| Literature DB >> 19370175 |
N Salvo1, S Hadi, J Napolskikh, P Goh, E Sinclair, E Chow.
Abstract
Approximately 27% of North American cancer deaths are attributable to cancer of the lung. Many lung cancers are found at an advanced stage, rendering the tumours inoperable and the patients palliative. Common symptoms associated with palliative lung cancer include cough, hemoptysis, and dyspnea, all of which can significantly debilitate and diminish quality of life (QOL). In studies of the effects of cancer therapies, the frequent evaluative endpoints are survival and local control; however, it is imperative that clinical trials with palliative patients also have a QOL focus when a cure is unattainable. We conducted a literature review to investigate the use of QOL instrument tools in trials studying QOL or symptom palliation of primary lung cancer or lung metastases through the use of radiotherapy. We identified forty-three studies: nineteen used a QOL tool, and twenty-four examined symptom palliation without the use of a QOL instrument. The European Organization for Research and Treatment of Cancer (eortc) QLQ-C30 survey was the most commonly used QOL questionnaire (in thirteen of twenty trials). Of those thirteen studies, eight also incorporated the lung-specific QOL survey eortc QLQ-LC13 (or the eortc QLQ-LC17). A second lung-specific survey, the Functional Assessment of Cancer Therapy-Lung (fact-L) was used in only two of the twenty trials. In total, only ten of forty-three trials (23%) used a lung-specific QOL tool, suggesting that QOL was of low priority as an endpoint and that measures created for lung cancer patients are underused. We encourage investigators in future trials to include specific QOL instruments such as the eortc QLQ-LC13 or the fact-L for studies in palliative thoracic radiotherapy because those instruments provide a measure of QOL specific to patients with lung cancer or lung metastases.Entities:
Keywords: Lung cancer; eortc qlq-C30; eortc qlq-LC13; fact-L; qol instrument; quality of life; review
Year: 2009 PMID: 19370175 PMCID: PMC2669235 DOI: 10.3747/co.v16i2.376
Source DB: PubMed Journal: Curr Oncol ISSN: 1198-0052 Impact factor: 3.677
Patients with inoperable non-small-cell lung cancer (nsclc) treated with palliative radiotherapy
| Reference | Type | Study Purpose | Arms | Pts ( | Median survival | Assessment tools Performance | Other | Measures of | |
|---|---|---|---|---|---|---|---|---|---|
| Simpson | To evaluate 3 | A: 40 Gy split course in 4 weeks
| 316 | A: 6.2 months
| None | Study designed: self-report either complete relief or relative relief by patient | 0 | ||
| Kaasa | A: Combination chemotherapy
| 95 | Not stated | Study designed: 29 variables; only psychosocial well-being and global | None | 0 | |||
| Teo | To compare a hypofractionated scheme with traditional fractionation | A: 45 Gy/18 fr
| 291 | Not stated | None | Study designed: subjective responses in thoracic symptoms to changes | 0 | ||
| Randomized prospective | To determine if a shorter treatment course of | A: 17 Gy/2 fr
| 369 | A: 179 days
| None | Study designed: 4-point scale to rate symptoms | 0 | ||
| Regan | Prospective | Correlate physician rating of | A: 30 Gy/10 fr
| 40 | 30 Days | 1 | |||
| Investigate whether a single fraction can provide palliation as good as that provided by 2 fractions | A: 17 Gy/2 fr
| 233 | A: 100 days
| None | Study designed: daily dairy for first 6 months: 4-point scale to rate symptoms | 0 | |||
| Omand and Meredith, 1994 | Prospective | To assess frequency of acute side effects of short-term | A: 10 Gy/1 fr
| 61 | Not stated | None | None | Study designed: percentage improvement in symptoms | 0 |
| Abratt | Randomized prospective | To evaluate the dose–response effect on survival of patients with good performance status | A: 35 Gy/10 fr
| 84 | A: 8.5 months
| None | Study designed: physician graded symptom improvements | 0 | |
| Macbeth | Randomized (multicentre) | To compare palliative with more-intensive | A: 17 Gy/2 fr
| 509 | A: 7 months
| None | 0 | ||
| Ball | Prospective | To assess the effect of adding continuous-infusion fluorouracil to palliative | A: 20 Gy/5 fr
| 200 | A: 6 months
| Study-designed questionnaire | Study-designed questionnaire to detect symptom palliation | 1 | |
| Gava | Prospective (multicentre) | To assess the indications for | A: Radical range: 30Gy–70Gy
| A: 109
| Not stated | Study designed | None | ||
| Lutz | Retrospective | To measure symptom palliation in patients treated with | 30 Gy/10–12 fr | 54 | 4 Months | None | 1 | ||
| Vyas | Retrospective | To evaluate response in patients receiving palliative | 17 Gy/2 fr | 37 | Not stated | None | Not stated | Study designed: patients asked to grade percentage improvement in symptoms | 0 |
| Donato | Prospective | To examine the results obtained with a fractionated | A: 20 Gy/5 fr (1 treatment)
| 52 | Not stated | None | Study designed: subjective patient assessment of symptoms | 0 | |
| Langendijk | Prospective | To see the association between prognostic factors and | A: Curative schedule: 70 Gy in 7 weeks B: Radical schedule: 60 Gy in 6 weeks C: Palliative schedule: 30 Gy in 4 weeks | 262 | A: 19.1 months
| None | 2 | ||
| Langendijk | Prospective | To investigate changes in symptoms and | 30 Gy/in 4 weeks | 65 | Not stated | who | None | 2 | |
| Nestle | Randomized prospective | To see if there is a difference between palliative and more intensive treatment | A: 60 Gy/30 fr
| 152 | A: 8.3 months
| None | Study designed: | 0 | |
| Schaafsma and Coy, 2000 | Prospective | To estimate the effect of high-dose | 30 Gy/10 fr | 54 | 266 Days | None | 1 | ||
| Auchter | Prospective | To evaluate | 57.6 Gy/36 fr over 15 days | 30 | 13 Months | None | 1 | ||
| BCentingoz | Retrospective | To retrospectively evaluate the treatment effects of | Median dose: 30 Gy/1–23 fr | 115 | 30 Weeks | None | Study designed: subjective palliation rates in one of three groups: near total response, improvement, or no response | 0 | |
| Langendijk | Prospective | To evaluate changes in | 60 Gy total dose | 164 | 8.5 Months | None | 2 | ||
| Bejzak | Comparison of 2 fractionation schedules on palliation of symptoms | A: 10 Gy/1 fr
| 230 | A: 4.2 months
| 1 | ||||
| Falk et al., 2002 29 | To determine if patients should be given palliative | A: 17 Gy/2 fr
| 230 | A: 240 days
| None | 0 | |||
| Nihei | Retrospective | To investigate the outcome of | 30 Gy/10 fr | 24 | Responders: 192 days
| None | None | Study designed:
| 0 |
| Borthwick | Prospective | To gain an understanding of fatigue in patients receiving | A: Radical:
| 53 | Not stated | None | Not stated | Study designed: daily card with 9 questions relating to fatigue | 0 |
| Kramer | Compare various fractions of | A: 16 GY/2 fr
| 297 | Not stated | None | 0 | |||
| Senkus–Konefka | Randomized prospective | To compare two palliative | A: 20 Gy/5 fr
| 100 | A: 5.3 months
| None | Study designed: patient-reported symptom relief on a 4-point scale | 0 | |
| Sundstrøm | Randomized prospective | To compare the course of symptoms and | 17 Gy/2 fr
| 395 | NSym: 11.8 months
| None | 2 | ||
| Sundstrøm | Randomized | To examine the predictive value of baseline | A: 17 Gy/2 fr
| 301 | A: 9.2 Months
| None | 2 | ||
| Temel | Prospective | To assess the feasibility of early palliative care in patients with newly diagnosed | Not stated | 51 | 9.0 Months | 2 |
Pts = patients; qol = quality of life; rct = randomized clinical trial; xrt = external-beam radiotherapy; kps = Karnofsky performance status; fr = fractions; who = World Health Organization; mrc = Medical Research Council; eortc = European Organization for Research and Treatment of Cancer; ecog = Eastern Cooperative Oncology Group; hads = Hospital Anxiety and Depression Scale; rscl = Rotterdam symptom checklist; swog = Southwest Oncology Group; lcss = Lung Cancer Symptom Scale; rt = radiotherapy; qald = quality-adjusted life-day; hr = health-related.
Patients with symptomatic lung cancer treated with endobronchial brachytherapy (ebb) as compared with external-beam radiotherapy (xrt) with or without ebb
| Reference | Type | Study Purpose | Arms | Pts ( | Median survival | Assessment tools Performance | Other ( | Measures of | |
|---|---|---|---|---|---|---|---|---|---|
| Stout | To compare | A: 30 Gy/8 fr | 99 | A: 287 days
| None | Study designed: 4-point scoring system to monitor performance status and 9 key symptoms | 2 | ||
| Langendijk | To test that the addition of | A: | 95 | A: 8.5 months
| None | 2 | |||
| Mallick | Prospective | To test the hypothesis that palliative | A: 30 Gy/10 fr with | 95 | A: 10 months
| None | 2 | ||
| Mallick | Prospective | To compare the subjective and objective responses to 3 regimens for duration, | A: 30 Gy/10 fr with | 45 | Not stated | None | 2 |
Pts = patients; qol = quality of life; rct = randomized clinical trial; fr = fractions; who = World Health Organization; hads = Hospital Anxiety and Depression Scale; rscl = Rotterdam symptom checklist; eortc = European Organization for Research and Treatment of Cancer; kps = Karnofsky performance status.
Patients with inoperable lung cancer [other than non-small-cell lung cancer (nsclc)] treated with palliative radiotherapy
| Reference | Type | Study Purpose | Arms | Pts ( | Median survival | Assessment tools Performance | Other | Measures of | |
|---|---|---|---|---|---|---|---|---|---|
| Berry | Prospective | Compares | A: 40 Gy/20 fr or 36 Gy/12 fr
| A: 48
| 125 Days | None | None | Study designed: physicians recorded changes in patient symptoms | 0 |
| Collins | Prospective | To determine whether palliative | Range: 18 Gy/5 fr–48 Gy/10 fr (split course) | 96 | 38 Weeks | None | Study designed: symptom response questions | 0 | |
| MRC Lung Cancer Working Party, 1989 | To compare two policies of treatment | A: Combination chemotherapy and | 151 | A: 32 weeks
| None | Study designed: treatment reports and daily diary chart | 0 | ||
| Devereux | Prospective | To assess the incidence and severity of the immediate side effects of palliative | Range: 8 Gy/1 fr–60 Gy/30 fr | 118 | Not stated | None | None | Study designed: questionnaire to determine occurrence of symptoms 24 hours post treatment | 0 |
| Rees | Randomized prospective | To compare the symptomatic effects of two regimens of | A: 17 Gy/2 fr
| A: 111
| Not stated | None | Study designed: questionnaire to rate severity of symptoms | 0 | |
| Ampil | To see the effects of palliative | Range: 5–58 Gy (mean dose: 35 Gy) | 32 | 7 Months | None | Study designed: subjective response | 0 | ||
| Erridge | To determine whether palliation of chest symptoms was the same in two fractionation schedules | A: 10 Gy/1 fr
| 149 | A: 28.3 Weeks
| Spitzer’s | 1 | |||
| Turner | Prospective | To see if older people benefit from | A: “High dose”: (36/39 Gy in 12/13 fr)
| Elderly (>75 years): 83
| A: 9 months
| 2 | |||
| Hicsönmez | Evaluate efficacy of palliative | Not stated | 88 | Not stated | None | 1 |
Pts = patients; qol = quality of life; xrt = external-beam radiotherapy; fr = fractions; rt = radiotherapy; who = World Health Organization; mrc = Medical Research Council; rct = randomized clinical trial; swog = Southwest Oncology Group; hads = Hospital Anxiety and Depression Scale; ecog = Eastern Cooperative Oncology Group; sclc = small-cell lung cancer; eortc = European Organization for Research and Treatment of Cancer.
Frequency of instruments used in clinical trials measuring quality of life (qol) in patients with locally advanced lung cancer or lung metastases
| Instrument | Frequency |
|---|---|
| European Organization for Research and Treatment of Cancer ( | |
| General cancer questionnaire ( | 13 |
| Lung cancer questionnaire ( | 7 |
| Lung cancer questionnaire ( | 1 |
| Functional Assessment of Cancer Therapy ( | |
| General questionnaire ( | 1 |
| Lung questionnaire ( | 2 |
| Spitzer | 1 |
| Hospital Anxiety and Depression Scale ( | 5 |
| Rotterdam Symptom Checklist ( | 4 |
| Study-designed | 3 |
| Lung Cancer Symptom Scale ( | 2 |
| Study-designed symptom palliation questionnaire | 19 |
Use of validated or study-designed tools in forty-three studies
| Questionnaire type | ||||
|---|---|---|---|---|
| Symptom palliation | Quality of life | |||
| ( | (%) | ( | (%) | |
| Validated | 9 | 21 | 16 | 37 |
| Study-designed | 21 | 49 | 3 | 7 |
| Total | 30 | 70 | 19 | 44 |
Six studies used both a qol and a symptom palliation tool.
FIGURE 1Questionnaire use in all identified studies.