Stage IV lung carcinoids: spectrum and evolution of proliferation rate, focusing on variants with elevated proliferation indices

The spectrum and evolution of proliferation rates in stage IV lung carcinoids is poorly defined. In particular, there are limited data on the prevalence and characteristics of tumors exceeding the standard upper proliferative criteria—as defined largely based on early-stage carcinoids—in metastatic...

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Veröffentlicht in:Modern pathology 2019-08, Vol.32 (8), p.1106-1122
Hauptverfasser: Rekhtman, Natasha, Desmeules, Patrice, Litvak, Anna M., Pietanza, Maria C., Santos-Zabala, Maria Lauren, Ni, Ai, Montecalvo, Joseph, Chang, Jason C., Beras, Amanda, Preeshagul, Isabel R., Sabari, Joshua K., Rudin, Charles M., Ladanyi, Marc, Klimstra, David S., Travis, William D., Lai, Wei-Chu
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Sprache:eng
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Zusammenfassung:The spectrum and evolution of proliferation rates in stage IV lung carcinoids is poorly defined. In particular, there are limited data on the prevalence and characteristics of tumors exceeding the standard upper proliferative criteria—as defined largely based on early-stage carcinoids—in metastatic setting. Sixty-six patients with stage IV lung carcinoids were identified, and all evaluable samples ( n  = 132; mean 2 samples per patient) were analyzed for mitotic counts and Ki-67 rate. Clinicopathologic and genomic features associated with elevated proliferation rates (>10 mitoses per 2 mm 2 and/or >20% hot-spot Ki-67), and evolution of proliferation rates in serial specimens were analyzed. We found that mitoses and/or Ki-67 exceeded the standard criteria in 35 of 132 (27%) samples, primarily (31/35 cases) at  metastatic sites. Although neuroendocrine neoplasms with >10 mitoses per 2 mm 2 are currently regarded as de facto neuroendocrine carcinomas, the notion that these cases are part of the spectrum of carcinoids was supported by (1) well-differentiated morphology, (2) conventional proliferation rates in other samples from same patient, (3) genetic characteristics, including the lack of RB1 / TP53 alterations in all tested samples ( n  = 19), and (4) median overall survival of 2.7 years, compared to
ISSN:0893-3952
1530-0285
1530-0285
DOI:10.1038/s41379-019-0248-2