Primary breast diffuse large B‐cell lymphoma in the rituximab era: Therapeutic strategies and patterns of failure

Abstract

Primary breast diffuse large B‐cell lymphoma (PB‐DLBCL) is a rare subtype of DLBCL with limited data on patterns of failure. This multicenter study aimed to define the optimum treatment strategy and patterns of failure for PB‐DLBCL patients. We retrospectively reviewed data on 108 PB‐DLBCL patients from 21 Chinese medical centers. Only patients with localized disease (involvement of breast and localized lymph nodes) were included. After a median follow‐up of 3.2 years, 32% of patients developed progression or relapse. A continuous pattern of relapse was observed, characterized by frequent late relapses in the contralateral breast and central nervous system (CNS). Although rituximab significantly reduced the overall cumulative risk of progression or relapse (5‐year cumulative risk 57% vs 24%, P = .029), it had limited effect on the reduction of breast relapse (P = .46). Consolidative radiotherapy significantly decreased the risk of breast relapse, even in the subgroup of patients treated with rituximab (5‐year cumulative risk 21.2% vs 0%, P = .012). A continuous risk of CNS progression or relapse up to 8.2 years from diagnosis was observed (10‐year cumulative risk 28.3%), with a median time to CNS relapse of 3.1 years. Neither rituximab nor prophylactic intrathecal chemotherapy significantly decreased the risk of CNS relapse. In summary, our study indicates that PB‐DLBCL has a continuous pattern of relapse, especially with frequent late relapses in the CNS and contralateral breast. Rituximab and RT confer complementary benefit in the reduction of relapse. However, neither the addition of rituximab nor prophylactic intrathecal chemotherapy could effectively prevent CNS relapse for PB‐DLBCL patients.

Abbreviations

CHOP

cyclophosphamide, doxorubicin, vincristine, and prednisone

CI

confidence interval

CNS

central nervous system

CT

chemotherapy

DLBCL

diffuse large B‐cell lymphoma

GCB

germinal center B‐cell like

IPI

International Prognostic Index

IT

intrathecal chemotherapy

NHL

non‐Hodgkin's lymphoma

OS

overall survival

PB‐DLBCL

primary breast diffuse large B‐cell lymphoma

PFS

progression‐free survival

R‐CHOP

rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone

RT

radiation therapy

1. INTRODUCTION

Primary breast lymphoma is a rare subtype of NHL representing an estimated 1% of all NHL and less than 3% of extranodal lymphomas.1, 2, 3 Its definition was first proposed in 1972 by Wiseman and Liao as a malignant lymphoma involving predominantly the breast with or without ipsilateral locoregional lymph nodes.4 By this definition, most primary breast lymphoma patients are classified as stage I or II based on the Ann Arbor Staging System, with the exception of bilateral breast lymphoma, which is considered as stage IV by some investigators.5 The most common histology is DLBCL, although diverse lymphoma subtypes have been reported.1, 2, 3

As a rare subentity of DLBCL, PB‐DLBCL has been shown to display characteristic patterns of relapse distinct from those of nodal DLBCL.5 Particularly, a high frequency of extranodal relapses in the breast and CNS has been reported in previous studies.6, 7, 8, 9, 10 However, due to the rarity of this disease, the current published reports on PB‐DLBCL comprise predominantly small retrospective series, with only a few large cohort studies reported so far. Thus, it is unsurprising that the patterns of relapse reported for PB‐DLBCL are not consistent across all studies. One major area of controversy is the risk of CNS relapse, which ranges widely from 5% to 19% in the published work.6, 7, 8, 9, 10 As a result, there is currently no consensus among clinicians with respect to the routine use of prophylactic CNS therapy in PB‐DLBCL patients.

The incorporation of rituximab into CT has led to a paradigm shift in the treatment of DLBCL, with a number of phase III studies reporting significant survival benefit of R‐CHOP vs CHOP as first‐line therapy of DLBCL patients.11, 12 This benefit from rituximab has also challenged the value of consolidative RT in the treatment of limited‐stage DLBCL, as results from one randomized controlled trial have shown that consolidative RT could not offer additional benefit for early stage DLBCL patients treated in the rituximab era.13 However, in the case of PB‐DLBCL, only a few studies have evaluated the role of rituximab, and most of them did not show an advantage in PFS or OS.7, 14, 15 Given this uncertain benefit of rituximab, whether consolidative RT is beneficial for PB‐DLBCL patients who have been treated with rituximab‐containing regimens remains unclear.

At present, most reports of PB‐DLBCL were from Western countries or regions, with a scarcity of data reported for Chinese patients. In light of the unresolved clinical issues mentioned above and the lack of large PB‐DLBCL series reported from China, a multicentric collaborative effort was initiated by the Leukemia and Lymphoma Committee of the Chinese Geriatric Oncology Society, in order to further elucidate the patterns of progression or relapse and the impact of different treatments on the risk of relapse in PB‐DLBCL patients.

2. MATERIALS AND METHODS

Data were collected on patients with primary breast DLBCL diagnosed between January 2000 and December 2015 from 21 Chinese medical centers. Institutional review board approval was obtained at each site. Eligibility criteria required confirmed a pathological diagnosis of DLBCL according to the 2001 or 2008 WHO classification of lymphoid neoplasms and disease localized to one or both breasts with or without ipsilateral regional (axillary and/or supraclavicular) lymph node involvement. Patients with systemic disease with breast involvement or transformed DLBCL from low‐grade lymphoma and patients who did not receive any treatment after diagnosis were excluded. A study‐specific data collection form was completed for each case. Collected data included patient and tumor characteristics, results of diagnostic tests, staging workup, treatments, time and sites of disease progression or relapse, and clinical outcomes. Available immunohistochemistry data obtained from the diagnostic specimens were reported from each of the participating centers. Staging workup included computed tomography scans of the neck, chest, abdomen, and pelvis and bone marrow smear and biopsy. In addition, whole‐body PET computed tomography, cerebrospinal fluid cytology test, and brain MRI were carried out in 18.5%, 22%, and 3% of patients at diagnosis, respectively. Patients were staged according to the Ann Arbor system.16 Patients with bilateral breast involvement were classified as stage IV in this study. The IPI was determined using all the available information.

Time to progression or relapse was measured from the date of diagnosis to the date of first progression or relapse. Progression‐free survival was measured from the date of diagnosis until the date of disease progression or death from any cause. Overall survival was measured from the date of diagnosis to the date of death or last follow‐up. The median follow‐up time was calculated by the reverse Kaplan‐Meier method.17 Cumulative incidence of progression or relapse at each site (eg nodal sites, breast, and CNS) was calculated by competing risk analysis using Fine and Gray's proportional hazard model.18 In this analysis, death without the prespecified site of relapse was defined as the competing risk. Both PFS and OS were estimated according to the Kaplan‐Meier method. Log‐rank test and Cox regression methods were used to analyze time‐to‐event data. A two‐tailed P value <0.05 was considered statistically significant. Analyses were carried out using the SPSS 19.0 package (IBM, Chicago, IL, USA) and the R language version 3.4.3.

3. RESULTS

3.1. Patients’ characteristics

One‐hundred and eight patients who met the eligibility criteria were included. The baseline characteristics are shown in Table 1. All patients were female, with a median age of 47 years (range, 16‐85 years). The most common presentation was an ipsilateral breast painless palpable mass, with right breast involvement more common than left (59% vs 35%). Bilateral breast involvement was present in 5.6% of patients at diagnosis. The median tumor size was 3.7 cm (range, 1.2‐12.8 cm), and regional nodal involvement was present in 39% of patients. Among the 91 patients with available information on IPI, 78 patients (86%) had a low IPI score of 0 or 1, with 48 patients (53%) in the very good risk group (IPI 0). Among the 89 patients in whom immunohistochemistry was available, CD10 was positive in 31%, BCL6 was positive in 74%, and MUM1 was positive in 82%. Fifty‐nine patients (66%) were classified as non‐GCB phenotype and 30 patients (34%) as GCB type according to the algorithms described by Hans et al.19 CD5 was positive in 9 patients (10%), and the median Ki‐67 index was 80%.

Table 1.

Clinical characteristics of 108 Chinese patients with primary breast diffuse large B‐cell lymphoma, at presentation

Parameters		No. (%)
Age	Median	47
	Range	16‐85
Sex	Female	108 (100)
ECOG‐PS	0	76 (70.4)
	1	26 (24.1)
	2	3 (2.8)
	Unknown	3 (2.8)
Presence of B symptoms		5 (4.6)
Primary site of lymphoma	Left breast	38 (35.2)
	Right breast	64 (59.3)
	Bilateral	6 (5.6)
Tumor size	Median	3.7 cm
	Range	1.2‐12.8 cm
Nodal sites involvement	None	66 (61.1)
	Axillary only	32 (29.6)
	Supraclavicular ± axillary	10 (9.3)
Ann Arbor stage	IE	62 (57.4)
	IIE	40 (37.0)
	IV	6 (5.6)
LDH	Normal	74 (68.5)
	Elevated	18 (16.7)
	Unknown	16 (14.8)
IPI	0	48 (44.4)
	1	30 (27.8)
	2	11 (10.2)
	3	2 (1.9)
	Unknown	17 (15.7)

IPI, International Prognostic Index; LDH, lactate dehydrogenase; PS, performance status.

3.2. Treatment

The front‐line therapy is summarized in Table 2. All patients received anthracycline‐containing CT, with CHOP or CHOP‐like regimens being the most common (77%). A minority of patients (23%) with high‐risk features (eg IPI ≥2, activated B‐cell type) were treated with cyclophosphamide, doxorubicin, vincristine, etoposide, and prednisone, or etoposide, doxorubicin, and vincristine by 96‐hour continuous infusion, cyclophosphamide, and prednisone. Epidoxorubicin or liposomal doxorubicin was used instead of doxorubicin in some patients. The median number of cycles of chemotherapy was 6 (range, 1‐8), with 92% of patients receiving at least 4 cycles of chemotherapy. Rituximab was routinely recommended to all PB‐DLBCL patients in this study. However, due to patients’ varying economic status (eg a proportion of patients with low income could not afford rituximab), only 61% of cases received rituximab in addition to chemotherapy. Consolidative radiation therapy to the involved breast with or without ipsilateral regional nodes was used in 36% of patients with a median dose of 45 Gy (range, 30‐50 Gy), including 2 patients who also received additional prophylactic RT to the contralateral breast. Prophylactic CNS CT was given to 48 (44%) patients; 44 patients received IT and the other 4 patients received systemic high‐dose methotrexate in combination with IT. Of the 6 patients with stage IV disease, 3 received prophylactic IT. Regimens for IT consisted of methotrexate 10‐15 mg plus dexamethasone 10 mg, or cytarabine 50 mg plus dexamethasone 10 mg. The median number of doses of IT was 4 (range, 1‐8). There was no significant difference in baseline clinical characteristics between patients treated with and without rituximab (Table S1) or between patients treated with and without prophylactic IT (Table S2). Mastectomy was carried out in 19% of patients.

Table 2.

Primary therapy of Chinese patients with primary breast diffuse large B‐cell lymphoma (n = 108)

		N.	%
Chemotherapy	CHOP	83	76.9
	CHOEP	14	13.0
	EPOCH	10	9.3
	BACOP	1	0.9
Rituximab	Yes	66	61.1
	No	42	38.9
RT	Yes	39	36.1
	No	69	63.9
Mastectomya	Yes	21	19.4
	No	87	80.6
CNS prophylaxis	IT only	44	40.0
	IT+HD MTX	4	4.4
	None	60	55.6

Including modified/radical mastectomy and simple mastectomy, excluding lumpectomy or excisional biopsy.

BACOP, bleomycin, cyclophosphamide, doxorubicin, vincristine, and prednisone; CHOEP, cyclophosphamide, doxorubicin, vincristine, etoposide, and prednisone; CHOP, cyclophosphamide, doxorubicin, vincristine, and prednisone; CNS, central nervous system; EPOCH, etoposide, doxorubicin, and vincristine (96‐hour continuous infusion), cyclophosphamide, and prednisone; HD MTX, high‐dose methotrexate; IT, intrathecal chemotherapy; RT, radiotherapy.

3.3. Patterns of progression or relapse

At a median follow‐up of 3.2 years (range, 0.1‐11.5 years), 35 (32%) patients developed disease progression or relapse, with 18 patients having 2 or more sites of involvement at first relapse. The median time to first progression or relapse was 1.5 years (range, 0.2‐8.2 years). The time to first progression or relapse was more than 3 years in 10 patients and more than 5 years in 6 patients. The estimated 2‐, 5‐, and 10‐year cumulative risks of all progression or relapse were 20.0%, 37.0%, and 61.6%, respectively (Figure 1A). Information regarding relapse sites is shown in Table 3. The most common site of first progression or relapse was the lymph nodes (43%), followed by the breast (41%) and CNS (24%). Extranodal relapse (n = 25) was more common than relapse confined to only nodal sites (n = 10). There was no significant difference in the cumulative risk of nodal relapse between patients with and without nodal involvement at initial diagnosis (5‐year cumulative risk of nodal relapse, 15.3% vs 21.2%, P = .69; Figure S1A).

Figure 1.

Risk of relapse among 108 Chinese women with primary breast diffuse large B‐cell lymphoma. A, Cumulative risk of relapse at all sites, breast, and central nervous system (CNS). B, Cumulative risk of CNS relapse in patients with unilateral and bilateral breast involvement at initial diagnosis

Table 3.

Anatomic sites of first relapse in 35 Chinese patients with primary breast diffuse large B‐cell lymphoma

Relapse sites	Overall	Relapse ≤3 years from diagnosis	Relapse >3 years from diagnosis
Patients	35	25	10
Extranodal relapse	25	17	8
Total CNS relapse	8	4	4
Brain relapse	6	2	4
Leptomeningeal relapse	1	1	0
Unknown	1	1	0
Total breast relapse	14	10	4
Ipsilateral breast relapse	8	8	0
Contralateral breast relapse	6	2	4
Extranodal sites other than CNS and breast	7	7	0
Bone marrow	2	2	0
Bone	2	2	0
Other sitesa	3	3	0
Nodal relapseb	15	12	3
Regional nodal relapse	8	6	2
Distant nodal relapse	13	10	3

^aIncluding kidney, adnexa of uterus, and soft tissue.

^bNodal‐only relapse was observed in 10 patients.

CNS, central nervous system.

Breast progression or relapse was observed in a total of 16 patients, including 2 patients with breast relapses occurring during salvage therapy. The estimated 5‐ and 10‐year cumulative risks of all breast progression or relapse were 20.0% and 26.9%, respectively (Figure 1A). All ipsilateral breast relapses occurred within the first 3 years following diagnosis, whereas contralateral breast relapses tended to occur later with a median time to relapse of 4.6 years (range, 0.4‐5.6 years).

Central nervous system progression or relapse developed in a total of 11 patients, including 3 patients whose CNS relapse occurred during salvage treatment. The median time to CNS progression or relapse was 3.1 years (range, 0.2‐8.2 years). The estimated 2‐year, 5‐year, and 10‐year cumulative risks of all CNS progression or relapse were 4.3%, 12.5%, and 28.3%, respectively (Figure 1A). Central nervous system relapse was reported in 8 stage I patients, 1 stage II, and 2 stage IV patients. Brain parenchymal relapse was observed in 8 patients, leptomeningeal relapse in 1 patient, and the specific sites of CNS relapse in the other 2 patients were unknown. Six patients developed isolated CNS relapse without concurrent systemic disease, whereas the remaining 5 patients had CNS disease accompanied by relapse or progression in other sites. Bilateral breast involvement at initial diagnosis was associated with a significantly increased risk of early CNS progression (1‐year cumulative risk 33.3% vs 1.0%, P = .037; Figure 1B), whereas neither regional nodal involvement nor tumor size larger than 5 cm was associated with a higher risk of CNS relapse (Figure S1B,C). Notably, of the 9 patients with CD5 positivity, only 1 patient developed CNS relapse.

When patterns of progression or relapse were analyzed according to the cell‐of‐origin classification, there was no significant difference in the cumulative risk of overall progression or relapse or site‐specific progression or relapse (eg nodal, breast, and CNS relapse) between GCB and non‐GCB subtypes, although a trend towards higher risk of nodal relapse was observed for the non‐GCB subtype (P = .057; Figure S2). When relapse sites were analyzed according to the time to relapse, there is a major difference in the distribution of relapse sites between early relapse and late relapse (Table 3). In the patients (n = 25) whose first relapse occurred within 3 years from initial diagnosis, the most common sites of relapse were the lymph nodes and ipsilateral breast. In the patients (n = 10) whose first relapse occurred more than 3 years from diagnosis, the predominant sites of relapse were the contralateral breast and CNS.

3.4. Impact of treatment methods on patterns of progression or relapse

3.4.1. Rituximab

The addition of rituximab significantly reduced the overall cumulative risk of progression or relapse in patients with PB‐DLBCL (P = .029; Figure 2A). The estimated 5‐year cumulative risk of progression or relapse in patients treated with rituximab and without rituximab was 24% and 57%, respectively. In relapse site‐specific analyses, rituximab was associated with significantly decreased risk of nodal relapse (5‐year cumulative risk, 35.5% vs 10.0%, P = .012; Figure 2B) but not a significant reduction in the risk of extranodal relapse (P = .117; Figure 2C). In particular, rituximab did not mitigate the cumulative risk of relapse in the breast (P = .46; Figure 2D) or in the CNS (P = .72; Figure 2E).

Figure 2.

Risk of relapse among 108 Chinese women with primary breast diffuse large B‐cell lymphoma. Cumulative risk at all sites (A), nodal sites (B), extranodal sites (C), breast (D), and CNS (E) according to the use of rituximab

3.4.2. Consolidative RT

Consolidative RT was associated with a significant reduction in the overall cumulative risk of relapse (P = .042; Figure 3A). In site‐specific analyses, RT significantly reduced the cumulative risk of relapse in both the ipsilateral and the contralateral breast (5‐year cumulative risk, 32.7% vs 0.0%, P < .001; Figure 3B). Notably, in the subgroup of patients treated with rituximab, RT was still associated with a significant reduction in the risk of breast relapse (5‐year cumulative risk, 21.2% vs 0.0%, P = .012; Figure 3C). No significant associations between RT and the risk of nodal relapse (P = .146) or CNS relapse (P = .714) were observed (Figure S3). Secondary malignancy was observed in 1 patient receiving consolidative RT who developed breast carcinoma with squamous and chondroid metaplasia on the involved side of breast 5 years later.

Figure 3.

A, Cumulative risk of relapse at all sites in 108 Chinese women with primary breast diffuse large B‐cell lymphoma, according to the use of consolidative radiotherapy (RT). B,C, Cumulative risk of breast relapse according to the use of consolidative RT in the entire cohort (B) and in the subgroup of patients treated with rituximab (C). D, Cumulative risk of central nervous system (CNS) relapse according to the use of prophylactic intrathecal chemotherapy (IT)

3.4.3. Prophylactic IT

Overall, CNS progression or relapse occurred in 3 of 48 patients who received prophylactic IT and 8 of 60 patients without IT prophylaxis, with no significant difference in the rates of relapse between the two groups (6.3% vs 13.3%, P = .374). In the univariate analysis, prophylactic IT was not associated with a significant reduction in the cumulative risk of CNS relapse (P = .975; Figure 3D).

3.4.4. Mastectomy

Mastectomy was not associated with a significant reduction in the overall cumulative risk of progression or relapse (P = .48) compared with biopsy or lumpectomy only, nor did mastectomy decrease the risks of relapse in the breast (P = .94) or CNS (P = .21) (Figure S4).

3.5. Survival and prognostic factors

The median PFS for the entire cohort was 6.3 years (95% CI, 4.2‐8.4 years), and the median OS was not reached. The 5‐year PFS and 5‐year OS were 61.2% (95% CI, 49.0‐73.4%) and 77.3% (95% CI, 66.1‐88.5%), respectively (Figure 4).

Figure 4.

Progression‐free survival (PFS) and overall survival (OS) among Chinese women with primary breast diffuse large B‐cell lymphoma (n = 108)

Results of prognostic factor analyses are detailed in Table 4. In multivariate analyses, IPI, rituximab, and RT were significantly associated with PFS. International Prognostic Index was the only significant prognostic factor associated with OS. Regional nodal involvement and tumor size larger than 5 cm were not associated with significant changes in PFS or OS.

Table 4.

Multivariate analyses of predictive factors for progression‐free survival (PFS) and overall survival (OS) in Chinese patients with primary breast diffuse large B‐cell lymphoma

Factor	PFS			OS
	HR	95% CI	P value	HR	95% CI	P value
IPI	2.06	1.18‐3.60	.012	4.52	1.64‐12.79	.008
Regional nodal involvement	1.23	0.50‐3.07	.655	0.57	0.09‐3.66	.550
Rituximab	0.33	0.12‐0.92	.028	1.04	0.19‐5.72	.969
RT	0.29	0.10‐0.80	.034	0.50	0.09‐2.88	.439
IT	0.71	0.27‐1.91	.502	0.41	0.04‐3.94	.439
Mastectomy	0.45	0.15‐1.30	.141	0.44	0.07‐2.83	.389

Bold values indicate statistically significant factors.

CI, confidence interval; HR, hazard ratio; IPI, International Prognostic Index; IT, intrathecal chemotherapy; RT, radiotherapy.

4. DISCUSSION

As the largest case series of PB‐DLBCL in the rituximab era to date, our study revealed a continuous pattern of relapse for PB‐DLBCL, which is largely attributable to frequent late relapses in the CNS and contralateral breast. In addition, our study revealed for the first time the differential effect of rituximab on nodal and extranodal relapse and the complementary benefit of rituximab and RT in the management of PB‐DLBCL. The underlying biology and clinical implications of these findings are discussed below.

The correlation between pathological characteristics and patterns of failure in PB‐DLBCL has not been extensively studied. Previous reports have shown the predominance of non‐GCB type in PB‐DLBCL, yet reported treatment outcomes were similar between the GCB and non‐GCB patients.20, 21 Consistent with these reports, our analysis found no significant difference in patterns of failure between GCB and non‐GCB subgroups, suggesting that cell‐of‐origin classification has limited prognostic value for PB‐DLBCL. CD5 positivity was observed in 10% of our cases, similar to the prevalence of CD5 positivity reported in the general DLBCL population (5%‐10%).22 Furthermore, the incidence of CNS relapse was similar between the CD5‐positive cases and the remainder of the cohort, indicating that CD5 positivity might not be the main cause of the high CNS relapse rate in PB‐DLBCL.

The benefit of rituximab in the treatment of PB‐DLBCL has been controversial. Two multicenter studies found no significant improvement in PFS or OS from the addition of rituximab,7, 14 whereas another small retrospective series reported significantly better 5‐year OS for PB‐DLBCL patients treated with R‐CHOP vs CHOP alone.23 Interestingly, our analysis revealed a differential effect of rituximab against nodal and extranodal (mainly breast and CNS) relapse. Whereas rituximab significantly decreased the risk of systemic nodal relapse, it showed limited benefit against breast and CNS relapse. A possible reason why rituximab could not effectively reduce CNS relapse might be related to its poor penetration across the blood‐brain barrier. Previous pharmacokinetic studies revealed that levels of rituximab in the cerebrospinal fluid are only 0.1% of matched serum levels following an i.v. dose.24 In published clinical studies, the impact of rituximab on CNS relapse of DLBCL was also controversial.25, 26 Villa et al26 suggested that the beneficial effect of rituximab against CNS relapse might be through superior eradication of systemic disease, which secondarily contributes to a reduction of late CNS relapse, rather than a direct CNS prophylactic effect. As none of our patients had systemic disease at initial diagnosis, and the majority of patients (6 of 11) developed isolated CNS relapse with no concurrent systemic disease, the CNS prophylactic effect of rituximab in this setting might be limited. In terms of breast relapse, there is currently no evidence of a “blood‐breast barrier” restricting the passage of i.v. rituximab into the breast tissue. However, as breast relapse can be considered as “local relapse” in PB‐DLBCL, this observation suggests systemic immunochemotherapy alone might be insufficient to achieve optimal local tumor control. Given these considerations, additional therapies to reduce local breast relapse and CNS relapse should be considered in the management of PB‐DLBCL patients who received rituximab‐containing regimens.

The benefit of consolidative RT for the treatment of PB‐DLBCL has been confirmed by randomized controlled trial in the prerituximab era,8 yet the role of RT for PB‐DLBCL patients receiving rituximab‐based regimens remains largely unknown. Our study showed that consolidative RT significantly reduced the risk of breast relapse, even in those who had received rituximab, suggesting the beneficial effect of RT in PB‐DLBCL patients treated with rituximab‐containing regimens. This finding is in line with the abovementioned assumption that immunochemotherapy alone is insufficient to achieve optimal local tumor control, and suggests a complementary benefit between rituximab and RT in the management of PB‐DLBCL. However, our finding seems to be at odds with results of a recently published phase III study that reported no significant difference in event‐free survival and OS between limited‐stage DLBCL patients treated with R‐CHOP with and without RT.13 This discrepancy could be explained by the different patterns of relapse between PB‐DLBCL and DLBCL in general. Relapses in this phase III study were predominantly systemic, and the incidence of local relapse (1.5%) was much lower compared with that of our cohort. Therefore, the high incidence of local breast relapse and the limited effect of rituximab on the reduction of breast recurrence might contribute to the benefit of RT observed in our PB‐DLBCL patients. Another interesting observation is that RT to the involved breast seemed to reduce the risk of contralateral relapse, given that only a few cases received prophylactic RT to contralateral breast in our study. This finding suggests that the risk of contralateral breast relapse is to a large extent associated with local tumor control. Studies into the lymphatic system of breast have revealed the existence of lymphatic channels cross‐linking bilateral breast, which might allow direct lymphatic drainage from one breast to the other.27 Therefore, it is reasonable to postulate that by improving local tumor control, consolidative RT could decrease the likelihood of late lymphatic metastasis of residue disease to the contralateral breast. Although these hypotheses should be regarded as only suggestive due to the lack of sound evidence, they are worthy of further exploration.

The risk of CNS relapse in PB‐DLBCL remains controversial with the reported rates of CNS relapse ranging from 5% to 19.6% (see Table S3).1, 6, 7, 8, 9, 10, 14 In our study, we observed a rate of CNS relapse of 10% with an estimated 10‐year cumulative risk of 28.3%, which is comparable to that of primary testicular DLBCL.28, 29 Notably, in contrast to the general observation that CNS relapse in DLBCL occurred early (median, 6.7‐8.1 months),30, 31, 32, 33 the PB‐DLBCL patients in our study showed a persistent risk of CNS relapse occurring up to 8.2 years after initial diagnosis (median, 3.1 years). In addition, our study showed for the first time that synchronous bilateral breast involvement was significantly associated with a higher risk of early CNS progression compared with patients with unilateral breast disease. However, it is noteworthy that, although patients with unilateral breast lymphoma had a low incidence of CNS progression in the first few years, this risk accumulated gradually, reaching up to 28% at 10 years, suggesting that CNS relapse is still a major cause of treatment failure for these patients. Based on these findings, more effective strategies for CNS prophylaxis against PB‐DLBCL need to be explored.

The optimum strategy of CNS prophylaxis in PB‐DLBCL has not been established. Rituximab seems to be ineffective against CNS relapse, as discussed above. Furthermore, we found no significant difference in the risk of CNS relapse between patients with and without IT prophylaxis. This finding is in line with several other studies of DLBCL that suggested the inadequate efficacy of intrathecal prophylactic chemotherapy in preventing CNS disease.30, 32, 33 As brain parenchymal relapse was more common than leptomeningeal relapse in PB‐DLBCL, a more promising option would be systemic CNS chemotherapy prophylaxis such as high‐dose i.v. methotrexate. However, because only 4 patients received high‐dose i.v. methotrexate in our cohort, the efficacy of this approach could not be determined.

As the largest study of PB‐DLBCL in a Chinese population, our cohort shares some common clinical characteristics with PB‐DLBCL reports from other East Asian countries or regions (eg South Korea, Japan, and Taiwan),14, 34, 35, 36 yet these clinical characteristics seem to be distinct from non‐Asian PB‐DLBCL reports. These differences include an earlier age of disease onset (median age, 47‐57 years vs 62‐64 years),6, 7 the different prognostic impact of regional nodal involvement (eg regional nodal involvement is associated with worse prognosis in non‐Asian reports but not East Asian ones),5 and different patterns of CNS relapse (eg continuous relapse vs early relapse).7, 14 Taken together, these findings suggest a possibility of racial difference in the biology of PB‐DLBCL between the East Asian and non‐Asian populations. Although these findings need to be validated by further evidence, they are hypothesis‐generating and warrant further investigation.

Although both rituximab and RT decreased disease relapse and improved PFS in our study, they were not associated with significant changes in OS. This result might be due to the limited duration of follow‐up in the present study. Given the favorable prognosis of PB‐DLBCL (median OS, 8‐14 years)6, 7 and the pattern of frequent late relapse, it is possible that a 3.2‐year follow‐up might be insufficient to detect a significant survival difference between different treatment groups. In addition, the majority of patients who had disease progression received multiple lines of salvage therapy, including the use of rituximab and autologous/allogeneic stem cell transplant, which might also impact the survival outcome.

Several limitations need to be noted in this study. First, evaluation of CNS involvement was not carried out in all patients at diagnosis, which could have resulted in understaging and inclusion of some patients with occult CNS disease. However, patients with occult CNS involvement at diagnosis typically develop clinical CNS progression early (usually earlier than 1 year from diagnosis), whereas our cohort was characterized by frequent late CNS relapse, thus the likelihood of initial CNS involvement for the patients who developed CNS relapse in our series is not very high. Second, the relatively limited follow‐up duration could mask the long‐term survival difference of patients receiving different treatments. Finally, a central pathology review was not undertaken, which might have an undefined impact given the possible interobserver variability among pathologists. However, all pathologists worked at centers with expertise in the management of lymphoma in our study.

In conclusion, our study provides a comprehensive analysis of clinical features, patterns of failure, and the effect of various therapeutic strategies on the pattern of relapse in a large cohort of Chinese PB‐DLBCL patients. Based on our results, a combination of immunochemotherapy with consolidative RT and CNS prophylaxis could be the optimum treatment choice for patients with newly diagnosed PB‐DLBCL. One major challenge is to explore effective strategies of CNS prophylaxis because neither rituximab nor prophylactic IT decreased the risk of CNS relapse in PB‐DLBCL patients.

CONFLICT OF INTEREST

The authors have no conflict of interest.

Supporting information

 

 

 

 

 

 

 

Hu S, Song Y, Sun X, et al. Primary breast diffuse large B‐cell lymphoma in the rituximab era: Therapeutic strategies and patterns of failure. Cancer Sci. 2018;109:3943–3952. 10.1111/cas.13828