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

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5536 General Poster Session (Board #21D), Sat, 1:15 PM-5:15 PM<br />

Gingival cancer: 11 year follow-up at Karolinska University Hospital (2000-<br />

2010). Presenting Author: Rusana Simonoska, Department <strong>of</strong> ENT, Karolinska<br />

Institutet/Karolinska University Hospital, Stockholm, Sweden<br />

Background: In Sweden, approximately 500-600 cases <strong>of</strong> oral cancer are<br />

diagnosed every year. These include cancer <strong>of</strong> the gingiva, retromolar<br />

trigonum, bucca, hard palate, tongue and floor <strong>of</strong> the mouth. Each year,<br />

around 15 cases <strong>of</strong> gingival cancer (GC) are diagnosed in the Stockholm<br />

region. The goal <strong>of</strong> this study was to study the onset <strong>of</strong> symptoms,<br />

treatment, prognosis, and sequelae <strong>of</strong> GC in order to optimize the<br />

treatment. Methods: The study consists <strong>of</strong> a retrospective review <strong>of</strong> medical<br />

records <strong>of</strong> all diagnosed cases <strong>of</strong> GC in Stockholm region between<br />

2000-2010, identified through the ENT-clinic Karolinska Hospital patient<br />

database. Results: Our retrospective study comprised 156 patients diagnosed<br />

with GC. The average age was 72 years sharing equally between the<br />

sexes, 50% were smokers. 98% had a squamous cell carcinoma (scc).<br />

Presenting symptoms were <strong>of</strong>ten lump or ulceration in the gums, pain,<br />

bleeding or discomfort/misfit <strong>of</strong> dentures. Around 30% had premalignant<br />

lessons in the oral cavity before diagnosis. 3/4-th <strong>of</strong> all GC was localized in<br />

the lower jaw. 66% <strong>of</strong> the GC-patients presented as aT4 cancer. At<br />

presentation, 26% had a regional metastasis and <strong>of</strong> those 90% had their<br />

primary tumor in the lower jaw. Six cases had bilateral neck disease. 81%<br />

<strong>of</strong> the patients with regional metastasis had low to medium grade <strong>of</strong> scc<br />

differentiation <strong>of</strong> the primary tumor. 84% <strong>of</strong> all patients with regional<br />

metastasis had a T4 primary tumor. Neck dissection was performed in 38%<br />

(n�59). Of these 35 cases where staging neck, i.e. N0 at presentation and<br />

in 7 cases (20%) a positive neck disease was found. The risk for second<br />

primary was 15%. The overall 5-year survival was 24%. Conclusions:<br />

Advanced age and high number <strong>of</strong> T4 cancer at diagnosis partly explains<br />

the poor survival statistics. Almost 30% <strong>of</strong> the patients in our material have<br />

had premalignant lessons in the oral cavity before the cancer diagnosis and<br />

are at high risk for new tumors (second primary); therefore patients with GC<br />

should be followed up for at least 5 years, possibly longer in the presence <strong>of</strong><br />

premalignant lessons. GC <strong>of</strong> the lower jaw is more likely to metastasize than<br />

GC <strong>of</strong> the upper jaw. Due to 20% occult metastasis occurrence in the<br />

staging neck cases, we recommend staging neck dissection for patients<br />

with GC.<br />

5538 General Poster Session (Board #21F), Sat, 1:15 PM-5:15 PM<br />

A phase II study <strong>of</strong> sorafenib in combination with cisplatin and 5-fluorouracil<br />

in the treatment <strong>of</strong> recurrent or metastatic nasopharyngeal carcinoma.<br />

Presenting Author: Cong Xue, Sun Yat-sen University Cancer Center,<br />

Guangzhou, China<br />

Background: Nasopharyngeal carcinoma (NPC) is a disease with distinctive<br />

epidemiology and clinical behavior compared with Head and neck cancer<br />

(HNC) and more common in South-East Asia. Sorafenib monotherapy has<br />

been shown modest anticancer activity in HNC and NPC (C Elser et al; JCO<br />

2007). This study was to evaluate the efficacy and tolerability <strong>of</strong> sorafenib<br />

combined with cisplatin and 5-fluorouracil (5-FU) for patients with recurrent<br />

or metastatic NPC. Methods: A phase II, single arm clinical trial was<br />

conducted in three centers in China. Chemotherapy-naive histologically<br />

confirmed NPC patients with recurrent or metastatic disease were enrolled.<br />

Patients received oral sorafenib 400mg bid continuously until disease<br />

progression or unacceptable toxicity, cisplatin 80mg/m2 intravenously (iv)<br />

on day 1-5, and 5-FU 400mg/m2 iv infusion for 96 hours on day 1.<br />

Treatment was repeated every 21 days for a maximum <strong>of</strong> 6 cycles. Results:<br />

54 patients were enrolled. Most patients were with bone metastases<br />

(70.0%), followed by liver (56%) and lung metastases (56%). The median<br />

chemotherapy administrated was 4.0 cycles (range, 2-6cycles). The<br />

disease control rate (DCR) reached 90.7%, including one complete<br />

response (CR), 41 partial responses (PR) and 7 stable diseases (SD).<br />

Median PFS was 7.2 months (95% CI 6.8-8.4 months) and median OS was<br />

11.8 months (95% CI 10.6-18.7 months). Tumor cavitation after treatment<br />

was observed in 32.1% <strong>of</strong> patients with lung metastases. Decreased<br />

percentage <strong>of</strong> contrast update in responder patients (PR and CR) with liver<br />

metastases was also observed by Contrast-Enhanced Doppler ultrasound.<br />

The major toxicities include hand foot syndrome (HFS), myelo-suppression<br />

and gastrointestinal reaction.Dose reduction <strong>of</strong> sorafenib was required in<br />

22 patients (40.7%) and dose interruption in 14 patients (25.9%) because<br />

<strong>of</strong> toxicity. Conclusions: Sorafenib combined with cisplatin and 5-FU has an<br />

encouraging efficacy pr<strong>of</strong>ile with tolerable toxicity. Further randomized<br />

studies are needed to confirm the clinical benefit <strong>of</strong> sorafenib combined<br />

with chemotherapy in recurrent or metastatic NPC.<br />

Head and Neck Cancer<br />

365s<br />

5537 General Poster Session (Board #21E), Sat, 1:15 PM-5:15 PM<br />

Efficacy <strong>of</strong> concurrent cetuximab (C225) versus 5-fluorouracil/carboplatin<br />

(5FU/CBDCA) or cisplatin (CDDP) with intensity-modulated radiation<br />

therapy (IMRT) for locally advanced head and neck cancer (LAHNSCC).<br />

Presenting Author: Lauren Quinn Shapiro, Memorial Sloan-Kettering Cancer<br />

Center, New York, NY<br />

Background: We reported inferior outcomes for LAHNSCC patients (pts)<br />

that received concurrent C225 vs. high-dose CDDP with IMRT (IJROBP<br />

2011; 81:915). Prior to FDA approval <strong>of</strong> C225 for LAHNSCC, non-CDDP<br />

candidates at our institution were treated with 5FU/CBDCA (JNCI 1999;<br />

91:2081). The purpose <strong>of</strong> this study was to compare the outcomes <strong>of</strong><br />

concurrent C225 vs. 5FU/CBDCA vs. CDDP with IMRT for LAHNSCC.<br />

Methods: Retrospective review <strong>of</strong> records was performed for pts treated at<br />

MSKCC with concurrent C225 (n�49) vs. 5FU/CBDCA (n�52) vs. highdose<br />

CDDP (n�259) and IMRT from 11/02 to 04/08. Overall survival (OS),<br />

locoregional failure-free survival (LRFS), and late toxicity for all pts and<br />

oropharyngeal subset were obtained. Outcomes were analyzed using<br />

univariate/multivariate Cox proportional hazards model or competing-risks<br />

analysis. Multivariate OS analysis was confirmed by propensity score<br />

adjustment. Results: Pts were similar with regard to site, overall stage, and<br />

alcohol/tobacco history. Compared to pts treated with CDDP, those who<br />

received C225 or 5FU/CBDCA were older, with lower performance status,<br />

higher Charlson score, higher T stage, and worse renal function. With<br />

median follow-up <strong>of</strong> 53.1 months for survivors, the 4-year OS was 40.9%<br />

(95% CI 26.0-55.2%) for C225 vs. 70.2% (95% CI 55.5-80.9%) for<br />

5FU/CBDCA vs. 86.9% (95% CI 82.0-90.6%) for CDDP. Compared with<br />

CDDP, C225 (hazard ratio [HR] 4.01, p�0.0001) but not 5FU/CBDCA (HR<br />

1.54, p�0.15) was associated with worse OS on multivariate analysis.<br />

Propensity score analysis yielded a HR <strong>of</strong> 2.76 (p�0.01) for treatment with<br />

C225 vs. platinum-based chemotherapy. 4-year actuarial LRF for 5FU/<br />

CBDCA was similar to CDDP (9.7% vs. 6.3%, HR 1.51, p�0.42 by Gray’s<br />

method) and significantly lower than C225 (40.2%, HR 4.95, p�0.002).<br />

Late toxicity was as follows: C225 (6.1%) vs. CDDP (7.7%) vs. 5FU/CBDCA<br />

(21.2%). Conclusions: After adjusting for independent risk factors, there<br />

was no significant difference in OS or LRFS between 5FU/CBDCA and<br />

high-dose CDDP, but C225/RT resulted in significantly inferior OS and<br />

LRFS. Late toxicity was worst with 5FU/CBDCA.<br />

5539 General Poster Session (Board #21G), Sat, 1:15 PM-5:15 PM<br />

Patterns <strong>of</strong> care in elderly patients with squamous cell carcinoma <strong>of</strong> the<br />

head and neck: A SEER-Medicare analysis. Presenting Author: Noam<br />

Avraham Vanderwalde, Department <strong>of</strong> Radiation Oncology, University <strong>of</strong><br />

North Carolina at Chapel Hill, Chapel Hill, NC<br />

Background: Head and neck squamous cell carcinoma (HNSCC) is predominantly<br />

a disease <strong>of</strong> the elderly, however age and co-morbidity may affect<br />

therapy decisions. The purpose <strong>of</strong> this study was to assess the patterns <strong>of</strong><br />

care <strong>of</strong> elderly HNSCC patients and identify factors associated with<br />

non-receipt <strong>of</strong> surgery and chemoradiation (CRT). Methods: Using the<br />

Surveillance, Epidemiology, and End Results (SEER)-Medicare linked<br />

database (1992-2007) we identified a retrospective cohort <strong>of</strong> nonmetastatic<br />

HNSCC patients and categorized them into treatment cohorts.<br />

Comparisons were made between surgery vs. non-surgery, and CRT vs.<br />

non-CRT cohorts. Multivariate logistic regression models examined factors<br />

associated with non-receipt <strong>of</strong> treatment. Variables included tumor location,<br />

stage, year <strong>of</strong> diagnosis, age, gender, marital status, race, comorbidity,<br />

race-comorbidity interaction, SEER region, socioeconomic variables,<br />

and hospital affiliations. Results: The final cohort <strong>of</strong> 11,336 were 63%<br />

male and 83% white. 52% had no co-morbidities, 44% had oral cavity<br />

HNSCC, 52% were diagnosed between 2002 and 2007, 58% had surgery,<br />

and 21% received CRT. For the CRT vs. non-CRT model, increasing age<br />

(OR � 0.93; 95% CI 0.92 -0.94) and non-whites with co-morbidity (OR �<br />

0.71; 95% CI 0.55 – 0.92) were associated with decreased likelihood <strong>of</strong><br />

receiving CRT. More advanced staged disease, oropharyngeal tumor location,<br />

and diagnosis after 2002 were associated with increased likelihood <strong>of</strong><br />

receiving CRT. For the surgery versus non-surgery model, age was not<br />

associated with receipt <strong>of</strong> surgery (OR 0.99; 95% CI 0.99-1.00), nor was<br />

existence <strong>of</strong> comorbidity in white patients (OR 0.97; 95% CI 0.88-1.05).<br />

However, recent year <strong>of</strong> diagnosis, non-oral cavity tumor location, and<br />

advanced stage were all associated with reduced likelihood <strong>of</strong> receiving<br />

surgery. During the 15 year surveillance period, patients were less likely to<br />

receive surgery, and CRT was used more <strong>of</strong>ten. Conclusions: Age may<br />

influence the non-receipt <strong>of</strong> CRT in this elderly cohort but does not appear<br />

to be significantly associated with the non-receipt <strong>of</strong> surgery. There has<br />

been an increasing trend in the receipt <strong>of</strong> CRT with a decrease in surgery<br />

over the past 15 years.<br />

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