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A B S T R A C T S

S77

Conclusion:

To improve the efficiency of clinical research

in geriatric oncology, it is essential to conduct elderly specific

phase II clinical trials using appropriate methodologies by

taking into account the heterogeneity of this population. The

use of these adaptive phase II designs permits to reduce the

sample size. Recruitment duration, that is a major cause of

early stopping in elderly specific clinical trials, can also be

shortened. The use of sequential adaptive designs allows

the possibility to select a subpopulation that could benefit

(or not) from the experimental treatment at the end of the

first or the second stage. From a scientific point of view, this

would permit to conclude the efficacy or the feasibility of the

experimental treatment in a subgroup of interest. From an

ethical point of view, this would limit the exposure time of

particular subgroup of patients to inadequate treatments.

Disclosure of interest:

None declared

Keywords:

Design, elderly, heterogeneity, Phase II clinical

trial

P070

HOME-BASED PREHABILITATION AND REHABILITATION TO

OPTIMIZE PHYSICAL FITNESS AND TREATMENT OUTCOMES

IN PATIENTS WITH NON-SMALL CELL LUNG CANCER : A

SYSTEMATIC REVIEW

E. J. Driessen

1,

*, M. E. Peeters

2

, B. C. Bongers

3

, H. A. Maas

4

,

G. P. Bootsma

5

, N. L. van Meeteren

6

, M. L. Janssen-Heijnen

1

1

Epidemiology, VieCuri Medical Centre, Venlo,

2

Physical Therapy,

Knooppunt Centre for Health, Baarlo,

3

Epidemiology, CAPHRI

School for Public Health and Primary Care, Maastricht University,

Maastricht,

4

Geriatric Medicine, Elisabeth-TweeSteden Hospital,

Tilburg,

5

Pulmonology, Zuyderland Medical Centre, Heerlen,

6

Topsector Life Sciences and Health, Health Holland, The Hague,

Netherlands

Introduction:

Patients with non-small cell lung cancer

(NSCLC) are often old, vulnerable and at risk for complications.

Standard curative treatments lead to adverse events in

50% of patients and frequently require hospitalization.

Prehabilitation (therapeutic exercise training before

treatment) and rehabilitation (training during and after

treatment) bare the potential to optimize physical fitness

through increasing the physiological reserve, leading to better

treatment tolerance and even survival. However, training may

be limited due to multimorbidity, physical limitations and

accessability to services. Personalized training in a home-

based setting might overcome these barriers and enhance

motivation and adherence, especially for vulnerable and older

patients. However, a systematic overview regarding feasibility

and effectiveness of home-based (p)rehabilitation for NSCLC

patients is currently lacking.

Objectives:

To determine the feasibility and effectiveness of

home-based (p)rehabilitation in NSCLC patients by evaluating

physical fitness, adherence and treatment tolerance in a

systematic review.

Methods:

The PRISMA and Cochrane guidelines were

followed. Studies were included from databases PubMed,

Medline, Embase and PEDro (January 2000-April 2016). Two

reviewers independently searched and selected studies based

on PICO (NSCLC, (p)rehabilitation, home-based, physical

fitness), full text and by reference tracking. Data regarding

study characteristics, outcomes, methodological quality

(Cochrane risk of bias tool) and therapeutic validity (CONTENT

scale) were independently assessed as well. Interobserver

agreement was assessed with Cohens’ Kappa.

Results:

Eleven studies were included (437 NSCLC patients,

mean age 59-72 years). Nine of ten rehabilitation studies

(90%) and one prehabilitation study, consisting of aerobic and

strength exercises, described (significantly) improved physical

fitness (28-65 meter improved 6-minute walking distance

[5.2-43%]). Three studies (27%) assessed home-based training

alone and eight (73%) combined home-based, intramural

and/or extramural training. Only 6 studies (55%) had home-

based supervision and 4 (36%) were personalized. Exercise

compliance varied strongly (8.7-125%) as well as dropout (0-

65%). Treatment tolerance was described in 6 studies (55%)

and was not significantly lower for controls. Methodological

Fig. 1 (abstract P068) – Stopping rules of Parashar design / G1 : G8

14 /G2 : G8

14 / S1(S2): number of success in G1(G2).