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STRONG ASSOCIATION BETWEEN HERPES SIMPLEX VIRUS AND CHEMOTHERAPY-INDUCED ORAL MUCOSITIS IN PATIENTS WITH HEMATOLOGIC MALIGNANCIES UNDERGOING INTENSIVE CHEMOTHERAPY OR STEM CELL TRANSPLANTATION
Author(s): ,
Junshik Hong
Affiliations:
Department of Internal Medicine,Seoul National University Hospital,Seoul,Korea, Republic Of
,
Hee-Kyung Park
Affiliations:
Department of Oral Medicine and Oral Diagnosis,Seoul National University Dental Hospital,Seoul,Korea, Republic Of
,
Hyunkyung Park
Affiliations:
Department of Internal Medicine,Inha University Hospital,Incheon,Korea, Republic Of
,
Dong-Yeop Shin
Affiliations:
Department of Internal Medicine,Seoul National University Hospital,Seoul,Korea, Republic Of
,
Youngil Koh
Affiliations:
Department of Internal Medicine,Seoul National University Hospital,Seoul,Korea, Republic Of
,
Sung-Soo Yoon
Affiliations:
Department of Internal Medicine,Seoul National University Hospital,Seoul,Korea, Republic Of
,
Ji-Yeob Choi
Affiliations:
Department of Preventive Medicine,Seoul National University College of Medicine,Seoul,Korea, Republic Of
,
Youngnim Choi
Affiliations:
Department of Immunology and Molecular Microbiology,School of Dentistry and Dental Research Institute, Seoul National University,Seoul,Korea, Republic Of
Inho Kim
Affiliations:
Department of Internal Medicine,Seoul National University Hospital,Seoul,Korea, Republic Of
(Abstract release date: 05/17/18) EHA Library. Hong J. 06/14/18; 216872; PB2387
Dr. Junshik Hong
Dr. Junshik Hong
Contributions
Abstract

Abstract: PB2387

Type: Publication Only

Background
A link between oral cavity infections and chemotherapy-induced oral mucositis (CIOM) in patients with hematological malignancies (HMs) undergoing intensive chemotherapy (IC) or hematopoietic stem cell transplantation (HSCT) has been suggested. However, conclusive data are lacking, and there are no current guidelines for the prophylactic use of antimicrobials to prevent CIOM in these populations. 

Aims
The aim of the current study was to prospectively determine the prevalence of HSV reactivation and colonization with Candida as well as the relationship between such oral microbial factors and CIOM development in patients with HM undergoing IC or HSCT.

Methods
Patients aged ≥19 years with HM undergoing IC or HSCT were enrolled. Each patient was evaluated for HSV and Candida in the oral cavity along with CIOM at baseline as well as the second, third, and fourth weeks. To evaluate the reactivation of HSV-1 and -2 in oral keratinocytes, a sample was obtained by placing a sterilized  Transfer Membrane on the buccal mucosa. If CIOM developed, the sampling site included the CIOM lesions. DNA was isolated from the sampled membrane and reactivation of HSV-1 and -2 was determined by PCR using the HSV 1/2 PCR kit. At every evaluation (baseline, week 2, week 3, and week 4), CIOM presence was estimated and graded according to the WHO oral toxicity scale and the NCI-CTCAE), version 3.0. For the semiquantitative evaluation of the severity of CIOM, the reticulation, erythema, and ulceration (REU) scoring method for oral lichen planus or oral lichenoid lesions was applied.  

Results
Seventy presentations among 56 patients were analyzed. CIOM was observed in 23 presentations (32.9%), with a higher incidence associated with HSCT (17 of 35 presentations, 48.6%) than with IC (6 of 35 presentations, 8.6%). Reactivation of HSV-1 was significantly associated with an increased incidence of CIOM and a higher 'reticulation, erythema, and ulceration' score after adjusting for age, sex, type of disease, and treatment stage. A higher HSV-1 viral load was associated with increased and more severe incidents of CIOM. The presence of Candida was not associated with CIOM.

Conclusion
HSV reactivation in the oral cavity is highly associated with CIOM in patients with HM undergoing high-dose chemotherapy, independent of age, sex, treatment stage, and type of disease.  A prospective trial to evaluate the effect of prophylactic acyclovir on CIOM prevention in HM patients receiving induction chemotherapy or autologous HSCT is therefore warranted.

Session topic: 36. Quality of life, palliative care, ethics and health economics

Keyword(s): Hematological malignancy, Herpesvirus, Mucositis

Abstract: PB2387

Type: Publication Only

Background
A link between oral cavity infections and chemotherapy-induced oral mucositis (CIOM) in patients with hematological malignancies (HMs) undergoing intensive chemotherapy (IC) or hematopoietic stem cell transplantation (HSCT) has been suggested. However, conclusive data are lacking, and there are no current guidelines for the prophylactic use of antimicrobials to prevent CIOM in these populations. 

Aims
The aim of the current study was to prospectively determine the prevalence of HSV reactivation and colonization with Candida as well as the relationship between such oral microbial factors and CIOM development in patients with HM undergoing IC or HSCT.

Methods
Patients aged ≥19 years with HM undergoing IC or HSCT were enrolled. Each patient was evaluated for HSV and Candida in the oral cavity along with CIOM at baseline as well as the second, third, and fourth weeks. To evaluate the reactivation of HSV-1 and -2 in oral keratinocytes, a sample was obtained by placing a sterilized  Transfer Membrane on the buccal mucosa. If CIOM developed, the sampling site included the CIOM lesions. DNA was isolated from the sampled membrane and reactivation of HSV-1 and -2 was determined by PCR using the HSV 1/2 PCR kit. At every evaluation (baseline, week 2, week 3, and week 4), CIOM presence was estimated and graded according to the WHO oral toxicity scale and the NCI-CTCAE), version 3.0. For the semiquantitative evaluation of the severity of CIOM, the reticulation, erythema, and ulceration (REU) scoring method for oral lichen planus or oral lichenoid lesions was applied.  

Results
Seventy presentations among 56 patients were analyzed. CIOM was observed in 23 presentations (32.9%), with a higher incidence associated with HSCT (17 of 35 presentations, 48.6%) than with IC (6 of 35 presentations, 8.6%). Reactivation of HSV-1 was significantly associated with an increased incidence of CIOM and a higher 'reticulation, erythema, and ulceration' score after adjusting for age, sex, type of disease, and treatment stage. A higher HSV-1 viral load was associated with increased and more severe incidents of CIOM. The presence of Candida was not associated with CIOM.

Conclusion
HSV reactivation in the oral cavity is highly associated with CIOM in patients with HM undergoing high-dose chemotherapy, independent of age, sex, treatment stage, and type of disease.  A prospective trial to evaluate the effect of prophylactic acyclovir on CIOM prevention in HM patients receiving induction chemotherapy or autologous HSCT is therefore warranted.

Session topic: 36. Quality of life, palliative care, ethics and health economics

Keyword(s): Hematological malignancy, Herpesvirus, Mucositis

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