morphology and risk stratification. Am J Surg Pathol. 2011;35(2):161–76.CrossRef
18.
go back to reference Musella A, De Felice F, Kyriacou AK, et al. Perivascular epithelioid cell neoplasm (PEComa) of the uterus: a systematic review. Int J Surg (Lond, Engl). 2015;19:1–5.CrossRef Musella A, De Felice F, Kyriacou AK, et al. Perivascular epithelioid cell neoplasm (PEComa) of the uterus: a systematic review. Int J Surg (Lond, Engl). 2015;19:1–5.CrossRef
19.
go back to reference Zheng S, Bi XG, Song QK, et al. A suggestion for pathological grossing and reporting based on prognostic indicators of malignancies from a pooled analysis of renal epithelioid angiomyolipoma. Int Urol Nephrol. 2015;47(10):1643–51.CrossRef Zheng S, Bi XG, Song QK, et al. A suggestion for pathological grossing and reporting based on prognostic indicators of malignancies from a pooled analysis of renal epithelioid angiomyolipoma. Int Urol Nephrol. 2015;47(10):1643–51.CrossRef
20.
go back to reference Yang L, Feng XL, Shen S, et al. Clinicopathological analysis of 156 patients with angiomyolipoma originating from different organs. Oncol Lett. 2012;3(3):586–90.CrossRef Yang L, Feng XL, Shen S, et al. Clinicopathological analysis of 156 patients with angiomyolipoma originating from different organs. Oncol Lett. 2012;3(3):586–90.CrossRef
21.
go back to reference Cho NH, Shim HS, Choi YD, et al. Estrogen receptor is significantly associated with the epithelioid variants of renal angiomyolipoma: a clinicopathological and immunohistochemical study of 67 cases. Pathol Int. 2004;54(7):510–5.CrossRef Cho NH, Shim HS, Choi YD, et al. Estrogen receptor is significantly associated with the epithelioid variants of renal angiomyolipoma: a clinicopathological and immunohistochemical study of 67 cases. Pathol Int. 2004;54(7):510–5.CrossRef
22.
go back to reference Luo D, Gou J, Yang L, et al. Epithelioid angiomyolipoma with involvement of inferior vena cava as a tumor thrombus: a case report. Kaohsiung J Med Sci. 2011;27(2):72–5.CrossRef Luo D, Gou J, Yang L, et al. Epithelioid angiomyolipoma with involvement of inferior vena cava as a tumor thrombus: a case report. Kaohsiung J Med Sci. 2011;27(2):72–5.CrossRef
23.
go back to reference D’Antonio A, Caleo A, Caleo O, et al. Monotypic epithelioid angiomyolipoma of the adrenal gland: an unusual site for a rare extrarenal tumor. Ann Diagn Pathol. 2009;13(5):347–50.CrossRef D’Antonio A, Caleo A, Caleo O, et al. Monotypic epithelioid angiomyolipoma of the adrenal gland: an unusual site for a rare extrarenal tumor. Ann Diagn Pathol. 2009;13(5):347–50.CrossRef
24.
go back to reference Jinzaki M, Tanimoto A, Narimatsu Y, et al. Angiomyolipoma: imaging findings in lesions with minimal fat. Radiology. 1997;205(2):497–502.CrossRef Jinzaki M, Tanimoto A, Narimatsu Y, et al. Angiomyolipoma: imaging findings in lesions with minimal fat. Radiology. 1997;205(2):497–502.CrossRef
25.
go back to reference Adanur S, Keskin E, Ziypak T, et al. Renal epithelioid angiomyolipoma mimicking urothelial carcinoma of the upper urinary tract. Archivio italiano di urologia, andrologia : organo ufficiale [di] Societa italiana di ecografia urologica e nefrologica. 2014;86(3):235–6.CrossRef Adanur S, Keskin E, Ziypak T, et al. Renal epithelioid angiomyolipoma mimicking urothelial carcinoma of the upper urinary tract. Archivio italiano di urologia, andrologia : organo ufficiale [di] Societa italiana di ecografia urologica e nefrologica. 2014;86(3):235–6.CrossRef
26.
go back to reference Gerdes J, Schwab U, Lemke H, et al. Production of a mouse monoclonal antibody reactive with a human nuclear antigen associated with cell proliferation. Int J Cancer. 1983;31(1):13–20.CrossRef Gerdes J, Schwab U, Lemke H, et al. Production of a mouse monoclonal antibody reactive with a human nuclear antigen associated with cell proliferation. Int J Cancer. 1983;31(1):13–20.CrossRef
27.
go back to reference Urruticoechea A, Smith IE, Dowsett M. Proliferation marker Ki-67 in early breast cancer. J Clin Oncol Off J Am Soc Clin Oncol. 2005;23(28):7212–20.CrossRef Urruticoechea A, Smith IE, Dowsett M. Proliferation marker Ki-67 in early breast cancer. J Clin Oncol Off J Am Soc Clin Oncol. 2005;23(28):7212–20.CrossRef
28.
go back to reference Ooi SM, Vivian JB, Cohen RJ. The use of the Ki-67 marker in the pathological diagnosis of the epithelioid variant of renal angiomyolipoma. Int Urol Nephrol. 2009;41(3):559–65.CrossRef Ooi SM, Vivian JB, Cohen RJ. The use of the Ki-67 marker in the pathological diagnosis of the epithelioid variant of renal angiomyolipoma. Int Urol Nephrol. 2009;41(3):559–65.CrossRef
29.
go back to reference Xu C, Jiang XZ, Zhao HF, et al. The applicability of Ki-67 marker for renal epithelioid angiomyolipoma: experience of ten cases from a single center. Neoplasma. 2013;60(2):209–14.CrossRef Xu C, Jiang XZ, Zhao HF, et al. The applicability of Ki-67 marker for renal epithelioid angiomyolipoma: experience of ten cases from a single center. Neoplasma. 2013;60(2):209–14.CrossRef
30.
go back to reference Li W, Guo L, Bi X, et al. Immunohistochemistry of p53 and Ki-67 and p53 mutation analysis in renal epithelioid angiomyolipoma. Int J Clin Exp Pathol. 2015;8(8):9446–51.PubMedPubMedCentral Li W, Guo L, Bi X, et al. Immunohistochemistry of p53 and Ki-67 and p53 mutation analysis in renal epithelioid angiomyolipoma. Int J Clin Exp Pathol. 2015;8(8):9446–51.PubMedPubMedCentral
Metadata
Title
♣Evaluation of clinicopathological profiles and development of a risk model in renal epithelioid angiomyolipoma patients: a large-scale retrospective cohort study
Authors
Aihetaimujiang Anwaier
Wen-Hao Xu
Xi Tian
Tao Ding
Jia-Qi Su
Yue Wang
Yuan-Yuan Qu
Hai-Liang Zhang
Ding-Wei Ye
Publication date
01-12-2022
Publisher
BioMed Central
Published in
BMC Urology / Issue 1/2022
Electronic ISSN: 1471-2490
DOI
https://doi.org/10.1186/s12894-022-01101-9

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