Skip to main content
Erschienen in: Annals of Surgical Oncology 1/2007

01.01.2007

Characteristics and Treatment of Metaplastic Breast Cancer: Analysis of 892 Cases from the National Cancer Data Base

verfasst von: Christopher M. Pezzi, MD, Lina Patel-Parekh, MHA, CHE, Karin Cole, MD, Jan Franko, MD, PhD, V. Suzanne Klimberg, MD, Kirby Bland, MD

Erschienen in: Annals of Surgical Oncology | Ausgabe 1/2007

Einloggen, um Zugang zu erhalten

Abstract

Background

Metaplastic breast cancer (MBC) is characterized by various combinations of adenocarcinoma, mesenchymal, and other epithelial components. It was officially recognized as a distinct pathologic diagnosis in 2000. With few published reports, we hypothesized that MBC may have markedly different characteristics at presentation than typical infiltrating ductal carcinoma (IDC) and may be managed differently.

Methods

Data from patients with MBC and IDC reported to the National Cancer Database from January 2001 through December 2003 were reviewed for year of diagnosis, patient age, race/ethnicity, tumor size, nodal status, American Joint Committee on Cancer (AJCC) stage, tumor grade, hormone receptor status, and initial treatment, and were analyzed statistically by the Pearson χ2 test.

Results

A total of 892 patients with MBC and 255,164 patients with IDC were identified. The group with MBC was older (mean age, 61.1 vs. 59.7 years; P = .001), had a significantly increased proportion of African American (14.1%, 126 of 892, vs. 10.2%, 25,900 of 255,164; odds ratio [OR], 1.455, P = .001) and Hispanic patients (5.5%, 49 of 892 vs. 3.9%, 9,947 of 255,164; OR, 1.817, P = .001), had fewer T1 tumors (29.5% vs. 65.2%), more N0 tumors (78.1% vs. 65.7%, OR, .5, P = .001), more poorly or undifferentiated tumors (67.8% vs. 38.8%), and fewer estrogen receptor–positive tumors (11.3% vs. 74.1%, OR, 22.4, P = .001) than the IDC group. Patients with MBC were treated with breast-conserving surgery less frequently than patients with IDC (38.5% vs. 55.8%, OR, 2.0, P = .001) because of the larger tumor size. Chemotherapy was used more often for patients with MBC (53.4% vs. 42.1%, OR, 1.6, P = .001) because of more advanced AJCC stage.

Conclusions

MBC is a rare tumor with different characteristics than IDC: it presents with larger tumor size, less nodal involvement, higher tumor grade, and hormone receptor negativity. Patients with MBC are treated more aggressively than IDC (more often with mastectomy and chemotherapy) because of a higher stage at presentation, but are being treated by the same principles as IDC. Follow-up will determine the long-term results of the current treatment.
Anhänge
Nur mit Berechtigung zugänglich
Literatur
1.
Zurück zum Zitat Fritz A, Percy C, Jack A, Solin LH, eds. (2000) International Classification of Diseases of Oncology. 3rd ed. Geneva: World Health Organization. Fritz A, Percy C, Jack A, Solin LH, eds. (2000) International Classification of Diseases of Oncology. 3rd ed. Geneva: World Health Organization.
2.
Zurück zum Zitat Pitts WC, Rojas VA, Gaffey MJ, et al. Carcinomas with metaplasia and sarcomas of the breast. Am J Clin Pathol 1991; 95:623–32PubMed Pitts WC, Rojas VA, Gaffey MJ, et al. Carcinomas with metaplasia and sarcomas of the breast. Am J Clin Pathol 1991; 95:623–32PubMed
3.
Zurück zum Zitat Kurian KM, Al-Nafussi Al. Sarcomatoid/metaplastic carcinoma of the breast: a clinicopathological study of 12 cases. Histopathology 2002; 40:58–64PubMedCrossRef Kurian KM, Al-Nafussi Al. Sarcomatoid/metaplastic carcinoma of the breast: a clinicopathological study of 12 cases. Histopathology 2002; 40:58–64PubMedCrossRef
4.
Zurück zum Zitat Johnson TL, Kini SR. Metaplastic breast carcinoma: a cytohistologic and clinical study of 10 cases. Diagn Cytopathol 1996; 14:226–32PubMedCrossRef Johnson TL, Kini SR. Metaplastic breast carcinoma: a cytohistologic and clinical study of 10 cases. Diagn Cytopathol 1996; 14:226–32PubMedCrossRef
5.
Zurück zum Zitat Gobbi H, Simpson JF, Borowsky A, Jensen RA, Page DL. Metaplastic breast tumors with a dominant fibromatosis-like phenotype have a high risk of local recurrence. Cancer 1999; 85:2170–82PubMedCrossRef Gobbi H, Simpson JF, Borowsky A, Jensen RA, Page DL. Metaplastic breast tumors with a dominant fibromatosis-like phenotype have a high risk of local recurrence. Cancer 1999; 85:2170–82PubMedCrossRef
6.
Zurück zum Zitat Chao TC, Wang CS, Chen SC, Chen MF. Metaplastic carcinomas of the breast. J Surg Oncol 1999 ; 71:220–5PubMedCrossRef Chao TC, Wang CS, Chen SC, Chen MF. Metaplastic carcinomas of the breast. J Surg Oncol 1999 ; 71:220–5PubMedCrossRef
7.
Zurück zum Zitat Bellino R, Arisio R, D’Addato F, et al. Metaplastic breast carcinoma: pathology and clinical outcome. Anticancer Res 2003; 23:669–73PubMed Bellino R, Arisio R, D’Addato F, et al. Metaplastic breast carcinoma: pathology and clinical outcome. Anticancer Res 2003; 23:669–73PubMed
8.
Zurück zum Zitat Wargotz ES, Norris HJ. Metaplastic carcinomas of the breast. I. Matrix-producing carcinoma. Hum Pathol 1989; 20:628–35PubMedCrossRef Wargotz ES, Norris HJ. Metaplastic carcinomas of the breast. I. Matrix-producing carcinoma. Hum Pathol 1989; 20:628–35PubMedCrossRef
9.
Zurück zum Zitat Wargotz ES, Deos PH, Norris HJ. Metaplastic carcinomas of the breast. II. Spindle cell carcinoma. Hum Pathol 1989; 20:732–40PubMedCrossRef Wargotz ES, Deos PH, Norris HJ. Metaplastic carcinomas of the breast. II. Spindle cell carcinoma. Hum Pathol 1989; 20:732–40PubMedCrossRef
10.
Zurück zum Zitat Wargotz ES, Norris HJ. Metaplastic carcinomas of the breast. III. Carcinosarcoma. Cancer 1989; 64:1490–9PubMedCrossRef Wargotz ES, Norris HJ. Metaplastic carcinomas of the breast. III. Carcinosarcoma. Cancer 1989; 64:1490–9PubMedCrossRef
11.
Zurück zum Zitat Wargotz ES, Norris HJ. Metaplastic carcinomas of the breast. IV. Squamous cell carcinoma of ductal origin. Cancer 1990; 65:272–6PubMedCrossRef Wargotz ES, Norris HJ. Metaplastic carcinomas of the breast. IV. Squamous cell carcinoma of ductal origin. Cancer 1990; 65:272–6PubMedCrossRef
12.
Zurück zum Zitat Wargotz ES, Norris HJ. Metaplastic carcinomas of the breast: V. Metaplastic carcinoma with osteoclastic giant cells. Hum Pathol 1990; 21:1142–50PubMedCrossRef Wargotz ES, Norris HJ. Metaplastic carcinomas of the breast: V. Metaplastic carcinoma with osteoclastic giant cells. Hum Pathol 1990; 21:1142–50PubMedCrossRef
13.
Zurück zum Zitat Park JM, Han BK, Moon WK, et al. Metaplastic carcinoma of the breast: mammographic and sonographic findings. J Clin Ultrasound 2000; 28:179–86PubMedCrossRef Park JM, Han BK, Moon WK, et al. Metaplastic carcinoma of the breast: mammographic and sonographic findings. J Clin Ultrasound 2000; 28:179–86PubMedCrossRef
14.
Zurück zum Zitat Gunhan-Bilgen I, Memis A, Ustun EE, Zekioglu O, Ozdemir N. Metaplastic carcinoma of the breast: clinical, mammographic, and sonographic findings with histopathologic correlation. Am J Roentgenol 2002; 178:1421–5 Gunhan-Bilgen I, Memis A, Ustun EE, Zekioglu O, Ozdemir N. Metaplastic carcinoma of the breast: clinical, mammographic, and sonographic findings with histopathologic correlation. Am J Roentgenol 2002; 178:1421–5
15.
Zurück zum Zitat Rayson D, Adjei AA, Suman VJ, Wold LE, Ingle JN. Metaplastic breast cancer: prognosis and response to systemic therapy. Ann Oncol 1999; 10:413–9PubMedCrossRef Rayson D, Adjei AA, Suman VJ, Wold LE, Ingle JN. Metaplastic breast cancer: prognosis and response to systemic therapy. Ann Oncol 1999; 10:413–9PubMedCrossRef
16.
Zurück zum Zitat Oberman HA. Metaplastic carcinoma of the breast: a clinicopathologic study of 29 patients. Am J Surg Pathol 1987; 11:918–29PubMedCrossRef Oberman HA. Metaplastic carcinoma of the breast: a clinicopathologic study of 29 patients. Am J Surg Pathol 1987; 11:918–29PubMedCrossRef
17.
Zurück zum Zitat Saxena S, Bansal A, Mohil RS, Bhatnagar D. Metaplastic carcinoma of the breast—a rare breast tumour. Indian J Pathol Microbiol 2004; 47:217–20PubMed Saxena S, Bansal A, Mohil RS, Bhatnagar D. Metaplastic carcinoma of the breast—a rare breast tumour. Indian J Pathol Microbiol 2004; 47:217–20PubMed
18.
Zurück zum Zitat Huvos AG, Lucas JC Jr, Foote FW Jr. Metaplastic breast carcinoma: rare form of mammary cancer. NY State J Med 1973; 73:1078–82 Huvos AG, Lucas JC Jr, Foote FW Jr. Metaplastic breast carcinoma: rare form of mammary cancer. NY State J Med 1973; 73:1078–82
19.
Zurück zum Zitat Grechi G, Pagnini P. Study of mammary gland neoplasms with an osteocartilaginous component. I. Cartilaginous metaplastic epiphenomena in the course of connective tissue malignancy. Arch De Vecchi Anat Patol 1965; 46:277–303PubMed Grechi G, Pagnini P. Study of mammary gland neoplasms with an osteocartilaginous component. I. Cartilaginous metaplastic epiphenomena in the course of connective tissue malignancy. Arch De Vecchi Anat Patol 1965; 46:277–303PubMed
Metadaten
Titel
Characteristics and Treatment of Metaplastic Breast Cancer: Analysis of 892 Cases from the National Cancer Data Base
verfasst von
Christopher M. Pezzi, MD
Lina Patel-Parekh, MHA, CHE
Karin Cole, MD
Jan Franko, MD, PhD
V. Suzanne Klimberg, MD
Kirby Bland, MD
Publikationsdatum
01.01.2007
Verlag
Springer-Verlag
Erschienen in
Annals of Surgical Oncology / Ausgabe 1/2007
Print ISSN: 1068-9265
Elektronische ISSN: 1534-4681
DOI
https://doi.org/10.1245/s10434-006-9124-7

Weitere Artikel der Ausgabe 1/2007

Annals of Surgical Oncology 1/2007 Zur Ausgabe

Update Chirurgie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.

S3-Leitlinie „Diagnostik und Therapie des Karpaltunnelsyndroms“

Karpaltunnelsyndrom BDC Leitlinien Webinare
CME: 2 Punkte

Prof. Dr. med. Gregor Antoniadis Das Karpaltunnelsyndrom ist die häufigste Kompressionsneuropathie peripherer Nerven. Obwohl die Anamnese mit dem nächtlichen Einschlafen der Hand (Brachialgia parästhetica nocturna) sehr typisch ist, ist eine klinisch-neurologische Untersuchung und Elektroneurografie in manchen Fällen auch eine Neurosonografie erforderlich. Im Anfangsstadium sind konservative Maßnahmen (Handgelenksschiene, Ergotherapie) empfehlenswert. Bei nicht Ansprechen der konservativen Therapie oder Auftreten von neurologischen Ausfällen ist eine Dekompression des N. medianus am Karpaltunnel indiziert.

Prof. Dr. med. Gregor Antoniadis
Berufsverband der Deutschen Chirurgie e.V.

S2e-Leitlinie „Distale Radiusfraktur“

Radiusfraktur BDC Leitlinien Webinare
CME: 2 Punkte

Dr. med. Benjamin Meyknecht, PD Dr. med. Oliver Pieske Das Webinar S2e-Leitlinie „Distale Radiusfraktur“ beschäftigt sich mit Fragen und Antworten zu Diagnostik und Klassifikation sowie Möglichkeiten des Ausschlusses von Zusatzverletzungen. Die Referenten erläutern, welche Frakturen konservativ behandelt werden können und wie. Das Webinar beantwortet die Frage nach aktuellen operativen Therapiekonzepten: Welcher Zugang, welches Osteosynthesematerial? Auf was muss bei der Nachbehandlung der distalen Radiusfraktur geachtet werden?

PD Dr. med. Oliver Pieske
Dr. med. Benjamin Meyknecht
Berufsverband der Deutschen Chirurgie e.V.

S1-Leitlinie „Empfehlungen zur Therapie der akuten Appendizitis bei Erwachsenen“

Appendizitis BDC Leitlinien Webinare
CME: 2 Punkte

Dr. med. Mihailo Andric
Inhalte des Webinars zur S1-Leitlinie „Empfehlungen zur Therapie der akuten Appendizitis bei Erwachsenen“ sind die Darstellung des Projektes und des Erstellungswegs zur S1-Leitlinie, die Erläuterung der klinischen Relevanz der Klassifikation EAES 2015, die wissenschaftliche Begründung der wichtigsten Empfehlungen und die Darstellung stadiengerechter Therapieoptionen.

Dr. med. Mihailo Andric
Berufsverband der Deutschen Chirurgie e.V.