Annual Meeting Proceedings Part 1 - American Society of Clinical ...
Annual Meeting Proceedings Part 1 - American Society of Clinical ...
Annual Meeting Proceedings Part 1 - American Society of Clinical ...
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9146 General Poster Session (Board #51D), Sat, 8:00 AM-12:00 PM<br />
Lifetime traumas and their influence on advanced cancer patients’ illness<br />
understanding and likelihood <strong>of</strong> end-<strong>of</strong>-life discussions. Presenting Author:<br />
Elizabeth L. Kacel, Dana-Farber Cancer Institute, Boston, MA<br />
Background: Research on posttraumatic stress in cancer patients has<br />
focused on patient reactions to their cancer diagnosis. Few studies have<br />
examined the impact <strong>of</strong> lifetime traumatic events prior to diagnosis on how<br />
advanced cancer patients understand the life-threatening nature <strong>of</strong> their<br />
illness and how likely they are to discuss their end-<strong>of</strong>-life (EOL) wishes with<br />
their oncology providers. Methods: The Coping with Cancer (CwC) is an<br />
NCI-funded prospective, multi-institutional cohort study <strong>of</strong> advanced<br />
cancer patients and their caregivers. <strong>Part</strong>icipants were recruited from<br />
September 2002 to February 2008 from six comprehensive cancer centers<br />
across the United States. Lifetime traumas were captured by the number <strong>of</strong><br />
events reported in response to the Structured <strong>Clinical</strong> Interview for the<br />
DSM-IV (SCID) Lifetime Posttraumatic Stress Disorder question that<br />
probed for “extremely upsetting” life events. Associations between patient<br />
characteristics and number <strong>of</strong> lifetime traumas were estimated as odds<br />
ratios using ordinal logistic regression. Associations between number <strong>of</strong><br />
lifetime traumatic exposures, controlling for confounding patient characteristics,<br />
and patient Terminal Illness Acknowledgement (TIA) and reports <strong>of</strong><br />
EOL discussions were estimated as odds ratios using multiple logistic<br />
regression. Results: After adjusting for race, education, and recruitment<br />
site, the number <strong>of</strong> lifetime traumas patients reported remained significantly<br />
associated with TIA (OR � 1.25, p � .034) and discussion <strong>of</strong> EOL<br />
wishes (OR � 1.29, p � .013). Conclusions: The greater the number <strong>of</strong><br />
traumatic experiences reported by cancer patients the more likely they are<br />
to acknowledge that they are terminally ill and discuss their end-<strong>of</strong>-life<br />
wishes with their oncology providers. The impact <strong>of</strong> witnessing or experiencing<br />
serious or life-threatening events in the past appears to improve<br />
advanced cancer patients’ abilities to understand the seriousness <strong>of</strong> their<br />
condition and increases the likelihood that they will discuss their preferences<br />
for care at the end <strong>of</strong> life with their doctors.<br />
TPS9148 General Poster Session (Board #51F), Sat, 8:00 AM-12:00 PM<br />
Prospective and working memory decline as a result <strong>of</strong> impaired sleep<br />
and/or impared blood glucose in breast cancer patients during chemotherapy<br />
treatment. Presenting Author: Liliana Moyers-Ruiz, Bournemouth<br />
University/ Royal Bournemouth Hospital, Bournemouth, United Kingdom<br />
Background: Breast cancer patients might develop impaired sleep patterns<br />
during chemotherapy, and impaired cognitive function has been associated<br />
with sleep patterns disruption. It has been suggested that sleepiness (sleep<br />
tendency) in cancer patients is prevalent and causes distress in the<br />
patient’s quality <strong>of</strong> life, that and their cognitive abilities are also affected.<br />
Furthermore, increased blood glucose levels among women undergoing<br />
chemotherapy may contrubute to memory deficits in breast cancer patients.<br />
It is proposed that Prospective and Working Memory are being<br />
affected by the disturbance <strong>of</strong> these biological factors over the course <strong>of</strong><br />
chemotherapy. Methods: Ninety participants will be invited to take part in<br />
the study. Thirty will be breast cancer patients receiving chemotherapy<br />
treatment, thirty breast cancer patients receiving treatment other than<br />
chemotheray, and thirty healthy controls. Measures <strong>of</strong> sleep and sleepiness,<br />
will be administered at 4 testing sessions during a 9-month period,<br />
along with a neuropsychological battery. Additionally, blood samples will<br />
be analysed. Eight <strong>of</strong> planned 60 cancer patients have been enrolled, and<br />
four <strong>of</strong> them have completed the second testing session. For the assessment<br />
<strong>of</strong> sleep/wake activity, participants will be required to wear a sleeping<br />
monitor (sensewear armband) for 7 days. Pupil dilatation to observe<br />
sleepiness will be meassured by using a Pupillometry developed at Poole<br />
hospital in the UK. Prospective Memory will be assessed using CAMPROMT<br />
test to analyse if this is a more sensitive measure for mild cognitive<br />
impairment. Discussion: Impairment on variables such as sleep, sleepiness<br />
and glucose have not been studied within the context <strong>of</strong> Chemo-Brain on<br />
breast cancer patients.Therefore we want to observe whether impaired<br />
sleep and sleepiness, and impaired glucose levels are at the core <strong>of</strong><br />
Prospective and Working Memory decline in Chemo-Brain patients in order<br />
to find a cause-and-effect relationship as a consequence <strong>of</strong> chemotherapy.<br />
Patient and Survivor Care<br />
603s<br />
TPS9147 General Poster Session (Board #51E), Sat, 8:00 AM-12:00 PM<br />
Using cancer patient stories to “power” communication modules. Presenting<br />
Author: Forrest Lang, East Tennessee State University, Johnson City,<br />
TN<br />
Background: Caring for patients with cancer poses great challenges to<br />
doctors’ communication skills. This project, funded by NIH-NCI, represents<br />
an innovative collaboration between ETSU faculty in medical oncology,<br />
family medicine, and storytelling. The team secures patients’ and<br />
caregivers’ cooperation in recording stories <strong>of</strong> their journeys with illness.<br />
These are the focus <strong>of</strong> a set <strong>of</strong> cancer communication modules, to be<br />
<strong>of</strong>fered as educational experiences for medical students, residents, and<br />
oncology fellows. The modules in development address 1) breaking bad<br />
news, 2) living through treatment, 3) transitioning from curative to<br />
palliative care, 4) communicating with family, and 5) sensitivity to issues <strong>of</strong><br />
religion and spirituality. Methods: A collaborative inter-pr<strong>of</strong>essional team<br />
developed an interview protocol to facilitate sharing <strong>of</strong> cancer-themed<br />
narratives. Video records are transcribed and coded using N-Vivo 8. The<br />
rating team meets to identify video clips that speak powerfully to positive,<br />
negative, or ambivalent aspects <strong>of</strong> cancer communication. Selected patients<br />
are brought together into “story circles,” where additional narratives<br />
are gathered. The module development team uses these stories to create<br />
empathic involvement in viewers, and to sensitize them to effective and<br />
ineffective communication strategies and challenges surrounding critical<br />
moments in patients’ lived experience <strong>of</strong> cancer. Modules effectiveness is<br />
tested with 1) Family Medicine and Internal Medicine residents, 2) medical<br />
oncology fellows and 3) multi-pr<strong>of</strong>essionals health students just completing<br />
a communication courses. Assessment includes a pre-test and post-test<br />
OSCE addressing a number <strong>of</strong> the challenging cancer communication<br />
moments. Eighty-four <strong>of</strong> a projected 100 patient interviews and twelve<br />
physician//faculty interviews have been recorded, and all have agreed to the<br />
use <strong>of</strong> their interview materials. Representative examples <strong>of</strong> recorded<br />
cancer stories will be presented to demonstrate their evocative and<br />
pedagogical value. Opportunities will be discussed for further uses <strong>of</strong> these<br />
and similar stories in collaborations between medicine and the arts and<br />
humanities.<br />
TPS9149^ General Poster Session (Board #51G), Sat, 8:00 AM-12:00 PM<br />
CATCH: A randomized trial comparing tinzaparin versus warfarin for<br />
treatment <strong>of</strong> acute venous thromboembolism (VTE) in cancer patients.<br />
Presenting Author: Agnes Y. Lee, University <strong>of</strong> British Columbia, Vancouver,<br />
BC, Canada<br />
Background: VTE is a major cause <strong>of</strong> morbidity and mortality in cancer<br />
patients. LMWHs have been shown to be superior to warfarin in one<br />
randomized study, but adequately powered confirmatory studies have not<br />
been conducted and warfarin continues to be widely used for treatment <strong>of</strong><br />
cancer-associated VTE. Methods: We are conducting an open-label, randomized<br />
trial <strong>of</strong> tinzaparin versus warfarin in 900 patients with active cancer<br />
and symptomatic proximal deep vein thrombosis (DVT) and/or pulmonary<br />
embolism (PE). Tinzaparin is given at full treatment doses (175 IU/kg once<br />
daily) for 6 months in the experimental arm and initial tinzaparin treatment<br />
for 5-10 days followed by dose-adjusted warfarin (target INR 2.0-3.0) is<br />
given for 6 months in the control arm. The primary composite outcome is<br />
time to recurrent VTE event, including incidentally diagnosed VTE and fatal<br />
PE. Baseline characteristics will be analysed for their ability to predict the<br />
risk for recurrent VTE or bleeding. In particular, the parameters <strong>of</strong> the<br />
Khorana scale and Wells rule will be tested for their usefulness in<br />
predicting recurrent VTE. Predictive biomarkers will be tested including<br />
D-dimer and Tissue Factor. Assessment <strong>of</strong> post-thrombotic syndrome<br />
(PTS), quality <strong>of</strong> life and healthcare resource utilization will also be<br />
performed. The trial is recruiting in � 160 sites in �25 countries in 4<br />
continents (NCT01130025). As <strong>of</strong> Jan 2012, 135 sites were activated for<br />
study enrolment and 228 patients have been enrolled. We anticipate<br />
completion <strong>of</strong> enrolment in Jan 2013. The results obtained from this study<br />
will add significantly to the knowledge on the efficacy, safety and<br />
cost-effectiveness <strong>of</strong> LMWH to prevent recurrent VTE. Important prospective<br />
data on the clinical significance <strong>of</strong> incidental VTE in patients with<br />
active cancer will be generated, and analyses <strong>of</strong> risk stratification parameters<br />
will add important information that may help to further tailor therapy.<br />
The study <strong>of</strong> PTS, which has not previously been done in this selected<br />
patient population, will add to the evidence that tinzaparin significantly<br />
reduces the incidence <strong>of</strong> PTS and leg ulcers (Hull et al, Am J Med<br />
2009;122:762-9).<br />
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