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Poster display session: Biomarkers, Gynaecological cancers, Haematological malignancies, Immunotherapy of cancer, New diagnostic tools, NSCLC - early stage, locally advanced & metastatic, SCLC, Thoracic malignancies, Translational research

3016 - Histology and detectability on ring-type dedicated breast PET in breast cancer

Date

20 Oct 2018

Session

Poster display session: Biomarkers, Gynaecological cancers, Haematological malignancies, Immunotherapy of cancer, New diagnostic tools, NSCLC - early stage, locally advanced & metastatic, SCLC, Thoracic malignancies, Translational research

Topics

Staging and Imaging

Tumour Site

Breast Cancer

Presenters

Yuri Kimura

Citation

Annals of Oncology (2018) 29 (suppl_8): viii479-viii482. 10.1093/annonc/mdy294

Authors

Y. Kimura1, S. Sasada1, N. Goda1, K. Kajitani1, A. Emi1, N. Masumoto1, T. Kadoya1, R. Haruta1, T. Kataoka1, M. Okada2

Author affiliations

  • 1 Breast Surgery, Hiroshima University Hospital, 734-8551 - Hiroshima/JP
  • 2 Surgical oncology, Hiroshima University, 734-8551 - Hiroshima/JP

Resources

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Abstract 3016

Background

Although dedicated breast PET (DbPET) visualizes sub-centimeter breast cancer lesions and intratumoral heterogeneity, the impact of histology on the detectability of DbPET remains unknown.

Methods

This study included 455 patients with breast cancer, who underwent whole-body PET (WBPET) and ring-type DbPET between January 2016 and March 2018. The relationship of histology and sensitivities of WBPET and DbPET for breast cancer was assessed.

Results

The median patient age was 57 years and histology was as follows: 82 (18.0%) noninvasive carcinoma, 18 (4.0%) microinvasive carcinoma, 305 (67.0%) invasive carcinoma with no special type, 9 (2.0%) invasive lobular carcinoma, and 41 (9.0%) other types. The sensitivity of WBPET and DbPET was 74.5% and 93.2%, respectively. The sensitivities of each histology on WBPET/DbPET were 41.5%/78.0%, 72.2%/100%, 83.9%/96.7%, 44.4%/88.9%, and 78.0%/95.1%, respectively (Table). The sensitivity was low on WBPET in noninvasive, microinvasive, invasive lobular, mucinous and tubular carcinomas. Lobular carcinoma in situ had low sensitivity on both WBPET and DbPET imaging. In the multivariate analysis, undetectable tumor factors on WBPET were sub-centimeter tumor size (Odds ratio [OR] = 6.04, P < 0.001) and histology (OR = 1.69, P = 0.08); for DbPET, Ki-67 labeling index was an undetectable tumor factor (OR = 4.32, P = 0.039).Table: 1343P

Sensitivities of whole-body and dedicated breast PET according to histology

NSensitivity (%)P
WbPETDbPET
Total455339 (74.5)424 (93.2)< 0.001
Noninvasive carcinoma8234 (41.5)64 (78.0)< 0.001
Ductal carcinoma in situ7232 (44.4)61 (84.7)< 0.001
Lobular carcinoma in situ81 (12.5)2 (25.0)1
Others21 (50.0)1 (50.0)1
Microinvasive carcinoma1813 (72.2)18 (100)0.046
Invasive carcinoma of no special type305256 (83.9)295 (96.7)< 0.001
Invasive lobular carcinoma94 (44.4)8 (88.9)0.131
Others4132 (78.0)39 (95.1)0.048
Mucinous carcinoma1913 (68.4)18 (94.7)0.09
Tubular carcinoma53 (60.0)4 (80.0)0.444
Carcinoma with apocrine differentiation55 (100)5 (100)1
Invasive micropapillary carcinoma55 (100)5 (100)1
Others76 (85.7)7 (100)1

Conclusions

Breast cancers with the specific histological subtypes are hard to detect on WBPET. DbPET can overcome the factors for weak WBPET detectability, such as tumor size and histology, and might prevent the overdiagnosis of lobular carcinoma in situ.

Clinical trial identification

Legal entity responsible for the study

Hiroshima University.

Funding

Has not received any funding.

Editorial Acknowledgement

Disclosure

All authors have declared no conflicts of interest.

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