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E-Poster Display

908P - Impact of serum galactomannan assay on diagnosis and outcome of invasive fungal infections in high risk febrile neutropenia: A prospective cohort study

Date

17 Sep 2020

Session

E-Poster Display

Topics

Tumour Site

Haematological Malignancies

Presenters

VIRAJ NEVREKAR

Citation

Annals of Oncology (2020) 31 (suppl_4): S590-S598. 10.1016/annonc/annonc261

Authors

V.V. NEVREKAR1, P. Choudhary1, A. TIWARI2, V. SURYAPRAKASH1, A. UPADHYAY1

Author affiliations

  • 1 Medical Oncology, AIIMS - All India Institute of Medical Sciences, 110029 - New Delhi/IN
  • 2 Medical Oncology, SHALBY HOSPITAL INDORE, 452003 - INDORE/IN

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Abstract 908P

Background

Invasive Aspergillosis (IA) is a major cause of early mortality in acute leukemia and stem cell transplants. Establishing a proven histo pathological diagnosis is often difficult in these patients. European organization for research and treatment of cancer (EORTC) classifies diagnosis of IA into proven, probable and possible.

Methods

Episodes of febrile neutropenia (FN) among inpatients aged ≥18 years with acute leukemia or those undergoing Hematopoietic stem cell transplantation (HSCT) were prospectively evaluated over 2 years (N=200). Serum galactomannan was analyzed on day 0, 4, 7 and then weekly till fever persisted. High Resolution Computed Tomography (HRCT) of chest was done on day 4 of fever. Optical density Index (ODI) > 0.5 for ≥ 2 samples was defined as positive. IA was diagnosed as per EORTC 2008 guidelines.

Results

Among 200 enrolled FN episodes, IA was diagnosed in 61 episodes (30.5%): Possible 27 (13.5%), Probable IA 34 (17%), Proven IA 0 (0%). 55.7% (27/61) of possible cases were reclassified as probable based on positive Galactomannan (GM) assay. False positivity rate was 49% but dropped t0 26% when positivity cut off of GM was increased to > 1 ODI. GM assay was able to detect 73% of probable IA cases earlier than CT scans. Use of antifungal was similar in GM positive and negative cases. However, episodes with positive GM had significantly higher use of > 1 antifungals. Overall mortality in all the enrolled episodes was 66 (33%). The mortality in those tested positive for GM was 33 (47.8%) and was 33 (50.7%) in those who tested negative. It was not statistically significant.

Conclusions

In a high risk population of acute leukemia and HSCT, GM assay could identify probable IA earlier than HRCT Chest. Although high number of false positives is a concern; it can be overcome by increasing cut off to 1, especially with known confounders.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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