CONTEMPORARY MANAGEMENT OF RENAL ANGIOMYOLIPOMA

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CONTEMPORARY MANAGEMENT OF RENAL ANGIOMYOLIPOMA Stephen A. Boorjian, MD Professor of Urology Vice Chair of Research Director, Urologic Oncology Fellowship Department of Urology Mayo Clinic, Rochester, MN Fourteenth International Kidney Cancer Symposium Miami, Florida, USA November 6-7, 2015 www.kidneycancersymposium.com

OUTLINE OF TALK Overview of renal angiomyolipoma (AML) Management of AML AML in the setting of tuberous sclerosis Future directions

ANGIOMYOLIPOMA: BACKGROUND Benign tumor composed of blood vessels, smooth muscle, and fat triphasic histology (can be monophasic) Belong to PEComa (perivascular epithelioid cell) family of tumors arise from single progenitor cell 80% sporadic; 20% in the setting of tuberous sclerosis Mean age at diagnosis = 45-55 yrs Female > male incidence Express hormone receptors (esp. ERb, AR) Boorjian SA et al, Urology 2008

DIAGNOSIS OF AML Fat-containing lesion with no calcification on non-enhanced CT < 10 HU Fat-poor AML (ddx vs RCC): MRI Biopsy AML characterized by expression of HMB-45

MANAGEMENT OF RENAL AML Observation for most cases (often incidental dx) Intervention if: Symptoms Pain Hematuria Hemorrhage (Wunderlich s syndrome) Concern for malignancy on imaging (rare) Prophylactic (controversial) Prevention of subsequent symptoms, bleeding

INDICATIONS FOR PROPHYLACTIC INTERVENTION FOR RENAL AML Size > 4 cm increased risk of growth, sxs/bleeding AML enlarges develop aneurysms with weak, elastin-poor walls rupture Risk of bleeding: 51% if > 4cm versus 15% if < 4 cm 4 cm cut-off challenged 8 cm cut-off Presence of aneurysm within AML > 5 mm Females of childbearing age Oesterling JE et al, J Urol 1986 Nelson CP et al, J Urol 2002 Dickinson M et al, Clin Nephrol 1998 Koh KB et al, Scan J Urol Nephrol 1996 Yamakado K et al, Radiology 2002 AMLs may grow/bleed during pregnancy, with oral contraceptive use (hormone receptors) Boorjian SA et al, Urology 2008

MANAGEMENT OPTIONS FOR RENAL AML Selective transarterial angioembolization Variety of agents (ethanol, coil, microparticle) Surgical resection (esp. if concern for malignancy) Partial nephrectomy (preferred if surgery undertaken) Radical nephrectomy Ablation (RFA/Cryo) Feasibility reported, albeit limited data to date KEY = RENAL FUNCTION PRESERVATION

Re-treatment required in 20-30% Persistent pain, hemorrhage, persistence or increase in lesion size, lesion revascularization Requires continued surveillance after treatment Frequency, imaging modality not well established Cost implications? Ramon J et al, Eur Urol 2009 Villalta JD et al, J Urol 2011 Murray TE et al, J Urol 2015 ANGIOEMBOLIZATION FOR RENAL AML Preferred management for patient presenting with acute bleed Option for management in elective setting Affords renal function preservation Post-embolization syndrome (flank pain, fever)

58 patients treated with partial nephrectomy Median tumor size = 3.9 cm Median postoperative follow-up = 8 years 12% 30-day complication rate Median pre/post op creatinine = 1.0/1.1 mg/dl No new-onset CKD Urology 2007

AML ASSOCIATED WITH TUBEROUS SCLEROSIS

TUBEROUS SCLEROSIS Autosomal dominant Renal AML in up to 80% of patients Can cause CKD/ESRD Pulmonary LAM in ~ 30% TS-AML Diagnosed at younger age (20-35) than sporadic Often multiple, bilateral tumors Consider renal function preservation!

Roach ES et al, J Child Neurol 2004;19:643 El-Hashemite N et al, Lancet 2003;361:1348 MOLECULAR BIOLOGY OF TS AML TS - mutation in tumor suppressor genes TSC1 (hamartin) or TSC2 (tuberin) Hamartin-tuberin complex negatively regulates activity of mtor Mutations in TSC1 or TSC2 genes mtor activation --> cell growth/proliferation Upregulation of mtor found in TS AML Therefore the rationale exists for

Phase III trial of 118 TS patients with 3 cm AML 1 endpoint: 50% reduction in AML volume Response rate = 42% (everolimus) vs 0% (placebo) Maintained regardless of age, gender, race Median time to response = 2.9 months Well tolerated; mostly grade 1-2 AE, no increased rate of discontinuation in everolimus arm FDA-approved for this indication Lancet 2013

FUTURE DIRECTIONS IN RENAL AML TREATMENT?

SAGE (Sporadic AML Growth Kinetics while on Everolimus) Ongoing phase II trial Concept = reset the biological clock and thereby delaying/reducing need for intervention 1 objective = efficacy/tolerability of everolimus in reducing tumor volume of sporadic AML 3 cm 2 objectives = HRQoL, growth kinetics, rate of intervention PI = Rob Uzzo

CONCLUSIONS Consider AML in ddx of solid renal mass Fat on imaging; may be fat-poor (MRI, bx HMB45) Intervention if symptoms, concern for malignancy Size (> 4 cm? > 8 cm? aneurysm presence?) Age/pregnancy status Relatively poor data for prophylactic intervention counsel patients accordingly Options = angioembolization, partial nephrectomy Consider patient age + comorbidities (renal function) Everolimus for TS-associated AMLs

THANK YOU