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410 <strong>EAPC</strong> Abstracts<br />

35 Oral Presentation<br />

Cachexia<br />

A novel Cachexia Classification for Palliative Cancer Care:<br />

Synthesis of systematic literature review and nominal experts’<br />

focus group<br />

Authors: Florian Strasser Dept. Internal Medicine & Palliative Care Centre<br />

Oncological Palliative Medicine, Section Oncology SWITZERLAND<br />

Aurelius Omlin Oncological Palliative Medicine, Cantonal Hospital<br />

St. Gallen SWITZERLAND<br />

Jochen Walker Oncological Palliative Medicine and Surgery, Cantonal<br />

Hospital St.Gallen SWITZERLAND<br />

David Blum Oncological Palliative Medicine, Cantonal Hospital St.Gallen<br />

SWITZERLAND<br />

Ken Fearon Surgical Oncology, Royal Infirmary of Edinburgh Edinburgh<br />

UNITED KINGDOM<br />

repesenting the EPCRC<br />

Background: The current definition of cancer cachexia (weight loss,<br />

anorexia) does poorly guide practice. To monitor clinical decisions, alleviate<br />

suffering and develop tailored anti-cachexia interventions, a novel cachexia<br />

classification system, adjusted for palliative care, is required. Methods: A<br />

SLR (1976–2007) was performed (Pubmed, Cochrane, Embase, PsycINFO,<br />

CinAhl; search strings: cachexia, cancer, classification). Inclusion criteria:<br />

system or factor to classify patients with cachexia or to predict response to<br />

anticachectic treatment. Data extraction (2 raters) applied a formalized list,<br />

considering results of the first FG. Scoring for quality (Hawker) is done.<br />

Nominal FG of 12 academic cachexia experts discussed in 2 rounds “Which<br />

factors guide clinical decision making for cachexia management in daily<br />

practice” Key findings from the first round and the SLR were presented in<br />

the second round. Collaboration with a non-cancer specific wasting/cachexia<br />

consensus group was achieved. The final synthesis includes eligibility criteria<br />

and stratification factors from registered anti-cachexia trials and applies<br />

a structured Delphi-type review process. Results: Of 9817 citations,<br />

126 papers (7 systems, 112 factors; 7913 patients [50% GI, 20% lung cancer])<br />

were included. 4 systems combined anthropometrics (AM), nutritional<br />

intake (NI), symptoms (SY) and inflammation (INF), 2 systems AM/NI and<br />

either SY or INF, 1 added REE and hormones. All systems challenge the old<br />

definition. Of the single factors, AM, INF, muscle strenght and ghrelin classify<br />

cachexia in most studies, whereas NI, SY, metabolic alterations, REE,<br />

and leptin are variably reported. Responders in 84 anticachexia trials were<br />

not identified by factors. Consensus appears in cachexia as ongoing loss of<br />

muscle mass with 3 domains: depleted muscle protein, decreased ability to<br />

eat, and a catabolic drive. Symptoms are in all domains. Conclusions: A<br />

novel, pragmatic CCS-PC hold promise for care and research.<br />

36 Invited Lecture<br />

Systematic Reviews – what they can and what they can’t do<br />

Systematic reviews: an essential tool or a fashionable foible<br />

Authors: Lukas Radbruch Department of Palliative Medicine University of<br />

Aachen GERMANY<br />

Research in palliative care faces many barriers, among them physical frailty<br />

and cognitive impairment as well as a general reluctance of clinical staff to<br />

recruit patients, as clinical trials are felt to be in contradiction with the holistic,<br />

caring philosophy of palliative care. Sample sizes of published studies<br />

are small, with wide variations in the study populations. This has led to an<br />

increasing use of systematic review in an attempt to collate high quality<br />

information from these studies. The use of systematic reviews is also fostered<br />

by the rise of evidence-based medicine (EBM), as systematic reviews<br />

are on the top of the scoring lists of EBM. Systematic reviews allow for a<br />

quick and comprehensive apprehension of the available literature.<br />

However, there are some drawbacks to the new fashion of EBM. User as<br />

well as authors of systematic reviews often forget that the absence of evidence<br />

does not equal the evidence of absent efficacy. Many reviews start<br />

high with elaborate search strategies and inclusion criteria, and end modestly<br />

with only a few papers (which could not be compared) found useful for<br />

their remit. Many reviews end with the stereotypical statement: there is not<br />

enough evidence. There is an inherent danger from this position, as it may<br />

lead decision makers to focus on those treatments only which have been<br />

proven effective with EBM. This means that decisions focus on systematic<br />

reviews and the randomized trials that generated them, and users forget that<br />

other evidence is also acknowledged in EBM, though on a lower level.<br />

Even the much maligned expert opinion is part of EBM, if no (randomized)<br />

trials are available. There may be good reasons why there are no randomized<br />

trials. For example the evidence from randomized trials on the efficacy<br />

of morphine is scarce, but running such a trial today would be unnecessary<br />

and inacceptable from an ethical point of view. We have to take care<br />

that we use systematic reviews where we need them, but not as a means to<br />

end all discussions.<br />

37 Invited Lecture<br />

Systematic Reviews – what they can and what they can’t do<br />

Cochrane reviews in palliative care: where is the evidence<br />

Common errors and problems with systematic reviews in palliative<br />

care and how to overcome<br />

Authors: Phil J. Wiffen Churchill Hospital, Pain Research Unit Pain,<br />

Palliative & Supportive Care CRG UNITED KINGDOM<br />

This lecture will present an overview of what we currently have in terms of<br />

systematic reviews and controlled trials. Current challenges include a lack<br />

of suitable data for analysis, continued use of practices that have been<br />

shown to be ineffective or have little supporting evidence, challenges of<br />

extrapolation of results from outside palliative care and imperfect methodology<br />

to get the best from qualitative data. The goal of developing a systematic<br />

review for the major issues in palliative care is not an impossible dream<br />

but will need to stimulate a higher standard of research and development of<br />

collaborative research groups that can recruit larger numbers of participants<br />

for trials.<br />

38 Invited Lecture<br />

Systematic Reviews – what they can and what they can’t do<br />

Drug treatment of cancer-related fatigue. An example of a<br />

Cochrane review and of the problems with extrapolating<br />

results from cancer to palliative care<br />

Authors: Paddy Stone Division of Mental Health St George’s Hospital<br />

Medical School UNITED KINGDOM<br />

This presentation will discuss the difficulties of using the results of a<br />

Cochrane systematic review in routine clinical practice. The presentation<br />

will be illustrated with the example of a recently conducted review and<br />

meta-analysis of randomised controlled trials for patients with cancerrelated<br />

fatigue (full results presented elsewhere). The author will explain<br />

how the review group settled on inclusion and exclusion criteria for the systematic<br />

review. These were based on a study quality standard requiring randomisation<br />

of treatment as a minimum. The impact of using different search<br />

strategies will be discussed. The chosen search strategy identified over<br />

5000 abstracts with 116 being short-listed for potential inclusion. Only<br />

45 studies fully met the inclusion criteria. It was decided only to analyse<br />

studies that used multi-item outcome measures – thus 27 trials were included<br />

in the meta-analysis. The rigorous criteria used in Cochrane reviews led<br />

to the exclusion of drug treatments examined only in phase 2 studies. Many<br />

studies of palliative care patients fell into this category and were excluded<br />

at the screening stage. The discussion of selected results will focus on how<br />

the findings can be applied in clinical practice. The populations studied<br />

were mainly receiving active treatment. The majority of the data comes<br />

from trials of anaemic cancer patients receiving erythrocyte colony growth<br />

factors such as erythropoietin. It is unclear how these results can be applied<br />

to a palliative care population without further study. The author will discuss

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