Intracranial radiotherapy with or without immune checkpoint inhibition for brain metastases: a systematic review and meta-analysis.

BACKGROUND: With the development of immunotherapy in recent years, the prognosis of patients is expected to improve due to immune checkpoint inhibition (ICI) combined with radiotherapy (RT). However, studies on combination therapy (ICI + intracranial RT) have reported inconsistent results, and it is unclear whether the combination has increased toxicity. By analyzing the latest relevant literature, we performed a meta-analysis to further clarify the effectiveness and safety of intracranial RT combined with ICI in patients with brain metastases (BMs).
METHODS: We searched PubMed, Embase and the Cochrane Library for published studies that compared the efficacy and safety of intracranial RT combined with ICI versus intracranial RT alone in the treatment of BMs. Overall survival (OS), local brain failure (LBF), distant brain failure (DBF), and radiation necrosis (RN) were pooled with the use of the hazard ratio (HR) or odds ratio (OR).
RESULTS: A total of 26 retrospective observation cohort studies were included, and over 1,500 patients who received ICI and intracranial RT were evaluated. Compared with intracranial RT alone, RT combined with ICI significantly improved OS in patients with BMs [HR =0.55, 95% confidence interval (CI): 0.48-0.64, P<0.001 when OS was defined from the date of diagnosis of BMs; HR =0.45, 95% CI: 0.39-0.52, P<0.001 when OS was defined from the date of RT], though the risk of RN was similar to that of RT alone (HR =1.27, 95% CI: 0.58-2.79, P=0.55). However, significant improvement in LBF and DBF was not obtained with RT combined with ICI (1-year LBF: OR =1.71, 95% CI: 0.38-7.67, P=0.48; LBF: HR =0.49, 95% CI: 0.28-0.87, P=0.01; 1-year DBF: OR =1.05, 95% CI: 0.47-2.33, P=0.90).
CONCLUSIONS: ICI combined with intracranial RT confers a significant OS benefit for patients with BMs without significantly increasing treatment-related toxicity, but further research regarding the specific details of combined treatment application is needed to improve the survival and quality of life of patients with BMs. 2020 Translational Cancer Research. All rights reserved.

Introduction

Brain metastasis (BM) is the most common type of intracranial tumor and mainly originates from melanoma and lung cancer. As patients with BM have a short survival time, improving the treatment effect for BMs has gradually become a major focus of research. At present, immunotherapy shows good therapeutic prospects for malignant tumors. However, its role in BMs has been overlooked, as it is generally believed that antitumor drugs exert minimal efficacy through the blood-brain barrier (BBB). Nonetheless, recent data have shown that the BBB can be destroyed by BMs, tumor-infiltrating lymphocytes (TILs) are significant in BMs, and the brain is no longer a strict “immune privilege” environment (1). Indeed, a certain level of BBB permeability of immune checkpoint inhibition (ICI) has been reported in BM (2). Clinical trials (CheckMate 017 and CheckMate 057) have also indicated that some patients with BMs experience improved overall survival (OS) after using nivolumab (3). Furthermore, an increasing number of studies have reported a certain response rate for intracranial tumors with various immune checkpoint inhibitors, possibly enhancing the survival time of patients (1,4-6).

Studies have revealed that radiotherapy (RT), as a mainstay in the treatment of BMs, is able to promote antitumor immune effects by inducing immunogenic cell death, exposing tumor-associated antigens, activating dendritic cells, reprogramming the tumor microenvironment, and enhancing expression of intercellular adhesion molecule-1 (ICAM-1), Fas and major histocompatibility complex I (MHCI) (7,8). Additionally, based on preclinical models, high-dose fractionated RT is immunogenic, potentially opening the BBB to facilitate the entry of immune checkpoint inhibitors and TILs into BMs (9). Moreover, some studies have found that RT can upregulate expression of PD-L1 and suppress antitumor immune effects (10). Interestingly, both the immune-enhancing effects and upregulation of PD-L1 expression after intracranial RT can theoretically increase the efficacy of immunotherapy. Therefore, RT combined with ICI may offer favorable benefits to patients with BMs.

Accordingly, the synergistic antitumor effect of RT and ICI in BMs is gradually being investigated. To date, quite a few studies have demonstrated that combination treatment is effective (11), though some have shown that combination therapy only improves the tumor regression rate and has no obvious effect on OS (12). Indeed, a small number of studies report that combined treatment has no significant advantage on either OS or the local control of intracranial BMs (13-16). In this systematic review and meta-analysis (SRMA), we aimed to further evaluate the efficacy and safety of ICI and intracranial RT combination therapy. We present the following article in accordance with the PRISMA reporting checklist (available at http://dx.doi.org/10.21037/tcr-20-902).

Methods

Search strategy and selection criteria

We conducted a literature search in PubMed, Embase and the Cochrane Library from inception to November 2019. We used “immune checkpoint inhibition”, “immunotherapy”, “intracranial radiotherapy”, “radiation”, “stereotactic radiosurgery”, and “brain metastases” as key words for our search.

The inclusion criteria of our search were designed around the “PICOS” principle, as follows: Population, patients with BMs; Intervention, ICI with intracranial RT; Comparison, intracranial RT alone; Outcome, the hazard ratio (HR) of OS, local brain failure (LBF) or radiation necrosis (RN); and Study, randomized trial or cohort study. All articles were independently reviewed by two investigators.

Exclusion criteria for the included articles were as follows: (I) repeated publication of data; (II) not a comparative study; (III) not published in English or Chinese; (IV) not treating BMs or including extracranial radiation; (V) not ICI combined with RT vs. RT alone; and (VI) not reported HRs for OS, LBF or RN.

Data extraction and quality assessment

Two investigators independently extracted the following data from each study: the publication year, number of institutions, type of study design, study period, number and median age of enrolled patients, median follow-up time, primary carcinoma of BM, radiation type, regimens of ICI, and outcomes of the various groups. Outcomes were extracted as follows: HRs for OS, LBF or RN and the incidence of 1-year LBF or 1-year DBF. When disagreements occurred, discussions were made with a third author to reach a consensus.

The quality of the studies (e.g., selection, comparability, and outcome) included was assessed using the Newcastle-Ottawa Scale (NOS) by two independent investigators. The total score was 9, with 1–5 being of low quality and 6–9 of high quality. Disagreements were discussed with a third author to reach a consensus.

Data analyses and statistical methods

Meta-analyses were conducted with RevMan 5.3 software (The Nordic Cochrane Center, Cochrane Collaboration). HRs were used to evaluate OS (primary endpoint), LBF and RN. Subgroup analyses were applied to assess the results for patients with different RT forms and primary tumor types. The incidence of 1-year LBF and 1-year DBF was evaluated through the odds ratio (OR). All data were extracted from the studies, and the 95% CI was collected. When I2<33, the fixed-effects (FE) model was employed to pool the outcomes of the studies included in the meta-analysis; when I2≥33, the random-effects (RE) model was applied. The outcomes are shown as forest plots, which also represent the heterogeneity statistics. Heterogeneity was estimated through the chi-squared test and I2 statistics, whereby the larger I2 was, the greater was the heterogeneity; I2=0% was considered no heterogeneity, and I2>50% was considered high heterogeneity. Significance was set at P<0.05. A funnel plot was used to assess publication biases for primary outcomes. Each study was removed sequentially for sensitivity analysis. If bias was suspected, the pooled effect size was recalculated with the trim-and-fill method.

Results

Included studies and study quality

A total of 1,785 relevant studies were retrieved from databases, and 1,295 articles remained after eliminating duplicate studies using literature management software. We removed 1,012 papers by abstract screening and then assessed the full texts of the remaining papers using the selection criteria. Ultimately, 26 retrospective observational cohort studies were included (), and over 1,500 patients who received combination treatment of ICI and intracranial RT were assessed. summarizes the main baseline characteristics and survival outcomes. The cohort studies that we included were generally of high quality, with NOS scores greater than 6 ().

Figure 1

The flow diagram described our process of selection studies. We finally included 26 retrospective cohort studies involving approximately 1,500 patients who received a combination of ICI and intracranial RT. BM, brain metastases; DBF, distant brain failure; ICI, immune checkpoint inhibition; LBF, local brain failure; N, number; RN, radiation necrosis.

Table 1

Summary of main baseline characteristics and efficacy outcomes

Study	Institution	Design	Study period	N (total/IT + RT)	Median age (years)	Median FU (months)	BM primary	RT	ICI	Arm	OS
											Defines	Median (months)	HR (95% CI)
Acharya 2017	1	ROCS	2006–2016	72/18	61 IT + RT/56 RT	8.9	Melanoma	SRS	CTLA-4/PD-1	IT + RT vs. RT	From RT	12.6 PD-1/2.1 CTLA-4 vs. –	0.53 (0.23–1.22)
Ahmed 2016.1	1	ROCS	2007–2015	96/46	60 PD-1/67 CTLA-4/62.5 CT	7.4	Melanoma	SRS	CTLA-4/PD-1	CTLA-4 + RT vs. CT + RT	From RT	8.9 (all pts)	0.32 (0.16–0.67)
										PD-1 + RT vs. CT + RT			0.29 (0.14–0.63)
Ahmed 2016.2	1	ROCS	2005–2015	104/55	NR	NR	Melanoma	SRS	IPI/PD-1	PD-1 + RT vs. CT + RT	From RT	NR	0.43 (0.22–0.79)
										PD-1 + RT vs. CT + RT	From BM diagnosis	NR	0.45 (0.23–0.84)
An 2017	1	ROCS	2007–2014	99/35	62.5	15.5	Melanoma	SRS	IPI/PD-1	IT + RT vs. RT	From RT	NR	0.53 (0.21–1.30)
Chen 2018	1	ROCS	2010–2016	260/79	NR	9.2	NSCLC/melanoma/RCC	SRS	IPI/PD-1	IT + RT vs. RT (Con.)	From BM diagnosis	24.7 vs. 12.9	0.37 (0.20–0.70)
Choong 2017	1	ROCS	2010–2015	108/39	64.3	8.6	Melanoma	SRS	IPI/PD-1	IT + RT vs. RT	From RT	7.5 CTLA-4/20.4 PD-1 vs. 10.8	0.51 (0.25–1.05)
Diao 2018.1	1	ROCS	2006–2015	72/-	61	6.58	Melanoma	SRS	IPI	IT + RT vs. RT (Con.)	NR	NR	NR
										IT + RT vs. RT (non-Con.)
Diao 2018.2	1	ROCS	2006–2015	91/51	62	7.4	Melanoma	SRS	IPI	IT + RT vs. RT (Con.)	From RT	15.1 vs. 7.8	0.60 (0.32–1.11)
										IT + RT vs. RT (non-Con.)			0.51 (0.28–0.92)
Gabani 2018	1	ROCS	2011–2013	1,104/192	62	6.4	Melanoma	SRS/WBRT	IPI/PD-1	IT + RT vs. RT	From BM diagnosis	11.1 vs. 6.2	NR
										IT + RT vs. RT		NR	0.54 (0.42–0.69)
										T + RT vs. RT		17.0 vs. 11.9	NR
Gaudy-Marqueste 2017	1	ROCS	2010–2015	179/75	59.3	9.8	Melanoma	SRS	IPI/PD-1	BRAFmut: IT + RT vs. RT	From RT	14.82 (TT + IT)	0.13 (0.04–0.39)
										BRAFwt: IPI + RT vs. RT; PD-1 + RT vs. RT; IPI + PD-1 + RT vs. RT		8.62 vs. 2.29	0.18 (0.07–0.44)
												12.26 vs. 2.29	0.16 (0.05–0.48)
												14.07 vs. 2.29	0.28 (0.16–1.38)
Glenn 2019	1	ROCS	NR	352/176	NR	NR	NR	SRS	CTLA-4/PD-1	IT + RT vs. RT	NR	NR	NR
Goel 2017	1	ROCS	2011–2015	51/21	NR	NR	Melanoma	SRS	CTLA-4/PD-1	IT + RT vs. RT	NR	32.4 vs. 13.2	0.40 (0.17–0.94)
Henson 2016	1	ROCS	2000–2015	123	63	NR	Melanoma	SRS	IPI/PD-1	IT + RT vs. RT	NR	NR	0.51 (0.32–0.82)
Kaidar-Person 2017	1	ROCS	2007–2015	58/29	57 IT + RT/62 RT	12	Melanoma	SRS	IPI/PD-1	IT + RT vs. RT	From RT	15 vs. 5.5	0.34 (0.19–0.6)
Kim 2017	1	ROCS	1997–2015	1,650/19	61	NR	NSCLC/breast/renal/melanoma/gastrointestinal/others	SRS	CTLA-4/PD-1	IT + RT vs. RT	NR	NR	NR
Knisely 2012	1	ROCS	002–2010	77/27	61	12.17	Melanoma	SRS	IPI	IT + RT vs. RT	From RT	21.3 vs. 4.9	0.61 (0.33–1.10)
Kotecha 2018	1	ROCS	1987–2014	366/32	60 BRAFmut/64 BRAFwt	5	Melanoma	SRS	CTLA-4/PD-1	IT + RT vs. RT	From BM diagnosis	6	0.67 (0.44–0.99)
Lanier 2019	1	ROCS	2013–2018	271/101	63 IT + RT/67 RT	29.9	Lung cancer/melanoma	SRS	IPI/PD-1/PD-L1	IT + RT vs. RT	From RT	15.9 vs. 6.1	0.61 (0.45–0.83)
Nguyen 2017	1	ROCS	2008–2017	69/50	NR	NR	Melanoma	SRS	IPI/PD-1	IT + RT vs. RT	From RT	9.9 vs. 3.29	0.23 (0.05–0.99)
Nguyen 2018	1	ROCS	2008–2017	68/49	NR	35.35	Melanoma	SRS	IPI/PD-1	IT + RT vs. RT	From RT	8.65 vs. 3.29	0.48 (0.27–0.85)
										IPI + RT vs. RT		6.43 vs. 3.29	0.25 (0.10–0.67)
										PD-1 + RT vs. RT		23.51 vs. 3.29	0.09 (0.03–0.30)
Patel 2017	1	ROCS	2009–2013	54/20	60.1	7.3	Melanoma	SRS	IPI	IT + RT vs. RT	NR	NR	1.07 (0.56–2.06)
Rauschenberg 2019	1	ROCS	2014–2016	208/139	60.1	7.3	Melanoma	SRS/WBRT	CTLA-4/PD-1	RT + IT vs. RT + TT	From RT	14.8 vs. 9.8	0.31 (0.16–0.59)
Shepard 2019	1	ROCS	2012–2018	51/17	64.43 IT + RT/64.1 RT	7.0 IT + RT/10.4 RT	NSCLC	SRS	PD-1/PD-L1	IT + RT vs. RT	From RT	Not reached vs. 15.9	0.99 (0.39–2.52)
Silk 2013	1	ROCS	2005–2012	70/33	56.6 IT + RT/57.7 RT	10	Melanoma	SRS/WBRT	IPI	IT + RT vs. RT	From RT	18.3 vs. 5.3	0.43 (0.24–0.78)
										IT + SRS vs. SRS		NR	0.31 (0.13–0.75)
										IT + WBRT vs. WBRT		NR	0.56 (0.25–1.23)
Stokes 2017	1	ROCS	2010–2013	1,287/185	NR	35.8	Melanoma	SRS/WBRT	IPI/PD-1	IT + RT vs. RT	From BM diagnosis	10.8 vs. 6.1	0.57 (0.47–0.70)
										IT + WBRT vs. WBRT		NR	0.51 (0.39–0.66)
										IT + SRS vs. SRS		NR	0.74 (0.54–0.99)
Yusuf 2017	1	ROCS	2008–2015	51/18	63.6	1.5/4/5	Melanoma	SRS	CTLA-4/PD-1	IT + RT vs. RT	NR	NR	NR

BM, brain metastases; BRAFmut, BRAF-mutated; BRAFwt, BRAF-wild-type; Con., concurrent; CT, chemotherapy; CTLA-4, cytotoxic T-lymphocyte-associated protein 4; FU, follow up; IPI, ipilimumab; IT, immunotherapy; non-Con., non-concurrent; NR, not reported; NSCLC, non-small cell lung cancer; PD-1, programmed cell death protein 1; PD-L1, programmed cell death protein ligand 1; peri-SRS, patients treated with SRS within 12 weeks of ICT administration; pts, patients; RCC, renal cell carcinoma; ROCS, retrospective observational cohort study; RT, radiotherapy; SRS, stereotactic radiosurgery; TT, target therapy; WBRT, whole brain radiotherapy.

Table S1

The Newcastle-Ottawa Scale (NOS) to evaluate the studies included

Study	Selection					Comparability		Outcomes			NOS score	Quality
	1	2	3	4		5		6	7	8
Acharya 2017 (22)	*	*	*	–		**		*	*	*	8	High
Ahmed 2016.1 (23)	*	*	*	–		**		*	*	*	8	High
Ahmed 2016.2 (18)	*	*	*	–		**		*	–	*	7	High
An 2017 (24)	*	*	*	–		**		*	*	*	8	High
Chen 2018 (19)	*	*	*	–		**		*	*	*	8	High
Choong 2017 (25)	*	*	*	–		**		*	*	*	8	High
Diao 2018.1 (38)	*	*	*	–		**		*	*	*	8	High
Diao 2018.2 (26)	*	*	*	–		**		*	*	*	8	High
Gabani 2018 (20)	*	*	*	–		**		*	*	*	8	High
Gaudy-Marqueste 2017 (27)	*	*	*	–		*		*	*	*	7	High
Glenn 2019 (41)	*	*	*	–		*		*	–	*	6	High
Goel 2017 (35)	*	*	*	–		*		*	–	*	6	High
Henson 2016 (36)	*	*	*	–		*		*	–	*	6	High
Kaidar-Person 2017 (28)	*	*	*	–		**		*	*	*	8	High
Kim 2017 (40)	*	*	*			**		*	–	*	7	High
Knisely 2012 (29)	*	*	*	–		**		*	*	*	8	High
Kotecha 2018 (17)	*	*	*	–		**		*	*	*	8	High
Lanier 2019 (30)	*	*	*	–		**		*	–	*	7	High
Nguyen 2018 (32)	*	*	*	–		*		*	–	*	6	High
Nguyen 2017 (31)	*	*	*	–		*		*	*	*	7	High
Patel 2017 (37)	*	*	*	–		**		*	*	*	8	High
Rauschenberg 2019 (33)	*	*	*	–		**		*	*	*	8	High
Shepard 2019 (12)	*	*	*	–		**		*	*	*	8	High
Silk 2013 (34)	*	*	*	–		**		*	*	*	8	High
Stokes 2017 (21)	*	*	*	–		**		*	*	*	8	High
Yusuf 2017 (39)	*	*	*	–		**		*	*	*	8	High

Notes: 1. Representativeness of the exposed cohort; 2. Selection of the non-exposed cohort; 3. Ascertainment of exposure; 4. Demonstration that outcome of interest was not present at start of study; 5. Comparability of cohorts on the basis of the design or analysis; 6. Assessment of outcome; 7. Was follow-up long enough for outcomes to occur; 8. Adequacy of follow-up of cohorts.

OS

The HR of OS was calculated in 22 studies, and OS was defined from the date of diagnosis of BMs (n=5) (17-21) or the date of intracranial RT (n=15 studies) (12,18,22-34). As statistical heterogeneity among the study outcomes was not high (I2=0%; I2=29%, respectively), the FE model was applied. The pooled HR demonstrated that the use of ICI significantly lowered the risk of death, regardless of whether OS was defined from the date of diagnosis of BMs or the date of RT (HR =0.55, 95% CI: 0.48–0.64, P<0.001; HR =0.45, 95% CI: 0.39–0.52, P<0.001, respectively) (). OS was not clearly defined in three studies [Goel 2017 (35), HR =0.40, 95% CI: 0.17–0.94; Henson 2016 (36), HR =0.51, 95% CI: 0.32–0.82; Patel 2017 (37), HR =1.07, 95% CI: 0.56–2.06]; therefore, these studies were not included in the pooled HR. Through subgroup analysis (), we also found that ICI significantly reduced the risk of death when combined with stereotactic radiosurgery (SRS), and the pooled HR of OS in the SRS subgroup was 0.46 (95% CI: 0.39–0.53, P<0.001, I2=31%) and 0.59 (95% CI: 0.44–0.80, P<0.001, I2=41%, RE model, ) when OS was defined from the date of RT (n=14 studies) and the diagnosis of BMs (n=4 studies), respectively. When ICI was combined with whole-brain radiotherapy (WBRT), there was no obvious difference in survival when OS was defined from the date of RT (n=1 study, HR =0.56, 95% CI: 0.25–1.23, P=0.15). When OS was defined from the date of diagnosis of BMs, combination therapy appeared to have a survival advantage in the WBRT subgroup (n=2 studies, HR =0.53, 95% CI: 0.44–0.63, P<0.001, I2=0%). Additionally, compared to RT alone, the OS benefit (defined from the date of RT) of combination therapy was significant in both the melanoma subgroup (n=13 studies) and in the other cancer subgroup (lung cancer and/or melanoma and/or renal cell carcinoma, n=2 studies), with pooled HRs of 0.40 and 0.64, respectively (95% CI: 0.34–0.47, P<0.001, I2=8%; 95% CI: 0.48–0.86, P=0.003, I2=0%, respectively).

Figure 2

Forest plot for OS. Compared with RT alone, ICI combined with RT significantly reduced the risk of death (whether OS was defined from the date of BMs diagnosis or the date of RT). This survival benefit was reflected in malignant melanoma or other tumors (such as lung cancer). RT for patients who benefited from combination therapy included SRS or WBRT. It should be noted that in some patients receiving WBRT combined with ICI, the OS benefit was not significantly, when OS is defined as the beginning of radiotherapy. ICI, immune checkpoint inhibition; BMs, brain metastases; OS, overall survival; RT, radiotherapy; SRS, stereotactic radiosurgery; WBRT, whole brain radiotherapy.

Figure 3

Forest plot for OS. SRS combined with ICI also showed OS advantages compared with SRS alone, when OS is defined as starting from the diagnosis of BMs. ICI, immune checkpoint inhibition; SRS, stereotactic radiosurgery; BMs, brain metastases.

LBF

LBF was defined as the date of first tumor progression in the radiation field, and LBF was evaluated in 7 studies. Three of the studies calculated the incidence of 1-year LBF for 420 patients (26,28,30), and heterogeneity between the results was high (I2=84%). RE model analysis revealed no significant difference in 1-year LBF between the two groups (OR =1.71, 95% CI: 0.38–7.67, P=0.48) (). Interestingly, four other studies with some heterogeneity (I2=51%) calculated the HR of LBF (17,22,38,39) and found that combination therapy may be a favorable predictor of LBF risk reduction (HR =0.49, 95% CI: 0.28–0.87, P=0.01, RE model) ().

Figure 4

Forest plot for 1-year LBF. There was no significant difference in 1-year LBF between the ICI combined with RT group and RT alone group. ICI, immune checkpoint inhibition; RT, radiotherapy; LBF, local brain failure.

Figure 5

Forest plot for the pooled HR of LBF. The combination of ICI and RT may be a favorable predictor of LBF risk reduction. HR, hazard ratio; LBF, local brain failure; ICI, immune checkpoint inhibition; RT, radiotherapy.

Distant brain failure (DBF)

DBF was defined as the emergence of a new BM or tumor progression outside the prior radiation treatment field in the brain. Seven articles (n=671 patients) assessed DBF (12,18,23,26,28,30,37). An RE model was used for the meta-analysis due to high heterogeneity (I2=73%), and the outcomes suggested no significant advantage in 1-year DBF between patients who received combination therapy and those who received RT alone (OR =1.05, 95% CI: 0.47–2.33, P=0.90) ().

Figure 6

Forest plot for 1-year DBF. There was no significant advantage in 1-year DBF between patients who received combination therapy and those who received RT alone. DBF, distant brain failure; RT, radiotherapy.

Toxicity

RN was defined based on pathological and/or radiographic evidence, and enhanced circular lesions usually indicate RN. Short-term follow-up using an institutional algorithm, positron emission tomography (PET), cerebral blood volume MRI, or surgical assessment (biopsy or resection) is essential for distinguishing tumor recurrence or progression from RN. Five studies analyzed RN, three of which included the HR (17,40,41). The RE model was used because of high heterogeneity (I2=49%), and the pooled HR of RN showed no significant difference in RN between the two groups (HR =1.27, 95% CI: 0.58–2.79, P=0.55), revealing that combination therapy did not increase the risk of RN ().

Figure 7

Forest plot for the pooled HR of RN. ICI combined with RT did not increase the risk of RN. HR, hazard ratio; ICI, immune checkpoint inhibition; RT, radiotherapy; RN, radiation necrosis.

Publication bias and sensitivity analysis

A funnel plot was constructed for OS (defined from the date of RT). The funnel plots were basically symmetrical, suggesting no significant publication bias (). Sensitivity analysis was performed by removing each study sequentially, with consistent outcomes.

Figure 8

Funnel plot for OS defined from the date of RT. There was no significant publication bias. OS, overall survival; RT, radiotherapy.

Discussion

Although some studies have shown that ICI combined with RT can bring clinical benefits to patients with BMs and that the toxicity is acceptable, no large-scale randomized controlled trial (RCT) has yet to confirm this finding. Therefore, the clinical effect and toxicity of combined therapy need to be further examined to improve the level of evidence and guide clinical practice. A previous meta-analysis that included studies before April 2018 evaluated the efficacy and safety of combination therapy for BMs (42), in which the primary endpoints were the median OS and 1- and 2-year OS rates. Because ICI combined with RT for BMs has become a focus and outcomes of related studies have been released successively, we designed and implemented this meta-analysis to include the latest research outcomes. The primary endpoint of this meta-analysis was the pooled HR for OS, which is highly capable of assessing survival benefits; the toxicity of combined therapy was assessed at the same time. This meta-analysis provides the latest data on the safety of treatment and its impact on patients’ quality of life.

This meta-analysis indicated that in terms of OS benefits, combination therapy conferred a significant OS benefit compared with RT alone, regardless of whether OS was defined from the date of BM diagnosis or the date of RT (HR =0.55, P<0.001; HR =0.45, P<0.001, respectively), especially when combined with SRS (HR =0.46, P<0.001). No statistically significant difference in the OR of 1-year LBF (OR =1.71, P=0.48) or 1-year DBF (OR =1.05, P=0.90) was found between the two groups, which suggests no corresponding significant trends in LBF or DBF. However, when the pooled HR was calculated to assess LBF, the combination therapy appeared to achieve better local control (HR =0.49, P=0.01). Although no significant improvement in intracranial control was found, there was still a survival advantage in the ICI group, indicating that these survival benefits may result from improvements in systemic disease control. This was consistent with the finding that the main limiting survival factor for patients with BMs is systemic disease rather than intracranial disease (26,43). Overall, there is no consensus to date on whether combination therapy will have better intracranial control. Some studies have reported no significant differences in LBF or DBF (37,44,45), whereas others have revealed that the appropriate timing of combination therapy might improve LBF or DBF (24,38,46). Nevertheless, most of these studies were retrospective and showed interstudy heterogeneity. Thus, further prospective studies are needed to further investigate intracranial control. Moreover, this meta-analysis detected no significant difference in RN risk between the two groups, indicating that combination therapy is generally safe and acceptable, consistent with previous studies (47).

When we analyzed the research, we found that the level of PD-L1 expression in tumors, which is closely related to the efficacy of immunotherapy, appeared to have no significant correlation with the efficacy of combination therapy. This may be partly due to the apparent heterogeneity of PD-L1 in tumor tissues and the influence of specific antibodies used in immunohistochemistry (12). Notably, PD-L1 expression levels may change significantly during treatment. For example, animal trials have shown that PD-L1 expression increases after RT (48). Furthermore, clinical trials (e.g., the PEMBRO-RT study) comparing the efficacy of pembrolizumab with the combination of pembrolizumab and stereotactic body radiotherapy (SBRT) found that in the combination treatment group, PD-L1-negative advanced lung cancer patients had greater benefits than did PD-L1-positive patients (49). Therefore, it is highly possible that more patients may benefit from the combination of ICI and RT.

According to this meta-analysis, combination therapy was used mainly in patients with melanoma and non-small cell lung cancer (NSCLC), the treatment of which was associated with the mutation status of key driver genes. There is also evidence that BRAF mutation (BRAFmut) is a positive prognostic factor for melanoma (i.e., prolonged OS) when patients receive ICI and intracranial RT (33). Gaudy-Marqueste et al. studied the effect of ICI and/or targeted therapy (TT) on the survival of 179 patients with melanoma BMs who received intracranial SRS and found that BRAF wild-type (BRAFwt) patients who received anti-PD-1 or BRAFmut patients who received anti-PD-1 and BRAF inhibition (BRAFi) therapy had the best OS (12.26 and 14.82 months, respectively) (27). Furthermore, the multivariate analysis of Kotecha et al. (17) showed BRAFi and anti-PD-1/CTLA-4 therapies to be significantly associated with OS and BRAFmut status to be a predictor of a low risk of RN (HR =0.27, 95% CI: 0.07–0.84). Notably, outcomes in their study may have been affected by imbalanced baseline data. Additionally, Cinausero et al. found that in nonsquamous NSCLC, patients with KRAS mutation (KRASmut) had a better response to PD-1 inhibition than did patients with KRAS wild-type (KRASwt), with prolonged progression-free survival (PFS) and OS. These authors considered KRAS mutations and deletions in ERBB family genes (including EGFR, ERBB2 and ERBB4) to be favorable predictors for PD-1 inhibition (50). These outcomes suggest that the detection of tumor-specific driver genes in different tumors during the combination of ICI and RT may help predict the efficacy of such combined therapy. We will further focus on related research in this area.

Although combination therapy may improve the OS of patients, different disease-specific grading prognostic factors (DS-GPAs) may lead to different efficacies of combination therapy. The latest versions of melanoma DS-GPA (melanoma-molGPA) (51) and lung cancer DS-GPA (lung-molGPA) (52) share four important survival prognostic factors: age, Karnofsky performance status (KPS) score, extracranial metastases and number of BMs. Additionally, melanoma-molGPA includes BRAF status, and lung-molGPA includes EGFR and ALK statuses. Multivariate analysis has shown that higher DS-GPA scores, such as young age, no extracranial metastases, high KPS scores and few BMs, are significantly related to improved OS (17,27). Moreover, retrospective studies have found that patients with a KPS <90 (9) or <80 (Singh et al. 2019) or patients with lung-mol GPA score <1.5 (13) often have poor OS.

By analyzing the extracted literature in detail, we found that when ICI was combined with RT, the specific strategy of RT used (such as selection of the RT form, irradiation field, and timing and sequence of the combination therapy) also affected efficacy. Regarding the RT form, there were limited data available for WBRT, and no consensus concerning whether WBRT combined with ICI could achieve similar survival benefits was reached (20,21,33,34). Regardless, this meta-analysis did reveal that SRS combined with ICI conferred a marked survival advantage for patients (HR =0.46, P<0.001; HR =0.59, P<0.001, when OS was defined from the date of RT or the date of diagnosis of BMs, respectively). The synergistic effect between RT and immunotherapy depends on the activation of immune cells (such as T lymphocytes), which are easily killed by RT. Moreover, RT kills not only TILs but also peripheral blood lymphocytes passing through the irradiation field and may induce lymphopenia. Of note, there are emerging data revealing that severe lymphopenia is associated with a poor prognosis in patients with different tumors (53-55). Therefore, the size of the radiation field should be reasonably limited when investigating combination therapy (7). We also need to pay attention to the timing of combination therapy. For instance, a preclinical study by Dovedi et al. using mouse models (56) indicated that the PD-L1 expression level gradually increased after RT, reached a peak after 72 hours, and gradually decreased after 7 days. Their study also showed that compared with the RT-only group, ICI on the 1st or 5th day of the RT cycle improved OS but that no advantage was obtained with sequential treatment with ICI 7 days after RT completion. Subsequent analysis of the PACIFIC study also revealed that patients who received ICI within 14 days after the last RT before randomization benefited more than those who received ICI later (48). Additionally, many retrospective analyses suggest that concurrent combination therapy can better improve the prognosis of patients with BMs than can nonconcurrent therapy (57,58). Regarding the combination sequence, some scholars retrospectively analyzed 139 melanoma patients with BMs who received ICI within 6 weeks of RT and found no significant difference in the median survival time, regardless of whether ICI was used before, during or after RT (P=0.72) (33). However, more data are needed to clarify the timing and sequence of combination therapy. Nonetheless, studies on the toxicity and side effects of immunotherapy combined with RT report that neither the timing nor sequence of combination therapy significantly increase the risk of toxicity (47).

Strengths and limitations

The main limitations of our study are as follows: (I) The studies included in this meta-analysis are all retrospective, and the results were limited by the preference of institutional treatment options. In some studies, the number of patients was small, patients were poorly matched, baseline data were incomplete, the timing of combination therapy differed, and the primary tumor types included were not sufficiently comprehensive. Overall, our analysis and findings are hypothesis generating, and large prospective randomized clinical trials will further validate the efficacy and safety of combination therapy. (II) The studies included a long-time span. The treatment strategy of ICI has gradually changed with its development, which may have affected the results. (III) The populations involved were not comprehensive, and whether different populations have similar effects needs further research. (IV) There were insufficient data for in-depth analyses of OS, LBF and DBF, and more clinical data are needed to screen the best beneficiaries and support the effect of combination therapy on intracranial control. (V) In our study, combination therapy toxicity was evaluated mainly through RN, and more data are needed to evaluate intratumoral bleeding and other acute or chronic toxicities.

Conclusions

In our meta-analysis, the combination of ICI and intracranial RT for patients with BMs was associated with prolonged OS, and toxicity was tolerable. However, the efficacy of intracranial control needs further study. In the era of immunotherapy, larger prospective randomized trials are needed to further explore the strategy of combination therapy and optimize the combination plan to prolong the survival of patients and improve their quality of life.