Better survival of patients with oligo- compared with polymetastatic cancers:  a systematic review and meta-analysis of 173 studies

Introduction

The vast majority of metastatic solid tumors are incurable, and despite the evolution of treatments, patients ultimately die because of their disease. The modern concept of oligometastatic (OM) state was initially developed in 1995¹ to describe patients with a low burden of disease (e.g. one to five metastases) with a potential for cure with local ablative treatments. This assumption also relies on the hypothesis that metastatic spread follows a hierarchical pattern in time and number of localizations.² In some circumstances, the 8^th Tumor Node Metastasis (TNM) staging system distinguishes between patients with a single metastasis and those with multiple such metastases. Large consensus on the definition and management of OM patients is currently lacking. Recently, advances in imaging and local ablative therapies have permitted the treatment of these patients with additional locoregional treatment in addition to systemic therapies, and some patients may be cured and attain long term survival.³ This scenario has been best elucidated in prostate, kidney, lung and melanomas.^4,5 In these settings oligometastatic cancers may be treated in oligoprogressive sites continuing systemic therapy that control the remaining disease. Also, oligometastatic tumors at presentation can receive local treatments on the primary tumor and on any single oligometastases. In the SABR-COMET randomized study median overall survival (OS) was 28 months (95% CI 19-33) in the control group versus 41 months (26-not reached) in the stereotactic body radiotherapy to all metastases group (hazard ratio 0.57, 95% CI 0.30-1.10; P = .09).⁶

The aim of this systematic review and meta-analysis was to investigate and establish the prognostic survival of OM compared to non-OM solid tumors. In particular, we evaluated if patients with oligometastatic solid tumors do better than patients with non-oligometastatic tumors defined as tumors with up to three to five metastatic sites.

Methods

This study followed the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guidelines.

Results

Among the publications retrieved using electronic search (n = 7510), 173 studies were eligible for meta-analysis, for a total of 104,234 patients¹⁰ (Figure 1). Baseline characteristics of the included studies and treatments received are presented in Table 1.

Figure 1. Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) 2020 flow diagram showing the process of study inclusion.

Progression-free survival was better in patients with OM disease (HR = 0.62, 95% CI 0.57–0.68; P < .01; n = 69 studies; Figure 2). Additionally, in the OS analysis, OM cancers were associated with a better OS (HR = 0.65, 95% CI 0.62–0.68; P < .01; n = 161 studies; Figure 3). Results were significant for all analyzed disease subgroups except biliary tract cancer and cervical cancer (only three studies included). In colorectal (CRC), breast, non-small cell lung cancer (NSCLC) and renal cell carcinoma (RCC), which constituted the more representative series, the reduction in the risk of death for OM patients were 35, 38, 30 and 42%, respectively (Figure 3). Timing of onset did not influence the risk of death. Most studies reported OS analysis for up to three metastases (152 out of 161 studies). After exclusion of eight studies that reported outcomes for up to five metastases the final results remained unchanged (HR = 0.64, 95%CI 0.61-0.67; P < .01). No cut-off was associated with a better outcome (1 vs 2 vs 1-2 vs 1-3 metastases).

Figure 2. Progression-free survival of oligo- compared to non-oligometastatic cancers.

Figure 3. Overall survival of oligo- compared to non-oligometastatic cancers.

Risk of bias through Begg's funnel plot was not significant for the OS analysis. Conversely, Egger's test showed evidence of bias (P < .01) (Figure 4). Trim and Fill analysis incorporated 29 missing studies. The overall effect measure (95% CI) based on this analysis was 0.7 (0.67-0.73), which became slightly weaker compared to the originally reported overall effect measure. Compared with cancers with more than three to five metastases, high-certainty evidence indicates OM tumors are associated with better prognosis in particular for CRC, breast, NSCLC and RCC.

Figure 4. Funnel plot of publication bias for overall survival analysis showing standard error by log hazard ratio.

Discussion

The definition of oligometastatic refers to malignancies with a limited metastatic spread which may be amenable of radical treatment for both primary and each distant site, and that generally have a better prognosis compared to polymetastatic cancers. A very recently published paper clearly explains the timely clonal evolution of somatic mutations and consequently the metastatic process of many cancer types.¹¹ It may be hypothesized that OM cancer is associated with a more indolent spread and therefore may represent a less fatal disease. With the expansion of the oncological armamentarium, many efforts have been made over the years to improve outcomes of patients with minimal metastatic burden.

We have performed the most exhaustive systematic review of the literature to quantify the prognostic value of OM stage in various cancers. Overall, OM cancer patients have a risk of death and progression that is a third less than the polymetastatic counterpart. The OM state is frequently calculated as an independent favorable prognostic variable, which means that these patients do well independent from other clinical-pathological characteristics. The effect size was calculated from 173 studies including more than 100,000 patients. The final results were similar in all the most frequent histologies including CRC, breast cancer, NSCLC, RCC and sarcoma with inferior survival in OM gastric, melanoma and head and neck cancers.

There is evidence from randomized clinical trials^12-14 that ablative therapies improve survival in patients with OM cancer. For example, in some cancers small randomized studies^12-20 already provide evidence of survival improvement in patients that received both systemic and local therapies compared to those that received systemic therapies alone. As a matter of fact, resection of colorectal cancer liver metastases nowadays represents an essential curative option and a primary endpoint in multiple clinical trails.¹² Furthermore, Gomez et al.¹³ found that in OM NSCLCs, adding local consolidative therapy to active oligometastases and to primary disease may improve OS from 17 to 41 months. Also, in RCC the treatment of indolent lung metastases may permit delaying the start of systemic treatment and obtain an excellent control.¹⁴ A large burden of evidence now supports local therapy for minimal oligoprogressive cancers treated with targeted therapies or immunotherapy. Here, metastases-directed therapy could delay the switch of systematic therapy by radical local treatment of all progressive metastatic sites.^15,16 With the advent of immunotherapy, the combination of immune check point inhibitors and radiotherapy to single OM lesions may facilitate a potentiation of the immune response, increasing the chances of achieving an abscopal effect. This term describes an event in which focalized radiotherapy discharge systemic anti-tumoral action that can result in distant responses.¹⁷ For example, in lung cancer the combination has a good safety profile and achieves high rates of local control and greater chances of obtaining abscopal responses than radiotherapy alone, with a relevant impact on outcome.¹⁸ Oligometastatic cancers can also regarded as extended locoregional disease if, after proper conversion therapy, all sites of metastases and primary tumor may be radically resected with curative purposes. Such a strategy has been employed in largely incurable cancers ad gastric and pancreatic carcinomas.^19,20

This meta-analysis has several limitations. First, our review does not evaluate the absolute benefit of any local treatment and the prognosis and management of oligoprogressive disease or down staged polymetastases to an OM state. Second, the literature search covered a large lifetime span and may include older series where radiological evaluation did not include more advanced modalities that can now increase the accuracy of oligometastases detection. Finally, the optimal number of lesions defining the OM state cannot be defined in this paper.

A consensus paper of EORTC and ESTRO societies attempted to provide definitions of various OM conditions either naïve or attained after therapy and either synchronous or metachronous.²¹

Some large, randomized studies have included local therapies for OM cancers. An NRG Oncology randomized phase II/III trial study compares therapy with stereotactic radiosurgery and/or surgery with standard of care therapy alone in treating patients with breast cancer that has one or two locations in the body (limited metastatic) that are previously untreated. The PREST study will assess the efficacy of ablative radiotherapy (stereotactic body radiotherapy applied to all oligometastases) administered to all tumor sites (metastases and prostate if applicable), in oligometastatic hormone-sensitive prostate cancer patients. Finally, an ECOG-ACRIn phase III study compared standard chemotherapy to consolidative radiotherapy in patients with oligometastatic HER2 negative esophageal and gastric adenocarcinoma (https://clinicaltrials.gov/ct2/show/NCT02364557; https://clinicaltrials.gov/ct2/show/NCT04115007; https://clinicaltrials.gov/ct2/show/NCT04248452).

Conclusions

In conclusion, this meta-analysis tried to quantify the prognosis associated with OM compared to cancers with more extensive diffusion. Based on our findings, we suggest that every metastatic patient should be accurately evaluated for the number of distant sites of disease, and a treatment strategy that involves both the primary and the metastases should be carefully considered. Also, we propose that these patients should be stratified when included in clinical trials.

Data availability