Journal Thoracic Oncology
WCLC2016-Abstract-Book_vF-WEB_revNov17-1
WCLC2016-Abstract-Book_vF-WEB_revNov17-1
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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