Frontiers in Oncology (Dec 2022)

Impact of differing methodologies for serum miRNA-371a-3p assessment in stage I testicular germ cell cancer recurrence

  • Ailsa J. Christiansen,
  • Ailsa J. Christiansen,
  • João Lobo,
  • João Lobo,
  • João Lobo,
  • Christian D. Fankhauser,
  • Christian D. Fankhauser,
  • Christian Rothermundt,
  • Richard Cathomas,
  • Aashil A. Batavia,
  • Josias B. Grogg,
  • Arnoud J. Templeton,
  • Anita Hirschi-Blickenstorfer,
  • Anja Lorch,
  • Silke Gillessen,
  • Silke Gillessen,
  • Silke Gillessen,
  • Silke Gillessen,
  • Holger Moch,
  • Jörg Beyer,
  • Thomas Hermanns

DOI
https://doi.org/10.3389/fonc.2022.1056823
Journal volume & issue
Vol. 12

Abstract

Read online

IntroductionCurrent evidence shows that serum miR-371a-3p can identify disease recurrence in testicular germ cell tumour (TGCT) patients and correlates with tumour load. Despite convincing evidence showing the advantages of including miR-371a-3p testing to complement and overcome the classical serum tumour markers limitations, the successful introduction of a serum miRNA based test into clinical practice has been impeded by a lack of consensus regarding optimal methodologies and lack of a universal protocol and thresholds. Herein, we investigate two quantitative real-time PCR (qRT-PCR) based pipelines in detecting disease recurrence in stage I TGCT patients under active surveillance, and compare the sensitivity and specificity for each method.MethodsSequential serum samples collected from 33 stage I TGCT patients undergoing active surveillance were analysed for miR-371a-3p via qRT-PCR with and without an amplification step included.ResultsUsing a pre-amplified protocol, all known recurrences were detected via elevated miR-371a-3p expression, while without pre-amplification, we failed to detect recurrence in 3/10 known recurrence patients. For pre-amplified analysis, sensitivity and specificity was 90% and 94.4% respectively. Without amplification, sensitivity dropped to 60%, but exhibited 100% specificity.DiscussionWe conclude that incorporating pre-amplification increases sensitivity of miR-371a-3p detection, but produces more false positive results. The ideal protocol for quantification of miR-371a-3p still needs to be determined. TGCT patients undergoing active surveillance may benefit from serum miR-371a-3p quantification with earlier detection of recurrences compared to current standard methods. However, larger cross-institutional studies where samples are processed and data is analysed in a standardised manner are required prior to its routine clinical implementation.

Keywords