What is Pleomorphic Lobular Carcinoma. Nicole Massoll M.D. University of Arkansas for Medical Sciences

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Transcription:

What is Pleomorphic Lobular Carcinoma Nicole Massoll M.D. University of Arkansas for Medical Sciences

Objectives Distinguish Pleomorphic from classic invasive lobular Histologic features Cytologic features Molecular pattern Immunohistochemical pattern Does it make a difference?

History Invasive pleomorphic lobular carcinoma was described by Page in 1987 as a distinct variant of classic invasive lobular carcinoma. Maintaining the loosely cohesive growth pattern, but unique cytologic features Other names used to describe pleomorphic lobular have been: myoid and histiocytoid Presumed apocrine differentiation (GCDFP-15 reactive) Today classic lobular is about 5-15% of invasive breast cancers while the pleomorphic variant is less than 1%

Histologic Features Tumor cells grow in single files or loosely cohesive clusters through the stroma. Linear strands Targetoid appearance around ducts Trabecular Frequent intracytoplasmic lumen Both are E-Cadherin negative by IHC PLC is often grade II-III; while classic lobular is grade I- II. Can be seen with classic LCIS (80%)or PLCIS (35%), mixed (15%)

Linear and strands and single tumor cells Histology

Targetoid pattern of tumor infiltration Histology

Cytologic Features Cytologic features distinguish pleomorphic from classic invasive lobular carcinoma Enlarged nuclei (4x a lymphocyte) Greater nuclear irregularity Hyperchromsia Prominent nucleoli Increased eosinophilic cytoplasm Increased mitotic activity

Abundant eosinophilic cytoplasm Cytoplasmic lumens Cytology

Cytology Hyperchromatic nuclei Enlarged, irregular, hyperchromatic nuclei with prominent nucleoli

Immunohistochemistry Pleomorphic lobular is more likely to be Estrogen and Progesterone Receptor negative more often than classic lobular. Pleomorphic lobular has a Ki-67 rate of greater than 10% Loss of E-Cadherin in greater than 90% of classical and 80% of pleomorphic lobular carcinomas Both are generally Her-2 negative Pleomorphic lobular is often reactive to P53 while classical is not

Invasive Lobular Carcinoma A. H&E; B. Estrogen Receptor reactive; C. Her-2 negative; D. Ki-67 negative

Invasive Pleomorphic Lobular Carcinoma A. H&E; B. Estrogen Receptor negative; C. Her-2 negative; D. Ki-67 reactive

Molecular Both classic and pleomorphic demonstrate loss of E-Cadherin expression through loss of CDH1 gene (loss of 16q) Classic and pleomorphic exhibit gains of 1q in the majority of cases Classic and pleomorphic have los of beta Catenin PLC is similar to high-grade IDC, with chromosomal gains on 8p, 8q,13q and losses on 1p, 8p, 12p, 14q, 18q, 19p, and 19q

Molecular

Patient and Tumor Characteristics (PLC vs. ILC) PLC (n=52) ILC (n=298) P-value Median age, years (range) 59 (36-86) 61 (34-89) 0.300 Median tumor size, mm (range) 20(2-75) 15(1-90) <0.001 Multicentric/multifocal (%) 29 (58.0%) 147 (49.3%) 0.453 Lymphovascular invasion (LVI) 10(19.2%) 3(1.0%) <0.001 Median No. of positive nodes (range) 1(0-19) 0(0-37) 0.027 Number with positive nodes 30 (57.7%) 135 (45.3%) 0.132 ER-positive 50/52 (96.1%) 273/290 (94.1%) 0.749 Mastectomy rate (%) 33(63.5%) 115 (38.6%) 0.001 LVI, lymphovascular invasion; PLC, pleomorphic lobular carcinoma; ILC, invasive lobular carcinoma

What does this Really Mean

Roswell Park Cancer Institute Study PLC was in general larger at time of diagnosis and more likely to develop metastases than ILC and IDC. Rate of recurrence was higher for PLC (11.5%) vs ILC (3.7%) PLC had a recurrence free survival similar to IDC

Roswell Park Cancer Institute Study Conclusions: PLC is a unique distinctive breast cancer Morphology, negative E-cadherin, and lacking basal keratins similar to ILC Aggressive clinical behavior, occasional HER2+ and triple negative, high rate of p53 reactivity resembling IDC

Follow-up, Recurrence and Disease Status Data (PLC vs. ILC) PLC (n=52) ILC (n=298) P-value Mean follow-up, years (range) 3.8 (0-9.3) 4.4 (0.1-9.3) 0.076 Distant recurrence (%) 6(11.5%) 11(3.7%) 0.027 Any recurrence (%) 6 (11.5%) 15 (5.0%) 0.120 Time to 1 st recurrence, years (range) 2.2 (0.2-4.2) 2.7 (1.5-4.0) 0.519 NED (%) 44 (84.6%) 273 (91.6%) 0.110 PLC, pleomorphic lobular carcinoma; ILC, invasive lobular carcinoma C. Buchanan, L. Flynn, M. Murray et al. Is Pleomorphic Lobular Carcinoma Really a Distinct Entity? J Sur Onc. 2008; 314-317.

Patient and tumor characteristics (PLC vs. ILC) PLC (n=7) ILC (n=58) P Age (y) 35-69 30-88.20 Grade I 0/7 11/58.59 II 5/7 47/58.62 III 2/7 0/58.01 LVI present 2/7 7/58.25 Lymph node Unknown 0/7 4/58 >.99 N0 4/7 37/58.70 N1a 1/7 12/58 >.99 N2a 0/7 2/58 >.99 N3a 2/7 3/58.09 LVI indicates lymphovascular invasion C. Buchanan, L. Flynn, M. Murray et al. Is Pleomorphic Lobular Carcinoma Really a Distinct Entity? J Sur Onc. 2008; 314-317.

Patient and tumor characteristics (PLC vs. ILC) continued PLC (n=7) ILC (n=58) P ER > 1% 4/7 All positive.001 Her-2 All negative All negative >.99 Ki-67 > 10% 5/7 7/58.002 Follow-up (median, 29mo) None 1/7 2/58.30 NED 5/7 51/58.25 Metastases 1/7 4/58.45 Deceased 0/7 1/58 >.99 NED, no evidence of disease C. Buchanan, L. Flynn, M. Murray et al. Is Pleomorphic Lobular Carcinoma Really a Distinct Entity? J Sur Onc. 2008; 314-317

Summary PLC is a unique variant of ILC It lacks E-cadherin generally, similary to ILC Histologically it is similar to ILC It has more aggressive features similar to high grade IDC It has mixed molecular finding between ILB and IDC

Summary Distinguishing Pleomorphic Lobular carcinoma as a distinct variant of Classic Lobular carcinoma DOES MAKE A DIFFERENCE!

References M. Jacobs, F. Fan, O. Tawfik et al. Clinicopathologic and biomarker analysis of invasive pleomorphic lobular carcinoma as compared with invasive classic lobular carcinoma: an experience in our institution and review of the literature. J Ann Diag Path. 2011; 185-189. C. Buchanan, L. Flynn, M. Murray et al. Is Pleomorphic Lobular Carcinoma Really a Distinct Entity? J Sur Onc. 2008; 314-317. L. Monhollen, C. Morrison, F. Ademuyiwa et al. Pleomorphic lobular carcinoma: a distinctive clinical and molecular breast cancer type. Hist. 2012; 61, 365-377. B. Yoder, E. Wilkinson, N. Massoll. Molecular and morphologic distinctions between infiltrating ductal and lobular carcinoma of the breast. Breast J. 2007 Mar-Apr;13(2):172-9.