Skip to main content
Erschienen in: International Journal of Clinical Oncology 6/2010

01.12.2010 | Original Article

Value of PET-FDG in primary breast cancer based on histopathological and immunohistochemical prognostic factors

verfasst von: Pierre Heudel, Sebastien Cimarelli, Anthony Montella, Catherine Bouteille, Thomas Mognetti

Erschienen in: International Journal of Clinical Oncology | Ausgabe 6/2010

Einloggen, um Zugang zu erhalten

Abstract

Background

The aim of the study was to analyze in breast tumors the correlation between [18F]fluorodeoxyglucose (FDG) uptake assessed by positron emission tomography (PET) and histopathological and immunohistochemical prognostic factors.

Methods

FDG-PET combined with computed tomography (CT) was performed before surgery in 45 women with biopsy-proven primary breast cancer. The standardized uptake value (SUV) was compared with histopathological findings after surgery.

Results

A positive relationship was found between SUV and histological grade (p < 0.0001), histological type (p = 0.001), tumor size (p < 0.0435), estrogen receptor status (p < 0.0005), and progesterone receptor status (p = 0.002). FDG-PET/CT revealed unknown distant metastatic lesions in 2 of 12 patients with triple-negative breast cancer. The sensitivity of FDG-PET/CT for detecting axillary lymph node metastases was, respectively, 21% and 100% for pN1 and pN2 cases, whereas specificity was 100% for pN0.

Conclusion

SUV, a preoperative and noninvasive metabolic parameter, correlates with other known prognostic factors in breast cancer. This study provides valuable insight into the usefulness of FDG-PET/CT for preoperative staging of patients with triple-negative and poorly differentiated breast tumors but not for evaluating axillary lymph nodes and lobular carcinomas.
Literatur
2.
Zurück zum Zitat Early Breast Cancer Trialists’ Collaborative Group (2005) Effects of chemotherapy and hormonal therapy for early breast cancer on recurrence and 15-year survival: an overview of the randomised trials. Lancet 365:1687–1717CrossRef Early Breast Cancer Trialists’ Collaborative Group (2005) Effects of chemotherapy and hormonal therapy for early breast cancer on recurrence and 15-year survival: an overview of the randomised trials. Lancet 365:1687–1717CrossRef
3.
Zurück zum Zitat Wahl RL, Siegel BA, Coleman RE et al (2004) Prospective multicenter study of axillary nodal staging by positron emission tomography in breast cancer: a report of the staging breast cancer with PET Study Group. J Clin Oncol 22:277–285PubMedCrossRef Wahl RL, Siegel BA, Coleman RE et al (2004) Prospective multicenter study of axillary nodal staging by positron emission tomography in breast cancer: a report of the staging breast cancer with PET Study Group. J Clin Oncol 22:277–285PubMedCrossRef
4.
Zurück zum Zitat Veronesi U, De Cicco C, Galimberti VE et al (2007) A comparative study on the value of FDG-PET and sentinel node biopsy to identify occult axillary metastases. Ann Oncol 18:473–478PubMedCrossRef Veronesi U, De Cicco C, Galimberti VE et al (2007) A comparative study on the value of FDG-PET and sentinel node biopsy to identify occult axillary metastases. Ann Oncol 18:473–478PubMedCrossRef
5.
Zurück zum Zitat Heusner TA, Kuemmel S, Hahn S et al (2009) Diagnostic value of full-dose FDG-PET/CT for axillary lymph node staging in breast cancer patients. Eur J Nucl Med Mol Imaging 36:1543–1550PubMedCrossRef Heusner TA, Kuemmel S, Hahn S et al (2009) Diagnostic value of full-dose FDG-PET/CT for axillary lymph node staging in breast cancer patients. Eur J Nucl Med Mol Imaging 36:1543–1550PubMedCrossRef
6.
Zurück zum Zitat Avril N, Rose CA, Schelling M et al (2000) Breast imaging with positron emission tomography and fluorine-18 fluorodeoxyglucose: use and limitations. J Clin Oncol 18:3495–3502PubMed Avril N, Rose CA, Schelling M et al (2000) Breast imaging with positron emission tomography and fluorine-18 fluorodeoxyglucose: use and limitations. J Clin Oncol 18:3495–3502PubMed
7.
Zurück zum Zitat Dose Schwarz J, Bader M, Jenicke L et al (2005) Early prediction of response to chemotherapy in metastatic breast cancer using sequential 18F-FDG PET. J Nucl Med 467:1144–1150 Dose Schwarz J, Bader M, Jenicke L et al (2005) Early prediction of response to chemotherapy in metastatic breast cancer using sequential 18F-FDG PET. J Nucl Med 467:1144–1150
8.
Zurück zum Zitat Avril N, Schelling M, Dose J et al (1999) Utility of PET in breast cancer. Clin Positron Imaging 2:261–271PubMedCrossRef Avril N, Schelling M, Dose J et al (1999) Utility of PET in breast cancer. Clin Positron Imaging 2:261–271PubMedCrossRef
9.
Zurück zum Zitat Baum RP, Przetak C (2001) Evaluation of therapy response in breast and ovarian cancer patients by positron emission tomography (PET). Q J Nucl Med 45:257–268PubMed Baum RP, Przetak C (2001) Evaluation of therapy response in breast and ovarian cancer patients by positron emission tomography (PET). Q J Nucl Med 45:257–268PubMed
10.
Zurück zum Zitat Wilcoxon F (1945) Individual comparisons by ranking methods. Biometrics Bull 1:80–83CrossRef Wilcoxon F (1945) Individual comparisons by ranking methods. Biometrics Bull 1:80–83CrossRef
11.
Zurück zum Zitat Kruskal WH, Wallis WA (1952) Use of ranks in one-criterion variance analysis. J Am Stat Assoc 47:583–621CrossRef Kruskal WH, Wallis WA (1952) Use of ranks in one-criterion variance analysis. J Am Stat Assoc 47:583–621CrossRef
12.
Zurück zum Zitat Singletary SE, Allred C, Ashley P et al (2002) Revision of the American joint Committee on cancer staging system for breast cancer. J Clin Oncol 20:3628–3636PubMedCrossRef Singletary SE, Allred C, Ashley P et al (2002) Revision of the American joint Committee on cancer staging system for breast cancer. J Clin Oncol 20:3628–3636PubMedCrossRef
13.
Zurück zum Zitat Oshida M, Uno K, Suzuki M et al (1998) Predicting the prognoses of breast carcinoma patients with positron emission tomography using 2-deoxy-2-fluoro[18F]-d-glucose. Cancer 82:2227–2234PubMedCrossRef Oshida M, Uno K, Suzuki M et al (1998) Predicting the prognoses of breast carcinoma patients with positron emission tomography using 2-deoxy-2-fluoro[18F]-d-glucose. Cancer 82:2227–2234PubMedCrossRef
14.
Zurück zum Zitat Avril N, Menzel M, Dose J et al (2001) Glucose metabolism of breast cancer assessed by 18F-FDG PET: histologic and immunohistochemical tissue analysis. J Nucl Med 42:9–16PubMed Avril N, Menzel M, Dose J et al (2001) Glucose metabolism of breast cancer assessed by 18F-FDG PET: histologic and immunohistochemical tissue analysis. J Nucl Med 42:9–16PubMed
15.
Zurück zum Zitat Bos R, van Der Hoeven JJ, van Der Wall E et al (2002) Biologic correlates of (18)fluorodeoxyglucose uptake in human breast cancer measured by positron emission tomography. J Clin Oncol 20:379–387PubMedCrossRef Bos R, van Der Hoeven JJ, van Der Wall E et al (2002) Biologic correlates of (18)fluorodeoxyglucose uptake in human breast cancer measured by positron emission tomography. J Clin Oncol 20:379–387PubMedCrossRef
16.
Zurück zum Zitat Buck A, Schirrmeister H, Kuhn T et al (2002) FDG uptake in breast cancer: correlation with biological and clinical prognostic parameters. Eur J Nucl Med Mol Imaging 29:1317–1323PubMedCrossRef Buck A, Schirrmeister H, Kuhn T et al (2002) FDG uptake in breast cancer: correlation with biological and clinical prognostic parameters. Eur J Nucl Med Mol Imaging 29:1317–1323PubMedCrossRef
17.
Zurück zum Zitat Cermik TF, Mavi A, Basu S et al (2008) Impact of FDG PET on the preoperative staging of newly diagnosed breast cancer. Eur J Nucl Med Mol Imaging 35:475–483PubMedCrossRef Cermik TF, Mavi A, Basu S et al (2008) Impact of FDG PET on the preoperative staging of newly diagnosed breast cancer. Eur J Nucl Med Mol Imaging 35:475–483PubMedCrossRef
18.
Zurück zum Zitat Avril N, Bense S, Ziegler SI et al (1997) Breast imaging with fluorine-18-FDG PET: quantitative image analysis. J Nucl Med 38:1186–1191PubMed Avril N, Bense S, Ziegler SI et al (1997) Breast imaging with fluorine-18-FDG PET: quantitative image analysis. J Nucl Med 38:1186–1191PubMed
19.
Zurück zum Zitat Crowe JP, Adler LP, Shenk RR et al (1994) Positron emission tomography and breast masses: comparison with clinical, mammographic, and pathological findings. Ann Surg Oncol 1:132–140PubMedCrossRef Crowe JP, Adler LP, Shenk RR et al (1994) Positron emission tomography and breast masses: comparison with clinical, mammographic, and pathological findings. Ann Surg Oncol 1:132–140PubMedCrossRef
20.
Zurück zum Zitat Inoue T, Yutani K, Taguchi T et al (2004) Preoperative evaluation of prognosis in breast cancer patients by [(18)F]2-deoxy-2-fluoro-d-glucose-positron emission tomography. J Cancer Res Clin Oncol 130:273–278PubMedCrossRef Inoue T, Yutani K, Taguchi T et al (2004) Preoperative evaluation of prognosis in breast cancer patients by [(18)F]2-deoxy-2-fluoro-d-glucose-positron emission tomography. J Cancer Res Clin Oncol 130:273–278PubMedCrossRef
21.
Zurück zum Zitat Gil-Rendo A, Martinez-Regueira F, Zornoza G et al (2009) Association between [18F]fluorodeoxyglucose uptake and prognostic parameters in breast cancer. Br J Surg 96:166–170PubMedCrossRef Gil-Rendo A, Martinez-Regueira F, Zornoza G et al (2009) Association between [18F]fluorodeoxyglucose uptake and prognostic parameters in breast cancer. Br J Surg 96:166–170PubMedCrossRef
22.
Zurück zum Zitat Basu S, Chen W, Tchou J et al (2008) Comparison of triple-negative and estrogen receptor-positive/progesterone receptor-positive/HER2-negative breast carcinoma using quantitative fluorine-18 fluorodeoxyglucose/positron emission tomography imaging parameters: a potentially useful method for disease characterization. Cancer 112:995–1000PubMedCrossRef Basu S, Chen W, Tchou J et al (2008) Comparison of triple-negative and estrogen receptor-positive/progesterone receptor-positive/HER2-negative breast carcinoma using quantitative fluorine-18 fluorodeoxyglucose/positron emission tomography imaging parameters: a potentially useful method for disease characterization. Cancer 112:995–1000PubMedCrossRef
23.
Zurück zum Zitat Carey LA, Perou CM, Livasy CA et al (2006) Race, breast cancer subtypes, and survival in the Carolina Breast cancer Study. J Am Med Assoc 295:2492–2502CrossRef Carey LA, Perou CM, Livasy CA et al (2006) Race, breast cancer subtypes, and survival in the Carolina Breast cancer Study. J Am Med Assoc 295:2492–2502CrossRef
24.
Zurück zum Zitat Bauer KR, Brown M, Cress RD et al (2007) Descriptive analysis of oestrogen receptor-negative, progesterone receptor-negative and HER 2-negative invasive breast cancer, the so called triple negative phenotype: a population-based study from the California cancer Registry. Cancer 109:1721–1728PubMedCrossRef Bauer KR, Brown M, Cress RD et al (2007) Descriptive analysis of oestrogen receptor-negative, progesterone receptor-negative and HER 2-negative invasive breast cancer, the so called triple negative phenotype: a population-based study from the California cancer Registry. Cancer 109:1721–1728PubMedCrossRef
25.
Zurück zum Zitat Kim J, Lee J, Chang E et al (2009) Selective sentinel node plus additional non-sentinel node biopsy based on an FDG PET/CT scan in early breast cancer patients: single institutional experience. World J Surg 33:943–949PubMedCrossRef Kim J, Lee J, Chang E et al (2009) Selective sentinel node plus additional non-sentinel node biopsy based on an FDG PET/CT scan in early breast cancer patients: single institutional experience. World J Surg 33:943–949PubMedCrossRef
Metadaten
Titel
Value of PET-FDG in primary breast cancer based on histopathological and immunohistochemical prognostic factors
verfasst von
Pierre Heudel
Sebastien Cimarelli
Anthony Montella
Catherine Bouteille
Thomas Mognetti
Publikationsdatum
01.12.2010
Verlag
Springer Japan
Erschienen in
International Journal of Clinical Oncology / Ausgabe 6/2010
Print ISSN: 1341-9625
Elektronische ISSN: 1437-7772
DOI
https://doi.org/10.1007/s10147-010-0120-3

Weitere Artikel der Ausgabe 6/2010

International Journal of Clinical Oncology 6/2010 Zur Ausgabe

Adjuvante Immuntherapie verlängert Leben bei RCC

25.04.2024 Nierenkarzinom Nachrichten

Nun gibt es auch Resultate zum Gesamtüberleben: Eine adjuvante Pembrolizumab-Therapie konnte in einer Phase-3-Studie das Leben von Menschen mit Nierenzellkarzinom deutlich verlängern. Die Sterberate war im Vergleich zu Placebo um 38% geringer.

Alectinib verbessert krankheitsfreies Überleben bei ALK-positivem NSCLC

25.04.2024 NSCLC Nachrichten

Das Risiko für Rezidiv oder Tod von Patienten und Patientinnen mit reseziertem ALK-positivem NSCLC ist unter einer adjuvanten Therapie mit dem Tyrosinkinase-Inhibitor Alectinib signifikant geringer als unter platinbasierter Chemotherapie.

Bei Senioren mit Prostatakarzinom auf Anämie achten!

24.04.2024 DGIM 2024 Nachrichten

Patienten, die zur Behandlung ihres Prostatakarzinoms eine Androgendeprivationstherapie erhalten, entwickeln nicht selten eine Anämie. Wer ältere Patienten internistisch mitbetreut, sollte auf diese Nebenwirkung achten.

ICI-Therapie in der Schwangerschaft wird gut toleriert

Müssen sich Schwangere einer Krebstherapie unterziehen, rufen Immuncheckpointinhibitoren offenbar nicht mehr unerwünschte Wirkungen hervor als andere Mittel gegen Krebs.

Update Onkologie

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