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Journal Thoracic Oncology

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Abstracts <strong>Journal</strong> of <strong>Thoracic</strong> <strong>Oncology</strong> • Volume 12 Issue S1 January 2017<br />

of consultations with different healthcare staff providing distinct specialist<br />

services. The topics discussed included diagnostic information about<br />

mesothelioma, treatment options and consequences, trials processes and<br />

logistics, and legal and financial information regarding classification of MPM<br />

as an industrial disease. Despite feeling well informed about their treatment<br />

some participants reported not being prepared for the full extent of the<br />

problems they experienced. Both chemotherapy and surgery were challenging<br />

treatments although they were associated with different physical effects.<br />

Adverse consequences of treatment were described including neutropenic<br />

sepsis and dehydration post chemotherapy, and bleeding, prolonged<br />

pneumothorax and infection post-surgery. For most participants pain and<br />

breathlessness were experienced post-surgery while nausea, anorexia, taste<br />

changes and constipation were associated with chemotherapy. Fatigue that<br />

impacted on daily living was experienced by both groups. Interventions to<br />

manage the consequences of treatment were recounted; some had been<br />

recommended by healthcare staff while others had been developed by<br />

patients from their own initiative. Participants reported struggling to cope<br />

with the effect of treatment whilst trying to deal with the broader context of<br />

coming to terms with their illness. Uncertainty was expressed in relation to<br />

treatment plans (exacerbated by the logistics surrounding participation in a<br />

clinical trial), severity and duration of side effects, rehabilitation and recovery<br />

and treatment outcomes. Participants employed a number of strategies<br />

to help with coping. These included ‘playing things down’, ‘weighing the<br />

balance’, ‘managing expectations’, ‘taking control’ ‘manning up’ and ‘trust in<br />

the doctor and/or treatment’. Many of these strategies facilitated staying<br />

positive, maintaining hope and finding comfort which was important to<br />

participants. Family members played a key role in coping. A diverse range of<br />

healthcare staff provided information, advice and practical interventions<br />

across the care pathway from community, surgical, respiratory and oncology<br />

services. Discussion: Patient’s perspectives on the experience of receiving<br />

radical surgery and/or chemotherapy for mesothelioma were identified by<br />

the study. This provided valuable insights into their impact on patient’s<br />

feelings about their illness and treatment and how they coped with the<br />

challenges they were presented with. Multiple sources of uncertainty were<br />

expressed by participants. The contribution of healthcare staff to supporting<br />

coping and providing information and advice was appraised positively by<br />

participants. However, we identified that fragmentation could occur due to<br />

the diverse services involved in providing care with no single point of contact<br />

or co-ordination. Conclusion: Understanding the patient’s perspective of the<br />

challenges associated with treatment, alongside their strategies for coping,<br />

provides insights for the services that can support patients undergoing<br />

arduous treatments for mesothelioma. The study reveals ways to facilitate<br />

strategies to help patients manage the condition, as well as treatment sideeffects.<br />

Interventions to reduce uncertainty have been identified as a priority<br />

for service improvement.<br />

Keywords: Radical surgery, Mesothelioma, patient experience, Qualitative<br />

research<br />

NU03: SUPPORTING PATIENTS RECEIVING TREATMENT<br />

TUESDAY, DECEMBER 6, 2016 - 11:00-12:30<br />

NU03.03 EHEALTH AND REMOTE PATIENT MONITORING AND<br />

SUPPORTIVE CARE IN THORACIC ONCOLOGY<br />

Roma Maguire<br />

School of Health Sciences, University of Surrey, Glasgow/United Kingdom<br />

Lung cancer is the commonest cancer worldwide with 1.6 million people<br />

diagnosed each year. People with lung cancer experience a high level of<br />

supportive care needs and many of these needs are unmet. Systematic<br />

supportive care is therefore vital in this patient group. Patient Reported<br />

Outcome Measures (PROMs) can be used to identify the supportive care needs<br />

of people with lung cancer and the collection of PROMs data is reported to<br />

have a number of positive effects on patient outcomes. Enhancing the utility<br />

of PROMs within clinical practice is the use of health technologies that have<br />

the ability to collect PROM data remotely from patients in their own homes<br />

and send this information in ‘real time’ immediately to relevant health/social<br />

care professionals for subsequent intervention. The Advanced Symptom<br />

Management System is one of the most evolved remote patient monitoring<br />

systems in cancer care. This presentation will initially focus on remote<br />

patient monitoring within the context of lung cancer before considering the<br />

implications for the future and the ultimate vision of connected health for all.<br />

Keywords: Technology, connected health, lung cancer, supportive care<br />

NU03: SUPPORTING PATIENTS RECEIVING TREATMENT<br />

TUESDAY, DECEMBER 6, 2016 - 11:00-12:30<br />

THERAPY<br />

Tanja Cufer<br />

Medical <strong>Oncology</strong> Unit, University Clinic Golnik, Golnik/Slovenia<br />

Introduction Systemic therapy (ST) with chemotherapy (Cht), targeted agents<br />

or immunotherapy (IT) represents the mainstay therapy for patients with<br />

advanced lung cancer; while adjuvant systemic therapy is recommended in<br />

a majority of patients with operable and locally advanced disease. The goal<br />

of ST is to prolong life without compromising quality of life (QoL). Despite<br />

the ability of ST to prolong life or even cure patients, QoL and life span might<br />

be compromised due treatment toxicity. In addition, uncontrolled adverse<br />

events (AEs) might lead to treatment interruption or discontinuation.<br />

Therefore, effective management of adverse events of anti-cancer drugs, the<br />

so-called “supportive care to systemic therapy” is extremely important for a<br />

true benefit, i.e. treatment effectiveness in a routine practice. During the last<br />

decade several improvements in prevention, treatment and amelioration of<br />

ST AEs been achieved. To implement them in everyday clinic practice a good<br />

understanding of adverse events, supportive care measures and professional<br />

skills of all team members are needed. Registered nurses, specialized in the<br />

oncology, the so called “oncology nurses” are key providers of supportive care<br />

in everyday clinical practice. Supportive care for prevention and treatment<br />

of adverse events Chemotherapy-induced nausea and vomiting (CINV)<br />

has been a priority in the supportive care of cancer patients ever since the<br />

first use of Cht (1). The introduction of 5-HT3 and NK1 antagonists into<br />

anti-emetic therapy resulted in much better control of CINV in lung cancer<br />

patients receiving highly emetogenic, platinum-based therapy. With proper<br />

use of available drugs complete control of vomiting could be achieved in<br />

up to 90% of these patients. However, despite the efficacy of new antiemetic<br />

therapies a proper us of anti-emetics and other preventive measures<br />

are vital. Chemotherapy-induced neutropenia with febrile neutropenia<br />

(FN) as its ultimate and most serious complication are often observed in<br />

patients receiving Cht. The risk of FN can be predicted by assessing patient<br />

characteristics and mylotoxicity of the Cht regimen; and granulocyte-colonystimulating<br />

factors (G-CSF) can be used to prevent it (2). Even thought,<br />

most of the regimens for lung cancer do not classify to high, i.e. more than<br />

20% risk of febrile neutropenia, the primary prophylaxis with G-CSF is often<br />

necessary due to high comorbidity index, poor PS or extensive disease often<br />

present in lung cancer patients. In case of FN, a risk-base approach provided<br />

by MASCC helps us to decide which patients need hospitalization and which<br />

can be treated by antimicrobial therapy at home (3). Oral mucositis and<br />

diarrhea related to mucosal damage are frequent complications of Cht as<br />

well as targeted therapy with TKIs that can significantly affect patient’s QoL<br />

and the ability to deliver full doses and complete therapy. Oral care protocols<br />

are essential components in prevention and treatment of stomatitis, while<br />

intensive local therapy protocols with antibiotics, anesthetics and/or<br />

corticosteroids help to ameliorative symptoms (4). Diarrhea is quite common<br />

in lung cancer patients receiving Cht with an even higher occurrence in<br />

patients treated with TKIs (5). It could be life threatening in elderly, fragile<br />

patients and in patients with concurrent neutropenia, thus requiring a rapid<br />

and effective control. When dietary strategy does not work, or when patients<br />

present with severe grade 3/4 diarrhea pharmacologic intervention with<br />

loperamide or even somatostatin analogues should be initiated quickly. Skin<br />

changes (rash, dry skin, paronychia) are the most frequent AEs associated<br />

with targeted therapy for lung cancer next to diarrhea. Even though, they<br />

are usually mild or moderate they hava negative impact on patient’s QoL<br />

and might lead to dose modifications or even discontinuation. Prophylactic<br />

measures with regular use of moisturizing products, sunshine protection and<br />

careful skin hygiene are necessary. In case of severe but still localized changes<br />

topical corticosteroids/antibiotics are indicated while a severe and prolonged<br />

toxicity usually requires TKIs dose interruptions (6). Fatigue is a common<br />

symptom reported in up to 80% of LC patients. In most cases it is impossible<br />

to distinguish to what extend it is the adverse event of ST and to what of<br />

disease. It is increasingly reported in patients receiving targeted therapy or<br />

immunotherapy, and major improvements in recognition and treatment of<br />

fatigue have been achieved recently (7). Immunotherapy with checkpoint<br />

inhibitors (CPIs) represents a novel approach. By breaking of immune<br />

self-tolerance it might lead to autoimmune/inflammatory adverse events,<br />

designated as immune-related adverse events (irAEs), mainly including rash,<br />

diarrhea, hepatitis and endocrinopathies (8). Although most of irAEs are of<br />

low grade, some of them progress rapidly and prompt medical attention with<br />

treatment interruption and the administration of glucocorticoids is critical.<br />

Implications for nursing <strong>Oncology</strong> nurses should have in-depth knowledge on<br />

adverse events of systemic therapy and must be familiar with the supportive<br />

care protocols. Nursing interventions for prevention and treatment of<br />

particular adverse events are presented in Table 1. <strong>Oncology</strong> nurses play a<br />

key role in continuous education of patients, their families and caregivers<br />

on adverse events. They are valuable members of the multidisciplinary team<br />

performing ongoing assessment of AEs and monitoring of patients and<br />

actively discussing potential solutions and improvements with other team<br />

members, thus providing a high-quality patient-centered care.<br />

NU03.04 SUPPORTIVE CARE IN PATIENTS RECEIVING SYSTEMIC<br />

S104 <strong>Journal</strong> of <strong>Thoracic</strong> <strong>Oncology</strong> • Volume 12 Issue S1 January 2017

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