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Poster display session: Breast cancer - early stage, locally advanced & metastatic, CNS tumours, Developmental therapeutics, Genitourinary tumours - prostate & non-prostate, Palliative care, Psycho-oncology, Public health policy, Sarcoma, Supportive care

3324 - Plasma miR-371a-3p for detection of non-teratomatous viable germ cell tumor in testicular cancer

Date

22 Oct 2018

Session

Poster display session: Breast cancer - early stage, locally advanced & metastatic, CNS tumours, Developmental therapeutics, Genitourinary tumours - prostate & non-prostate, Palliative care, Psycho-oncology, Public health policy, Sarcoma, Supportive care

Topics

Tumour Site

Malignant Germ-Cell Tumours of the Adult Male

Presenters

Lucia Nappi

Citation

Annals of Oncology (2018) 29 (suppl_8): viii303-viii331. 10.1093/annonc/mdy283

Authors

L. Nappi1, M. Thi2, B.J. Eigl1, A. Lum3, D. Huntsman4, C. Martin5, B. O Neil5, D.J. Khalaf1, K.N. Chi1, M.E. Gleave6, A. So2, P. Black2, S. Daneshmand7, C.R. Nichols8, C.K. Kollmannsberger1

Author affiliations

  • 1 Medical Oncology, British Columbia Cancer Agency, V5Z 4E6 - Vancouver/CA
  • 2 Urologic Science, Vancouver Prostate Centre, V5n0c3 - Vancouver/CA
  • 3 Department Of Molecular Oncology, British Columbia Cancer Research Centre, Vancouver/CA
  • 4 Department Pathology And Laboratory Medicine, British Columbia Cancer Agency, V5Z 4E6 - Vancouver/CA
  • 5 Surgery, Huntsman Cancer Institute, Salt Lake City/US
  • 6 Urologic Science, University of British Columbia Faculty of Medicine, V6T 1Z3 - Vancouver/CA
  • 7 Urology, University of South California, Los Angeles/US
  • 8 Na, Testicular Cancer Commons, UT 84101 - Salt Lake Cty/US

Resources

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Abstract 3324

Background

Active surveillance for CSI testicular cancer is currently based on serial radiological imaging and classic tumor markers (β-HCG, AFP, LDH). The management of borderline suspicious tumor markers negative enlarging nodes and of the post-chemotherapy residual disease is challenging, and currently relies on clinical follow-up with imaging to establish patterns of growth or pathological confirmation with biopsy or retroperitoneal lymphadenectomy (RPLND). A blood-based approach to reliably identify patients with non teratoma viable GCT (NTVGCT) would be valuable.

Methods

Plasma miR-371a-3p (miR371) of pts with GCT was analyzed by RT-PCR. Spike-in cel-miR-39-3p and miR-30b-5p as internal controls. miR-451a and miR-23a-3p were used as quality control for the hemolysis. The miR371 expression was used to calculate its area under the ROC curve, sensitivity and specificity in detecting viable NTGCT.

Results

One hundred samples from 79 patients (44 CSI and 35 metastatic) were analyzed. Nineteen CSI pts presented suspicious enlarging nodes (≥ IIA) during surveillance and 8/19 had confirmed relapse. miR371 predicted the clinical relapse in 6/8 of pts while the 11 CSI pts with unconfirmed enlarging nodes were all negative for miR-371. miR371 was expressed in all the pre-chemotherapy metastatic pts and negative after chemotherapy (n = 25). miR371 was negative in all the pts with post-chemotherapy residual radiographic findings (n = 24). No residual NTVGCT was detected in any of these 24 pts by either pathology at resection (n = 16) or clinical follow-up (n = 8). The area under the ROC curve was 0.94, the sensitivity and specificity were 89% and 98%, respectively. The results showed a high concordance comparing 2 independent experiments conducted in house and in an outside lab (r = 0.98 and 0.87, respectively).

Conclusions

Detectable circulating miR371 expression predicts the presence of NTVGCT. If validated in larger real world settings, this may result in significant change in the practice for all patients with germ cell tumors by moving it to a biological rather than radiological decision base. These encouraging findings inform upcoming North American trials for further definition of miR371 operating characteristics in GCTs.

Clinical trial identification

Legal entity responsible for the study

Lucia Nappi.

Funding

GUMOC research grant 2017.

Editorial Acknowledgement

Disclosure

All authors have declared no conflicts of interest.

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