Concordance of non-invasive plasma cell-free DNA with invasive diagnostics for diagnosis of invasive fungal disease

Abstract

Background Mold plasma cell-free DNA (cfDNA) PCR is a promising non-invasive diagnostic modality for early diagnosis of invasive mold disease (IMD) in immunocompromised patients. Although mold cfDNA PCR has been shown to be highly accurate, the value of invasive procedures to collect specimens for conventional fungal diagnostics following plasma cfDNA testing remains unclear. Methods This retrospective single-center cohort study included patients with mold plasma cfDNA PCR performed 7 days before or 2 days after invasive specimen collection. Mold PCR detected Aspergillus species, Mucorales agents, Fusarium species, and Scedosporium species. Invasive procedures included tissue biopsy and bronchoscopy. The primary endpoint was the concordance of mold plasma cfDNA PCR results with results of conventional fungal tests performed on tissue and bronchoalveolar lavage fluid (BAL). Results Five hundred and six patients with mold plasma cfDNA PCR resulting ahead of invasive specimen (123 tissue and 426 BAL) results were included, and 437 (86.4%) were immunocompromised. After adjudicating discordant results based on the EORTC/MSGERC definitions for IMD, mold plasma cfDNA PCR and invasive test results were 88.5% (448/506) concordant. In proven cases, 64.7% (11/17) of negative mold plasma cfDNA PCR results occurred in patients with fungal sinusitis (8) and limb infection (3). Non-hematologic malignancy and non-neutropenic states were statistically associated with negative mold plasma cfDNA PCR in patients with proven or probable IMD. Conclusions Non-invasive mold plasma cfDNA PCR results were highly concordant with invasive specimen fungal test results, thus indicating risk-prone invasive specimen collection can be safely curtailed in immunocompromised patients with suspected IMD.