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

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6077 General Poster Session (Board #6B), Mon, 1:15 PM-5:15 PM<br />

Cost-effectiveness <strong>of</strong> biomarker-directed bevacizumab for first-line therapy<br />

<strong>of</strong> persons with metastatic colorectal cancer. Presenting Author: Kristin<br />

Berry, Fred Hutchinson Cancer Research Center, Seattle, WA<br />

Background: When added to first-line chemotherapy for metastatic colorectal<br />

cancer, bevacizumab provides a moderate survival increase, but is<br />

associated with significant adverse events and high cost. As only a minority<br />

<strong>of</strong> patients respond to antiangiogenic therapy, a diagnostic that identifies<br />

potential responders ex ante could potentially change the benefit to risk<br />

pr<strong>of</strong>ile <strong>of</strong> bevacizumab and likely improve cost-effectiveness. Since efforts<br />

to identify a predictive test have so far been unsuccessful, a novel strategy<br />

may be to measure tumor response after bevacizumab treatment initiation<br />

using an in vivo biomarker test to guide decisions on whether patients<br />

should continue treatment. The objective is to estimate the costeffectiveness<br />

<strong>of</strong> biomarker-directed use <strong>of</strong> bevacizumab in first-line treatment<br />

<strong>of</strong> metastatic colorectal cancer compared to standard care. Methods:<br />

The analysis takes the perspective <strong>of</strong> the US healthcare system. A decision<br />

model was built to estimate the incremental effect <strong>of</strong> adding bevacizumab<br />

to IFL, FOLFIRI, 5FU/LV and FOLOFOX/XELOX regimens. Survival data,<br />

estimated through a meta-analysis <strong>of</strong> four clinical trials, combined with<br />

utilities from the literature were used to calculate quality-adjusted life<br />

years (QALYs). Costs were based on Medicare reimbursement and expert<br />

opinion. Assumed performance characteristics <strong>of</strong> the biomarker technology<br />

(sensitivity, specificity – provided by our industry partner) were 75% and<br />

95% 10 days after commencement <strong>of</strong> bevacizumab. Results: The biomarkerdirected<br />

bevacizumab strategy dominated usual care, providing both an<br />

average per patient gain <strong>of</strong> 0.015 QALYs and a cost-savings <strong>of</strong> $21,038.<br />

The cost-effectiveness <strong>of</strong> the biomarker technology was most influenced by<br />

the cost <strong>of</strong> the test and colorectal cancer utilities. Variations in biomarker<br />

specificity and sensitivity changed the magnitude <strong>of</strong> cost-savings and<br />

benefit gain but did not change the overall result <strong>of</strong> dominance. Conclusions:<br />

Modeling predicts that a validated marker which could identify responders<br />

to bevacizumab will save money and improve quality-adjusted life years.<br />

The results support additional investment in identifying such a diagnostic.<br />

6079 General Poster Session (Board #6D), Mon, 1:15 PM-5:15 PM<br />

Surveillance after potentially curative breast cancer treatment: The impact<br />

<strong>of</strong> HMOs. Presenting Author: Robert J. Avino, Saint Louis University, St.<br />

Louis , MO<br />

Background: Over 230,000 new cases <strong>of</strong> breast cancer are diagnosed in the<br />

US annually. Most patients receive curative-intent treatment. Posttreatment<br />

surveillance is commonly done. We have previously documented<br />

dramatic variation in surveillance intensity among ASCO experts. The only<br />

surveillance modalities endorsed by ASCO for asymptomatic patients are<br />

<strong>of</strong>fice visit and mammogram. It is commonly believed that health maintenance<br />

organizations (HMOs) restrict test utilization. We sought to determine<br />

the effect <strong>of</strong> HMO penetration rate on the known variation in<br />

surveillance strategies. Methods: The 3245 ASCO members who indicated<br />

that breast cancer was a major clinical focus <strong>of</strong> their practice were surveyed<br />

regarding their surveillance practices. Members were asked to consider 4<br />

idealized clinical vignettes and indicate their surveillance plan for each. A<br />

menu <strong>of</strong> 12 testing modalities was <strong>of</strong>fered. Practice patterns were stratified<br />

by HMO penetration rate (0-14%, 14-22%, 22-33%, 33-61%) in each<br />

physician’s practice location. Repeated-measures ANOVA was employed<br />

for analysis. Results: Of the ASCO members surveyed, 1012 responded;<br />

915 were evaluable. The modalities most frequently recommended were<br />

<strong>of</strong>fice visit, CBC, liver function tests (LFTs), and diagnostic mammogram.<br />

There was significant variation (p�0.05) in the recommended frequency <strong>of</strong><br />

utilization <strong>of</strong> diagnostic mammogram, but in no other modalities. For<br />

example, in year 1, diagnostic mammogram was recommended 1.9 � 1.8<br />

(mean �SD) times for the 0-14% penetration rate cohort and 1.5 � 1.1<br />

times for the 14-22% cohort. Conclusions: We found little evidence that<br />

HMOs restrict test utilization. The HMO penetration rate in the clinician’s<br />

practice location cannot account for the overall variation we have documented<br />

previously.<br />

Health Services Research<br />

401s<br />

6078 General Poster Session (Board #6C), Mon, 1:15 PM-5:15 PM<br />

Deviations from guideline-based therapy for febrile neutropenia in cancer<br />

patients. Presenting Author: Jason D. Wright, Columbia University College<br />

<strong>of</strong> Physicians and Surgeons, New York, NY<br />

Background: Febrile neutropenia (FN) is a common cause <strong>of</strong> morbidity in<br />

cancer patients. We examined guideline and non-guideline based care for<br />

cancer patients hospitalized with FN and examined how treatment influenced<br />

outcomes. Methods: The Perspective database was used to examine<br />

the treatment <strong>of</strong> solid tumor patients with FN from 2000-2010. To capture<br />

initial decision-making, we examined treatment within 48 hrs <strong>of</strong> admission.<br />

Based on evidence-based guidelines we determined the appropriate<br />

use <strong>of</strong> guideline-based antibiotics as well as use <strong>of</strong> treatments not routinely<br />

recommended, vancomycin and granulocyte-colony stimulating factors<br />

(GCSF). Hierarchical mixed effects models were developed to examine the<br />

influence <strong>of</strong> patient, physician, and hospital characteristics on the quality<br />

<strong>of</strong> treatment. Patients were stratified into low and high-risk groups and the<br />

effect <strong>of</strong> initial treatment on outcome (nursing home discharge and death)<br />

examined. Results: Among 25,231 patients with FN, within 48 hours <strong>of</strong><br />

admission blood cultures were obtained in 90%, guideline-based antibiotic<br />

administered to 79%, vancomycin to 37%, and GCSF to 63%. Patients<br />

treated at high-volume hospitals, by high-volume physicians and patients<br />

managed by hospitalists were more likely to receive guideline-based<br />

antibiotics (p�0.05). Vancomycin use increased with time from 17% in<br />

2000 to 55% in 2010 while GCSF use only decreased from 73% to 55%.<br />

Patients treated by internists and hospitalists were more likely to receive<br />

vancomycin; high-volume physicians were less likely to treat with both<br />

vancomycin and GCSF (p�0.05). Among patients who received GCSF,<br />

15% received only one dose and 22% received 2 doses <strong>of</strong> filgrastim.<br />

Among low-risk patients prompt initiation <strong>of</strong> guideline-based antibiotics<br />

decreased the risk <strong>of</strong> discharge to a nursing facility (OR�0.78; 95% CI,<br />

0.66-0.91) and death (OR�0.65; 95% CI, 0.50-0.85). Conclusions: There<br />

is substantial variability in the initial treatment for FN in cancer patients.<br />

While use <strong>of</strong> appropriate empiric antibiotics is high, use <strong>of</strong> non guidelinebased<br />

treatments such as vancomycin and GCSF are common. Physician<br />

and hospital factors are the most important predictors <strong>of</strong> both guideline and<br />

non guideline-based treatment.<br />

6080 General Poster Session (Board #6E), Mon, 1:15 PM-5:15 PM<br />

The relationship between symptom burden and perceived comorbidity in<br />

outpatients with common solid tumors. Presenting Author: Christine<br />

Ritchie, Unviersity <strong>of</strong> California, San Francisco, San Francisco, CA<br />

Background: Cancer patients have high symptom burden, but it is unclear<br />

whether comorbid conditions are associated with patient-reported symptom<br />

burden (the number and severity <strong>of</strong> symptoms). Methods: The Eastern<br />

Cooperative Oncology Group (ECOG) enrolled 3106 patients with invasive<br />

cancer <strong>of</strong> the breast, colon/rectum, prostate and lung, regardless <strong>of</strong> phase<br />

<strong>of</strong> care or stage <strong>of</strong> disease. At baseline, patients completed the M.D.<br />

Anderson Symptom Inventory (MDASI) and were also asked how bothered<br />

they were by difficulties related to health problems other than cancer.<br />

Symptom burden (SB) was defined as the number <strong>of</strong> symptoms scored 7 or<br />

higher on the 13-item MDASI physical scale. Variance-weighted least<br />

squares regression was used to identify factors associated with increasing<br />

levels <strong>of</strong> being bothered by comorbid conditions. Results: About 65% <strong>of</strong><br />

patients were at least a little bothered by symptoms associated with<br />

comorbidities. There was a strong association between increased bother by<br />

comorbidities and increased SB (p�0.0001). Among those not bothered<br />

by difficulties related to comorbidities, �1 symptom was rated 7 or worse<br />

by 29% <strong>of</strong> patients, compared to 51% in patients bothered by difficulties<br />

related to comorbidities (Fisher’s exact p�0.0001). Except for hair loss,<br />

the severity <strong>of</strong> all symptoms was higher in those patients reporting bother<br />

due to other perceived comorbidities. Factors associated with increased<br />

bother include SB (p�0.0001), taking medications for diabetes<br />

(p�0.0001), impaired ECOG performance status (p�0.03), older age<br />

(p�0.004), and being perceived by the clinician as having higher degree <strong>of</strong><br />

difficulty for providing care (p�0.0001). Conclusions: Symptom burden<br />

varies significantly according to the degree to which cancer patients<br />

perceive bother that they attribute to comorbid health problems. Perception<br />

<strong>of</strong> comorbidity is worth exploring as a stratification factor in symptom<br />

research and as an indicator for complexity in patient care.<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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