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Cancer program annual report 2010 - Evangelical Community Hospital

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Quality Measure Analysis<br />

Lymph node harvest:<br />

Regarding the first of the aforementioned quality<br />

measures—harvest and analysis of at least 12 lymph<br />

nodes in the resected specimen—<strong>Evangelical</strong> shows<br />

room for improvement: Of all cancers resected at<br />

<strong>Evangelical</strong>, 32 percent were found to have at least 12<br />

lymph nodes in the specimen. The above data include<br />

Stage 0 cancers, which, in essence, represent incidental<br />

findings of carcinoma in polyps<br />

resected endoscopically, which<br />

then go on to oncologic<br />

resection secondary to an<br />

inability to assess for complete<br />

excision on the colonoscopically<br />

resected specimen. One can<br />

argue that such scenarios<br />

should be excluded as there is<br />

no residual carcinoma identified<br />

on the final pathology;<br />

disregarding the Stage 0<br />

resections, however, results in only nominal elevation<br />

of percentage of specimens removed with the requisite<br />

number of lymph nodes: 43 percent.<br />

Lymph node harvests in<br />

excess of 12 nodes have<br />

been shown to increase<br />

survival as a result of<br />

their staging properties.<br />

The author of this <strong>report</strong> undertook analysis of the<br />

data available insofar as the impact of the surgeon,<br />

pathologist and site of the primary tumor was concerned<br />

regarding lymph node harvest. The data demonstrated<br />

no clear trend with respect to the impact of the surgeon<br />

or the pathologist in question. Regarding the site of<br />

the primary tumor, sigmoid resections demonstrated<br />

the largest lymph node harvest with an average of 23<br />

lymph nodes per specimen; this was followed closely by<br />

right colectomies, which demonstrated an average of<br />

14 lymph nodes per specimen.<br />

Discussions have ensued regarding the handling of<br />

pathologic specimens by the pathologists, and it has<br />

been determined that measures are in place to ensure<br />

maximal nodal harvest from the surgical specimen,<br />

namely that of de-fatting protocols to assist in the<br />

identification of mesenteric lymph nodes.<br />

Per the guidelines of the National Comprehensive<br />

<strong>Cancer</strong> Network (NCCN), lymph node harvests in excess<br />

of 12 nodes have been shown to increase survival<br />

as a result of their staging<br />

properties; counter-arguments<br />

would state that adequate<br />

lymph node harvest acts as a<br />

surrogate marker for adequate<br />

resection and, accordingly,<br />

inadequate nodal harvest<br />

reflects inadequate oncologic<br />

resection, thereby leading to<br />

inferior outcomes insofar as<br />

survival is concerned. While it<br />

is a fine point to argue, current<br />

guidelines do recommend for adjuvant chemotherapy in<br />

patients resected with inadequate nodal harvests; this,<br />

in essence, is an argument as to whether or not to treat<br />

Stage II cancers with fewer than 12 lymph nodes in the<br />

resected specimen.<br />

With the advent of novel assays such as the Oncotype<br />

dx colon cancer genomic assay, one could argue the<br />

value of lymph node harvest for Stage II colon cancers.<br />

In essence, the Oncotype dx colon cancer assay is<br />

a genomic assay that assesses the propensity of<br />

recurrence of the primary tumor following resection. A<br />

score is generated based on the assay results, and this<br />

score predicts the probability of local recurrence within<br />

a 36-month period. A lower score portends a lower<br />

likelihood of recurrence. This assay has been utilized by<br />

the author of this <strong>report</strong> to help determine the utility of<br />

adjuvant chemotherapy in Stage II colon cancers with<br />

a great degree of success (admittedly, though, with<br />

a very small cohort of patients). The advocacy of the<br />

NCCN insofar as KRAS mutation and mismatch repair<br />

gene testing is concerned pays homage to the potential<br />

significance of genetic markers and their impact on<br />

colon cancer treatment.<br />

Adjuvant chemotherapy for Stage III cancer:<br />

Eight patients under the age of 80 were surgically resected<br />

for Stage III disease and 100 percent of these patients<br />

were referred for evaluation by Medical Oncology for<br />

the consideration of adjuvant chemotherapy. Complete<br />

compliance in this regard is enthusiastically endorsed<br />

by the author, accompanied by an insatiable desire to<br />

<strong>report</strong> identical results in the ensuing years.<br />

Radiation therapy for rectal cancer:<br />

Zero out of one cases that fulfill the requirements of<br />

this benchmark were referred for radiation therapy. The<br />

precise details of the situation in question are unknown<br />

to the author, so insight into this clinical scenario is<br />

obscure. The benefit of neoadjuvant therapy in rectal<br />

cancer as it pertains to reductions in local recurrence has<br />

been unabashedly endorsed in the medical literature,<br />

and one would be hard pressed to argue against it; that<br />

12

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