What s New in Pathology of Genitourinary Tumors. Jiaoti Huang, MD, PhD Department of Pathology Duke University School of Medicine

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Transcription:

What s New in Pathology of Genitourinary Tumors Jiaoti Huang, MD, PhD Department of Pathology Duke University School of Medicine

Kidney Tumors Multilocular cystic renal neoplasm of low malignant potential Old name: Multilocular cystic renal cell carcinoma No death or metastasis

Multilocular cystic renal neoplasm of low malignant potential

Multilocular cystic renal neoplasm of low malignant potential

Hereditary leiomyomatosis and RCC-associated RCC Rare tumor Characteristic morphology Germline mutation in FH (encoding fumarate hydratase) at 1q42.3-q43 Poor prognosis with early metastasis

MiT family translocation carcinoma Harbor gene fusion involving TFE3 (Xp11 translocation) or TFEB (6:11 translocation) Originally discovered in young patients. Present in adults as well IHC or break-apart FISH

MiT family translocation carcinoma

Xp11 translocation RCC is similar to clear cell RCC in survival (worse than papillary RCC) Distant metastasis and older age predicts death ASPSCR1-TFE3 RCCs more likely to have regional nodal mets than PRCC-TFE3 RCCs Most nodal+ ASPSCR1-TFE3 RCC patients remain disease-free without adjuvant therapy T(6:11) RCCs are more indolent that Xp11 RCCs

Succinate dehydrogenase-deficient RCC Very rare. Between 14 and 76 years old (mean age=38; median age=35). M:F=1.8:1. Majority low grade. Hereditary, with mutation in a SDH gene (SDHB>SDHC>SDHA or SDHD) Personal or family history of SDH-deficient RCC, paraganglioma, GIST or pituitary adenoma may be present (autosomal dominant tumor syndrome) All patients should be offered genetic testing Confirmed by loss of SDHB expression on IHC

Succinate dehydrogenase-deficient RCC

Tubulocystic RCC Uncommon cystic renal epithelial malignancy Most incidentally discovered, 70% in left kidney Most present as a solitary, well-circumscribed multicystic mass. Gain of chromosome 7 and 17, and loss of the Y chromosome (close relationship with papillary RCC) Majority behave indolently.

Acquired cystic disease-associated RCC In the background of end stage renal disease and acquired cystic disease (long term hemodialysis). Variable architecture, microcysts and intratumoral oxalate crystals. Often multifocal and bilateral. Most are indolent.

Clear cell papillary RCC Typically detected incidentally. Morphologic overlap with clear cell RCC and papillary RCC. Molecular profile is distinct. Typically indolent.

Clear cell papillary RCC

Prostate Cancer: Prognostic grouping Divide prostate cancer into 5 different prognostic groups (Groups 1-5) Not a new grading system Re-grouping of Gleason grading system Group I (3+3), II (3+4), III (4+3), IV (4+4), and V (Combined score of 9 or 10) The premise is that indolent tumor would be group 1 instead of having 6 points

Measuring cancer length and percentage on biopsy cores

Measuring cancer length and percentage on biopsy cores

Metastatic Prostate Cancer Cancer kills patients by metastasis Bone, lymph nodes, visceral organs and soft tissue Little is known about metastatic tumors

SU2C/AACR/PCF West Coast Dream Teams UCLA, UCSF, UC Davis, UC Santa Cruz, OHSU, University of British Columbia Team consists of basic researchers, translational scientists, interventional radiologists, urologists, medical oncologists and pathologists.

Patient population Plan is to biopsy metastatic tumors from 300 men who have failed medical therapy. Tumor tissue is subjected to histologic examination, RNAseq (after LCM) and Iron Torrent study with a predetermined panel (whole exome sequencing planned).

West Coast Dream Team Biopsy Trial

Sites of Biopsy As Of May 16, 2016 (n=250)

Metastatic CRPC (Adenocarcinoma)

Metastatic CRPC (Adenocarcinoma)

Small cell carcinoma

Small cell carcinoma

Tumor type Adenocarcinoma IAC SCNC Cytoplasm Abundant Moderate to abundant Scant Nuclear chromatin Clumpy, vacuolated, open chromatin pattern Fine homogeneous chromatin pattern Fine homogeneous chromatin pattern Nuclear staining Light Dark Dark Nuclear shape Some degree of irregularity Round and regular Irregular Nuclear molding No No Yes Nucleoli Prominent macronucleoli Absent or central small nucleolus No nucleoli Crush artifact No No Yes Mitotic figures Rare Rare Common Glandular formation Obvious Vague No

A novel histologic variant of metastatic prostate cancer Adenocarcinoma IAC Small cell carcinoma

IAC carries a poor prognosis despite bland cytology

Overal Survival of Adeno vs Non-Adeno (SCNC+IAC)

IAC vs. Adeno 50-gene Signature (AUC = 0.802)

Master Regulator Signature Accuracies Signature 5-MR 360-MR 50-gene Dense Small Cell vs Not 0.801 0.847.755.894 Small Cell vs IAC 0.682 0.788.682.879 Small Cell vs Adeno 0.780 0.811.879.902 IAC vs Adeno 0.405 0.541.802.620 Adeno vs Not 0.509 0.705.764.575 As few as 5 regulators often accurate enough

Grant Support Department of Defense Prostate Cancer Research Program National Cancer Institute RO1 UCLA SPORE in Prostate Cancer Prostate Cancer Foundation SU2C-AACR-PCF West Coast Dream Team Award Acknowledgements Eric Small, UCSF Owen Witte, UCLA Rob Reiter, UCLA Matthew Rettig, UCLA George Thomas, OHSU Larry True, UW Josh Stuard Stand Up to Cancer Dream Team