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Annals of Oncology<br />
evidence should include: side effects, schedule of treatment, support services, storage,<br />
handling, disposal and interactions.<br />
Results: During <strong>the</strong> review period, 35 patients receiving OAT were identified. Of<br />
<strong>the</strong>se, 12 patients had documentation of education by a doctor (34%), 15 (43%) by a<br />
nurse. Documentary evidence of education about side effects was noted in 22 cases<br />
(63%), schedule of treatment in 16 cases (46%), support services in 16 (46%), safe<br />
storage in 3 cases (9%), safe disposal, safe handling and interactions in 2 cases each<br />
(6%). Recommendations: A standardised tool has been developed to enable<br />
healthcare staff to accurately document issues discussed during patient education for<br />
OAT. This is in <strong>the</strong> form of a checklist to ensure that all elements including safety,<br />
timing of medication, interactions, monitoring and support are documented<br />
accurately. All patients prescribed OAT will be referred to a nurse-led OAT clinic to<br />
facilitate education. Healthcare staff in <strong>the</strong> oncology department will be educated<br />
about <strong>the</strong> tool and clinic and, following a pilot period, a repeat audit will be<br />
performed to assess <strong>the</strong> effectiveness of <strong>the</strong> tool. These results will also be presented.<br />
Disclosure: All authors have declared no conflicts of interest.<br />
1635 INTENSIVE CARE AS A KEY PLAYER IN THE CHANGING<br />
PARADIGM OF MODERN CANCER CARE: A SINGLE<br />
INSTITUTION EXPERIENCE<br />
L.C. Connell 1 , F. Othman 2 , B. Marsh 2 , D.N. Carney 1 , J.A. McCaffrey 1 ,P.<br />
O Gorman 3 and C.M. Kelly 4<br />
1 Medical Oncology, Mater Misericordiae University Hospital, Dublin, IRELAND,<br />
2 Department of Intensive Care, Mater Misericordiae University Hospital, Dublin,<br />
IRELAND, 3 Haematology, Mater Misericordiae University Hospital, Dublin,<br />
IRELAND, 4 Medical Oncolgy, Mater Misericordiae University Hospital, Dublin,<br />
IRELAND<br />
Background: Many metastatic cancers are now treated similar to o<strong>the</strong>r chronic<br />
diseases. Expanding treatment options, increasing age; co-morbid illness; and<br />
improving cancer-specific survival means that decisions regarding <strong>the</strong> timeliness &<br />
appropriateness of transfer to <strong>the</strong> Intensive Care Unit (ICU) are complex. We sought<br />
to examine <strong>the</strong> clinical, demographic & outcome characteristics of oncology/<br />
haematology patients (pts) transferred to ICU at a large academic teaching hospital.<br />
Methods: Data was extracted from a prospectively maintained database for all pts<br />
with documented malignancy admitted to ICU between September 2009 &<br />
December 2011. Clinicopathological variables examined included; cancer type;<br />
tumour stage; time from diagnosis; age; co-morbidities; and treatment history. The<br />
Sequential Organ Failure Assessment (SOFA), an ICU-specific scoring system, was<br />
reviewed for each patient (pt). We report 30 day & 6-month mortality.<br />
Results: A total of 52 of an eligible 83 pts have been analysed in detail to date. The<br />
common cancer types were well represented; breast (11.5%),colorectal(11.5%), lung<br />
(11.5%) & acute leukaemia(19.2%). Mean age at time of ICU admission was 60 years<br />
(range 29-82). The maximum number of prior lines of chemo<strong>the</strong>rapy (CT) was 5<br />
(range 0-5). Approximately 50% of pts had metastatic disease at time of ICU<br />
admission. The most frequent reasons for admission were sepsis (n = 16, 31%) &<br />
respiratory distress (n = 15, 29 %). Use of mechanical ventilation, vasopressors &<br />
renal dialysis was 51.9%, 61.5% & 21.1% respectively. Four pts (7.7 %) received CT in<br />
<strong>the</strong> ICU setting. ICU-specific mortality was 28.8% (n = 15). Thirty-day and 6-month<br />
mortality rates were 38.5% & 61.5% respectively. Data on <strong>the</strong> remaining 31 pts is<br />
currently being analysed and will be available for presentation at <strong>the</strong> meeting.<br />
Conclusions: A significant proportion of pts admitted to ICU had advanced disease<br />
& had received multiple lines of CT previously. The ICU-specific mortality rate was<br />
lower than expected at 28.8% and may reflect stringent selection criteria. Pts<br />
transferred tended to have had long periods of disease remission/stabilisation or had<br />
a new diagnosis of malignancy with unknown CT sensitivity status. Analysis of pt<br />
selection at ward level is on-going and will identify o<strong>the</strong>r factors influencing ICU<br />
transfer decisions.<br />
Disclosure: All authors have declared no conflicts of interest.<br />
1636 A PROSPECTIVE STUDY OF SUBACUTE THYROID<br />
DYSFUNCTION FOLLOWING SUPRACLAVICULAR<br />
IRRADIATION IN THE MANAGEMENT OF CARCINOMA OF THE<br />
BREAST<br />
S. Akyurek 1 , I. Babalioglu 1 , S. Yuksel 2 and S. Cakir Gokce 1<br />
1 Radiation Oncology, Ankara University School of Medicine, Ankara, TURKEY,<br />
2 Biostatistic, Ankara University School of Medicine, Ankara, TURKEY<br />
Purpose: To evaluate <strong>the</strong> relationship between irradiation and early thyroid<br />
dysfunction, focusing on radiation dose-volume factors.<br />
Patients and methods: Between December 2010 and January <strong>2012</strong> a total of 21<br />
patients with breast cancer received supraclavicular irradiation were evaluated<br />
Thyroid function tests, including serum thyroid stimulating hormone (TSH), free<br />
thyroxine (fT4), free triiodothyronine (fT3), were analyzed prior to irradiation and<br />
every three months <strong>the</strong> first year and <strong>the</strong>n 18th month after radio<strong>the</strong>rapy. Based on<br />
each patient’s dose volume histogram (DVH), total volume of <strong>the</strong> thyroid, mean<br />
radiation dose <strong>the</strong> thyroid and percentages of thyroid volume which received<br />
radiation doses 10-60Gy (V10-V60) were considered for statistical analysis.<br />
Results: Mean TSH levels before irradiation, at 3, 6, 9 and 12 months were 1.4 µIU/<br />
ml, 1.5 µIU/ml, 1.7 µIU/ml, 3.6 µIU/ml and 4.6 µIU/ml, respectively. Serum TSH<br />
levels did not change significantly at 3 and 6 months after irradiation (p = 0.1).<br />
However, a significant elevation was noted at 9 months (p = 0.005). Mean thyroid<br />
dose was 32 Gy (19-48 Gy) and mean thyroid volume was 35 cc (24-64 cc). Median<br />
values of V10-20-30-40-50-60 were 68%, 58%, 55%, 53%, 48% and 0%, respectively.<br />
With a median follow-up was 9 months (range, 3-18 months), only one patient (5%)<br />
developed clinical hypothyroidism requiring thyroid replacement treatment.<br />
Conclusion: According to early results of our study, irradiation of <strong>the</strong> thyroid<br />
develops early thyroid dysfunction. This damage is initially manifested within 9<br />
months after radio<strong>the</strong>rapy. However we could not analyze <strong>the</strong> radiation dose-volume<br />
factors of <strong>the</strong> peak level of serum TSH because of inefficient follow up time.<br />
Disclosure: All authors have declared no conflicts of interest.<br />
1637 COMBINATION OF SERUM PROCALCITONIN AND<br />
C-REACTIVE PROTEIN LEVEL AS A DIAGNOSTIC MARKER OF<br />
DISCRIMINATING INFECTION FROM NEOPLASTIC FEVER IN<br />
FEBRILE LUNG CANCER PATIENTS<br />
K. Miyamoto 1 , R. Seki 2 , D. Taniyama 1 , H. Kamata 1 and F. Sakamaki 1<br />
1 Pulmonary Medicine, Saiseikai Central Hospital, Minato-ku, Tokyo, JAPAN,<br />
2 Pathology, Saiseikai Central Hospital, Tokyo, JAPAN<br />
Background: Neoplastic fever in lung cancer is assessed on clinical course only, and<br />
is difficult to discriminate from infection.<br />
Objective: To evaluate <strong>the</strong> diagnostic role of procalcitonin (PCT) and C-reactive<br />
protein (CRP) in discriminating neoplastic fever and infection.<br />
Methods: We reviewed <strong>the</strong> medical records of 112 consecutive febrile episodes of 52<br />
patients (39 males, mean age 67.1y/o), who were diagnosed as lung cancer from<br />
November 2009 to April <strong>2012</strong> at our Saiseikai Central Hospital in Tokyo, Japan.<br />
Based on clinical, laboratory, and bacteriological results, patients were classified as<br />
having neoplastic fever (NF, n = 53), suspected or definite bacterial infection (BI, n = 59).<br />
Values of white blood cell count (WBC), PCT, and CRP were measured on day 1 of<br />
onset of fever. Microbiological specimen and radiological imaging study were also<br />
performed to diagnose infectious diseases or o<strong>the</strong>r febrile conditions.<br />
Results: The most common infection was pneumonia (38.4 %). Mean WBC (12000<br />
vs. 14800) were not statistically significant. Mean values of PCT were significantly<br />
higher in patients with BI compared with NF (0.14 vs. 3.95 ng/ml, p < 0.05). Mean<br />
values of CRP were also significantly higher in patients with BI compared with NF<br />
(8.6 vs. 15.2 mg/dl, p < 0.05). Combination of CRP level at <strong>the</strong> threshold value of<br />
10.2 mg/dl and PCT level at <strong>the</strong> threshold value of 0.32 ng/ml were <strong>the</strong> most<br />
sensitive from ROC curve for discriminating infection to neoplastic fever.<br />
Conclusions: Combination of PCT and CRP on <strong>the</strong> day of onset of fever is useful in<br />
discriminating neoplastic fever from infection in febrile lung cancer patients.<br />
Disclosure: All authors have declared no conflicts of interest.<br />
1639 INCIDENCE OF THROMBOEMBOLIC EVENTS IN PATIENTS<br />
TREATED WITH CISPLATIN-BASED CHEMOTHERAPY<br />
A.C. Fernandes 1 , S.R. Meireles 2 , I. Augusto 2 , L. Aguas 2 and M. Damasceno 2<br />
1 Oncologia Médica, Hospital de São João, Porto, PORTUGAL, 2 Medical<br />
Oncology Department, Hospital São João, Porto, PORTUGAL<br />
Introduction: Cancer patients on chemo<strong>the</strong>rapy have higher risk in developing<br />
thromboembolic events (TEE), with great impact on morbidity and mortality. The<br />
aim of this study is to determine <strong>the</strong> incidence of venous and arterial TEE in patients<br />
treated with cisplatin-based chemo<strong>the</strong>rapy. We also analysed <strong>the</strong> prognostic value of<br />
patientś baseline and treatment characteristics in predicting TEE occurrence.<br />
Methods: We performed a retrospective analysis of all patients with cancer treated<br />
with cisplatin-based chemo<strong>the</strong>rapy between January 1, 2011, and April 10, <strong>2012</strong>,<br />
with at least 4 weeks of follow-up after <strong>the</strong>ir last cisplatin dose. A TEE was<br />
considered cisplatin-associated if it occurred between <strong>the</strong> time of <strong>the</strong> first dose of<br />
cisplatin and 4 weeks after <strong>the</strong> last dose.<br />
Results: Among 141 patients, 27 (19.1%) experienced a TEE. The TEE observed<br />
were: deep vein thrombosis (DVT) in 9.9% (14), pulmonary embolism (PE) in 5.7%<br />
(8), DVT plus PE in 0.7% (4) and arterial thrombosis in 2.8%. The majority of<br />
patients (51.9%) had a TEE after 63 days, and after <strong>the</strong> 3 rd dose of cisplatin, with a<br />
cumulative dose of 160 mg/m 2 . By univariate analysis, active smoking (p = 0.016),<br />
hypertension (p = 0.007), site of cancer (p = 0.025), Khorana site of cancer (p =<br />
0.001), Khorana score (p = 0.049) and risk group (p = 0.04) were all identified as risk<br />
factors. However, by multivariate analysis, only hypertension (p = 0.18; HR 3.59; 95%<br />
CI, 1.25 to 10.34) and Khorana site of cancer (p = 0.03) retained statistic significance.<br />
Conclusion: As we expected, gastric and pancreatic cancers had <strong>the</strong> highest<br />
incidence of TEE. We verified a very high incidence of TEE in patients treated with<br />
cisplatin-based regimens, also described in o<strong>the</strong>r published studies. It is <strong>the</strong>refore<br />
Volume 23 | Supplement 9 | September <strong>2012</strong> doi:10.1093/annonc/mds416 | ix525