http://orcid.org/0000-0002-1211-4916
Correction
27 Apr 2021: de’Angelis N, Baldini C, Brustia R, Pessaux P, Sommacale D, et al. (2021) Correction: Surgical and regional treatments for colorectal cancer metastases in older patients: A systematic review and meta-analysis. PLOS ONE 16(4): e0251005. https://doi.org/10.1371/journal.pone.0251005 View correction
Figures
Abstract
Objective
The present study explored the existing literature to describe the outcomes of surgical and regional treatments for colorectal cancer metastases (mCRC) in older patients.
Methods
A literature search was conducted in PubMed, EMBASE, Cochrane and ClinicalTrials.gov for studies published since 2000 that investigated the short- and long-term outcomes of regional treatments (surgical or non-surgical) for mCRC in patients aged ≥65 years. Pooled data analyses were conducted by calculating the risk ratio (RR), mean differences (MD) and hazard ratio (HR) between older and younger patients or between two different approaches in older patients.
Results
After screening 266 articles, 29 were included in this review. These studies reported the outcomes of surgery (n = 19) and non-surgical local ablation treatments (n = 3) for CRC metastases in older vs. younger patients or compared the outcomes of different interventions in older patients (n = 7). When comparing older vs. younger patients undergoing liver surgery for mCRC, pooled data analysis showed higher postoperative mortality [RR = 2.53 (95%CI: 2.00–3.21)] and shorter overall survival [HR = 1.17 (95%CI: 1.07–1.18)] in older patients, whereas no differences in operative outcomes, postoperative complications and disease-free survival were found. When comparing laparoscopy vs. open surgery for liver resection in older mCRC patients, laparoscopy was associated with fewer postoperative complications [RR = 0.27 (95%CI: 0.10–0.73)].
Conclusion
Liver resection for mCRC should not be disregarded a priori in older patients, who show similar operative and postoperative outcomes as younger patients. However, clinicians should consider that they are at increased risk of postoperative mortality and have a worse overall survival, which may reflect comorbidities and frailty.
Citation: de’Angelis N, Baldini C, Brustia R, Pessaux P, Sommacale D, Laurent A, et al. (2020) Surgical and regional treatments for colorectal cancer metastases in older patients: A systematic review and meta-analysis. PLoS ONE 15(4): e0230914. https://doi.org/10.1371/journal.pone.0230914
Editor: Giuseppe Nigri, Sapienza University of Rome, ITALY
Received: November 15, 2019; Accepted: March 11, 2020; Published: April 22, 2020
Copyright: © 2020 de’Angelis et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: No funding or research grant was received to perform this systematic review and meta-analysis. No external financial support was received. The study was promoted by the Societé Francophone d’Oncogeriatrie (SoFOG), but no financial contribution was received from the scientific society. The authors’ affiliations (universities/hospitals) provided support exclusively in form of salaries and did not have any additional role in the study design, data collections and analyses, decision to publish, or preparation of the manuscript.
Competing interests: Pr P Pessaux is an orator for Integra and a co-founder of VirtualiSurg. This affiliation does not alter our adherence to PLOS ONE policies on sharing data and materials. All other authors have nothing to disclose, and all authors have declared that no competing interests exist in relation to the matter of this study.
Introduction
With the increase of life expectancy, the proportion of people aged 65 years and over has increased five-fold during the last 15 years [1]. Recent approaches have forecasted an increase in life expectancy by 4.4 years for both sexes by 2040, exceeding 85 years in many developed countries [2]. Indeed, although an increase in functional impairment and frailty is observed with aging, life expectancy for those aged between 80 years and 85 years is still 8 years [3–5], with a consequent greater chance for clinicians to diagnose diseases and treat patients at an advanced age.
Colorectal cancer (CRC) is the third most incident cancer in adults [6, 7] and the second most common cause of cancer-related death in Europe [8]. In 20–25% of cases, CRC presents with simultaneous liver metastases (American Joint Committee on Cancer [9], AJCC stage IV) and 85% of these lesions are not resectable at diagnosis [7, 10, 11]. Moreover, an additional 25–50% of CRC patients will develop metachronous metastases after the resection of the primary tumor, with the liver as the most frequent initial recurrence site [12–14]. In the case of metastatic CRC (mCRC), a multimodality treatment is required [15, 16]. Hepatectomy for colorectal liver metastasis (CRLM) offers the highest cure rate and is indicated for adult patients with primarily resectable disease or after downstaging chemotherapy [11, 17, 18], with a 5-year survival rate that ranges from 35% to 60% [19]. Alternative treatments include chemotherapy (CT) regimens, local ablation therapies, radio-embolization and hepatic intra-arterial chemotherapy [15, 20–22].
The yearly incidence of CRC has increased in people aged 75 years or older [23]. In France, 45% of new cases have occurred in patients aged 75 years or older [24]. In general, there is less frequency of chemotherapy or liver surgery for mCRC in older populations [25, 26]. Non-surgical therapies are favored in older patients with the assumption that advanced age and the presence of comorbidities yield a higher risk of surgical morbidity and mortality [14]. Age is often considered a risk factor for poorer postoperative outcomes; however, compelling evidence supports that it is not the actual chronological age of the patient that constitutes a risk for surgery but rather the quality of aging, comorbidity and the functional status that define the condition of frailty [27–29]. Therefore, caring for older patients with mCRC is an ongoing challenge and to date, there is still a lack of guidelines to support the decision of the optimal strategy for the management of mCRC in older patients (age ≥ 65 years)[14, 25, 30].
This study aimed to explore the current literature to i) describe the current trend of regional treatments for mCRC in older patients and ii) evaluate the clinical and oncological outcomes of surgery and regional treatment options in older vs. younger patients.
Methods
Study design
This is a systematic review and meta-analysis designed to describe and evaluate the outcomes of different regional treatments (i.e., surgery, radiofrequency, cryotherapy, microwave ablation, electroporation, and radioembolization) in the case of treatable mCRC in older patients. The present report is structured according to recommendations by the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines [31, 32], and the study protocol has been registered in the PROSPERO database (provisional registration number: 132956).
Eligibility criteria for study inclusion
Studies were eligible for inclusion if they met the criteria established by the following PICOS framework:
Patients: patients aged ≥65 years and diagnosed with mCRC (AJCC stage IV)[33, 34].
Intervention: regional treatments including curative-intent surgical resection, radioembolization, cryotherapy, microwave ablation, electroporation, regional hepatic intra-arterial chemotherapy, and chemoembolization for synchronous or metachronous mCRC [22].
Comparison: according to the patients’ age (e.g., surgical resection in older vs. surgical resection in younger patients) or the type of intervention (e.g., surgical resection vs. chemotherapy in older patients).
Outcomes: operative and postoperative outcomes (e.g., morbidity, mortality) and survival rates (overall survival, OS; disease-free survival, DFS).
Study design: randomized controlled trials (RCTs), non-randomized controlled trials (NRCTs), and observational case-control and cohort studies.
Search strategy
Relevant human studies were identified up to March 2019 from the following online available databases: MEDLINE (through PubMed), EMBASE, Cochrane Library, and ClinicalTrials.gov register. For each database, a specific research equation was formulated using the following key words and/or MeSH terms: metastatic colorectal cancer, metastasis, elderly, older, age ≥65, age ≥70, age ≥80, surgery, surgical resection, liver resection, metastasectomy, radiofrequency ablation, radioembolization, local ablation treatment, cryotherapy, microwave ablation, electroporation, regional treatment. In addition, manual searches in the references sections of eligible studies and relevant review articles were crosschecked to identify additional records. The literature search was limited to the time frame January 2000 –March 2019, and only English literature was considered.
Study selection
A parallel, double blind screening procedure of titles and abstracts was carried out by two reviewers (NdeA and EL). To enhance sensitivity, records were removed only if both reviewers excluded the record at the title/abstract level. The reviewers’ consistency was assessed by the kappa test. Subsequently, both reviewers performed a full-text analysis of the articles and proceeded to the final selection phase. Any disagreement between the two reviewers was resolved by consensus with a third reviewer (CB).
Data extraction and quality assessment
The following variables were extracted from the selected articles and collected in an excel spreadsheet: authors, year of publication, journal, country, study time frame, study design, patient population, type of regional treatments, type of surgical procedure, intraoperative and postoperative outcomes, 90-day morbidity (overall postoperative complications; type and severity of postoperative complications according to Dindo-Clavien classification, including pulmonary complications, hepatic complications, and major complications) and 30-, 60- or 90-day mortality, survival (overall, disease-free, cancer-specific) at any reported time point (1, 2, 3, 5 years or more after the intervention).
The risk of bias was assessed using the Newcastle–Ottawa Scale (NOS) for case-control and cohort studies [35]. Both data extraction and the quality assessment of the study were performed by the two reviewers (NdeA and EL) independently and compared to reach a consensus (if necessary) with the third reviewer (CB).
Pooled data analyses
Data from the included studies were used for a qualitative and quantitative synthesis according to the patients’ age or the type of intervention. For binary outcomes, the risk ratio (RR) and 95% confidence intervals (CI) were estimated using the Mantel-Haenszel method. For continuous data, the mean differences and 95%CI were estimated using inverse variance weighting. Outcome measures were extracted as the mean (SD) or median (interquartile range) as provided. To calculate the mean values from the median, we applied the method described by Hozo et al. [36].
To compare OS and DFS between older and younger patient groups or between different types of interventions for mCRC, we calculated the hazard ratio (HR) and 95%CI as described by Tierney et al. [37]. Heterogeneity was assessed by the I2 statistic, and values of 25%, 50%, and 75% were considered low, moderate, and high heterogeneity, respectively [38, 39]. Random effect model was used as considered a more precise estimator when there is in between study heterogeneity in true effects. Whenever indicated, sensitivity analyses were performed to test degree of certainty of the results. A p<0.05 identifies significant pooled effects. Meta-analyses were performed using the Cochrane Collaboration software, RevMan (Version 5.3).
Results
Literature search and selection
Results of the literature review in the considered databases and the step-by-step study selection are shown in Fig 1. Overall, the combined search on the different databases identified 266 articles. After removing duplicates and non-pertinent studies upon title and abstract, 146 articles underwent a full-text evaluation. Of these, 124 were excluded because they were not pertinent to the review question. Finally, 29 articles were selected and eligible for pooled data analyses (availability of outcome data). The two reviewers had an optimal interexaminer agreement in the selection process (kappa: 0.978).
Study characteristics
Studies were published predominantly after 2013 (62% of the studies), whereas no study was published before 2004 (S1 Fig). These studies were conducted in Europe (n = 15), North America (n = 7), Asia and the Pacific (n = 7). There was no RCT. All of the studies were retrospective, of which 7 were population-based cohort studies [25, 26, 40–44], 16 retrospective analyses of patient cohorts [45–60], 4 case-control studies [61–64], and 2 propensity score matched (PSM) case-control studies [65, 66]. Overall, 5 studies (17.8%) were multicentric [48, 49, 51, 59, 66]. The study time frames spanned from 1986 to 2017, with a mean of 9.64 years (range: 8 months-22 years).
Twenty-two studies compared the outcomes of local ablation therapies in older patients vs. younger patients. Of these, 19 studies reported the outcomes of surgical resection for CRC metastases (Table 1). Specifically, 16 studies focused on liver resection for CRLM [40, 45, 47, 50–52, 54–57, 59–64], and 3 studies investigated the outcomes of multimodality treatments, including surgical resection for CRC metastases [25, 42, 44]. Only 3 studies reported the outcomes of non-surgical regional treatments (including radioembolization [RE], radiofrequency ablation [RFA], and high-dose-rate brachytherapy [HDR-BT]) for mCRC in older vs. younger patients (Table 2)[49, 53, 58]. The remaining 7 studies compared the outcomes of different types of regional interventions in older patients [26, 41, 43, 46, 48, 65, 66](Table 3).
Definition of older patients
The definition of older patients largely varied among the studies. The majority of the studies (55.1%) used an age cut-off of ≥70 years [46, 47, 49, 50, 52–59, 62–64, 66] to define older people. Two studies defined older patients aged ≥65 years[41, 65] and 6 patients aged ≥75 years [25, 26, 40, 43, 45, 48, 51, 60, 61]. One study defined older patients as those aged ≥80 years[42] or ≥85 years [44] and compared them to younger patients. Few studies compared more than 2 age groups, with a category of very old patients, whose age cut-off varied from 75 to 85 years old [44, 51, 61]. For the sake of clarity, the terminology has been unified as older vs. younger patients in the present systematic review, although in each study different terms were used (e.g., old, older, elderly, non-elderly, young, younger patients).
Scores of general status or comorbidity were reported in only 48.2% of the studies. Eight studies used the Charlson Comorbidity Index (CCI)[25, 40, 41, 43, 52, 53, 62, 64], 5 studies used the Eastern Cooperative Oncology Group Performance Status (ECOG-PS) [44, 48, 49, 58, 63], and one study used the Prognostic Nutritional Index (PNI)[57]. None of the studies reported frailty status or morbidity, mood, cognitive function or social environment parameters in older patients.
Outcomes of surgical resection of mCRC in older vs. younger patients
The 19 studies that reported on the outcomes of surgical resection for CRC metastases presented different study designs, populations, and settings (Table 1). Overall, the outcomes of liver resection for CRLM were investigated in 7579 older patients, 179 very old patients, and 15904 younger patients [25, 40, 42, 44, 45, 47, 50–52, 54–57, 59–64, 67]. The use of portal vein embolization before surgery was reported in 5 studies [45, 54, 61, 63, 64], which was not applied differently between older and younger patients.
Although the disease stage was not systematically reported, the metastases characteristics were described in the majority of the studies (84.2%), with seldom differences between the groups. However, older patients usually presented with comorbidities, greater ASA score, and lower treatment rate than younger patients. In general, older patients were less likely to undergo major liver resection and less likely to receive perioperative chemotherapy.
Ten studies found similar postoperative complication rates between older and younger patients [47, 48, 51, 52, 56, 57, 61–64], whereas 5 studies reported a higher incidence of postoperative complications in the older [50, 54, 55, 59, 60]. Four studies did not report morbidity rates [25, 40, 42, 44]. Similarly, 12 studies reported a similar postoperative mortality between older and younger patients [45, 47, 50–52, 55–57, 61–64], whereas a significantly higher postoperative mortality was observed in 4 studies [40, 54, 59, 60]. In the majority of the studies (11/18, 61.1%), older patients had a worse overall survival compared to younger patients [25, 40, 42, 44, 47, 54, 55, 57, 59, 62]. However, the majority of the studies found that age was not an independent predictor of OS and DFS, supporting the conclusion that the advanced chronologic age should not be regarded as a medical contraindication to hepatic resection for CRLM.
Meta-analyses were performed by the patients’ age group and as a global comparison between older and younger patients. Eleven studies compared patients aged ≥70 years vs. patients aged <70 years [47, 50, 52, 54–57, 59, 62–64], and 5 studies were selected to compare patients aged ≥75 years vs. patients aged <75 years [40, 45, 51, 60, 61].
The operative time was significantly shorter in older patients, whereas no age-related difference was found for the transfusion rate and R0 resection (Fig 2). Blood loss was estimated in only 6 studies comparing 337 patients aged ≥70 years vs. 839 patients aged <70 years [50, 52, 56, 57, 62, 64]. Pooled data analysis showed a non significant difference between the groups (MD: 14.85 [95%CI: -8.59; 38.27], p = 0.21; I2: 44%) (S2 Fig).
The following outcomes were analyzed: a. operative time (min); b. transfusion rate (n); and c. R0 resection (n).
Postoperative bile leak and liver failure were not different between older and younger patients undergoing liver resection for CRLM (S3 Fig). Pulmonary complications were evaluated in 6 studies comparing 397 patients aged ≥70 years vs. 1096 patients aged <70 years [54, 56, 57, 62–64] and were not different between the groups (RR: 1.75 [95%CI: 0.69; 4.44], p = 0.24; I2: 66%) (S4 Fig). The rates of overall postoperative complications (Fig 3A), as well as the occurrence of major postoperative complications (classified as Dindo-Clavien III or more) (S5 Fig) and the overall hospital stay (Fig 3B), were similar between older and younger patients. Conversely, a significantly higher postoperative mortality was observed in older patients (RR: 2.53), overall and when considering age cut-off of ≥70 years old or ≥75 years old (Fig 3C). Concerning the survival analysis, older patients had a worse survival compared with younger patients but a similar DFS (Fig 4).
The following outcomes were analyzed: a. overall postoperative complications (n), b. hospital stay (days), and c. mortality (n).
The following outcomes were analyzed: a. overall survival and b. disease-free survival.
Outcomes of non-surgical local ablation of mCRC in older vs. younger patients
The outcomes of yttrium-90-labeled resin microsphere radioembolization (90Y-RE) were assessed in 3 studies involving a total of 809 patients [49, 53, 58] and were compared between older (≥70 years old) and younger patients (<70 years old) (Table 2). 90Y-RE was indicated for patients with CRLM who were refractory, exhausted or declined standard CT regimens [49, 58], or patients with diffuse, liver-dominant involvement [53]. Overall, 90Y-RE was equally well tolerated in both the older and younger patient groups, with no different rate and severity of adverse events. Mortality at 90 days ranged between 12.5% to 18.1%, without differences related to the age group [49, 58]. Median survival did not reach 1 year after 90Y-RE (range: 6.5–9.7 months)[49, 53, 58] independent of the age group. Although older patients appeared to be less likely to receive more than 1 90Y-RE procedure and a lower liver volume was treated, all 3 studies concluded that age alone should not be a discriminating factor for the use of 90Y-RE in the management of mCRC [49, 53, 58]. Pooled data analysis was possible only for postoperative mortality. Based on two studies [49, 58], including 204 older patients vs. 510 younger patients, the postoperative mortality rate post 90Y-RE was not different between the groups (RR: 1.39 [95%CI: 0.95, 2.02], p = 0.09; I2: 0%) (S6 Fig).
Only one study evaluated the outcomes of radiofrequency ablation (RFA) applied in 60 mCRC patients, and high-dose-rate brachytherapy (HDR-BT) applied in 192 mCRC patients [53]. For RE, local ablation was selected in potentially resectable metastases only if patients had an unfavorable performance status and/or severe comorbidities (resulting in a high risk of perioperative morbidity and mortality) or if patients refused surgery. RFA was preferentially applied for patients with single lesions up to 3 cm in diameter, whereas interstitial HDR-BT was applied for oligometastatic disease [53]. The median survival rate reported for RFA was 26.7 months for older patients vs. 24.3 months for younger patients, whereas it was 19.1 months for older patients vs. 18.2 months for younger patients receiving HDR-BT. No age-related differences were found, suggesting that local ablation treatments can be safely performed in older people, although the type of local ablation treatment seems to have no impact on OS. The presence of comorbidity, in particular moderate to severe renal insufficiency, appeared to negatively impact the outcomes of local therapies [53].
Outcomes of different treatments for mCRC in older patients
Comparisons at the intervention level included 1 study that compared first hepatectomy vs. repeated hepatectomy [46] in older patients (≥70 years old), 2 studies that compared hepatic resection vs. no hepatic resection for CRLM [26, 41], 2 studies that compared CT vs. other treatments (including surgery and multimodality treatments, MMT)[43, 48], and 2 studies that compared laparoscopic hepatectomy vs. open hepatectomy [65, 66] in older patients (Table 3). CRC metastases were highly heterogeneous in their presentation, in terms of number of lesions, size and type (synchronous or metachronous). Overall, survival was dependent on the patient’s age [26, 41, 43, 48] and was significantly better in patients who underwent hepatic resection for CRLM (based on 2 population-based studies, including 54736 patients)[26, 41].
The comparisons between laparoscopic and open surgery for the resection of CRLM in older patients (2 PSM studies, including 1160 patients before PSM and 608 patients after PSM) showed that the operative approach is not a predictor of 5-year OS and 5-year DFS [65, 66], although a significantly lower postoperative morbidity was associated with laparoscopic hepatectomy, particularly in the age groups < 80 years [66]. The meta-analytic approach was used to pool together data from these two studies and compare laparoscopy vs. open surgery [65, 66], reaching a total of 304 patients in the laparoscopic group and 304 patients in the open surgery group. The forest plots (Fig 5) show a significant difference in favor of laparoscopy for blood loss, hospital stay, and rate of major postoperative complications. The operative time was not different between the two surgical approaches. A sensitivity analysis was conducted pooling together data from the study by Zeng et al. [65](all patients aged ≤75 years) and a subsample of patients from the study of Martinez-Cecilia et al. [66] aged between 70 and 74 years (n = 356). This analysis confirmed the previous results for operative time (MD: 13.9 [95%CI: -39.93, 67.73]; p = 0.61; I2: 95%), blood loss (MD: -72.54 [95%CI: -100.19, -44.89]; p<0.001; I2: 93%), hospital stay (MD: -2.86 [95%CI: -4.55, 0.55]; p<0.0001; I2: 0%), and severe postoperative complication rate (RR = 0.27 [95%CI: 0.10, 0.73]; p = 0.01; I2: 0%) between laparoscopy and open surgery. OS and DFS were not different between the two surgical approaches (Fig 5E and 5F).
The following outcomes were analyzed: a. blood loss (mL); b. operative time (min); c. major postoperative complications (n); d. hospital stay (days); e. overall survival; and f. disease-free survival.
Study quality assessment
Fourteen studies were judged as having low quality and thus had a high risk of bias (S1 Table). The remaining studies scored ≥ 6 on the NOS.
Discussion
The present systematic review and meta-analysis comprised studies published in the last 19 years that investigated the outcomes of surgical and non-surgical regional treatments for mCRC in older patients. The qualitative synthesis revealed that the current pertinent literature is lacking RCTs while only retrospective studies with heterogonous study design, study populations, and study outcomes can be found. Notwithstanding, the review question remains extremely actual and critical, considering the increasing life expectancy of the general population and the compelling incidence of mCRC in older patients [5–8].
The treatment of mCRC requires a multidisciplinary approach that must include chemotherapy, surgery or other regional strategies to be curative [15, 16]. This results in a complex management burden by morbidity and adverse events that can be more frequent and severe in already frail patients. Indeed, it appears from the literature that although all treatments can be considered for older patients with mCRC, these patients are less likely to receive aggressive curative-intent therapies compared to younger ones [40, 42, 54, 57]. The main reason is found in the anticipated risk of mortality and morbidity that guides clinicians to choose a less aggressive approach. However, overall, the literature states that the patient’s advanced chronologic age cannot be considered as an absolute medical contraindication for regional treatments in case of mCRC [49, 58], including surgical resection of CRC metastases [51, 52, 55–57, 62, 64]. Pooled data analyses support this therapeutic attitude, since no difference was found in terms of operative parameters and postoperative complications between older (both aged ≥70 and 75 years) and younger patients. However, older patients are at 2 to 3-fold increased risk of postoperative mortality compared to younger patients. This finding may reflect the increased ASA score and comorbidity index usually observed in older patients undergoing treatments for mCRC and may reflect a lower likelihood of older patients to recover after postoperative complications. Indeed, in most of the studies, a significant imbalance between the two age groups was noted for these clinical variables, but their impact as covariates is hardly assessable. Notwithstanding it, we may hypothesize that although the estimated rate of postoperative complications is similar between older and younger patients, whenever a postoperative complication occurs, this is more likely to be fatal in the older patient group. Conversely, no significant age-related difference was noted for mortality rate after 90Y-RE.
Pooled survival analyses showed that older age is associated with worse survival after surgery for mCRC, as expected. However, disease-free survival rates appear not to be affected by the patients’ age. These data suggest that the risk of cancer recurrence is similar between older and younger patients, underlying a negligent impact of chronological age on DFS, and it can be interpreted as indirect proof of a similar success rate of CRLM surgical resection in both older and younger CRC patients.
Considering the surgical approach to liver resection, the two selected comparative studies demonstrated that there is no difference in terms of OS and DFS outcomes between open surgery and laparoscopy in older patients [65, 66]. However, open surgery is associated with a 2.6 times greater risk of major postoperative complications [65, 66] and overall postoperative morbidity compared to laparoscopy [66]. These findings are in accordance with the results of the OSLO-COMET RCT that demonstrated the superiority of laparoscopic liver resection for mCRC [68], and supports the use of laparoscopy also in selected older patients. Moreover, they corroborate the findings of a recent meta-analysis that evaluated the outcomes of all types of laparoscopic liver resection (for both benign and malignant lesions) in older patients, and reported significantly better intra-operative (e.g., bleeding) and postoperative outcomes (e.g., severe Dindo-Clavien complications) for laparoscopy vs. open surgery [69]. It must be noted that the surgical approach chosen may have a relevant impact on postoperative outcomes, especially in a higher-risk patient population such as older patients. Indeed, minimizing surgical trauma can facilitate the patient’s recovery and results in benefits from both the patient’s perspective and the healthcare system’s perspective. Thus, age should not be regarded as a contraindication for laparoscopy; rather, this approach should be preferred whenever an adequate surgeon’s proficiency and experience is insured [70].
The results of the present systematic review and meta-analysis should be interpreted in light of the study limitations, among which we must acknowledge the clinical heterogeneity of the included studies, the lack of a standardized age definition and outcomes, and the lack of variable adjustments on potential confounders such as the score of frailty. It is highly difficult to assess the potential bias linked to the selection of patients for whom the treatment is indicated. Moreover, all included studies have a retrospective design, which increases the risk of selection and reporting bias. However, we attempted to reduce other potential sources of bias by performing a literature search limited to the time period 2000–2019, which avoided important discrepancies that may be found when comparing treatment protocols and indications prior to the year 2000. Finally, the literature search and evaluation were performed by two independent and blind reviewers, a digestive surgeon and a geriatric oncology specialist, who were advised by a team of multidisciplinary contributors including oncologists, geriatrics, gastroenterologists, hepatologists, radiologists, and methodologists.
Key-points and future research perspectives
- Standardized treatment protocols and international guidelines are eagerly awaited in order to limit unjustified treatment differences based on the patient’s age.
- A standardized definition of older patient, comprising a validated evaluation of frailty, should be systematically used in studies focusing on the treatment of mCRC in order to allow a better comparability of study outcomes and provide a stronger evidence-based interpretation of study results.
- Whenever a curative-intent surgical resection for mCRC can be attempted, this should be encouraged and tailored to the patient’s performance status, comorbidity index and willingness to receive treatments rather than on age. These factors should be evaluated preoperatively in multidisciplinary meetings, which should involve oncologists, geriatrics, gastroenterologists, hepatologists, radiologists, and liver surgeons, to insure the best patient global management.
- Prospective single center or multicenter registers are required to assess patient-centered outcomes, such as the quality of life for CRC survivors with or without a recurrence of cancer. These outcomes are currently completely disregarded in the literature.
- Development of treatment protocols tailored to older patient populations will consequently have an impact on the economic burden of CRC, with direct and indirect medical costs that are expected to increase due to population changes alone [71]. In the case of mCRC, it is also extremely relevant to investigate the financial burden of cancer for the patients and their family to assist health care policy makers in their efforts to improve the quality of survivorship in older patients.
Conclusion
The present systematic review and meta-analysis suggest that older patients undergoing surgery and local ablation treatments for mCRC have similar operative outcomes and similar postoperative complication rates as younger patients. These treatment options should not be disregarded a priori in patients aged 65 years or more, but clinicians should be aware that older patients are at an increased risk of postoperative mortality and have a worse overall survival compared to younger patients. These two outcomes may reflect the competitive effects of comorbidity and frailty of the older population, which need to be further evaluated in future studies.
Supporting information
S1 Fig. Number of publications per year on the local ablation treatments for colorectal cancer metastases in elderly patients.
https://doi.org/10.1371/journal.pone.0230914.s002
(TIFF)
S2 Fig. Forest plots of estimated blood loss in older (≥70 years old) vs. younger patients (<70 years old) undergoing liver resection for CRLM.
https://doi.org/10.1371/journal.pone.0230914.s003
(TIFF)
S3 Fig. Forest plots of postoperative outcomes of liver resection for CRLM in older vs. younger patients.
The following outcomes were analyzed: a. bile leak (n) and b. liver failure (n).
https://doi.org/10.1371/journal.pone.0230914.s004
(TIFF)
S4 Fig. Forest plots of pulmonary complications in older (≥70 years old) vs. younger patients (<70 years old) after liver resection for CRLM.
https://doi.org/10.1371/journal.pone.0230914.s005
(TIFF)
S5 Fig. Forest plots of major postoperative complications (Dindo-Clavien III or more) after liver resection for CRLM in older vs. younger patients.
https://doi.org/10.1371/journal.pone.0230914.s006
(TIFF)
S6 Fig. Forest plots of mortality rate in older (≥70 years old) vs. younger patients (<70 years old) after Y90-RE for CRLM.
https://doi.org/10.1371/journal.pone.0230914.s007
(TIFF)
S1 Table. Study quality assessment using Newcastle-Ottawa scale (NOS).
https://doi.org/10.1371/journal.pone.0230914.s008
(DOCX)
Acknowledgments
The authors would like to thank the Societé Francophone d’Oncogeriatrie (SoFOG) for their support.
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