ALK rearranged renal cell carcinoma (ALK-RCC): a multi-institutional study of twelve cases with identification of novel partner genes CLIP1, KIF5B and KIAA1217.


Journal

Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
ISSN: 1530-0285
Titre abrégé: Mod Pathol
Pays: United States
ID NLM: 8806605

Informations de publication

Date de publication:
12 2020
Historique:
received: 19 02 2020
accepted: 15 05 2020
revised: 15 05 2020
pubmed: 30 5 2020
medline: 13 10 2021
entrez: 30 5 2020
Statut: ppublish

Résumé

ALK rearranged renal cell carcinoma (ALK-RCC) has recently been included in 2016 WHO classification as a provisional entity. In this study, we describe 12 ALK-RCCs from 8 institutions, with detailed clinical, pathological, immunohistochemical (IHC), fluorescence in situ hybridization (FISH), and next generation sequencing (NGS) analyses. Patients' age ranged from 25 to 68 years (mean, 46.3 years). Seven patients were females and five were males (M:F = 1:1.4). Tumor size ranged from 17 to 70 mm (mean 31.5, median 25 mm). The pTNM stage included: pT1a (n = 7), pT1b (n = 1), and pT3a (n = 4). Follow-up was available for 9/12 patients (range: 2 to 153 months; mean 37.6 months); 8 patients were alive without disease and one was alive with distant metastases. The tumors demonstrated heterogeneous, 'difficult to classify' morphology in 10/12 cases, typically showing diverse architectural and cellular morphologies, including papillary, tubular, tubulocystic, solid, sarcomatoid (spindle cell), rhabdoid, signet-ring cell, and intracytoplasmic vacuoles, often set in a mucinous background. Of the remaining two tumors, one showed morphology resembling mucinous tubular and spindle cell renal cell carcinoma (MTSC RCC-like) and one was indistinguishable from metanephric adenoma. One additional case also showed a focal metanephric adenoma-like area, in an otherwise heterogeneous tumor. By IHC, all tumors were diffusely positive for ALK and PAX8. In both cases with metanephric adenoma-like features, WT1 and ALK were coexpressed. ALK rearrangement was identified in 9/11 tumors by FISH. ALK fusion partners were identified by NGS in all 12 cases, including the previously reported: STRN (n = 3), TPM3 (n = 3), EML4 (n = 2), and PLEKHA7 (n = 1), and also three novel fusion partners: CLIP1 (n = 1), KIF5B (n = 1), and KIAA1217 (n = 1). ALK-RCC represents a genetically distinct entity showing a heterogeneous histomorphology, expanded herein to include unreported metanephric adenoma-like and MTSC RCC-like variants. We advocate a routine ALK IHC screening for "unclassifiable RCCs" with heterogeneous features.

Identifiants

pubmed: 32467651
doi: 10.1038/s41379-020-0578-0
pii: S0893-3952(22)00425-2
doi:

Substances chimiques

Biomarkers, Tumor 0
KIAA1217 protein, human 0
KIF5B protein, human 0
Microtubule-Associated Proteins 0
Neoplasm Proteins 0
Proteins 0
cytoplasmic linker protein 170 148349-95-5
ALK protein, human EC 2.7.10.1
Anaplastic Lymphoma Kinase EC 2.7.10.1
Kinesins EC 3.6.4.4

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2564-2579

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Auteurs

Naoto Kuroda (N)

Department of Diagnostic Pathology, Kochi Red Cross Hospital, Kochi, Japan.

Kiril Trpkov (K)

Department of Pathology and Laboratory Medicine, University of Calgary, Calgary, AB, Canada.

Yuan Gao (Y)

Department of Pathology and Laboratory Medicine, University of Calgary, Calgary, AB, Canada.

Maria Tretiakova (M)

Department of Pathology, University of Washington, School of Medicine, Seattle, WA, USA.

Yajuan J Liu (YJ)

Department of Pathology, University of Washington, School of Medicine, Seattle, WA, USA.

Monika Ulamec (M)

Ljudevit Jurak Pathology Department, University Clinical Hospital Center Sestre Milosrdice, Zagreb; Pathology Department, Medical Faculty, Zagreb, Croatia.

Kengo Takeuchi (K)

Division of Pathology and Pathology Project of Molecular Targets, The Cancer Institute, Japanese Foundation for Cancer Research, Tokyo, Japan.

Abbas Agaimy (A)

Institute of Pathology, Friedrich-Alexander University Erlangen-Nuremberg, University Hospital of Erlangen, Erlangen, Germany.

Christopher Przybycin (C)

Robert J. Tomsich Pathology and Laboratory Medicine Institute and Glickman Urological Institute, Cleveland Clinic, Cleveland, OH, USA.

Cristina Magi-Galluzzi (C)

Department of Pathology, School of Medicine, University of Alabama, Birmingham, AL, USA.

Soichiro Fushimi (S)

Department of Pathology, Himeji Red Cross Hospital, Hyogo, Japan.

Fumiyoshi Kojima (F)

Department of Human Pathology, Wakayama Medical University, Wakayama, Japan.

Malthide Sibony (M)

Anatomie et Cytologie Pathologiques, Cochin Hospital, Paris University, Paris, France.

Jen-Fan Hang (JF)

Department of Pathology and Laboratory Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.

Chin-Chen Pan (CC)

Department of Pathology and Laboratory Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.

Asli Yilmaz (A)

Department of Pathology and Laboratory Medicine, University of Calgary, Calgary, AB, Canada.

Farshid Siadat (F)

Department of Pathology and Laboratory Medicine, University of Calgary, Calgary, AB, Canada.

Emiko Sugawara (E)

Department of Pathology, Musashino Red Cross Hospital, Tokyo, Japan.

Pierre-Alexandre Just (PA)

Anatomie et Cytologie Pathologiques, Cochin Hospital, Paris University, Paris, France.

Nikola Ptakova (N)

Second Faculty of Medicine, Charles University, Prague, Czech Republic.
Department of Pathology, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.

Ondrej Hes (O)

Department of Pathology, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic. hes@biopticka.cz.

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Classifications MeSH