A Systematic Review of the Clinical Efficacy of Treatments in Relapsed or Refractory Diffuse Large B Cell Lymphoma.

INTRODUCTION: Novel treatment options are needed to improve outcomes in transplant-ineligible relapsed/refractory (R/R) diffuse large B cell lymphoma (DLBCL). This systematic literature review evaluated clinical evidence on treatments for patients with R/R DLBCL ineligible for, or relapsed following, stem cell transplantation.
METHODS: We assessed the feasibility of conducting an indirect treatment comparison (ITC) or network meta-analysis (NMA) to evaluate the relative efficacy and safety of polatuzumab vedotin in combination with bendamustine + rituximab versus other relevant treatments.
RESULTS: Thirty-seven studies were identified, of which 20 were eligible [seven randomized, controlled trials (RCTs); 13 observational/single-arm trials]. Due to a lack of RCTs, an ITC/NMA summary of the relative efficacy and safety of the treatment options was not possible. Only two of the seven RCTs had positive outcomes.
CONCLUSIONS: These findings highlight the paucity of published RCTs to establish the comparative efficacy of treatments for transplant-ineligible R/R DLBCL and lack of standard of care in this setting.

Key Summary Points

Digital Features

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Introduction

Comprising approximately one-third of non-Hodgkin lymphoma (NHL), diffuse large B cell lymphoma (DLBCL) is the most common NHL subtype, with an estimated 5.6 per 100,000 men and women diagnosed annually in the US and 6.6 per 100,000 in Europe [1-3]. Standard first-line therapy for DLBCL is rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone [4, 5]. For patients who do not respond to first-line therapy, high-dose chemotherapy followed by autologous stem cell transplantation (SCT) represents a second option for cure [4, 5]. However, for patients who either relapse after or are not eligible for SCT due to refractory disease or frailty, treatment outcomes are poor [6]. Furthermore, even if some patients are eligible for transplant, very few actually benefit from this treatment [6]. Response rates to subsequent therapies range from 10–35% in most cases [6-10]; thus, novel treatment options are urgently needed to improve outcomes in transplant-ineligible relapsed/refractory (R/R) DLBCL.

Polatuzumab vedotin (pola) is an antibody-drug conjugate that has been demonstrated to prolong survival in combination with bendamustine + rituximab (BR) compared with BR alone in a phase 1b/2 multicenter, open-label study of patients with transplant-ineligible R/R DLBCL (NCT02257567) [11]. Pola, in combination with BR (pola-BR), was approved by the US Food and Drug Administration for third-line or later treatment of R/R DLBCL [12]. The European Commission granted conditional marketing authorization for pola-BR for second-line or later treatment for patients with R/R DLBCL who are not candidates for hematopoietic SCT [13], and the Australian health authorities approved pola-BR for second-line or later treatment. These approvals were based on the randomized phase 2 response data from the GO29365 study [11, 14]. A recently published structured review examined the efficacy of treatment beyond frontline therapy for patients with transplant-ineligible aggressive B cell NHL (aNHL) [15]. The aim of our clinical systematic literature review (SLR) was to identify current clinical evidence on pharmacologic options for the specific population of patients with R/R DLBCL who were ineligible for, or relapsed following SCT. A secondary objective was to assess the feasibility of conducting an indirect treatment comparison (ITC) or network meta-analysis (NMA) to evaluate the relative efficacy and safety of pola-BR versus other relevant treatments for R/R DLBCL.

Methods

This article is based on previously conducted studies and does not contain any studies with human participants or animals performed by any of the authors.

Search Strategy

Electronic databases (Embase®, MEDLINE®, and The Cochrane Library) were searched for relevant English-language publications on 10 June 2019 using a predefined search string (see the appendix in the electronic supplementary material). In addition, conference proceedings were screened from January 2015 to June 2019 from the following congresses: European Hematology Association, International Conference on Malignant Lymphoma, American Society of Hematology, American Society of Clinical Oncology, European Society for Medical Oncology, International Society for Pharmacoeconomics and Outcomes Research Annual and European Meetings, Health Technology Assessment International, and Society for Medical Decision Making. Finally, clinical trial registries and health technology assessment submissions were also searched.

Eligibility Criteria

The eligibility criteria applied were in the form of PICOS (population, intervention, comparators, outcomes and study design). Table S1 in the electronic supplementary material shows the predefined inclusion criteria for the SLR. Briefly, English-language randomized, controlled trials (RCTs) and prospective or comparative observational studies in adults with R/R DLBCL receiving licensed or investigational treatments as second- or later-line therapy were included. Pre-clinical/in vitro studies, trials of first-line treatments or non-pharmacologic therapies, reviews/editorials, case reports/case series, and retrospective single-arm studies were excluded.

Study Selection and Data Extraction

Identified citations were initially reviewed by two independent reviewers to assess eligibility on the basis of title and abstract. Full publications of potentially relevant citations were then obtained and examined in full to identify publications eligible for inclusion in the SLR. Disputes regarding eligibility were resolved through discussion between reviewers. Citations identified by hand searching of reference lists from included publications and also relevant SLRs were also screened. Non-English-language articles with an English abstract were assessed individually for inclusion. Relevant data from included studies were extracted into pre-designed tables in Microsoft® Excel. A quality assessment of included RCTs and observational studies was performed using the Cochrane Collaboration tool and the Downs and Black checklist [16], respectively. The Cochrane tool assesses the risk of bias across categories and studies, and by outcomes [progression-free survival (PFS), complete response (CR)]. The Downs and Black checklist scores studies based on five subscales, including reporting, external validity, bias, confounding and power.

Network-Building Analysis

Prior to data extraction, a network-building exercise was conducted to identify whether a connected network of evidence could be constructed from the identified studies. Matching Adjusted Indirect Comparisons is a method for comparing single-arm studies, and was used to establish links to interventions not connected to the network through RCTs; these data will be reported separately. A post-hoc supplementary process was then carried out, whereby studies not meeting the SLR protocol criteria were re-evaluated to see whether they could be used to help construct a connected network of evidence to provide links between comparators and fill data gaps.

Results

Search Results

Overall, the SLR identified 37 studies of patients with R/R DLBCL (103 publications); of these, 20 studies (66 publications) met the eligibility criteria (Fig. 1), including seven RCTs [11, 17–22] and 13 prospective, observational or single-arm trials [9, 23–34]. Table S2 in the electronic supplementary material summarizes the studies included in the SLR. The 20 studies included in the review provided data on 13 different interventions (Table 1). The sample size of the included studies varied from 14 patients [31] to 338 patients [20], with 11 studies having a sample size of < 60 patients [9, 22–26, 28, 29, 31, 32, 34]. Median follow-up varied from four.Seven [28] to 65.0 months [26]. At the time of literature searching, three studies were published only as a conference abstract [11, 22, 30]. Of the 20 eligible studies, 15 included transplant-ineligible patients and two were considered to be in a transplant-ineligible population because they included elderly frail patients [17, 18]. Another three studies included transplantation- or chemotherapy-relapsed patients.

Fig. 1

PRISMA flow diagram of included studies. PRISMA Preferred Reporting Items for Systematic Reviews and Meta-Analyses; SCT stem cell transplant

Table 1

Outcomes for each of the interventions covered by the 19 included studies identified by the systematic literature review

Intervention	No. studies	ORR, %	CR %	Median PFS, months	Median OS, months	EFS, %	Median DOR, months	References
Axicabtagene ciloleucel	1	82	58	7.3h	NR		8.1	[27]
BR	2	46–63	15–37	3.6–6.7	NR [30]		17.3	[28, 32]
GDP	1a	63 (vs 55)	29 (vs 38)	17.1 (vs 6.0)i	17.0 (vs 7.0)	19.6 (vs 11.1)j		[17]
Gemcitabine + vinorelbine	1	50	14		12.9			[29]
ESHAP	1b	62 (vs 60)	37 (vs 36)					[18]
Inotuzumab ozogamicin + R	1c	41 (vs 44)	13 (vs 13)	3.7 (vs 3.5)	9.5 (vs 9.5)			[20]
Lenalidomide	4d	19–28	7–12	13.6 (vs 7.9) weeks	7.1		10.6	[9, 19, 24, 33]
Lenalidomide + R	1	35	35		NR		16.5	[34]
Pixantrone	1e	37 (vs 14)	11 (vs 0)	5.3 (vs 2.6)	10.2 (vs 7.6)			[19, 35]
Pixantrone + R	1f	62 (vs 44)	36 (vs 22)	7.3 (vs 6.3)	13.3 (vs 19.6)			[22]
Pola-BR	1g	48.0 (vs 18)	42.5 (vs 15)	7.6 (vs 2.0)	12.4 (vs 4.7)	31.6 (vs 5.3)k	10.3 (vs 4.1)	[11]
R-GemOx	3	44–73	34–73	5.0–NR	5.7–11.0			[23, 25, 26]
Tisagenlecleucel	2	50–54	40–43	2.9–3.2	11.1–22.2		NR	[30, 31]

BR, bendamustine plus rituximab; CR, complete response; DOR, duration of response; EFS, event-free survival; ESHAP, etoposide, methylprednisolone, cytosine arabinoside, platinum; GDP, gemcitabine, dexamethasone, cisplatin; GemOx, gemcitabine, oxaliplatin; NR, not reached; ORR, objective response rate; OS, overall survival; PFS, progression-free survival; pola, polatuzumab vedotin; R, rituximab

aIn this trial, GDP was compared with ESHAP

bIn this trial, ESHAP was compared with R-ESHAP

cIn this trial, inotuzumab ozogamicin plus rituximab was compared with the investigator’s choice of treatment (inotuzumab ozogamicin plus rituximab)

dIn this trial, lenalidomide was compared with the investigator’s choice of treatment (gemcitabine, rituximab, etoposide, or oxaliplatin)

eIn this trial, pixantrone was compared with the investigator’s choice of treatment (vinorelbine, oxaliplatin, ifosfamide, etoposide, mitoxantrone, or gemcitabine)

fIn this trial, pixantrone plus rituximab was compared with gemcitabine plus rituximab

gIn this trial, pola-BR was compared with BR

hIndependent review committee-assessed

iDigitized estimate from the Kaplan-Meier curve

jThree-year EFS rate shown

kOne-year EFS rates shown

An additional three RCTs [36-38] and 14 single-arm studies [39-52] were identified that did not meet the inclusion criteria for the SLR, but were potentially useful for the post-hoc network building exercise (see Fig. S1 in the electronic supplementary materials). The three RCTs did not meet the inclusion criteria for the SLR because they were in SCT-eligible patients [6, 37, 38].

Baseline Characteristics

Baseline characteristics in the studies are shown in Table 2. Median patient age across studies ranged from 51–74 years. The proportion of males was well balanced across studies, although five studies had > 65% male patients [11, 21, 27, 31, 33]. An imbalance was noted between studies in terms of disease severity, with some studies showing higher proportions of patients with Ann Arbor Stage III–IV disease and a International Prognostic Index score of 3–4 [11, 18, 26] than the other studies. Overall, Ann Arbor Stage III–IV disease affected 48–90% of patients. Among the eight studies that reported individual Ann Arbor disease stages, Stage III disease affected 6–36% of patients and Stage IV affected 4–87% [17, 18, 20, 22, 27–29, 34]. The number of prior lines of therapy varied from 1 to ≥ 4 (0–1 line, 3–68%; 2 lines, 20–44%; 3 lines, 12–31%; ≥ 4 lines, 13–35%).

Table 2

Baseline characteristics of the 19 included studies identified by the systematic literature review

Intervention	Reference	Median age (years)	Male sex (%)	Disease severity (%)	Prior lines of therapy (%)	Refractory status (%)	DOR to last therapy
Axicabtagene ciloleucel	[27]	58	67	IPI 0–2: 52 3 or 4: 48	≥ 3: 69	History of primary refractory disease: 26 Primary refractory at study entry: 2 Refractory to 2L + therapy: 77	N/A
BR	[28]	67	42.4	IPI 0, 1: 33.9 0–2: 35.6 Ann Arbor stage II: 30.5 III: 35.6 IV: 25.4	1 prior chemotherapy regimen: 64.4 2: 22.0 Prior rituximab: 96.6	N/A	N/A
	[32]	74	49	Ann Arbor stage I–II: 10 III–IV: 89	1: 51 2: 21 3: 13 > 3: 15 Prior rituximab: 95	N/A	N/A
GPD	[17]a	66.2	24	IPI 0, 1: 33 0–2: 69 3: 24 4: 7	NR	42	N/A
Gemcitabine + vinorelbine	[29]	65	59	IPI low risk: 41 Low intermediate: 36 High intermediate: 9 High risk: 14	1: 64 2: 32 3: 4.5	N/A	N/A
ESHAP	[18]a	51.8	28	IPI intermediate: 16 High: 37	1: 43 2: 10	N/A	N/A
Inotuzumab ozogamicin + R	[20, 53]a	70	56	sIPI 0–1: 16 2: 31 3: 32 4–5: 20	1 prior rituximab regimen: 53 2: 35 3: 12	N/A	N/A
Lenalidomide	[9]	65	51	IPI 0–1: 16.3 2: 44.9 3: 26.5 4–5: 12.2	1: 8 2: 16 3: 24 4: 27 ≥ 5: 24	Refractory to last therapy: 56 Rituximab refractory: 58 Refractory to last chemotherapy: 55	N/A
	[33]	66	64.5	IPI low risk: 20.3 Intermediate risk: 62.7 High risk: 17.1	Median prior regimens: 3	Refractory to last therapy: 44.2 Rituximab refractory: 53.9	N/A
	[24]	51	72	IPI low risk: 16 Intermediate risk: 68 High risk: 16	Median prior regimens: 2	Refractory to last therapy: 72	N/A
	[19]a	69	58.8	NR	1: 9.8 2: 41.2 ≥ 3: 49.0 ASCT: 25		N/A
Lenalidomide + R	[34]	74.2	52	Ann Arbor stage II: 22 III: 26 IV: 52	Median prior therapies: 3		N/A
Pixantrone	[21, 35]a	60	66	IPI 0–1: 30 2: 36  ≥ 3: 34	Median number of prior chemotherapy regimens: 3 Prior rituximab: 54 Prior stem cell transplant: 16	Refractory at baseline: 57	N/A
Pixantrone + R	[22]	73	43.6	IPI 0: 2 1: 13.1 2: 33  ≥ 3: 53.2 Ann Arbor stage I: 6.4 II: 19.9 III: 24.0 IV: 49.7	0: 4.8 1: 61.9 2: 21.8 3: 11.58 Prior SCT: 10.6		N/A
Pola-BR	[11]a	67	69.2	Ann Arbor stage III/IV: 84.6 IPI score 3–5: 53.8	Median 1: 28.2 2: 35.9  ≥ 3 35.9 Prior anti-CD20 agents: 97.4	Refractory to last treatment: 74.4	DOR to last treatment ≤ 12 months: 79.5
R-GemOx	[23]	64	67	Age-adjusted IPI: Low/Low-intermediate: 63 High/intermediate-high: 37	Median: 2 Prior rituximab: 57	Primary refractory: 13	Duration of last remission ≤ 1 year: 20  > 1 year: 67
	[25]	69	59	Ann Arbor stage III–IV: 75 Adjusted IPI > 1: 69	Mean number prior regimens: 1.72	59	N/A
	[26]	69	55	Secondary age-adjusted IPI 0–1: 31 2–3: 69	N/A	Primary refractory: 12	Duration of last remission ≥ 1 year: 46  < 1 year: 54
Tisagenlecleucel	[30, 31]	56	N/A	IPI ≥ 2: 73	2 Prior lines antineoplastic therapy: 44 3: 31 4–6: 20 Prior ASCT: 49	54	N/A

ASCT, autologous stem cell transplantation; BR, bendamustine plus rituximab; ESHAP, etoposide, methylprednisolone, cytosine arabinoside, platinum; GDP, gemcitabine, dexamethasone, cisplatin; GemOx, gemcitabine, oxaliplatin; IPI, International Prognostic Index; sIPI, second-line International Prognostic Index; pola, polatuzumab vedotin; R, rituximab

aBaseline characteristics for intervention cohort

Quality Assessment of Included Studies

Among the seven included RCTs, the studies by Sehn et al. [11] and Pettengell et al. [21] appeared to have the lowest risk for bias. This was based on the results of the quality assessment using the Cochrane critical appraisal tool.

Study Outcomes

Efficacy Outcomes

Endpoint definitions varied between studies (see Table S2 in the electronic supplementary materials) limiting potential comparisons. The International Working Group (IWG) 1999–NHL guidelines were the most commonly used criteria to define CR (Fig. 2). Across the included studies, overall response rate (ORR) was the most commonly reported outcome. All 20 studies reported ORR (Table 1; Table S2 in the electronic supplementary materials), with 12 studies measuring ORR as the primary outcome [9, 19, 23, 24, 26–28, 30–34]. The reported ORR for pola-BR was 48% compared with 18% in BR group (Table 1) [11]. Similarly, the ORR was higher with pixantrone than with the comparator of the investigator’s choice of treatment (37% vs. 14%; Table 1) [21]. ORR across studies varied between 19% with lenalidomide [9] and 82% with axicabtagene ciloceucel (Table 1) [27]. The second most commonly reported outcome was CR (Table 1; table S2 in the electronic supplementary materials). The reported CR rates were 43% and 15% for pola-BR vs. BR, respectively (Table 1) [11]. CR rates varied between 12% with lenalidomide [9] and 73% with rituximab + gemcitabine + oxaliplatin (R-GemOx; Table 1) [23].

Fig. 2

Assessment criteria used to assess complete response (by investigator) in the included studies. Pettengell et al. 2016 [21] included patients who were rituximab naïve and rituximab pretreated (54% of the pixantrone group and 56% of the comparator group received rituximab). CR complete response; IWG International Working Group

Twelve studies reported median PFS [11, 19–22, 25, 26, 28, 31, 32], which ranged from 2.6–17.1 months (Table 1). One of the most notable results was the longer median PFS with the addition of pola to BR at a median follow-up of 22.3 months [hazard ratio (HR) 0.34 (95% confidence interval (CI) 0.2–0.57); Table 1] [11]. Median PFS was higher with pixantrone than with the investigator’s choice comparator [HR 0.60 (95% CI 0.42–0.86), median follow-up 18 months] [21]. Similarly, in the PIX-306 trial median PFS was prolonged with pixantrone + rituximab compared with gemcitabine + rituximab, but the difference was not statistically significant [HR 0.85 (95% CI 0.64–1.14), median follow-up 18 months] [22]. Among chimeric antigen receptor T cell (CAR-T) therapies, median PFS was 2.9–3.2 months (median follow-up of 19.0 and 28.6 months, respectively) with tisagenlecleucel [30, 31], and 5.8 months (investigator assessed) and 7.3 months (independent review committee) with axicabtagene ciloleucel at a median follow-up of 15.4 months [27]. In addition, two studies reported 1-year PFS rates [11, 25]. The PFS rate at 1 year was 46% with pola-BR (vs. 13% with BR alone) [11], and 29% with R-GemOx [25].

Eleven studies reported median overall survival (OS) [11, 19–22, 25, 26, 29–32] with estimates ranging 5.0–22.2 months (Table 1; in two studies, median OS was not reached). An improvement in median OS was observed with the addition of pola to BR [HR 0.42 (95% CI 0.24–0.75)] [11]. Similarly, median OS for pixantrone was higher than the investigator’s choice comparator [HR 0.79 (95% CI 0.53–1.18)]; however, the difference was not statistically significant [21]. In the PIX-306 trial, median OS was lower with pixantrone + rituximab than with gemcitabine + rituximab [22]. Median OS for R-GemOx ranged from 9.1 [25] to 11.0 months [26], and median OS with tisagenlecleucel ranged from 11.1 [30] to 22.2 months [31]. In addition, three studies reported 1-year OS rates [11, 25, 30]. The OS rate at 1 year was 52% with pola-BR (vs. 24% with BR alone) [11], 48% with tisagenlecleucel [30], and 41% with R-GemOx [25].

Other reported secondary efficacy outcomes included event-free survival (two studies) [11, 17] and duration of response (seven studies) [11, 27, 30–34] (Table 1; Table S2 in the electronic supplementary materials).

Safety Outcomes

There was some variation in the safety results presented in the studies; therefore, direct comparisons were not feasible. Rates of any-cause adverse events (AEs) were similar with pola-BR vs. BR alone (100% vs. 97.4%) [11]. The most common Grade 3/5 AEs that were higher with addition of pola to BR were cytopenias, febrile neutropenia, and infections [11]. Grade 3/4 AEs occurring in > 5% of patients treated with gemcitabine, dexamethasone, and cisplatin were anemia and leukopenia [17]. Similarly, common Grade 3/4 AEs with R-GemOx were neutropenia (43%), peripheral neuropathy (7%), and thrombocytopenia (43%) [25]. In a single-arm study assessing the efficacy and safety of tisagenlecleucel, 86% of patients had Grade 3/4 AEs [30]. Furthermore, with axicabtagene ciloleucel, 67% and 27% of patients had Grade 3/4 neutropenia and febrile neutropenia, respectively [27]. Among the CAR-T therapies, rates of cytokine release syndrome and neurologic events (any grade) were lower with tisagenlecleucel than with axicabtagene ciloleucel (57% vs. 93%, and 20% vs. 64%, respectively) [27, 30]. Two patients treated with axicabtagene ciloleucel died because of AEs [27]; no treatment-related deaths were reported with tisagenlecleucel [30].

It was not possible to construct a connected network of evidence using data from either RCTs or the broader post-hoc study inclusion (Fig. S1 in the electronic supplementary materials). Because of this, conducting an NMA was deemed unfeasible.

Discussion

This SLR provides a summary of currently published evidence regarding treatments for R/R DLBCL. The findings from the review highlight that there is a paucity of published RCTs comparing alternative treatments for DLBCL, which is understandable since some of these therapies (e.g., pola, CAR-T therapies) have only been available for approximately 2 years. Only 10/37 studies (27%) were RCTs, including three that did not meet the inclusion criteria of transplant ineligibility, preventing implementation of an ITC or NMA. Furthermore, it was difficult to summarize the relative efficacy and safety of the different treatment options due to a lack of robust published evidence. Only two of the seven RCTs that met the inclusion criteria had positive outcomes (i.e. the intervention under study was more effective than the comparator in terms of response) [11, 21]; of those, one was in the second-line and beyond setting and one was in the third-line and beyond setting.

A limitation to the comparison of the interventions assessed in this review was the differences in the baseline characteristics of enrolled patients (Table 2). There were large differences in terms of median age, which ranged from 51 to 74 years [24, 34], and the proportion of male patients, ranging from 24 to 72% [17, 24]. There were also differences in terms of prior therapies patients received, and only five studies reported the proportion of patients who received prior rituximab treatment (Table 2), which ranged from 53 to 97% for inotuzumab ozogamicin and BR, respectively [20, 28]. The large variation in the refractory status of patients between studies also makes comparison of the interventions difficult due to the poor prognosis associated with refractory patients. Another limitation was the difference in grading criteria of cytokine release syndrome between the CAR-T trials. The axicabtagene ciloleucel trials used the Lee et al. (2014) criteria [54], whereas the tisagenleucel trials used the University of Pennsylvania (Penn) grading scale [55]. Due to differences in these two methods, the Penn criteria usually assign a higher grade of cytokine release syndrome compared with the Lee criteria, which impacts the comparability of safety data between different CAR-T trials [56].

The findings from this review are consistent with those of a recently published structured review, which concluded that the efficacy of current treatments is modest and there is an unmet need for novel, effective, and tolerable treatments for patients with R/R aNHL who are ineligible for or have failed SCT [15]. However, the review by Salles et al. [15] had slightly different eligibility criteria than the current review, for example, the review focused on patients with aNHL, while the current review focused on one subtype i.e., DLBCL. Furthermore, incorporation of three identified RCTs in transplant-eligible patients into the post-hoc network-building exercise in the current review allowed consideration of a broader population than in the earlier review, which focused on transplant-ineligible or failed SCT patients only [15]. The findings from this review are also consistent with a recently published real-world study by Ionescu-Ittu and colleagues [57], which analyzed second-line therapies for R/R DLBCL used in US clinical practice. The results showed heterogeneity, with 200 distinct therapy regimens used in 702 included patients [57], highlighting the unmet need in this treatment landscape.

Imaging assessment criteria have become more stringent over time [58-60]. Despite this, the recent study of pola-BR achieved among the highest CR in R/R DLBCL using the strictest response criteria [11]. Responses were assessed by CT, PET-CT, and bone marrow examination (if required to confirm CR) as per study protocol.

A strength of the current study is its systematic approach to literature searching. Despite this, the lack of published studies hampered any clinically meaningful analysis of outcomes. In addition, the differences in patient baseline characteristics and reported efficacy and safety outcomes made it difficult to compare results between the different interventions in the trials. Therefore, we recommend that an indirect comparison should be conducted to account for the differences in the trials in the DLBCL setting.

Conclusions

These findings highlight the paucity of published RCTs to establish the comparative efficacy of treatments for R/R DLBCL, and demonstrate a fragmented treatment landscape and lack of standard of care in this setting.

Below is the link to the electronic supplementary material.

Supplementary file1 (JPG 838 kb)

Supplementary file2 (DOCX 126 kb)

Why carry out this study?

Outcomes for patients with diffuse large B cell lymphoma (DLBCL) who relapse or are refractory (R/R) to first-line treatment are poor, especially those who are ineligible for stem cell transplantation (a standard second-line treatment).

The aim of our clinical systematic literature review was to identify clinical evidence on treatment options for these patients and to assess the feasibility of conducting an indirect treatment comparison (ITC) or network meta-analysis (NMA) to evaluate the relative efficacy and safety of polatuzumab vedotin plus bendamustine-rituximab (pola-BR; a recently approved second-line or later treatment) versus other treatments for R/R DLBCL.

What was learned from this study?

Thirty-seven studies were identified, of which 20 were eligible. Due to a lack of randomized controlled trials (RCTs; seven in total), an ITC/NMA summary of the relative efficacy and safety of the treatment options was not possible, and only two of the seven RCTs had positive outcomes.

These results highlight the lack of published RCTs to establish the comparative efficacy of treatments for transplant-ineligible R/R DLBCL and the lack of standard of care treatment in this setting.