Background
Cancer patients remain at substantial risk for developing serious infections despite significant advances in cancer therapy and supportive care. The treatment of malignant conditions with cytotoxic chemotherapy and radiation therapy has become increasingly effective, but it is associated with significant side affects, including toxicities to haemopoietic and non-haematopoietic tissues. Similarly neutropenia is still the most common pre-disposing factor, it is often superimposed on other immunological deficits (e.g. impaired cellular or humoral immunity) each of which is associated with a specific spectrum of infection. Bacterial infections predominate during the early phases of a neutropenic episode, whereas fungal infections occur more often in patients with prolonged neutropenia[
1,
2]. Beside neutropenia the chemotherapeutic agents and therapeutic radiation also disrupt the mucosal banner of the mouth, leading to severe oral mucositis, gingivitis, oral candidiasis, cellulitis and viral mucosal eruptions[
3‐
10]. The oral mucositis or inflammation of the oral mucosa is painful and is characterized by erythema, edema, and mucosal shedding, which can lead to ulceration and secondary infection[
11,
12]. Moreover, the oral cavity infections in cancer patients usually result from the combination of neutropenia and mucositis. In oral cavity infection the oral micro flora may be subsequently replaced by potentially pathogenic microorganisms, such as
Candida sp., (from 72% to 92%),
Candida carriage was reported common in cancer patients, with
C. albicans being the predominant species in patients who undergo radiotherapy for Head and neck[
13‐
17]. Oral colonization (up to 93%) and infection (up to 30%) are frequently noted in the patients[
18]. The main reason is that the irradiation-induced histological changes leading to oral mucositis, together with salivary quantitative and qualitative changes, have been reported to facilitate yeast growth[
13,
19]. Beside that a possible explanation for the higher predisposition of irradiated patients to candidosis is due to reduced phagocytic activity of salivary granulocytes against these micro-organisms[
20].
Similar to oral cavity infection, bloodstream infections (BSI) also remain serious complications in patients receiving antineoplastic therapy[
21]. Bloodstream infections (BSIs) occur due to the failure of the immune system and consequently disseminated the disease. The frequency of BSI infections, their epidemiology, and the invading organisms have changed in parallel with the evolution of medical care, particularly with the emergence of an increasingly ill and immunocompromised population of hospitalized patients who are often heavily dependant on medical support and indwelling devices[
22,
23]. Currently, slightly more than 50% of BSIs are hospital acquired[
24‐
28].
So, because of a weakened line of defense in oral cancer patients, the present prospective cohort study was carried out, with the aim of isolation, and identification of bacterial, fungal colonization from oral cavity and blood of radiotherapy, chemotherapy and radio chemotherapy treated patients. It is also important to be mentioned that our study was based on evaluation of colonization of fungal species only and did not consider the clinical aspects of the fungal species.
Methods
Study design
The present prospective cohort analysis was conducted on the patients undergoing treatment in the radiotherapy unit of Regional Cancer Institute, Pt. B.D. Sharma University of Health Sciences, Rohtak, Haryana, during the period of January 2007 to October 2009. A total of 186 patients with squamous cell carcinoma of oral cavity were analyzed in the study. The present study was approved by Human Ethical Committee of the University (M.D. University, Rohtak) and written consent was also taken from the patients.
Patient’s population
The patients were divided into three groups depending on their treatment protocol; each category was having 62 cases. First group patients were radiotherapy treated (RT) only (total dose of radiotherapy ranging from 51 to 60 grays in dose of 200cGY/day, 5 days a week), second group patients were given chemotherapy treated (CT) only (3 or 4 Courses of carboplatin, 5-FU, docetaxel/methotrexate/cisplatin given after 21 days gap) and third category patients were given radio chemotherapy simultaneously (RCT) (Between irradiation, chemotherapy courses of paclitaxel, carboplatin and 5-FU given).
Inclusion criteria
About 108 CFU/ml of bacteria and 105 CFU/ml of fungi cells were considered as pathogenic for the study. The main predisposing factors that can cause oral cavity and blood stream infection in the three studied groups were following:
Bloodstream infection (BSI): BSIs were defined, as isolation of a recognized pathogen (aerobic bacteria and fungi) from one or more blood cultures (BCs) that were unrelated to an infection at another site with, or without fever or hypotension[
29,
30].
Oral infection: Oral infection was defined as, isolation of recognized pathogens (aerobic bacteria and fungi) from one or more oral swab.
Episodes of BSI: Since any given patients could have a BSI more than once, so we use the term episode of BSI for each separate event[
29,
30].
Episode of bactermia: The isolation of one bactermia (unimicrobial) or more (polymicrobial) microorganisms in the same blood culture or in a separate blood culture obtained within 24–48 hours[
29,
30].
Neutropenia: Neutropenia was defined as, an ANC of less than 500 neutrophil/μL that may increase susceptibility to infection [29. 30].
Fever: Oral temperature of ≥ 38.5°C or more within a 24-hours period after initiation of therapy[
29,
30].
Anemia: A pathologic deficiency for oxygen-carrying hemoglobin in the red blood cells. In case of males Hb. < 14 g/dl and in case of females Hb. < 12 g/dl were considered as anemic cases[
31].
Community acquired infection: Any infection acquired before, or within 48 hours of admission to hospital and which was not related to any hospital procedure[
29,
30].
Nosocomial Infection: Nosocomial infection was defined as, at least one blood culture positive for significant pathogens in patients before, or within 48 hours of admission to hospital[
29,
30].
Catheter related infection: Infection was considered catheter related when at least one of following conditions were, meet (1) Isolation of same pathogens from catheter tip and blood. (2) Isolation of pathogens from a blood culture obtained from the catheter, but not from another blood obtained from peripheral vein at the same time[
29,
30].
Oral mucositis: WHO describe oral mucositis into 4 categories, like: grade 0- no change; grade 1 soreness/erythema; grade 2 erythema, ulcers, can eat solids; grade 3 ulcers, requires liquid diet only; grade 4 alimentation not possible[
30].
Exclusion criteria
Patients were excluded from the study if they had clinical or microbiological evidence of bloodstream infection of unknown origin. Patients who developed, fever within 24 hours after administration of chemotherapy and fever subsided within next 24 hours after completion of chemotherapy were also excluded from study. Common skin isolates, including Coryneforms and Bacillus species excluded from analysis. Coagulase negative Staphylococci (CoNS) were only considered as causative pathogens if two or more blood samples drawn on separate occasions showed the growth of the pathogen.
Clinical and laboratory data
The data on patient’s age, sex, underlying cancer, clinical stage of cancer, medications (antibiotics, cytotoxic drugs), fever, and exposure to radiotherapy or chemotherapy were recorded over the preceding 30 days and an invasive procedure performed over the proceeding 10 days. For every febrile episode of oral infection and blood cavity infection, the data on: date of onset, date of admission, sources of infection, presence of venous catheters and period of their insertion, result of complete blood count, severity and duration of neutropenia were collected.
Oral cavity specimen handling
Before antibiotics were started, Oral swab were taken by gently rubbing a sterile cotton swab over the labial mucosa, tongue and cancerous lesion[
32]. The swabs were incubated in sheep blood agar, saboured dextrose agar, macconkey agar, nutrient agar, and other selective media for primary isolation of the pathogens. These plates were than aerobically incubated for 24–48 hours at 37°C temperature for bacterial pathogens isolation and for 24–72 hours at 30°C in B.O.D. incubator for fungal species isolation.
Blood Specimen handling
Before antibiotics were started, blood samples (5 ml each) for cultures were obtained from each patient who developed, fever within 21 days following radiotherapy, chemotherapy and radio chemotherapy. One samples isolated from central venous catheter (if present) and other from peripheral vein. Blood cultures were drawn with a sterile system after a sterile pad was placed below the catheter hub and the hub was disinfected with 10% povidone–iodine. Blood samples were than transferred in culture bottles of brain heart infusion broth. Bottles were incubated at 37°C for 7 days. Simultaneously bottles showing positive growth index from blood culture were gram stained and sub cultured on sheep blood agar, saboured dextrose agar, macconkey agar and nutrient agar, simmon citrate agar and cetrimide agar plates. These plates were than aerobically incubated for 24–48 hours at 37°C temperature for bacterial pathogens isolation and for 24–72 hours at 30°C in B.O.D. incubator for fungal species isolation.
Microbial identifications
The bacterial pathogens were identified after appearance of growth on sub cultured, plates of blood and oral swab by standard microbiological and biochemical procedures. These biochemical tests include: Carbohydrates fermentation tests, urease tests, oxidase test, haemolysis of blood, catalase test, motility tests and growth pathogens on specific media etc. A preliminary examination of fungal colony on SDA was done through gram stained, smear, formation of germ tube, study of micro morphology, morphology on KOH stained smear, assimilation of carbon and nitrogen[
33‐
36].
All isolated pathogens were compared with MTCC standard strains like S. aureus with MTCC 96 strain, S. epidermidis MTCC 435 strain, P. vulgaris MTCC 426 strain, P. mirabilis MTCC 425 strain, E. coli MTCC 443 strain, K. pneumonia MTCC 109 strain, P. aeruginosa MTCC 741 strain, C. albicans 3017 strain and A. fumigatus 2550 strain.
Absolute neutrophils count
The absolute neutrophils count (ANC) was done by multiplying the total WBC count by percentage of neutrophils (segmented + band)[
37].
On the basis of ANC the patients were divided into two categories:
Neutropenia: When ANC was less than 500 (severe risk of infection).
Non neutropenia: When ANC was more than 500 (moderate risk of infection).
Basic statistical methods
Means values were reported ± standard deviation (SD). Continuous variables mean values were compared by ‘t’ tests. For independent samples difference in proportion of two groups were compared by chi – square test (with Yates correction) or Fisher’s exact test, when appropriate. All test of significance were two tailed. Alpha was set at 0.05. For the logistic regression odd ratio with 95% confidence interval (CI95) were calculated. Univariate analysis of dichotomous and ordinal variables was performed by using the procedures for matched data seta in the EpiInfo computer Programme (Epi 6.03: centre for disease control and prevention, USA). Conventional statistical methods were used to calculate means and standard deviation with the help of Microsoft excel 2007.
Discussion
This prospective cohort study is first from Haryana, India and is based on evaluation of the rate, risk factors and outcomes of treatment procedures between oral cancer patients. The present report describes colonization of bacterial and fungal infectious pathogens in oral cancer patients.
The colonization of microorganisms in cancer patients was found to occur in oropharynx as well as gastrointestinal system, urinary system and airways. Colonization starts within 48 hours of hospitalization[
38]. Number of studies proved that Neutropenia increases the microbial colonization[
39‐
41]. Our observation also illustrates that the colonization of microorganisms was higher in blood and oral cavity of neutropenic cases after chemotherapy, radio chemotherapy.
Nowadays, in most of hospitals, there is a shift of the microbial spectrum of cancer patients from gram-negative to gram positive, compared with the predominance of gram-negative species in the 1960s and 1970s[
42‐
46]. Nevertheless in developing countries there is a different situation where the predominant pathogens are gram-negative, the reason maybe the people cannot afford to give routinely prophylactic oral antibiotics, such as quinolones, and use less central lines. The predominance of gram negative bacteria in developing countries can also be explained with the help of various studies. A study was conducted on febrile neutropenic patients in a hospital from Lebanon and observed that the gram-negative bacteria were responsible for 78.8% (26/33) of bloodstream infections compared to 33.3% (11/33) gram-positive organisms. In the present study dominant gram negative bacteria were of
E. coli and
P. aeruginosa. A possible explanation of the observed high incidence of gram-negative infections in Lebanon was the relatively low proportion of indwelling catheters[
47]. Another study was carried in Malaysia observed that out of 120 episodes, 60.02% were gram-negative organisms of Enterobacteriaceae[
48]. A similar pattern of predominant gram-negative bacteria (61%) was seen in a study of hematologic malignancy patients from Brazil[
49]. Similar to above study we have also observed that main pathogen isolated from blood of group I and oral cavity of group II were of gram negative bacteria. This may be due to absence of use of catheter as a routine practice during the period of our analysis.
In our study
P. aeruginosa was the main gram negative bacteria in blood stream and
K. pneumonia was in oral cavity. Similar to our study the presence of
P. aeruginosa as an infectious pathogen was also observed by Raje et al.,[
50]. They reported
P. aeruginosa (28%) as a major pathogen in febrile neutropenic patients of acute lymphobalastic leukemia cases. Karim et al.,[
51] and Saghie et al.,[
52] were also observed presence of
P. aeruginosa in 31% and 38% respectively from febrile neutropenic cases. However our study showed the proportion of
P. aeruginosa was higher in non- neutropenic cases.
The present report also revealed the predominance of gram positive bacteria (
S. aureus and
S. epidermidis) in blood of group II, III and oral cavity of I, III group. The predominance of gram positive bacteria as infectious pathogen was also proved by other studies did in India. Jagarmuldi et al.,[
43] conducted a study on acute leukemia cases and observed 38.5% of
S. aureus infection in 240 febrile episodes and in other study
S. aureus (39%) infection was observed in blood after chemotherapy[
53]. The prevalence of gram positive bacteria may be due to that oral cancer patient were undergone treatment of high intensive chemotherapy, radio chemotherapy which may be led to damage of the mucosal barriers and increases the risk of infection with gram-positive oral (and GI) flora[
54]. In favor of that reason, we observed the significant predisposing factor for blood stream infection was the use of central venous line (P < .05) in group III, which may be facilitated the entry of organisms colonizing the skin into the bloodstream, and thus increase the rate of Staphylococcal infections in blood and oral cavity[
2,
43]. Our study also observed another significant predisposing factor of bloodstream infection in group III was nosocomial acquired (P < .01). The role of nosocomial acquisition of
S. aureus infection was also demonstrated in various studies did at five centers in Egypt and a provincial hospital in north east Thailand[
55,
56]. Nosocomial infection of
S. aureus in developing countries is probably common, the reasons for which may include lack of hand washbasins or hand washing, overcrowding in hospital wards and clinics, lack of infection control training or policies, the inability to isolate specific patients, and lack of diagnostic microbiology facilities[
56].
Another salient featured of our study was the colonization of
C. albicans as most significant oral cavity pathogens in group I and III patients.
C. albicans was isolated in group I neutropenic, non neutropenic cases in proportion of 45.90%, 48.78% respectively and in group III its proportion in neutropenic, non neutropenic cases was 28.2%, 27.72% respectively. The proportion of C
. albicans in group I i.e. radiotherapy treated, cases was similar to various studies conducted on oral candidiasis after radiotherapy and showed a wide variation ranging from 17 to 52.5%[
4,
17,
19,
57‐
60]. The colonization of C. albicans in oral cavity of radiotherapy treated, cases may be due to the reason that our patients were often unable to maintain satisfactory oral health and nutritional status during RT, mainly because of low income and educational level. This reasons of colonization of
C. albicans in oral cavity was also observed in study did in Brazilian patients undergoing head and neck radiotherapy[
17]. The pathogenesis of candidal infections is complex encompassing both fungi and host factors. Candidal colonisaion appears to be influenced by adherence mechanisms among fungi and oral epithelial cells. Radiotherapy-induced hyposalvation also encourages oral candidal colonization that often leads to oral candidiasis[
19].
We have also observed other reason of colonization of
C. albicans may be oral mucositis, which played a significant role in oral cavity infection of all three groups. Generally it is also accepted that oral mucositis, is of multifactorial origin, and it is ranged among 20% and 100% in patients receiving different types of cancer treatments[
61‐
65]. Other reason for the prevalence of mucositis in our study may be due to fluorinated 5-fluorouracil (5-FU) which was the most effective and frequently used antineoplastic agent for the treatment of oral cancer. There are others reports which also showed mucositis (4 to 74% for head and neck cancers) induced by 5-FU[
66,
67].
Some limitations were present in our study, first was that we did not take the clinical features of Oral candidosis in our patients i.e. we were not able to evaluate that whether the Oral candiasis remain confined to the oral cavity, or spread to oesophageal or more widely to cause systemic candidosis. This study also is limited to infections caused by aspergillosis and candidiasis. Although these two pathogens represent most of fungal infections, infections due to other fungal species may result an additional burden to the oral cancer cases.
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
All authors have equal contribution in study designs, experiment, data analysis and interpretation of data. Similarly all authors have critically reviewed the manuscript, approved of its contents and consented to its communication for publication.