| Literature DB >> 35805005 |
Sara Zuccarino1, Fiammetta Monacelli2,3, Rachele Antognoli4, Alessio Nencioni2,3, Fabio Monzani4, Francesca Ferrè1, Chiara Seghieri1, Raffaele Antonelli Incalzi5.
Abstract
The Comprehensive Geriatric Assessment (CGA) and the corresponding geriatric interventions are beneficial for community-dwelling older persons in terms of reduced mortality, disability, institutionalisation and healthcare utilisation. However, the value of CGA in the management of older cancer patients both in terms of clinical outcomes and in cost-effectiveness remains to be fully established, and CGA is still far from being routinely implemented in geriatric oncology. This narrative review aims to analyse the available evidence on the cost-effectiveness of CGA adopted in geriatric oncology, identify the relevant parameters used in the literature and provide recommendations for future research. The review was conducted using the PubMed and Cochrane databases, covering published studies without selection by the publication year. The extracted data were categorised according to the study design, participants and measures of cost-effectiveness, and the results are summarised to state the levels of evidence. The review conforms to the SANRA guidelines for quality assessment. Twenty-nine studies out of the thirty-seven assessed for eligibility met the inclusion criteria. Although there is a large heterogeneity, the overall evidence is consistent with the measurable benefits of CGA in terms of reducing the in-hospital length of stay and treatment toxicity, leaning toward a positive cost-effectiveness of the interventions and supporting CGA implementation in geriatric oncology clinical practice. More research employing full economic evaluations is needed to confirm this evidence and should focus on CGA implications both from patient-centred and healthcare system perspectives.Entities:
Keywords: CGA; cost-effectiveness; geriatric oncology; older adults
Year: 2022 PMID: 35805005 PMCID: PMC9265029 DOI: 10.3390/cancers14133235
Source DB: PubMed Journal: Cancers (Basel) ISSN: 2072-6694 Impact factor: 6.575
Recommendations in the CGA by scientific associations.
| Proponents | Target Population | Recommendations |
|---|---|---|
| The International Society of Geriatric Oncology (SIOG) [ | Cancer patients aged 70 or older |
adoption of CGA with further interventions and follow-up use of screening tools to identify those patients who need CGA and multidisciplinary approach, when facing a busy clinical practice the preferred screening tool may depend on the clinical situation |
| The European Society for Medical Oncology (ESMO) [ | Patients aged 70 or older with diffuse large B-cell lymphoma (DLBCL) |
CGA is recommended to aid patient’s categorisation into fit, vulnerable and terminally ill patients |
| The American Society of Clinical Oncology (ASCO) [ | Cancer patients aged 65 or older receiving chemotherapy |
CGA results should lay the basis of an integrated and individualised care plan CGA results should inform cancer management clinicians should consider CGA results when recommending chemotherapy the information from CGA should be provided to patients and caregivers to guide treatment decision making |
| The National Comprehensive Cancer Network (NCCN), U.S.A. [ | Older cancer patients |
implementation of pre-treatment evaluation using CGA when there are concerns about the patient’s ability to tolerate treatment or when issues are identified by a geriatric screening tool assessment using a geriatric screening tool only, when there are no concerns regarding a patient’s ability to tolerate therapy CGA should inform targeted interventions and a coordinated plan for cancer treatment |
| The Italian Society of Geriatrics and Gerontology (SIGG) [ | Cancer patients aged 65 or older |
CGA should be performed in all patients with cancer aged 65 or older as a second choice (whenever resources are limited), adoption of a ‘two-step approach’ (screening to select patients who need CGA) a closer interaction between geriatricians and oncologists (or haematologists) should take place to optimise the approach to cancer patients CGA should be performed by a trained geriatrician with the ability to detect and treat impairments in the different domains, possibly calling into play additional health professionals as needed |
| European Society of Surgical Oncology (ESSO) [ | Patients aged 70 or older with rectal cancer |
CGA and multidisciplinary evaluation to identify the main predictors of frailty and postoperative complications such as functional status, nutritional status and comorbidities |
| American College of Surgeons (ACS) (and the American Geriatrics Society—AGS) [ | Older cancer patients undergoing oncological surgery |
a preoperative frailty assessment is recommended for all older patients who are candidates to an oncological surgical procedure risk assessment for older patients; management of geriatric domains in the perioperative period, postoperative period and after discharge |
Figure 1Review diagram.
Studies conducted in surgical settings, main features and results.
| Authors | Participants | Type of Study | CGA and Geriatric Interventions | Effectiveness Measures Suitable for Cost-Effectiveness | Main Effect of CGA and Geriatric Interventions | Cost-Effectiveness Propensity |
|---|---|---|---|---|---|---|
| Nipp et al., 2022 [ | 98 patients (per-protocol) patients undergoing curative/palliative resections 30 intervecntion patients | RCT | Random assignment to PERI-OP or usual care. Patients assigned to PERI-OP met with a geriatrician preoperatively and postoperatively. Geriatricians communicated findings to surgical/oncology teams or (after surgery) to inpatient team. | Postoperative LoS | In per-protocol analyses, PERI-OP patients had shorter postoperative LoS (5.90 vs. 8.21 days, | Positive |
| Complications | In per-protocol analyses, differences in CD complication rates between PERI-OP and usual care group (6.7% vs. 20.6%, | Neutral | ||||
| Koh et al., 2021 [ | 81 patients 58 patients in intervention group sequential comparison with earlier cohort (non-PEERS) of 23 CRC patients of a similar age who underwent colorectal resections and managed by the same group of surgeons | Before-and-after | A structured multidisciplinary prehabilitation program prior to surgery: PEERS. The program included CGA, nutrition supplementation, resistance training, optimisation of cardiac risk for operation, optimisation of the discharge process to avoid institutionalisation. | QoL | PEERS group had significant improvement in median EQ-5D (0.70 pre-surgery to 0.80 6-months’ post-surgery, | Positive |
| Surgical complications | Rate of CD grade 3+ complications were similar between groups. No significant improvement of anthropometric and functional characteristics before and after PEERS. Both groups had similar 30-days’ morbidity rates (8.6% vs. 17.4%, | Neutral | ||||
| Shahrokni et al., 2020 [ | 1892 patients 1020 patients in intervention group | Retrospective | Geriatric co-management of care with pre-operative (electronic Rapid Fitness Assessment) and postoperative evaluations. | LoS | Patients in the geriatric co-management group were older compared with surgical service group. The intervention group had longer operative time and longer LoS. | Negative |
| Adverse surgical events | CD adverse surgical outcomes within 30 days of surgical treatment did not differ between groups. A higher proportion of patients in the geriatric co-management group were discharged home with home supportive services (18.0% vs. 13.6%, | Neutral | ||||
| van der Vlies et al., 2020 [ | 433 patients 127 frail patients in intervention arm (considered frail by clinical judgment or with G8 and 6-CIT) | Retrospective | Intervention: extended preoperative CGA. MDT estimated the risk of a surgical procedure and when patients were considered eligible for surgery, a prehabilitation program was initiated based on comorbidity and frailty characteristics. Control group: no preoperative MDT approach. | LoS | Readmission rates were similar between groups and most frequently caused by an infectious complication. No significant results were found for LoS and unplanned ICU admissions. | Neutral |
| Severity of postoperative complications | Despite at increased risk, MDT patients did not suffer more postoperative CD III-V complications than non-MDT patients (14.9% vs. 12.4%; | Neutral | ||||
| Janssen et al., 2019 [ | 627 patients 267 patients in the intervention group (CRC 73.8%, abdominal aortic aneurysm 26.2%) | Before-and-after | Prehabilitation group received interventions to improve physical health, nutritional status, factors of frailty and preoperative anaemia prior to surgery. During the outpatient visit, a nurse practitioner and a physiotherapist re-evaluated patient global health, fitness and frailty. The control group was not pre-habilitated. | In-hospital LoS | The prehabilitation group had a higher burden of comorbidities and was more physically and visually impaired at baseline. No effect of prehabilitation on LoS, readmissions, unplanned ICU admissions and LoS in ICU. | Neutral |
| Delirium | At adjusted logistic regression analysis, prehabilitation significantly reduced the incidence of delirium. No effect was observed for postoperative complications, institutionalisation and short-term mortality. | Positive | ||||
| Tarazona-Santabalbina et al., 2019 [ | 310 patients 203 patients in intervention group (GS) | Retrospective | In GS group, the geriatrician performed a CGA and established a care plan, then applied and monitored by the geriatrician and multidisciplinary team. Control group was assessed daily by the General Surgery Service in accordance with the usual practice criteria. | LoS | At baseline, patients in the GS group presented poorer clinical conditions than controls. LoS was similar in groups, but patients in the GS group stayed more frequently over ten days in hospital and were more frequently hospitalised and admitted to the ICU. No significant differences were observed between groups regarding readmissions and in-hospital and post-discharge mortality. | Neutral |
| Delirium | 54 patients experienced delirium (11.3% and 29.2% in GS and control group respectively, | Positive | ||||
| Ommundsen et al., 2018 [ | 122 frail patients Frailty is any of: (1) VES-13 > 2; (2) severe comorbidities; (3) cognitive impairment; (4) PP; (5) malnourishment 53 patients in intervention arm | RCT | CGA followed by a tailored intervention or usual care. | LoS | No differences in term of LoS between groups. No statistically significant differences between intervention and control group for reoperations (19% vs. 11%) or readmissions (16% vs. 6%). | Neutral |
| Severity of postoperative complications | In the secondary analyses, a statistically significant difference in favour of the intervention in terms of lower CD grade I–V complications ( | Positive | ||||
| Shipway et al., 2018 [ | 682 cancer patients (84% were cancer patients) 132 patients in intervention group | Before-and-after | Preoperative CGA and corresponding interventions, postoperative patient co-management by a geriatrician. Geriatrician involvement also in the definition of the postoperative discharge plan and in the implementation of a rehabilitation program. | LoS | Intervention was associated with a LoS significant reduction (by 3.1 days) for all surgical patients aged > 60 years, with esteemed cost savings of approximately £300,000/annum. In patients admitted electively for GI surgery, LoS reductions did not reach statistical significance, although a trend reduction was seen indicating possibly greater reduction with advancing age. | Positive |
| Medical complications | No statistically difference in term of medical complications (the reduction of LoS could reflect the prevalence of these). | Neutral | ||||
| Souwer et al., 2018 [ | 86 patients 86 patients in intervention cohort | Retrospective | Multidisciplinary pre- and rehabilitation (cohort 2014–2015): preoperative assessment with geriatric screening, subsequent CGA when indicated, rehabilitation care. Retrospectively identified historic control cohorts of patients operated at same centre (cohorts 2010–2011, 2012–2013). | LoS | The number of patients with a prolonged LoS (>14 days) decreased from 27% in 2010–2011 to 13% in 2012–2013 and 6% in 2014–2015 ( | Positive |
| Postoperative complications | Severe complications and cardiac complications after surgery were significantly reduced. Number of surgical and pulmonary complications did not differ between the three cohorts. Six patients in 2010–2011, seven in 2012–2013 and 11 in the study cohort received adjuvant CT. | Positive | ||||
| Ho et al., 2017 [ | 74 patients | RCT | All patients are randomised to either conventional surgical care or enhanced geriatric input. | LoS | The median LoS was statistically significantly shorter in the intervention group when compared to control (7.1 ± 4.0 days vs. 14.0 ± 10.9 days, | Positive |
| Postoperative complications | Postoperative complications were significantly lower in the intervention group (16.2% vs. 54.1%, | Positive | ||||
| Indrakusuma et al., 2015 [ | 100 patients | Retrospective cohort and match-control study | Patients from cohort ISAR + with a positive ISAR score were referred to the geriatric specialists for DOG assessment. | LoS | LoS was only statistically significant shorter in the cohort (ISAR+ vs. ISAR-) comparison (but since 2011 the use of laparoscopic resection increased, preoperative workup improved, and a postoperative fast track program was implemented). | Neutral |
| PoD | Compared with controls, DOG patients were older and underwent laparoscopic resection more often. Hearing and cognitive impairment were more prevalent among DOG patients, as history of delirium. Even if significantly more at risk for postoperative complications, DOG patients had comparable postoperative outcomes as controls in general/surgical and medical complications. DOG patients had similar outcomes in mortality and PoD compared to controls. | Positive | ||||
| Mak et al., 2014 [ | 78 patients 79 patients in intervention arm control group: registry (database of the same surgical department) | Prospective pilot study | Intervention group: perioperative assessment and active management of their pre-existing medical problems, nutritional status and social status were carried out. Patients were jointly managed perioperatively by the colorectal and geriatric teams with further input on discharge. Control group: standard care | LoS | The interventional group had shorter mean LoS (9.31 vs. 12.2 days; | Positive |
| Discharge destination | Discharge destination (i.e., home, nursing home or rehabilitation hospital) in both groups was not different. | Neutral | ||||
| Hempenius et al., 2013 [ | 260 frail patients 148 patients in the intervention group randomisation stratified by cancer type Frailty: GFI > 3 | RCT | Geriatric liaison intervention to prevent PoD: pre-operative CGA by a geriatric team, individual treatment plan, daily visits by a geriatric nurse during the hospital stay and advice on emerging medical problems. The intervention focused on best supportive care and the prevention of delirium. | LoS | Median LoS was 8 days in both groups. | Neutral |
| Postoperative complications | No significant difference between groups in number and type of complications. | Neutral |
Abbreviations: CD: Clavien-Dindo; CGA: Comprehensive Geriatric Assessment; CRC: Colorectal Cancer; EQ-5D: EuroQol-5 Dimension; G8: Geriatric 8; GFI: Groningen Frailty Indicator; GS: CGA-based care; GI: Gastrointestinal; ICU: Intensive Care Unit; ISAR: Identification of Seniors At Risk (questionnaire); LoS: Length of Stay; MDT: Multidisciplinary team; OS: Overall Survival; RCT: Randomised Controlled Trial; PEERS: Programme for Enhanced Elderly Recovery; PERI-OP: Perioperative geriatric intervention; PoD: Postoperative Delirium; QoL: Quality of Life; 6-CIT: 6-Item Cognitive Impairment Test. White rows: cost-sensitive measures (measures of patient health conditions leading to cost-increasing or cost-decreasing effects); grey rows: measures of effectiveness of CGA intervention (with estimation of costs in two studies [81,86]).
Studies conducted in medical settings, main features and results.
| Authors | Participants | Type of Study | CGA and Geriatric Interventions | Effectiveness Measures Suitable for Cost-Effectiveness | Main Effect of CGA and Geriatric Interventions | Cost-Effectiveness Propensity |
|---|---|---|---|---|---|---|
| Lund et al., 2021 [ | 142 frail patients Frailty: G8 ≤ 14 71 patients in intervention group | RCT | CGA-based intervention: CGA at the start of CT, follow-up after 2 months or more frequently if needed. Interventions included medication changes (62%), nutritional therapy (51%), physiotherapy (39%). | Hospitalisations | Hospitalisation during CT occurred with equal frequency in both groups. QoL (EORTC QLQ-C30, EORTC QLQ ELD-14) was better in intervention patients, with decreased burden of illness ( | Neutral |
| ADEs | Grade 3+ toxicity occurred in 39% of patients from the control arm and in 28% of patients from the CGA arm ( | Neutral | ||||
| Mohile et al., 2021 [ | 718 frail patients 349 patients in intervention arm | RCT | Intervention (CGA and CGA-guided management integrated into oncology care): patients completed CGA, oncologists received a tailored CGA summary and management recommendations. Usual care: patients completed CGA, no CGA summary or management recommendations were provided to oncologists (only alerts for significantly impaired scores on depression and cognitive screening were sent). | ADEs | A lower proportion of patients in intervention group had grade 3–5 ADEs compared with usual care group (51% vs. 71%), with a reduced risk of ADEs ( | Positive |
| Choukroun et al., 2021 [ | 51 frail outpatients patients with G8 score ≤14 median number of chronic comorbidities (excluding primary cancer) was 4.0 [high blood pressure (69%), dyslipidaemia (29%), chronic renal failure (27%), heart failure (25%) and type 2 diabetes (24%)]. | Prospective observational study | Five-stage process (outpatient): preparation phase; face-to-face pharmaceutical consultation with the patient; CGA performed by an ergotherapist and a geriatrician (geriatric tools; physical examination); pharmaceutical medication analysis (PP, PIM, DRP and DDI); final multidisciplinary medication review by the clinical pharmacist and a geriatrician team (recommendations to reduce DRP and optimise prescriptions). After the medication review, the proposals for prescription modification were sent to GPs and oncologists. | PIM | A significant decrease was observed in prevalence of PIM use and ADE risk. A not significant trend was observed for a lower number of medications. | Positive |
| DuMontier et al., 2020 [ | 160 frail/prefrail patients [per-protocol intervention and control ( 60 patients in intervention group 48 patients had at least one visit with a geriatrician | RCT | Prefrail and frail patients were randomised to standard oncologic care or standard care plus consultation with a geriatrician. Geriatrician provided individualised interventions, if indicated, he communicated with patient’s primary care provider and utilized referral systems (e.g., psychiatry). Follow-up was encouraged, but not required. Most common interventions fell within the comorbidity/PP domain (81%); followed by nutrition (54%); function/falls (48%); cognition (31%) and depression/mood (17%). | LoS | Consultation did not significantly reduce the incidence of ED visits, hospitalisations (6 months follow-up), or days in hospital. | Neutral |
| Discussion on EoL goals | Consultation did improve the odds of having EoL goals of care discussions (OR = 3.12, 95% CI: 1.03–9.41). | Positive | ||||
| Li et al., 2020 [ | 605 patients 402 patients in intervention arm | RCT | Before starting CT, both arms completed a baseline CGA and Fulmer SPICES assessment. In the intervention arm (GAIN), a geriatrics-trained multidisciplinary team (oncologist, nurse practitioner, social worker, physical/occupation therapist, nutritionist, and pharmacist) acted on CGA results and implemented interventions. In the control arm (SOC), CGA results were sent to treating oncologists for consideration without any input from the multidisciplinary team. | LoS | No significant differences were observed in ED visits, unplanned hospitalisations, average LoS, unplanned hospital readmissions and OS between groups. | Neutral |
| ADEs | Compared to SOC, GAIN arm experienced a significant 10.1% reduction in the incidence of grade 3+ CT-related toxic effects. Reductions were observed for hematologic-only toxic effects (8.0% reduction) as well as non-hematologic-only toxic effects (8.2% reduction). No significant differences in CT dose modifications or discontinuations. | Positive | ||||
| Nadaraja et al., 2020 [ | 96 patients 49 patients in intervention group | RCT | Control group: treatment decision based on oncologist’s clinical judgement. | Treatment completion | No impact on completion rate of planned oncologic treatment, but the intervention resulted in a borderline significant lower incidence of grade 3–4 toxicity. | Neutral |
| Nipp et al., 2020 [ | 62 patients 30 patients assigned to intervention group | RCT | Random assignment to usual care or intervention. Transdisciplinary intervention integrating geriatric and palliative care with oncology care (two visits with a geriatrician trained about geriatric-specific and palliative care issues and CGA). | QoL | Intervention patients presented less decrease in QoL decrement (FACT-G). | Positive |
| Symptom burden | Intervention patients had reduced number of moderate/severe symptoms and improved confidence in communication compared to usual care. | Positive | ||||
| Ørum et al, 2021 [ | 363 patients 152 patients in intervention arm | RCT | All patients received CGA at baseline performed by a multidisciplinary team with evaluation of patient health status. Intervention group received a tailored follow-up by a multidisciplinary team. Follow-up lasted 90 days, performed in-hospital (either in the outpatient clinic or during hospitalisation), in the patient own home, or as phone calls. | Hospitalisations | No significant impact on hospitalisation (47% of intervention vs. 55% of controls). | Neutral |
| Completion of planned treatment | No differences in ability to complete the treatment, ADLs or physical performance were found. | Neutral | ||||
| Soo et al., 2020 [ | 130 patients | RCT | Intervention group received integrated oncogeriatric care: CGA and management integrated with standard oncology care. The group was co-managed by a geriatrician during oncological treatment, undergoing a CGA, standardised personalised interventions and receiving referrals, supportive care information, encouragement of physical activity, management of comorbidities, medication reconciliation and advance care planning. Control group: managed by oncologist only, without input from geriatrician. | QoL | Significant differences favouring the intervention group over the usual care group were seen in QoL—assessed using EORTC QLQ-C30 and EORTC QLQ-ELD14 at 0, 12, 18 and 24 weeks—and unplanned hospital admissions (−1.2 admissions person-years in intervention group; 41% less) and ED visits (39% less). Intervention group presented significantly better ELFI than usual care group at all follow-ups. | Positive |
| Treatment discontinuation | Significant differences favouring the intervention group over the usual care group were seen in early treatment discontinuation (32.9% vs. 53.2%, respectively). | Positive | ||||
| Ramsdale et al., 2018 [ | 40 patients 20 patients in intervention arm | Descriptive comparison study (subset of patients enrolled in RCT) | All patients received CGA at baseline, prior to starting antineoplastic therapy. | Addressing PIM and PP | Physician-initiated discussions were higher in intervention (73% vs. 49%, | Positive |
| Magnuson et al., 2018 [ | 71 patients 37 patients in intervention group [recommendations for GA management interventions were relayed to the primary oncologist within the target time-frame in 34 patients (92%)]. | Prospective randomised pilot study | In intervention arm an algorithm was used to guide GA management recommendations. The coordinator scored the GA and identified impairments, then summarised GA impairments with management recommendations and delivered recommendations to the patient’s primary oncologist within 1 week of assessment. At the 3-month follow-up timepoint, the primary oncologist reported whether these recommendations had been implemented. | Hospitalisations | Prevalence of hospitalisation did not differ between the two groups. | Neutral |
| ADEs | Incidence of grade 3–5 CT toxicity did not differ between the two groups. | Neutral | ||||
| Puts et al., 2018 [ | 61 patients 31 patients allocated to intervention arm | RCT | Intervention: CGA, interventions, first follow up. 3 months after CGA, follow-up appointment if needed. Treating physician received the summary of findings and interventions that would be implemented by the clinical intervention team. | QoL | Slight benefit in QoL for intervention patients, but results at all timepoints presented no statistically significant difference. No significant differences in number of ED and GP visits, even if slightly lower rates in intervention group. | Neutral |
| IADL impairment | Fewer patients with IADL impairment ≥ 1 in intervention than in control group at baseline. At six months, the proportion of those with ≥ 1 IADL impairment was similar. | Neutral | ||||
| Corre et al, 2016 [ | 494 patients 243 patients in the intervention arm | RCT | All patients had a CGA performed by their regular cancer physician. | QoL | Although QoL utility scores at baseline were not different between the arms, they always were higher (although not significantly) in the CGA arm than in the standard arm at each subsequent evaluation, with no evident negative impact of the 23% of patients who received exclusive BSC. The difference in QoL utility scores was significant only at week 36 ( | Neutral |
| ADEs | Treatment objective response rate and disease control rate in CGA arm and control showed no difference. Intervention had significantly less all grade toxicity than control (85.6% vs. 93.4%, | Positive | ||||
| Kalsi et al., 2015 [ | 135 patients 65 patients in intervention group (2011–2013) 70 patients in observational control group (2010–2012). | Prospective cohort comparison study | The intervention group underwent risk stratification using a patient-completed screening questionnaire and high-risk patients received geriatrician-delivered CGA. The observational control group received standard oncology care. | CT outcome | Geriatrician-delivered CGA was associated with better outcomes. No significant trend for a lower grade 3+ toxicity rate in intervention (43.8% 3+ toxicity rate in the intervention group and 52.9% in the control). More participants in intervention completed treatment as planned ( | Positive |
| Bourdel-Marchasson et al., 2014 [ | 336 patients | RCT | The usual care received usual dietary recommendations. | Hospitalisation | Analyses were performed on an ITT basis. The intervention was no beneficial for hospitalisation (intervention presented not significantly lower hospitalisations) and 1 and 2-year mortality (similar in both groups). Cancer cachexia anti-anabolism may explain this lack of effect. The intervention did not modify the HRQoL changes in comparison with routine care. | Neutral |
| ADEs | Diet counselling was efficient in increasing dietary intake but had no beneficial effect on CT management (dosage, changes, arrest). | Neutral | ||||
| Rao et al., 2005 [ | 99 frail patients | Secondary analysis (of RCT) | Hospitalised on a medical or surgical ward, after stabilisation of acute illness, randomised to receive care in a geriatric inpatient unit/geriatric outpatient clinic/both/neither. | LoS | Geriatric evaluation and management inpatient units impacts the QoL (SF-36) in the management of bodily pain and mental and emotional health (no difference in SF-36 general scores between groups). These effects were achieved with no overall increase in hospitalisation or cost of care over the year of the study. No significant differences in LoS. No effect on mortality. | Neutral |
Abbreviations: ADLs: Activities of Daily Living; ADEs: Adverse Drug Events; AEs: Adverse Events; BSC: Best Supportive Care; CT: Chemotherapy; CGA: Comprehensive Geriatric Assessment; CRC: Colorectal cancer; DDI: Drug–Drug Interaction; DRP: Drug Related Problems; ED: Emergency Department; ELFI: Elderly Functional Index; EoL: End of Life; EQ-5D: EORTC: European Organisation for Research and Treatment of Cancer; EORTC QLQ-C30: EORTC Core Quality of Life Questionnaire; EORTC QLQ-ELD14: EORTC Quality of Life Questionnaire—Elderly Cancer Patients Module; EuroQoL-5 Dimension; EQ-5D-3L: 3-level version of EQ-5D; FACT-G: Functional Assessment of Cancer Therapy-General; GPs: General Practitioners; GU: genitourinary; HRQoL: Health-Related Quality of Life; IADLs: Instrumental Activities of Daily Living; ITT: Intention-To-Treat; KPS: Karnofsky PS; LoS: Length of Stay; MNA: Mini Nutritional Assessment; NSCLC: Non-Small-Cell Lung Cancer; OS: Overall Survival; PFS: Progression Free Survival; PIM: Potentially Inappropriate Medication; PP: polypharmacy; PS: Performance Status; RCT: Randomised Control Trial; RT: Radiotherapy; SF-36: Short Form-36 Health Survey; SPICES: Sleep disorders—Problems with eating/feeding–Incontinence–Confusion–Evidence of Falls–Skin Breakdown; TFFS: Treatment Failure-Free Survival; VES-13: Vulnerable Elders Survey. White rows: cost-sensitive measures (measures of patient health conditions leading to cost-increasing or cost-decreasing effects); grey rows: measures of effectiveness of CGA intervention (with the estimation of costs in two studies [81,86]).
Most recurrent reported measures for effectiveness of CGA interventions.
| Measures | Evidence in Identified Studies | ||||||||
|---|---|---|---|---|---|---|---|---|---|
|
| Nipp et al., 2022 [ | Koh et al., 2021 [ | DuMontier et al., 2020 [ | Li et al., 2020 [ | Shahrokni et al., 2020 [ | van der Vlies et al., 2020 [ | Janssen et al., 2019 [ | Tarazona-Santabalbina et al., 2019 [ | |
| positive | positive | neutral | neutral | negative | neutral | neutral | neutral | ||
| Ommundsen et al., 2018 [ | Shipway et al., 2018 [ | Souwer et al., 2018 [ | Ho et al., 2017 [ | Indrakusuma et al., 2015 [ | Mak et al., 2014 [ | Hempenius et al., 2013 [ | Rao et al.2005 [ | ||
| neutral | positive | positive | positive | neutral | positive | neutral | neutral | ||
|
| Lund et al., 2021 [ | Mohile et al., 2021 [ | Choukroun et al., 2021 [ | Li et al., 2020 [ | Nadaraja et al., 2020 [ | Magnuson et al., 2018 [ | Corre et al., 2016 [ | Kalsi et al., 2015 [ | Bourdel-Marchasson et al., 2014 [ |
| positive | positive | positive | positive | positive | neutral | positive | neutral | neutral | |
* Frail patients in the intervention group. Abbreviations: ADEs: Adverse Drug Events; LoS: Length of Stay; RCT: Randomised Control Trial.
Costs for hospitalisation and adverse events treatments.
| Country | Cost Estimates |
|---|---|
| United States [ | Median cost per day of inpatient visits for older patients with cancer: USD 2108—USD 3468 |
| United States [ | Direct cost of neutropenia per episode: USD 1893 (outpatient)/USD 2893 (inpatient)—USD 38,583 (febrile neutropenia hospitalisation) |
| UK and Europe [ | Direct cost of neutropenia per episode: USD 300 (non-febrile cases)—USD 32,395 (older breast cancer patients) |
| United States [ | Direct cost of thrombocytopenia per cycle/episode: USD 1035—USD 5328 |
| Europe [ | Direct cost of thrombocytopenia per cycle/episode: USD 790—USD 2523 |
| United States [ | Direct cost attributable of anaemia per year: USD 18,418—USD 69,478 |
| Canada and Europe [ | Total cost of anaemia per episode: USD 124—USD 2704 |
| United States and Europe [ | Average total cost per ICU/day: estimated at EUR 1200 |
| Europe [ | Direct costs per sepsis patient (ICU): estimates of EUR 23,000—EUR 29,000. |
| United States [ | Direct costs per sepsis patient (ICU): estimates of EUR 34,000 |
| United States [ | Costs for severe sepsis cancer hospitalisation: USD 27,400 |
| United States [ | Healthcare costs per delirious patient per year: USD 60,516—USD 64,421 |