The Role of Pulmonary Rehabilitation Programs in Patients with Lung Cancer: A Narrative Review
Abstract
1. Introduction
2. Materials and Methods
2.1. Study Design
2.2. Exclusion Criteria
2.3. Search Strategy
2.4. Study Selection
2.5. Data Extraction and Synthesis
2.6. Intervention Classification
3. Results
3.1. Preoperative Phase
3.2. Perioperative Phase
3.3. Postoperative Phase
3.3.1. Functional Recovery and Exercise Capacity
3.3.2. Pulmonary Function and Respiratory Mechanics
3.3.3. Symptoms of Dyspnoea and Cough
3.3.4. Health-Related Quality of Life and Psychological Outcomes
3.3.5. Postoperative Complications and Length of Stay
| Study (Year) | Design | Duration | Population | Intervention | Comparator | Main Outcomes | Key Results |
|---|---|---|---|---|---|---|---|
| [43] | Retrospective outpatient | 6 weeks | Post resection (n = 57 referred 52 completed) | PR (3–4 h, 3 days/week): endurance + strength + IMT + education | None | 6MWT, Wmax, PiMax, strength, CAT | ↑ 6MWT ↓ CAT no Aes 91% completion |
| [44] | Retrospective cohort | 3 weeks | Post-lobectomy NSCLC ± COPD | 3-week inpatient PR (6 days/week: breathing + cycling+ airway clearance + relaxation + education + psych + nutrition) | Basic postoperative physiotherapy and control standard care | 6MWT, SGRQ, spirometry, | ↑ 6MWT ↓ SGRQ spirometry ns |
| [45] | Prospective non-randomised cohort | 8 weeks | Post-resection NSCLC (n = 66) | Outpatient PR (2×/week) + home exercises | Breathing exercises only | 6MWD, dyspnoea, SGRQ/SF-36,HADS spirometry | PR: ↑ FVC ↑ 6MWD ↓ dyspnoea ↑ QoL control: small symptom gains only |
| [46] | RCT | 3 months | Post-VATS lobectomy (n = 88) | PR + albuterol nebuliser for 3 months | Albuterol only | PFTs, 6MWT, dyspnoea, chest-tube time, LOS | ↑ PF, ↓ dyspnoea ↓ LOS and tube time ↑ 6MWT |
| [47] | Prospective randomised controlled study | 14 days | NSCLC post-VATS lobectomy (n = 86) | Conventional PR + manual techniques (14 days) | Conventional PR only | PEF/FEV1/FEV1/FVC, 6MWT, PPCs, tube time, LOS | ↑ FEV1 and PEF ↓ tube time and LOS 6MWT/PPCs similar |
| [48] | Prospective cohort | 12 weeks | NSCLC post-treatment PR (mostly post-surgical) (n = 56) | Supervised PR (aerobic + resistance + RMT + education) | None | CPET (VO2peak etc.), RM strength, HRQoL, Borg | ↑ MIP PFTs ns HRQoL improved |
| [49] | Retrospective comparative cohort | Not mentioned | NSCLC post-VATS lobectomy (PR 81 vs. 195) | Post-op hospital + home PR (breathing + airway clearance + stretching + aerobic) | “Traditional rehab” | Cough + LCQ6-mo PFTs complications/LOS | ↓ Cough (day 3 and 6 months) ↑ LCQ6-mo ↑ PFTs complications/ LOS: ns |
3.4. Full Versus Partial Pulmonary Rehabilitation
| Study | Category | Exercise Capacity | Pulmonary Function | Symptoms (Dyspnoea/Cough/Fatigue) | HRQoL | PPCs | LOS/Recovery |
|---|---|---|---|---|---|---|---|
| [28] | Pre-op | — | ↑ DLCO ↓ VE/VCO2 | ↑ mood/↓ stress | ↑ | ↓ | ↓ |
| [33] | Pre-op | ↑ ISWT ↑ 5STS (better physical performance) | — | ↓ pre-op dyspnoea | ↑ global QoL fewer patients with QoL deterioration | — | ns |
| [34] | Pre-op | ↑ capacity | — | — | ↑ | — | ↓ LOS |
| [31] | Pre-op | ↑ performance | — | — | ↑ | ns | — |
| [30] | Pre-op | ↑ functional capacity | — | — | ↑ | ↓ | ↓ |
| [35] | Pre-op | ns recovery to baseline | — | ↑ | ↑ | — | → |
| [44] | post-op | ↑ 6MWD | ns | — | ↑ | — | — |
| [48] | Pre-op | ↑ exercise tolerance | ↑ ventilatory indices | ↑ | ↑ | — | → |
| [38] | Peri-op | ↑ 6MWD | ↑ FEV1/FVC | ↑ | ↑ nutrition | ↓ | ↓ |
| [40] | Peri-op | ↑ 6MWD | ↑ FEV1/FVC | — | — | ↓ | ↓ |
| [41] | Peri-op | — | — | ↑ cough strength | — | ns | ns |
| [36] | Peri-op | — | — | — | — | ↓ | ns |
| [39] | Peri-op | — | — | ↓ (QoL domain) | ↑ | ↓ | ↓ |
| [32] | Peri-op | — | ns | — | — | ↓ | ↓ |
| [46] | Peri-op | ↑ 6MWD | ↑ | ↓ dyspnoea index | — | — | — |
| [37] | Peri-op | — | ns | — | ↑ | ↓ | ns |
| [42] | Post-op | ↑ walking capacity | ns | ns | ns | ns | ns |
| [43] | Post-op | ↑ 6MWD | ↑ PiMax spirometry ns | ↓ CAT (improved respiratory symptoms incl. dyspnoea item) | — | — | — |
| [45] | Post-op | ↑ 6MWD | — | ↓ dyspnoea (mMRC) | ↑ | — | — |
| [47] | Post-op | ns | ↑ PEF, FEV1, FEV1/FVC | ↓ dyspnoea (Borg) | — | ns | ↓ |
| [49] | Post-op | — | ↑ lung function | ↓ cough | — | ns | ns |
| Study (Year) | Exercise Training (A) | Respiratory Component (B) | Education/Behaviour (C) | Nutrition/Psych (D) | Category (Final) |
|---|---|---|---|---|---|
| [28] | ✖ | ✔ | ✔ | ✔ | Partial PR |
| [33] | ✔ | ✖ | ✔ | ✖ | Partial PR |
| [34] | ✔ | ✔ | ✔ | ✖ | Full PR |
| [31] | ✔ | ✔ | ✔ | ✖ | Full PR |
| [32] | ✖ | ✔ | ✔ | ✖ | Partial PR |
| [35] | ✔ | ✖ | ✔ | ✔ | Partial PR |
| [30] | ✔ | ✔ | ✖ | ✖ | Partial PR |
| [41] | ✔ | ✔ | ✔ | ✖ | Full PR |
| [40] | ✔ | ✔ | ✔ | ✖ | Full PR |
| [38] | ✔ | ✔ | ✖ | ✔ | Full PR |
| [42] | ✔ | ✔ | ✔ | ✖ | Full PR |
| [39] | ✔ | ✔ | ✔ | ✖ | Full PR |
| [37] | ✖ | ✔ | ✔ | ✖ | Partial PR |
| [27] | ✔ | ✔ | ✔ | ✖ | Full PR |
| [44] | ✔ | ✔ | ✔ | ✔ | Full PR |
| [43] | ✔ | ✔ | ✔ | ✖ | Full PR |
| [45] | ✔ | ✔ | ✖ | ✖ | Partial PR |
| [47] | ✔ | ✔ | ✔ | ✖ | Full PR |
| [49] | ✔ | ✔ | ✖ | ✖ | Partial PR |
| [48] | ✔ | ✔ | ✔ | ✖ | Full PR |
| [46] | ✔ | ✔ | ✖ | ✖ | Partial PR |
4. Discussion
4.1. Overview of Main Findings
4.2. PR Completeness and Intervention Heterogeneity
4.3. Effects Across the Perioperative Continuum
4.4. Outcome Measurement Challenges and the Need for Standardisation
4.5. Barriers to Implementation of Pulmonary Rehabilitation
- Patient-related factors, including symptom burden, fatigue, anxiety and reduced motivation.
- Disease-related factors, such as advanced stage, comorbidities and treatment-related toxicity.
- Accessibility and distance, particularly for centre-based programmes.
- Adherence challenges, especially in unsupervised or home-based models.
- Organisational and resource constraints, including staffing and funding limitations.
- Lack of standardisation in PR content and outcome measurement.
4.6. Study Limitations
4.7. Clinical Implications and Future Directions
5. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
Abbreviations
| Abbreviation | Definition |
| RCT | Randomised controlled trial |
| IG | Intervention group |
| CG | Control group |
| LOS | Length of stay |
| PPCs | Postoperative pulmonary complications |
| ARDS | Acute respiratory distress syndrome |
| ERAS | Enhanced recovery after surgery |
| PHET | Preoperative home-based exercise training |
| PR | Pulmonary rehabilitation |
| IMT | Inspiratory muscle training |
| RMT | Respiratory muscle training |
| HIIT | High-intensity interval training |
| FITT | Frequency, Intensity, Time, Type |
| MICT | Moderate-intensity continuous training |
| BiPAP | Bilevel positive airway pressure |
| CPET | Cardiopulmonary exercise test |
| WR | Work rate |
| Wmax | Maximal workload |
| VE | Minute ventilation |
| VCO2 | Carbon dioxide production |
| MVV | Maximum voluntary ventilation |
| MIP | Maximal inspiratory pressure |
| MEP | Maximal expiratory pressure |
| PiMax | Maximal inspiratory pressure |
| Pemax | Maximal expiratory pressure |
| PEF | Peak expiratory flow |
| ABGs | Arterial blood gases |
| PFTs | Pulmonary function tests |
| FVC | Forced vital capacity |
| FEV1 | Forced expiratory volume in 1 s |
| FEV1%pred | Percentage of predicted FEV1 |
| 6MWD | 6 min walk distance |
| 6MWT | 6 min walk test |
| 5STS | Five-times sit-to-stand test |
| ISWT | Incremental shuttle walk test |
| POD | Postoperative day |
| SAEs | Serious adverse events |
| AEs | Acute exacerbations |
| NS | Non-significant |
| QoL | Quality of life |
| HRQoL | Health-related quality of life |
| SGRQ | St. George’s Respiratory Questionnaire |
| CAT | COPD Assessment Test |
| HADS | Hospital Anxiety and Depression Scale |
| FACT-L | Functional Assessment of Cancer Therapy–Lung |
| EQ-5D | EuroQol five dimensions questionnaire |
| EORTC QLQ-C30 | European Organisation for the Research and Treatment of Cancer Quality of Life Questionnaire |
| TNM | Tumour, Node, Metastasis |
| SCSS | Semiquantitative cough strength score |
| MGS | Melbourne Group Score |
| PSM | Propensity score matched |
| NSCLC | Non-small cell lung cancer |
| VATS | Video-assisted thoracoscopic surgery |
| MFS | Move For Surgery |
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| Study (Year) | Design | Duration | Population | Intervention | Comparator | Main Outcomes | Key Results |
|---|---|---|---|---|---|---|---|
| [28] | RCT | 14 days | High-risk lung resection candidates | Multimodal prehab (RMT/IMT + exercise + education + smoking cessation + psych + nutrition) | Usual care | PPCs, LOS, chest drain, CPET/VE/VCO2 | ↓ PPCs, ↓ LOS and chest drain ↓ VE/VCO2 slope ↑ QoL |
| [30] | Prospective RCT | 16-days alternate supervised exercise | NSCLC, planned VATS lobectomy | HIIT/MICT | Usual care | PPCs, LOS, QoL | ↓ PPCs ↓ LOS before surgery ↑ QoL ↑ functional capacity |
| [31] | Active-comparator RCT | 3 weeks/5 weeks | Adults with NSCLC presurgery | Supervised high-intensity multimodal prehab (interval aerobic + resistance + IMT + education) dense vs. distributed schedules | Active comparator (no usual care arm) | VO2peak, VE/VCO2, MIP, quad strength, QoL, PPCs | Physiology ↑ (VO2peak, MIP, strength), ↓ VE/VCO2, ↑ emotional QoL no diff. dense vs. distributed underpowered for PPCs |
| [32] | RCT | 7 days | Thoracotomy lung resections | Intensive supervised pre-op physio (≈3 h/day): breathing + BiPAP + education | None/usual | ABGs resp function, PPCs, LOS | ↓ LOS ↓ PPCs ABGs, respiratory function = ns |
| [33] | RCT | 4 weeks | NSCLC presurgery | Home-based exercise + education + weekly phone supervision | Usual care (+ attention calls) | HRQoL (QLQ-C30), ISWT, 5STS, postop exercise capacity, LOS | ↑ Global QoL pre- and post-op better function ↑ postop exercise capacity LOS = ns |
| [34] | Blinded single-site RCT | 3–4 weeks | Early-stage NSCLC for resection (≈51/arm) | Home-based “Move for Surgery” (activity tracker + breathing + lifestyle/education) | Usual care | Prolonged LOS > 5 days, LOS, HRQoL | ↓ Prolonged LOS (7% vs. 24%), LOS ↓ (~1.77 days) ↑ EQ-5D-5L pain ↓ POD1 |
| [35] | RCT | 4 weeks before the operation (PREHAB, n = 52) or 8 weeks after (REHAB, n = 43). | NSCLC resection | Home multimodal (aerobic + resistance + whey protein + anxiety-reduction) | Same programme delivered post-op | 6MWD over time | No between-group diff. recovery to baseline by 8 weeks > 75% regained capacity |
| Study (Year) | Design | Population | Intervention | Comparator | Main outcomes | Key Results |
|---|---|---|---|---|---|---|
| [36] | RCT | Patients scheduled for VATS | ERAS + PR nursing programme | ERAS alone | PPCs, chest drain removal time, LOS | ↓ PPCs, drain time and LOS ns |
| [37] | RCT | Older adults undergoing thoracoscopic surgery | Nurse-led peri-op breathing + airway clearance + education | Usual care | PPCs, EQ-5D, spirometry, LOS | PPCs ↓ (11.9%→3.7%) EQ-5D ↑ spirometry/LOS ns |
| [38] | Single-centre RCT | NSCLC scheduled thoracoscopic resection (n = 169) | Peri-op PR + individualised nutrition (start 2 weeks preop, restart 2 weeks postop; breathing trainer + walking + diet) | Usual care | FACT-L, spirometry, 6MWD, nutrition indices, PPCs, LOS, costs | Better QoL + improved pulmonary function/6MWD and nutritional indices ↓ PPCs/LOS/costs |
| [39] | PSM cohort | Lung cancer surgery patients receiving PR vs. not | PR (programme details in study) | Usual care | PPCs, LOS, QoL | ↓ PPCs ↓ LOS ↑ QoL |
| [40] | Cohort + PSM | NSCLC surgery cohort (n = 420 PSM 46 vs. 46) | PR (aerobic + strength + flexibility + IMT + education) | No PR | CPET, spirometry, HRQoL, muscle loss | FEV1/FVC and fitness ↑ less muscle loss symptoms/CAT better |
| [41] | Randomised prospective single-centre controlled trial | Smokers ≥ 20 pack-years candidates for lobectomy (n = 194) | Pre-op 3 days endurance + IMT postop IMT until discharge (ERAS in both) | ERAS only | PPCs, LOS/cost, drainage; cough strength, pain/fatigue walking distance POD1–2 | PPCs ns (24.5% vs. 33.0%), LOS, fatigue ns ↑ cough strength ↑ walking distance |
| [42] | Single-centre RCT (PUREAIR) | Thoracic surgery patients | Perioperative “rehab bundle” (early mobilisation, cough/breathing training etc.) | Usual care | Exercise capacity 1 m/6 m 6MWT, PFTs, PPCs, LOS, QoL, HADS | ↑ 6MWT PFTs, PPCs, LOS, QoL, HADS = ns |
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Andreadou, S.; Tanti, A.; Gkiliri, F.; Chatzikonstantinou, K.; Vatista, E.; Christakou, A. The Role of Pulmonary Rehabilitation Programs in Patients with Lung Cancer: A Narrative Review. BioMed 2026, 6, 8. https://doi.org/10.3390/biomed6010008
Andreadou S, Tanti A, Gkiliri F, Chatzikonstantinou K, Vatista E, Christakou A. The Role of Pulmonary Rehabilitation Programs in Patients with Lung Cancer: A Narrative Review. BioMed. 2026; 6(1):8. https://doi.org/10.3390/biomed6010008
Chicago/Turabian StyleAndreadou, Stiliani, Angeliki Tanti, Foteini Gkiliri, Kriton Chatzikonstantinou, Eleni Vatista, and Anna Christakou. 2026. "The Role of Pulmonary Rehabilitation Programs in Patients with Lung Cancer: A Narrative Review" BioMed 6, no. 1: 8. https://doi.org/10.3390/biomed6010008
APA StyleAndreadou, S., Tanti, A., Gkiliri, F., Chatzikonstantinou, K., Vatista, E., & Christakou, A. (2026). The Role of Pulmonary Rehabilitation Programs in Patients with Lung Cancer: A Narrative Review. BioMed, 6(1), 8. https://doi.org/10.3390/biomed6010008

