Thomas Staudinger1, Frédéric Pène2. 1. Intensive Care Unit, Department of Medicine I, Medical University of Vienna/General Hospital of Vienna, Vienna, Austria. 2. Medical Intensive Care Unit, Cochin Hospital, Assistance Publique, Hôpitaux de Paris, Paris, France.
CLASSICAL AND EMERGENT RISK FACTORS FOR INFECTIONS
Neutropenia due to myelosuppression by malignant infiltration or that which is more
commonly caused by cytotoxic chemotherapy remains the hallmark of immunodeficiency in
patients with cancer and is associated with a considerably increased risk for bacterial
or fungal infections. In addition to quantitative defects, neutrophils also exhibit
various functional defects in chemotaxis, phagocytosis, bactericidal capacity and
respiratory burst. The requirements of indwelling long-term central venous access,
non-selective cytotoxic activity on dividing cells and poor wound healing account for
the frequent impairment in skin and mucosal integrity. Nonetheless, the emergence of new
drugs that specifically target lymphocytes has broadened the spectrum of infectious
complications to include opportunistic fungal, parasitic and mycobacterial infections,
which are observed in patients with lymphoproliferative disorders.(
Interestingly, even a short course of stress-dose corticosteroids that is commonly
applied in cases of severe or refractory circulatory failure is likely to increase the
risk of intensive care unit (ICU)-acquired infections in hematological patients with
septic shock.( Most importantly, the
spectrum of pathogens responsible for severe infections has changed. Multi-resistant
Gram-negative bacteria, especially enterobacteriaceae like Klebsiella
or Serratia spp. together with Pseudomonas spp. and
others have emerged and exert a major impact on the outcomes of immunocompromised
patients for whom any delay in adequate antibiotherapy may be extremely
harmful.( Extensive
prophylaxis with azoles or echinocandins in hematologic patients has led to a shift in
the fungal spectrum to more resistant strains and to the emergence of rare
fungi.(In addition, some additional risk factors of infections are potentially involved in
patients with malignancies. Cancerpatients frequently require red blood cell
transfusions. Transfusion-related immunomodulation is likely to confer an additional
risk of infectious complications, as suggested by a recent meta-analysis of studies that
addressed the transfusion thresholds in various populations.( Furthermore, some inherited individual predispositions
that have been previously described in immunocompetent patients might confer an
increased susceptibility to severe infections in immunocompromised patients as well. A
deficiency in mannose-binding lectin has thus been associated with a higher incidence of
severe bacterial and fungal infections in patients with hematological malignancies.
Moreover, functional polymorphisms in TLR4 or long pentraxin PTX3 have been associated
with an increased risk of invasive aspergillosis in allogeneic stem cell transplant
recipients.(
PARTICULARITIES OF SEVERE SEPSIS IN CANCER PATIENTS
It is commonly assumed that the immune pathophysiology of severe sepsis incancerpatients is mostly linked to immune deficiency imposed by anticancer treatments. Recent
animal experiments have shed some light on the immunomodulatory impact of an underlying
malignancy on the host’s response to severe infections. Indeed, mice previously
subjected to tumor inoculation displayed an increased mortality to infectious challenges
through P. aeruginosa pneumonia or polymicrobial
peritonitis.( Changes in the behavior of immune cells, including
decreased apoptosis of lymphocytes or expansion of myeloid-derived suppressor cells, are
associated with impaired anti-infective responses in hosts with advanced malignant
diseases.Acute circulatory failure is the hallmark of septic shock and involves both macro- and
microcirculatory mechanisms. Myocardial systolic or diastolic dysfunction is frequently
encountered in cancerpatients with septic shock and demonstrates a strong prognostic
value in this setting.( However, an
assessment of the microcirculation in septicpatients with neutropenia and
thrombocytopenia did not reveal any differences compared with patients with normal blood
cell counts.(
CURRENT PROGNOSIS
The survival of cancerpatients who are admitted to the ICU for severe sepsis has
markedly improved over the last several decades and now exceeds 50%, an improvement that
has been accompanied by encouraging long-term survival rates and better quality of
life.( During the late
nineties, the 30-day mortality rate of cancerpatients who were admitted for septic
shock was reported to reach 65% to 72%, whereas subsequent series showed a dramatic
relative decline of 25% to 42%.( A similar trend was observed for
patients with neutropenia and severe sepsis for whom in-hospital mortality before and
after 2003 dropped from 59% to 43%.( Along this line, severe sepsis following chemotherapy that is
frequently linked with neutropenia was associated with an in-hospital survival rate of
55%.( A volume effect has
been demonstrated because survival rates were higher in specialized centers that treat
large numbers of patients.( The
causes of this improvement might include urgent anti-infective measures that were
implemented by the combination of broad-spectrum antibiotics with an aminoglycoside as
well as early removal of indwelling catheters; another cause may be adhesion to the
Surviving Sepsis Campaign guidelines. Generally, early recognition and aggressive
management of sepsis are certainly vital to the improvement of patient outcomes.
SEPSIS-LIKE SYNDROMES
Due to the relative uniformity of the inflammatory response, a number of non-infectious
acute inflammatory disorders may mimic sepsis inpatients with hematological
malignancies. Patients with acute monocytic leukemia frequently exhibit pulmonary
involvement as a result of leukostasis, pulmonary infiltration and acute lysis
pneumopathy.( Lymphoma may be
revealed by hemophagocytic lymphohistiocytosis.( Induction treatments may precipitate tumor lysis syndrome in
patients with high-grade hematological malignancies such as acute leukemia, Burkitt
lymphoma and anaplastic lymphoma but also rarely in aggressive and bulky solid tumors
such as small cell lung carcinoma. In addition to the common metabolic features and
acute renal failure, tumor lysis syndrome may result in multiple organ dysfunctions,
presumably driven by a massive release of pro-inflammatory cytokines.( Differentiation syndrome is a particular complication of acute
promyelocytic leukemia under induction treatments with all-transretinoic acid or
arsenic trioxide that are likely to induce the overwhelming activation of myeloid
cells.( Finally, some
complications of allogeneic stem cell transplantation, such as sinusoidal obstruction
syndrome, engraftment syndrome or graft-versus-host disease may result in systemic
inflammatory response and multiple organ dysfunctions.
THE UNDEREVALUATED CONSEQUENCES OF SEPSIS ON CANCER PROGNOSIS
Thus far, studies that have addressed the outcome of severe sepsis incancerpatients
have focused primarily on short-term vital status. Few studies have assessed the
long-term survival and none have assessed how sepsis and intensive care might impact the
prognosis of the malignancy. Intensive care is associated with potentially devastating
consequences through profound alterations in functional status or residual organ
dysfunctions that may clearly compromise the maintenance of appropriate anticancer
treatment in ICU survivors. Furthermore, sepsis is also likely to directly impact tumor
growth, although dual pro- and anti-tumoral effects have been reported. On the one hand,
some clinical data suggest that severe bacterial infections may further confer an
increased risk of cancer.( This
particular clinical situation was recently modeled in a double-hit animal model of
polymicrobial sepsis followed by tumor inoculation, in which post-septicmice exhibited
enhanced tumoral growth compared with control animals with respect to the expansion of
regulatory T-cells.( On the other
hand, some data suggest that a bacterial challenge might act as a vaccine in patients
with malignancies. As was recently explained, in 1924, Coley first described a case of
remission of sarcoma in a patient who experienced a streptococcal infection and where an
injection of a mixture of bacteria was able to induce remission in several patients with
malignancies.( Furthermore,
the modulation of the intestinal microbiota was recently shown to alter tumor growth in
mice.( Whether the frequent exposure to antibiotics might also
impact the anti-tumoral response in cancerpatients remains to be investigated.
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