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Annual Meeting Proceedings Part 1 - American Society of Clinical ...

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570s Patient and Survivor Care<br />

9012 <strong>Clinical</strong> Science Symposium, Sat, 3:00 PM-4:30 PM<br />

Prognostic factors <strong>of</strong> the loss <strong>of</strong> autonomy (LoA) in older patients with<br />

cancer receiving first-line chemotherapy. Presenting Author: Pierre-Louis<br />

Soubeyran, Institut Bergonie, Bordeaux, France<br />

Background: Actual data on prognostic geriatric factors <strong>of</strong> health outcomes<br />

are lacking. We aimed to examine whether a decrease in autonomy for<br />

activities <strong>of</strong> daily living (ADL) after a first cycle <strong>of</strong> chemotherapy influences<br />

elderly cancer pts prognosis, and to determine prognostic factors <strong>of</strong> this<br />

LoA from a range <strong>of</strong> biological and geriatric evaluation factors. Methods:<br />

Pts� 70 years receiving 1st-line chemotherapy for a range <strong>of</strong> cancers were<br />

included in this multicentre prospective study. A LoA was defined as a<br />

decrease <strong>of</strong> 0.5 or more points on the ADL scale between the beginning <strong>of</strong><br />

treatment and the 2nd cycle (ADL scored 6 to 0). The association between<br />

a LoA and OS was examined and prognostic factors were sought from the<br />

pre-treatment Geriatric Assessment data (CIRS-G, IADL, MNA, MMSE,<br />

GDS et Get up and Go) and from baseline biological and clinical information<br />

(age, sex, tumor extension and localization, performance status, BMI,<br />

weight loss, albumin, CRP, haemoglobin levels, leucocyte and platelet<br />

count, creatinine clearance). Pts completely dependent at baseline (ADL<br />

score 0) were excluded as a LoA was not possible. Results: Among 364 pts<br />

included, 299 pts were evaluable and 50 experienced a LoA. A LoA was<br />

significantly associated with an increased risk <strong>of</strong> death (RR 1.518,<br />

95%CI[1.079-2.135]). Biological and clinical factors were not associated<br />

with LoA but pre-treatment low GDS15, dependencies on the IADL, low<br />

MMS, slow Get Up and Go, low ECOG-PS and poor MNA were found to be<br />

prognostic <strong>of</strong> a LoA in univariate analyses. In the multivariate model, low<br />

GDS (OR 2.4, p�0.01, 95%CI [1.23-4.66]) and dependencies on the<br />

IADL (OR 3.0, p� 0.027, 95%CI � [1.13-9.09]) were independently<br />

associated with an increased risk <strong>of</strong> LoA. Conclusions: Our study underlines<br />

the close link between LoA during treatment and poorer prognosis <strong>of</strong> elderly<br />

pts with cancer. Pts with a pre-treatment low GDS15 and IADL-dependent<br />

were the most likely to experience LoA after the 1st chemotherapy cycle.<br />

This research suggests that the GDS15 and IADL should be included as<br />

part <strong>of</strong> any screening for elderly pts before treatment.<br />

9014 <strong>Clinical</strong> Science Symposium, Tue, 9:45 AM-11:15 AM<br />

Falls, physical performance deficits, and functional losses in cancer<br />

survivors with chemotherapy-induced neuropathy (CIPN): A University <strong>of</strong><br />

Rochester CCOP study. Presenting Author: Supriya Gupta Mohile, University<br />

<strong>of</strong> Rochester Medical Center, Rochester, NY<br />

Background: CIPN impairs quality <strong>of</strong> life in cancer survivors. Little is known<br />

about the prevalence <strong>of</strong> falls, physical performance (PP) deficits, and<br />

functional losses or their association with CIPN toxicities in cancer<br />

survivors. Methods: We conducted an analysis <strong>of</strong> baseline assessments from<br />

a phase III randomized clinical trial in cancer survivors with CIPN self<br />

reported pain scores <strong>of</strong> � 4 reflecting leg and foot pain from neuropathy<br />

over the past 24 hours on a scale from 0 (“no pain”) to 10 (“pain as bad as<br />

you can imagine”). Patients also completed EORTC QLQ-CIPN-20 sensory<br />

and motor scales for neuropathy toxicities and self reported falls in the<br />

previous 3 months. A PP deficit was defined as “a lot <strong>of</strong> difficulty” or<br />

“unable to do” any <strong>of</strong> 6 physical tasks (e.g., lifting objects, walking a<br />

quarter <strong>of</strong> a mile). Functional losses were defined as “a lot <strong>of</strong> difficulty” or<br />

“unable to do” any <strong>of</strong> 5 functional tasks (e.g., managing money, bathing).<br />

We examined the association <strong>of</strong> baseline characteristics and CIPN toxicities<br />

with falls, PP deficits and functional losses using logistic regression.<br />

Results: Of 421 patients, 11.9% experienced recent falls, 58.6% reported<br />

a PP deficit, and 26.6% reported a functional loss. Patients with falls<br />

and/or PP deficits were more likely to be older (mean age 60.9 vs 58.9,<br />

p�0.02), female (75.3% vs 65.2%, p�0.03) and have less education<br />

(�high school: 7.1% vs 0.6%, p�.01). Cancer and chemotherapy history<br />

were not different between groups. Patients with falls and/or PP deficits<br />

reported higher severity <strong>of</strong> CIPN toxicities: pain (6.82 vs 6.05, p�0.01),<br />

sensory (23.3 vs 19.6, p�0.01), and motor (17.4 vs 12.7, p�0.01). In<br />

multivariable analysis, factors associated with having a fall and/or PP<br />

deficit included: older age (OR 1.03, p�0.04), low education (OR 9.34,<br />

p�0.04), and motor toxicity (OR 1.21, p�0.01). Factors associated with<br />

functional losses included: non-white race (OR 3.16, p�0.01), Hispanic<br />

ethnicity (OR 5.32, p�0.05), motor toxicity (OR 1.19, p�0.01), and PP<br />

deficit (OR 4.94, p�.01). Conclusions: CIPN toxicities, primarily motor, are<br />

significantly associated with falls, physical performance deficits, and<br />

functional losses.<br />

CRA9013 <strong>Clinical</strong> Science Symposium, Tue, 9:45 AM-11:15 AM<br />

CALGB 170601: A phase III double blind trial <strong>of</strong> duloxetine to treat painful<br />

chemotherapy-induced peripheral neuropathy (CIPN). Presenting Author:<br />

Ellen M. Lavoie Smith, University <strong>of</strong> Michigan, Ann Arbor, MI<br />

The full, final text <strong>of</strong> this abstract will be available at<br />

abstract.asco.org at 12:01 AM (EDT) on Monday, June 4,<br />

2012, and in the <strong>Annual</strong> <strong>Meeting</strong> <strong>Proceedings</strong> online<br />

supplement to the June 20, 2012, issue <strong>of</strong> Journal <strong>of</strong><br />

<strong>Clinical</strong> Oncology. Onsite at the <strong>Meeting</strong>, this abstract will<br />

be printed in the Monday edition <strong>of</strong> ASCO Daily News.<br />

9015 <strong>Clinical</strong> Science Symposium, Tue, 9:45 AM-11:15 AM<br />

Rates and risks <strong>of</strong> suicidality in young adults (YAs) with advanced cancer.<br />

Presenting Author: Kelly Marie Trevino, Dana-Farber Cancer Institute,<br />

Boston, MA<br />

Background: Suicide rates in YA cancer patients are higher than in the<br />

general population. Although cancer is associated with a four-fold increase<br />

in the likelihood <strong>of</strong> a suicide attempt, little is known about suicidality in<br />

YAs with cancer. This study examined rates and clinical risk factors<br />

associated with suicidality in a sample <strong>of</strong> YAs with advanced cancer.<br />

Methods: Structured interviews were conducted between 4/2010 and<br />

9/2011 with 70 YA advanced cancer patients (range 20-40 yrs, M�33.97,<br />

SD�5.61) receiving care at the Dana-Farber Cancer Institute. Validated<br />

measures assessed suicidality (i.e., Yale Evaluation <strong>of</strong> Suicidality), quality<br />

<strong>of</strong> life, major depressive disorder, grief over cancer-related losses, and<br />

social support. Scores on the suicidality measure were dichotomized into<br />

positive screen � 1 and negative screen � 0. Chi-square, t-test, and<br />

logistic regression analyses evaluated the relationship between suicidality<br />

and participant characteristics and psychosocial variables, controlling for<br />

confounding variables. Results: Over one-fifth (21.4%) <strong>of</strong> the sample<br />

screened positive for suicidality. Female gender �2 (1, N � 70) � 4.95, p �<br />

.026), breast compared with other cancer diagnosis �2 (1, N � 70) � 5.66,<br />

p � .017), and better performance status (t(68) � 3.13, p � .01) were<br />

associated with lower rates <strong>of</strong> suicidality. <strong>Part</strong>icipants who met criteria for<br />

current (OR [95% CI] 8.67 [1.78, 42.22]) or lifetime major depressive<br />

disorder (5.38 [1.60, 18.12]) endorsed higher rates <strong>of</strong> suicidality. Better<br />

overall (.97 [.94, .99]), psychological (.93 [.87, .94]), and existential<br />

quality <strong>of</strong> life (.91 [.85, .98]) were associated with reduced suicidality risk.<br />

More severe grief was associated with greater risk (1.15 [1.04, 1.28])<br />

whereas greater social support was associated with lower suicidality risk<br />

(.85 [.74, .97]). Conclusions: YAs with advanced cancer reported higher<br />

rates <strong>of</strong> suicidality than observed in other age groups. Developmentally<br />

targeted interventions that promote physical function, effectively treat<br />

depression, improve quality <strong>of</strong> life and reduce grief, and provide opportunities<br />

for social support may reduce rates <strong>of</strong> and risk for suicidality in this<br />

population.<br />

Visit abstract.asco.org and search by abstract for the full list <strong>of</strong> abstract authors and their disclosure information.

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