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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6052 General Poster Session (Board #3A), Mon, 1:15 PM-5:15 PM<br />
Influence <strong>of</strong> comorbidity on guideline concordant care for breast cancer:<br />
Findings from the Center for Disease Control and Prevention National<br />
Program <strong>of</strong> Cancer Registry (NPCR) patterns <strong>of</strong> care study. Presenting<br />
Author: Gretchen Genevieve Kimmick, Duke University Medical Center,<br />
Durham, NC<br />
Background: Comorbidity burden predicts cancer treatment and may<br />
influence outcome. We explore the relationship <strong>of</strong> specific comorbid<br />
illnesses with receipt <strong>of</strong> guideline concordant care for early stage breast<br />
cancer. Methods: The NPCR’s Patterns <strong>of</strong> Care study reabstracted the<br />
medical records <strong>of</strong> breast cancer cases diagnosed in 2004 from 7 cancer<br />
registries. We included women with nonmetastatic in situ and invasive<br />
breast cancer, known hormone receptor status, node status, and tumor<br />
size. Guideline-concordant management, including surgery, radiation,<br />
chemotherapy and endocrine components, was based on NCCN guidelines<br />
using tumor size, nodal and hormone receptor status. Comorbidity was<br />
measured according to the Adult Comorbidity Evaluation Index (ACE).<br />
Multivariate logistic regression models were used to determine factors<br />
associated with guideline-concordant care, and included overall ACE<br />
scores and 26 separate ACE comorbidity categories, as well as age, race,<br />
hormone receptor status, and HER2 status. Results: The study sample<br />
included 6904 women (mean age 58.7 and range 20-99 years, 76% white,<br />
45% with ACE comorbidity score <strong>of</strong> 0, 70% ER and/or PR�, 13%<br />
HER2�). Overall, 64% received guideline-concordant care. Receipt <strong>of</strong><br />
guideline-concordant care varied by overall comorbidity burden (71% for<br />
none; 65% for minor; 63% for moderate; 50% for severe; p�0.05). The<br />
presence <strong>of</strong> hypertension (OR 1.26, 95% CI 1.08-1.48) predicted receipt<br />
<strong>of</strong> guideline concordant care, whereas, peripheral artery disease (OR 0.44,<br />
95% CI 0.21-0.93), diabetes (OR 0.78, 95% CI 0.63-0.97) and dementia<br />
(OR 0.31, 95% CI 0.13-0.74) predicted lack <strong>of</strong> guideline concordant care.<br />
Older age, black race, and hormone receptor positivity were associated with<br />
less, and HER2 positivity with receipt <strong>of</strong> more guideline-concordant care.<br />
Conclusions: Overall those with more comorbidity burden received less<br />
guideline-concordant care. However, the effects vary by specific conditions.<br />
The odds <strong>of</strong> receiving guideline-concordant care was greater in those<br />
with hypertension and less in those with peripheral arterial disease,<br />
diabetes, and dementia.<br />
6054 General Poster Session (Board #3C), Mon, 1:15 PM-5:15 PM<br />
A brief educational intervention to increase communication about complementary<br />
and alternative medicine (CAM) in community oncology settings.<br />
Presenting Author: Lorenzo Cohen, University <strong>of</strong> Texas M. D. Anderson<br />
Cancer Center, Houston, TX<br />
Background: The widespread use <strong>of</strong> CAM in academic oncology settings has<br />
been well documented. However, there is a lack <strong>of</strong> communication between<br />
patients and health care pr<strong>of</strong>essionals on CAM that may have negative<br />
health consequences. No comprehensive study <strong>of</strong> CAM use in community<br />
oncology settings exists. We examined the benefits <strong>of</strong> a brief educational<br />
intervention on nurse discussions <strong>of</strong> CAM with patients. Methods: A<br />
multi-site, randomized trial <strong>of</strong> an educational intervention (brief video,<br />
resource list) designed to encourage oncology nurses to discuss CAM use<br />
with their patients was conducted within the MD Anderson CCOP network.<br />
Nurses (N�175) and patients (baseline N�699 and different set <strong>of</strong><br />
patients after intervention N�650) completed questions about CAM use,<br />
communication, and knowledge. Results: Nurses were 97% female, 96%<br />
non-Hispanic white. Two months after the intervention, nurses in the<br />
intervention group reported that they were more likely to ask about CAM use<br />
than those in the control group (OR�4.2; p�.005) and asked more <strong>of</strong> their<br />
last 5 patients about CAM use (p�.003). No significant intervention effect<br />
was found for the proportion <strong>of</strong> patients in the clinic who indicated they<br />
were asked about CAM use after the intervention (OR�1.6, p�.10).<br />
Approximately 40% <strong>of</strong> patients reported using CAM following their cancer<br />
diagnosis yet the majority <strong>of</strong> nurses estimated less than 25% <strong>of</strong> their<br />
patients used CAM. Conclusions: CAM use in community-based oncology<br />
patients is high and there is an underestimation <strong>of</strong> use by the oncology<br />
nurses. This very brief intervention significantly improved how <strong>of</strong>ten nurses<br />
reported asking patients about their CAM use. However, the patients <strong>of</strong> the<br />
nurses did not reflect this change in communication. Additional types <strong>of</strong><br />
interventions are needed to increase communication between patients and<br />
nurses.<br />
Health Services Research<br />
395s<br />
6053 General Poster Session (Board #3B), Mon, 1:15 PM-5:15 PM<br />
Examining patient choices for metastatic breast cancer drugs. Presenting<br />
Author: Mary Lou Smith, Research Advocacy Network, Plano, TX<br />
Background: Patients with metastatic breast cancer face difficult drug<br />
decisions. Our previous research (ASCO Proc 2011, abstr 6044) focused<br />
on general benefit and toxicity showed that conjoint analysis (CA) allows<br />
patients to express preferences; our current research quantifies patient<br />
preference for specific drug pr<strong>of</strong>iles (capecitabine and paclitaxel). Methods:<br />
Research Advocacy Network and CBWhite conducted research using CA for<br />
DOD Center <strong>of</strong> Excellence for Individualization <strong>of</strong> Therapy in Breast Cancer.<br />
An online survey was sent by four breast cancer organizations (N�641).<br />
Questions elicited views on trade-<strong>of</strong>fs between benefit and type/severity/<br />
duration <strong>of</strong> toxicity. CA questions present pairs <strong>of</strong> hypothetical treatments<br />
and ask respondents their preferred alternative; a follow-up question asks<br />
whether the person would take the treatment if it were the only option<br />
available. Analysis <strong>of</strong> response patterns allows study <strong>of</strong> treatment preferences<br />
for combinations <strong>of</strong> benefit and described toxicity. Results: See table.<br />
Preferences show much greater attention to benefit than to toxicity. When<br />
CA is used to examine impact <strong>of</strong> biomarkers, focus on benefit continues.<br />
Paclitaxel pr<strong>of</strong>ile (IV) set with moderate PN lasting 1 year post treatment:<br />
with 33% benefit LH, 6% <strong>of</strong> respondents change treatment decision if<br />
biomarker predicts 27% vs 60% toxicity likelihood; with 27% toxicity LH,<br />
22% <strong>of</strong> respondents change treatment decision if biomarker predicts 20%<br />
vs 50% benefit likelihood. Conclusions: For patients with metastatic<br />
disease, CA shows much greater attention to benefit than toxicity, and high<br />
likelihood to take treatment with at least 30% chance <strong>of</strong> benefit for any<br />
toxicity tested here. These results suggest biomarkers (for the pr<strong>of</strong>iled<br />
drugs) predicting benefit are more likely to be used to affect patient<br />
treatment decisions than biomarkers for toxicity.<br />
Prediction <strong>of</strong> % selecting treatment with benefit and toxicity likelihood (LH)<br />
under two scenarios (N�641).<br />
10%<br />
Toxicity LH<br />
20% 40% 60%<br />
IV drug pr<strong>of</strong>ile—moderate peripheral neuropathy (PN) for 1 year<br />
Benefit LH<br />
20% N/A 77.4 72.3 65.3<br />
30% N/A 89.8 86.4 81.6<br />
50% N/A 97.1 96.1 94.3<br />
Oral drug pr<strong>of</strong>ile—moderate Hand-Foot Syndrome during treatment<br />
10% 67.6 65.2 60.8 N/A<br />
30% 94.7 93.0 91.4 N/A<br />
50% 99.0 98.3 97.4 N/A<br />
6055 General Poster Session (Board #3D), Mon, 1:15 PM-5:15 PM<br />
Self-reported conflicts <strong>of</strong> interest (sfCOI) <strong>of</strong> authors and the interpretation<br />
<strong>of</strong> randomized phase III trials (RCT) and related editorials (REd) in cancer<br />
research. Presenting Author: Giovanni Mendonca Bariani, Instituto do<br />
Cancer do Estado de Sao Paulo, Sao Paulo, Brazil<br />
Background: Growing participation from industry in cancer research has<br />
resulted in increased reporting <strong>of</strong> COI. We aimed to test any association<br />
between author’s conclusion and sfCOI in cancer studies. Methods: All RCT<br />
and REd published in 6 major cancer journals in a 3.5 year period were<br />
selected. Two investigators blinded to COI disclosure independently<br />
analyzed each RCT and REd, classifying authors’ conclusions as highly<br />
positive, positive, neutral, negative, and highly negative with respect to<br />
author’s opinion on the experimental therapy. The agreement rate between<br />
investigators for conclusion classification was 90% (consensus was achieved<br />
for the remaining 10%). We also collected data on study results, COI and<br />
sponsorship. COI was defined as any self-reported financial tie between<br />
author and industry except for research funds. Predictors <strong>of</strong> positive/highly<br />
positive conclusions <strong>of</strong> RCT and <strong>of</strong> REd were tested separately in logistic<br />
regression multivariable models. Results: From Jan 2008 to Oct 2011,<br />
1,485 articles were retrieved: 150 RCT and 140 REd were eligible. Among<br />
the RCT, 82 (55%) were positive, and 78 (52%) were entirely or partially<br />
funded by industry. Any sfCOI was present in 103 (69%) RCT and in 71<br />
(47%) REd. Conclusions <strong>of</strong> REd and RCT were: 7.3% and 11.3% highly<br />
positive, 42.7% and 57.3% positive, 8.0% and 2.0% neutral, 29.3% and<br />
18.7% negative, and 12.7% and 10.7% highly negative, respectively.<br />
Multivariable analysis showed that RCT positive result was the only<br />
significant predictor for positive conclusion by RCT authors (OR�109,<br />
95% CI: 21-567; p�0.001). The only factor associated with positive<br />
conclusions <strong>of</strong> REd authors was a positive conclusion by RCT author<br />
(OR�42, 95% CI: 7-244; p�0.001). While 64 (43%) RCT reported<br />
negative results, 103 (68.7%) RCT authors interpreted studies positively.<br />
Logistic regression for discordance between RCT result and RCT conclusion<br />
did not find any association with COI. Conclusions: Theinterpretation <strong>of</strong> RCT<br />
results by authors was not influenced by sfCOI or trial sponsorship. Authors<br />
<strong>of</strong> REd were not influenced by study results or by their sfCOI when<br />
discussing cancer RCT.<br />
Visit abstract.asco.org and search by abstract for the full list <strong>of</strong> abstract authors and their disclosure information.