Upward trend in follicular lymphoma among the Korean population: 10-year experience at a large tertiary institution

Article information

J Pathol Transl Med. 2021;55(5):330-337
Publication date (electronic) : 2021 September 2
doi : https://doi.org/10.4132/jptm.2021.07.25
1Department of Pathology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea
2Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea
Corresponding Author: Jooryung Huh, MD, PhD, Department of Pathology, Asan Medical Center, University of Ulsan College of Medicine, 88 Olympic-ro 43-gil, Songpa-gu, Seoul 05505, Korea Tel: +82-2-3010-4553, Fax: +82-2-472-7898, E-mail: jrhuh@amc.seoul.kr
Corresponding Author: Heounjeong Go, MD, PhD, Department of Pathology, Asan Medical Center, University of Ulsan College of Medicine, 88 Olympic-ro 43-gil, Songpa-gu, Seoul 05505, Korea Tel: +82-2-3010-5888, Fax: +82-2-472-7898, E-mail: damul37@amc.seoul.kr
Received 2021 April 13; Revised 2021 June 26; Accepted 2021 July 25.

Abstract

Background

Follicular lymphoma (FL) is the second most common non-Hodgkin lymphoma (NHL) in Western countries. However, it is relatively rare in Asia. This study examined epidemiologic characteristics of FL in South Korea, with an emphasis on recent trends of increase in cases.

Methods

We retrospectively examined 239 cases of newly diagnosed FL at a large tertiary institution in Korea (Asan Medical Center, Seoul, Republic of Korea) between 2008 and 2017. Age-adjusted incidence rates and clinicopathological variables were analyzed, and joinpoint regression analysis was used to identify the changes.

Results

The age-adjusted incidence of FL significantly increased during the study period (p = .034), and the ratio of (relative incidence) patients with FL to patients with NHL increased from 4.28% to 9.35% in the same period. Over the 10-year study assessment duration, the proportion of patients with stage III/IV FL (p = .035) and expression of BCL2 (p = .022) or BCL6 (p = .039) significantly increased. From 2013–2017, the proportion of patients with highrisk Follicular Lymphoma International Prognostic Index (FLIPI) score increased (21.5% to 28.7%), whereas that of low-risk FLIPI decreased (55.4% to 38.6%), although those results were not statistically significant (p = .066).

Conclusions

We found an increasing incidence of FL, with a disproportionate increase in the incidence of high-stage disease and recent changes in the clinicopathologic features of the Korean patient population.

Follicular lymphoma (FL) is the second most common non-Hodgkin lymphoma (NHL) in Western countries and accounts for 20% to 35% of all lymphomas [1,2]. In Asia, until recently, the incidence has been characteristically low, at approximately 5% to 10% of all lymphomas in most studies [3,4]. However, the relative proportion of FL in many Asian populations has increased rapidly in recent years, and FL is now the second most common low-grade B-cell lymphoma after mucosa-associated lymphoid tissue lymphoma in Asia [3,5-7]. The proportion of FL to NHL increased from 8.1% to 23.5% in China and 5% to 20% in Japan [3,4,7,8]; additionally, an increase in the proportion in Korea, from 3.4% to 4.8% between 1999 and 2012, has been reported [9,10].

FL is characterized by indolent clinical behavior, and most cases involve a low histologic grade and low-risk Follicular Lymphoma International Prognostic Index (FLIPI), which is determined based on the sum of points assigned for each of the following risk factors: age >60 years, elevated lactate dehydrogenase (LDH) level, hemoglobin (Hb) level <12 g/dL, Ann Arbor stage III/IV, and involvement of more than four nodal sites. Grade 3B FL or transformation to high-grade B-cell lymphoma significantly reduces survival [11,12]. However, due to the availability and broad use of rituximab, the incidence of transformation has been reduced, and the distribution of clinicopathologic features including histologic grade and FLIPI subgroup has changed, although the differences have not been reported consistently [12-14]. Most of the information in the literature is based on studies involving Caucasian patients, and characteristics of FL in East Asians have not been delineated well. In light of the recent increase in the incidence of FL in the Korean population, we investigated the trends in incidence of FL from 2008 to 2017, using data from a large tertiary institution in South Korea, and examined the clinicopathologic features of FL in the Korean population.

MATERIALS AND METHODS

Age-adjusted incidence rate of FL and frequency of FL and NHL

The age-adjusted incidence rate, which is a weighted average of the age-specific crude rate, was calculated using data from Korean Statistical Information Service (http://kosis.kr/index/index.do). The age-adjusted incidence rates per 100,000 were calculated by dividing the annual number of FL cases observed in a specific age group of patients treated at Asan Medical Center between 2008 and 2017, by the number of corresponding person-years of observation; the obtained result was multiplied by 100,000.

Additionally, we retrieved the total numbers of inpatients and of patients with NHL or FL treated at Asan Medical Center, Seoul, between 2008 and 2017, using the Asan BiomedicaL research Environment, i.e., ABLE, research information retrieval system. The annual frequency of patients with NHL or FL was calculated using the date of initial diagnosis.

Patient selection

A total of 239 patients diagnosed with FL between 2008 and 2017, at Asan Medical Center was included in this retrospective study. The study included patients from whom excisional (n= 215) and needle (n=24) biopsy specimens were collected before treatment. The following demographic and clinical data were collected by reviewing the patients’ medical records: age, sex, presence or absence of B symptoms (fever, night sweats, and weight loss), transformation to diffuse large B-cell lymphoma (DLBCL) (during follow-up), complete blood count, serum LDH level, bone marrow involvement, Ann Arbor stage, FLIPI risk group, and treatment modalities.

Pathological review and immunohistochemistry data

All cases were reviewed, and based on the revised 4th edition of the World Health Organization classification criteria, patients with testicular FL, duodenal-type FL, and pediatric-type FL were excluded [2]. The following pathological parameters were recorded: histologic grade (grades 1–2, grade 3A, and grade 3B), histologic pattern (follicular, follicular and diffuse, and diffuse), and immunophenotype (expression of BCL2, BCL6, CD10, or Ki-67). Immunohistochemical (IHC) staining was performed on whole slides using a fully automated IHC assay on a Ventana BenchMark XT Autostainer (Ventana Medical Systems, Woonsocket, RI, USA). Antibodies specific for the following markers were used: CD3 (clone PS1, mouse mAb, Novocastra, Newcastleupon-Tyne, UK), CD5 (clone 4C7, mouse mAb, Novocastra), CD20 (clone L26, mouse mAb, Novocastra), Ki-67 (mouse mAb, Dako, Glostrup, Denmark), CD10 (clone 56C6, mouse mAb, Novocastra), CD21 (clone 2G9, mouse mAb, Novocastra), BCL2 (clone E17, rabbit mAb, Cell Marque, Rocklin, CA, USA), and BCL6 (clone GI191E/A8, mouse mAb, Cell Marque). Immunostained slides from 239 FL cases were reviewed, and immunopositivity was defined as protein expression by ≥30% of the tumor cells [15-18]. Ki-67 proliferation index (PI) was assessed manually in neoplastic follicles, and a Ki-67 PI ≥ 30% was deemed as high expression [19-23].

Statistical analyses

Joinpoint regression analysis was performed to identify the changes in the incidence rates of FL at Asan Medical Center, using the Joinpoint Trend Analysis Software (ver. 4.8.0.1, Statistical Methodology and Application Branch, Surveillance Research Program, Division of Cancer Control and Population Sciences, National Cancer Institute). Joinpoint regression analysis usually is applied to study varying trends over time to identify the time point(s) at which the trends show significant changes [24-26]. Based on the trend analysis, we estimated the annual percentage change (APC) in the rates between trend-change points and the average annual percentage change (AAPC) for the entire study period. When there was no joinpoint (no significant change in trend), the APC was equal to AAPC.

Simple linear regression analysis was conducted to investigate changes in the proportion of clinicopathologic features of FL over the study period. Chi-square and Fisher exact tests were performed to evaluate the changes in clinicopathologic characteristics from 2008 to 2012, and from 2013 to 2017. In addition, overall survival (OS) was analyzed using the Kaplan-Meier method from the date of diagnosis to the date of death or the last followup visit, and data were compared using the log-rank test. All statistical analyses were conducted using SPSS software package ver. 18.0.0 (SPSS Statistics software, SPSS Inc., Chicago, IL, USA) and R ver. 3.6.3 (R Foundation for Statistical Computing, Vienna, Austria). Statistical significance was defined by p-value<.05.

RESULTS

Incidence of FL between 2008 and 2017

In total, 8,406 patients (0.17% of total inpatients) with NHL were treated at Asan Medical Center between 2008 and 2017, and 498 patients (0.01% of total inpatients and 5.92% of NHL) had FL. The proportion of FL patients (patients with FL/total inpatients) increased from 0.01% in 2008 to 0.02% in 2017, and the ratio of patients with FL to patients with NHL increased from 4.28% (26/607 cases) in 2008 to 9.35% (103/1102 cases) in 2017 (Supplementary Fig. S1).

Fig. 1 presents the increasing trend in the age-adjusted incidence rates of FL at Asan Medical Center between 2008 and 2017, and one joinpoint that was identified in 2010; the fastest increasing trend was observed in 2008–2010 (APC, 48.3; 95% confidence interval [CI], 9.0 to 101.7) and a moderately increasing trend was observed in 2010–2017 (APC, 10.1; 95% CI, 5.7 to 14.8) (p=.034) (Fig. 1).

Fig. 1.

Age-adjusted incidence rates of follicular lymphoma between 2008 and 2017.

Clinicopathologic characteristics during defined periods

The patients with FL (n=239) included in this study had a median age of 52.1 years (range, 17 to 82 years) with a male:female ratio of 1.13:1. The overall clinicopathologic characteristics and initial treatment modalities used for the 239 patients and changes in the baseline characteristics from 2008 to 2012 and 2013 to 2017 are summarized in Table 1. The proportion of patients aged >60 years significantly increased from 13.2% in 2008–2012 to 34.5% in 2013–2017 (p=.001) (Table 1). In 2013–2017, the proportion of patients with high-risk FLIPI (21.5% to 28.7%) and grade 3B FL (5.9% to 14.0%) increased but not at a statistically significant level (p=.270 and p=.077, respectively) (Table 1).

Baseline patient characteristics

Fig. 2 outlines the changes in the proportion of patients >60 years of age, with Hb level <12 g/dL, elevated LDH level, and involvement of more than four nodal sites, which were the factors included in FLIPI score. The proportion of patients aged >60 years significantly increased between 2008 and 2017 (R2=0.74, p<.001) (Fig. 2A). In contrast, the rates of patients with Hb level <12 g/dL remained stable (R2=–0.12, p=.959) (Fig. 2B). The proportion of patients with elevated LDH level sharply decreased between 2008 and 2013 (60.0% to 4.3%) and gradually increased to 25.0% in 2017; however, these changes were not statistically significant (R2=0.12, p=.173) (Fig. 2C). The proportion of patients with involvement of greater than four nodal sites rapidly decreased during 2008–2010 (66.7% to 41.7%), but increased to 75.6% in 2017 (R2=0.05, p=.258) (Fig. 2D).

Fig. 2.

Scatter plots with trend lines of the annual proportion of patients aged >60 years (A), with hemoglobin (Hb) level <12 g/dL (B), elevated lactate dehydrogenase (LDH) level (C), and involvement of more than four nodal sites (D).

Over 10 years, the proportion of patients with stage III/IV disease significantly increased (R2=0.36, p=.039) (Fig. 3A), as was observed on the joinpoint regression analysis (AAPC, 5.0; 95% CI, 0.4 to 9.7; p=.035) (Table 2). We found a decreasing trend in the number of cases of low-risk FLIPI (R2=0.23, p=.094) and a slightly increasing trend in the number of cases of grade 3B FL (R2=–0.20, p=.111), although the result was not statistically significant (Fig. 3B, C). Regarding histological pattern, the proportions of follicular pattern (R2=0.24, p=.086) and diffuse pattern (R2=0.15, p=.145) showed increasing trends, whereas follicular and diffuse patterns decreased (R2=0.34, p=.045) (Fig. 3D), and these variations were significant during 2008–2012 and 2013–2017 (p=.018) (Table 1).

Fig. 3.

Scatter plots with trend lines of the annual proportion of patients with follicular lymphoma: (A) Ann Arbor stage, (B) Follicular Lymphoma International Prognostic Index (FLIPI), (C) histologic grade, and (D) histologic pattern.

Trends in clinicopathologic characteristics of FL: average annual percentage change

For the IHC staining results, the rates of FL cases with BCL2 or BCL6 expression and those with Ki-67 PI ≥30% increased from 2008 to 2012 and from 2013 to 2017 (p=.086, p=.002, and p=.016, respectively) (Table 1). In the joinpoint regression analysis, the expression levels of BCL2 (AAPC, 2.6; 95% CI, 0.7 to 4.6, p=.022) and BCL6 (AAPC, 3.0; 95% CI, 0.4 to 5.7; p=.028) significantly increased over the 10 years (Table 2).

Since the 2000s, rituximab has been used widely, and a majority of the patients (54.4%) in this study underwent rituximab-based chemotherapy; however, the proportion of patients on a watch-and-wait strategy significantly increased by 8.8% in 2008–2012 and by 22.2% in 2013–2017, while there was a slight decrease in the number of patients on rituximab-based therapy (p=.049) (Table 1). There was no significant variation in other clinicopathologic features, e.g., sex, bone marrow involvement, transformation to DLBCL, and mortality, over the study period.

In survival analysis, during a median follow-up of 47 months (range, 0 to 222 months), 15 patients died, and the mean OS was 199 months. There was no significant OS difference between 2008–2012 and 2013–2017 (Supplementary Fig. S2).

DISCUSSION

The incidence rate of FL, which has been low in Korea, has increased in recent years. Lee et al. [9] studied 65,948 lymphoid diseases in the South Korean population and found increasing incidence of lymphoid malignancies (6.85% to 13.18%) and FL (0.22% to 0.39%) between 1999 and 2012. Kim et al. [27] studied epidemiologic changes in B-cell NHL in South Korea using the National Health Information Database and found that the incidence of FL has increased since 2006: the ratio of FL to NHL increased from 5.6% to 7.8% during 2006–2015, and the age-adjusted incidence of FL increased by 25% between 2011 and 2015. Similarly, in the current study, the incidence of FL significantly increased between 2008 and 2017, with an increasing ratio of FL:NHL. Although previous studies ascribed the low incidence of FL in Asian populations to ethnic differences, the recent trend of increased incidence rates might reflect the increasing adoption of a Westernized lifestyle by Asian populations [6,28].

Currently, the etiology of FL is not understood fully; however, age, sex, ethnicity, genetic, clinical and environmental factors including lifestyle can affect the development of FL. Multiple large cohort studies have investigated the influence of smoking, alcohol intake, obese or overweight status and their relationship to FL development; however, the results have been conflicting [29]. A population-based study by Le et al. [30] in Canada during 1992–2010, demonstrated that the incidence rate of FL increased, especially in concentrated industrial zones, suggesting that industrial exposures play an important role in the development of FL. Further, it has been reported that exposure to herbicides is associated with FL by causing a t(14;18)-translocation [30].

In the current study, we found an increasing trend of stage III/IV disease over 10 years, and that the proportions of highrisk FLIPI and grade 3B FL also increased between 2008–2012 and 2013–2017, although the results were not statistically significant. In a study by Conconi et al. [14] that included 281 FL cases from 1979 to 2007, the trend in the proportion of patients aged ≥60 years with stage III/IV disease and high-risk FLIPI scores increased over the study period, although the result was not statistically significant. Mozas et al. [13] studied 727 grade 1–3A FL cases reported between 1980 and 2017, and found that grade 1–2 disease showed a decreasing trend over time, while high-risk FLIPI showed an increasing trend in recent years. These findings can be attributed to the increasing life expectancy and increase in the number of patients that present with advanced FL status at initial diagnosis, as a majority of the patients are asymptomatic.

We also note that most patients with FL have stage III/IV disease, a low-risk FLIPI score, and grade 1–2 FL, and the findings are comparable to those in the Unites States, showing predominance of stage III/IV, low-risk FLIPI score, and grade 1–2, with similar results to our data [29,31]. Cho et al. [5] retrospectively analyzed clinical characteristics and pathologic features of BCL2 expression in 343 FL patients in Korea during1993–2013, and demonstrated that predominancy of stage III/IV, low-risk FLIPI score, and grade 1–2 FL, suggesting that there was no significant difference between Korean and Western populations.

In this study, BCL2 or BCL6 immunopositivity significantly increased over the study period. We investigated whether the expression of BCL2 or BCL6 was associated with histologic grade; however, those unexpected findings were not associated with changes in the proportion of histologic grade (Supplementary Table S1). Although several studies have shown that the expression of BCL2 was less common in high-grade FL, the relationship between expression of BCL2 or BCL6 and histologic grade was not definitive in most prior studies [32-35].

The proportion of FL cases with Ki-67 PI ≥30% and diffuse pattern significantly increased between 2008–2012 and 2013–2017, and was significantly correlated with histologic grade (Supplementary Table S1). Most prior studies have shown that higher Ki-PI or diffuse pattern in FL generally correlates with higher grade or poor prognosis, although several FL cases with low grade and high Ki-PI have been described [2,22,23,36]. In this study, Ki-PI was estimated manually and might have produced intra- and interobserver variability. However, recent studies using software–automated quantification of Ki-67 PI in FL have shown that high Ki-67 PI was associated with grade 3 FL or poor prognosis [19,21].

There were some limitations to this study. The low incidence of FL in our institutional series might have led to overestimation of the proportion of clinicopathologic features and inadequate statistical significance in the changes over the study period. FL has an indolent prognosis with a favorable outcome, and the number of events (e.g., death) per group was insufficient in the current study, in which large numbers of individuals were censored in the survival analysis. Thus, multicenter studies should be performed to precisely address the trends of FL in Korea. Our study was not a population-based study and lacks representativeness. However, we found an increase in the age-adjusted incidence rate of FL using data from a large tertiary institution, which is an accepted approach that can be adopted to allow better comparison [37,38]. In addition, the increasing incidence of FL and the ratio of FL to NHL observed in our data were similar to the trends observed in the National Health Information Database [27].

In conclusion, our study demonstrated an increase in the incidence rates of FL at a large tertiary institution in South Korea over the last 10 years, and we found recent changes in the clinicopathologic features of FL, an aspect that rarely has been studied.

Supplementary Materials

The Data Supplement is available with this article at https://doi.org/10.4132/jptm.2021.07.25.

Supplementary Table. S1.

Histologic grade and clinicopathologic characteristics of follicular lymphoma

Supplementary Fig. S1.

Annual proportion of follicular lymphoma (FL) between 2008 and 2017: (A) the proportion of patients with FL compared with the yearly number of inpatients and (B) the proportion of patients with FL to patients with non-Hodgkin lymphoma.

Supplementary Fig. S2.

Kaplan-Meier analyses of overall survival (OS) in patients with follicular lymphoma between 2008─2012 and 2013─2017.

Notes

Supplementary Information

The Data Supplement is available with this article at https://doi.org/10.4132/jptm.2021.07.25.

Ethics Statement

All procedures performed in the current study were approved by the Institutional Review Board (IRB) of Asan Medical Center with a waiver of informed consent (IRB No. 2019-0509) and performed in accordance with the principles of the Declaration of Helsinki.

Availability of Data and Material

The datasets generated or analyzed during the study are available from the corresponding author on reasonable request.

Code Availability

Not applicable.

Author Contributions

Conceptualization: MK, JH. Data curation: MK, HSH. Formal analysis: MK, HSH. Investigation: MK, HC, DHY, CS, HG. Methodology: MK, HSH, HC, HG. Project administration: HG, JH. Resources: MK, DHY, CS. Supervision: HG, CSP, JH. Validation: HSH, HG, CSP, JH. Visualization: MK, HSH. Writing—original draft: MK, HG, JH. Writing—review & editing: MK, HSH, HG, CSP, JH. Approval of final manuscript: all authors.

Conflicts of Interest

H.G., a contributing editor of the Journal of Pathology and Translational Medicine, was not involved in the editorial evaluation or decision to publish this article. All remaining authors have declared no conflicts of interest.

Funding Statement

No funding to declare.

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Article information Continued

Fig. 1.

Age-adjusted incidence rates of follicular lymphoma between 2008 and 2017.

Fig. 2.

Scatter plots with trend lines of the annual proportion of patients aged >60 years (A), with hemoglobin (Hb) level <12 g/dL (B), elevated lactate dehydrogenase (LDH) level (C), and involvement of more than four nodal sites (D).

Fig. 3.

Scatter plots with trend lines of the annual proportion of patients with follicular lymphoma: (A) Ann Arbor stage, (B) Follicular Lymphoma International Prognostic Index (FLIPI), (C) histologic grade, and (D) histologic pattern.

Table 1.

Baseline patient characteristics

Characteristic Total (n = 239) Year p-value
2008–2012 (n = 68) 2013–2017 (n = 171)
Age > 60 yr 68 (28.6) 9 (13.2) 59 (34.5) .001
Sex .267
 Male 127 (53.1) 40 (58.8) 87 (50.9)
 Female 112 (46.9) 28 (41.2) 84 (49.1)
B symptom .751
 Absent 212 (90.2) 62 (91.2) 150 (89.8)
 Present 23 (9.8) 6 (8.8) 17 (10.2)
Hb < 12 g/dL 41 (17.2) 12 (17.9) 29 (17.0) .861
Elevated LDH 46 (19.8) 15 (23.8) 31 (18.3) .353
Ann Arbor stage .111
 Stage I/II 90 (37.7) 31 (45.6) 59 (34.5)
 Stage III/IV 149 (62.3) 37 (54.4) 112 (65.5)
Bone marrow involvement 87 (37.8) 24 (35.8) 63 (38.7) .688
FLIPI .270
 Low to intermediate 173 (73.3) 51 (78.5) 122 (71.3)
 High 63 (26.7) 14 (21.5) 49 (28.7)
Histologic grade .077
 1–2/3A 211 (88.3) 64 (94.1) 147 (86.0)
 3B 28 (11.7) 4 (5.9) 24 (14.0)
Histologic pattern .018
 Follicular 207 (87.7) 56 (82.4) 151 (89.9)
 Follicular and diffuse 20 (8.5) 11 (16.2) 9 (5.4)
 Diffuse 9 (3.8) 1 (1.5) 8 (4.8)
BCL2 expression .086
 Negative 25 (11.3) 11 (16.9) 14 (8.9)
 Positive 197 (88.7) 54 (83.1) 143 (91.1)
BCL6 expression .002
 Negative 10 (4.3) 7 (11.1) 3 (1.8)
 Positive 222 (95.7) 56 (88.9) 166 (98.2)
CD10 expression .461
 Negative 44 (18.8) 14 (21.9) 30 (17.6)
 Positive 190 (81.2) 50 (78.1) 140 (82.4)
Ki–67 PI ≥ 30% 86 (37.9) 15 (25.0) 71 (42.5) .016
Treatment .049
 Watch-and-wait 44 (18.4) 6 (8.8) 38 (22.2)
 Rituximab-based 130 (54.4) 40 (58.8) 90 (52.6)
 Radiation monotherapy 30 (12.9) 11 (16.4) 19 (11.5)
Transformation to DLBCL 19 (8.0) 5 (7.4) 14 (8.2) .821
Deaths 15 (6.6) 6 (9.0) 9 (5.7) .387

Values are presented as number (%).

Hb, hemoglobin; LDH, lactate dehydrogenase; FLIPI, Follicular Lymphoma International Prognostic Index; Ki-67 PI, Ki-67 proliferation index; DLBCL, diffuse large B-cell lymphoma.

Table 2.

Trends in clinicopathologic characteristics of FL: average annual percentage change

Characteristic AAPC (95% CI) p-value
Age > 60 yr naa
Hb < 12 g/dL 1.0 (–0.91 to 12.2) .833
Elevated LDH –6.5 (–20.9 to 10.5) .378
> 4 nodal areas involved 6.6 (–5.5 to 20.2) .254
Ann Arbor stage
 Stage I/II –6.2 (–12.6 to 0.7) .070
 Stage III/IV 5.0 (0.4 to 9.7) .035
Bone marrow involvement 3.5 (–5.9 to 13.8) .455
FLIPI
 Low –5.3 (–10.8 to 0.6) .071
 Intermediate naa
 High 6.6 (–12.4 to 29.7) .486
Histologic grade
 1–2 –0.9 (–5.3 to 3.7) .661
 3A –4.7 (–16.3 to 8.6) .424
 3B naa
Histologic pattern
 Follicular 2.0 (–0.3 to 4.3) .120
 Follicular and diffuse naa
 Diffuse naa
BCL2-positive 2.6 (0.7 to 4.6) .022
BCL6-positive 3.0 (0.4 to 5.7) .028
CD10-positive 1.0 (–3.0 to 5.2) .666
Ki-67 PI ≥ 30% 5.4 (–5.4 to 17.3) .309
Treatment
 Watch-and-wait naa
 Rituximab-based 2.1 (–4.7 to 9.4) .550
 Radiation monotherapy naa
Transformation to DLBCL naa

FL, follicular lymphoma; AAPC, average annual percent change; CI, confidence interval; Hb, hemoglobin; LDH, lactate dehydrogenase; FLIPI, Follicular Lymphoma International Prognostic Index; Ki-67 PI, Ki-67 proliferation index; DLBCL, diffuse large B-cell lymphoma.

a

Not applicable due to zero case counts for some years.