Original Article
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Blood Res 2014; 49(1):
Published online March 31, 2014
https://doi.org/10.5045/br.2014.49.1.15
© The Korean Society of Hematology
Clinical features and treatment outcomes in patients with mantle cell lymphoma in Korea: Study by the Consortium for Improving Survival of Lymphoma
1Department of Hematology/Oncology, Internal Medicine, Kyungpook National University Hospital, Daegu, Korea.
2Department of Hematology/Oncology, Internal Medicine, Samsung Medical Center, Seoul, Korea.
3Department of Hematology/Oncology, Internal Medicine, Chonnam National University Hwasun Hospital, Hwasun, Korea.
4Department of Hematology/Oncology, Internal Medicine, Korea University Ansan Hospital, Ansan, Korea.
5Department of Hematology/Oncology, Internal Medicine, Keimyung University Dongsan Medical Center, Daegu, Korea.
6Department of Hematology/Oncology, Internal Medicine, Kosin University Gospel Hospital, Busan, Korea.
7Department of Hematology/Oncology, Internal Medicine, Inje University Busan Paik Hospital, Busan, Korea.
8Department of Hematology/Oncology, Internal Medicine, Soonchunhyang University Hospital, Seoul, Korea.
9Department of Hematology/Oncology, Internal Medicine, Wonkwang University Hospital, Iksan, Korea.
10Department of Hematology/Oncology, Internal Medicine, Chonbuk National University Hospital, Jeonju, Korea.
11Department of Hematology/Oncology, Internal Medicine, Yeungnam University Medical Center, Daegu, Korea.
12Department of Hematology/Oncology, Internal Medicine, Hallym University Scared Heart Hospital, Anyang, Korea.
13Department of Hematology/Oncology, Internal Medicine, Dong-A University Hospital, Busan, Korea.
14Department of Hematology/Oncology, Internal Medicine, Korea Cancer Center Hospital, Seoul, Korea.
15Department of Hematology/Oncology, Internal Medicine, Asan Medical Center, Seoul, Korea.
Correspondence to : Correspondence to Cheolwon Suh, M.D., Ph.D., Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, 88, Olympic-ro 43-gil, Songpa-gu, Seoul 138-736, Korea. Tel: +82-2-3010-3209, Fax: +82-2-3010-6961, csuh@amc.seoul.kr
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Background
We investigated the clinical features and treatment outcomes of patients with mantle cell lymphoma (MCL) in Korea.
Methods
We retrospectively analyzed the clinical characteristics and prognosis of 131 patients diagnosed with MCL between January 2004 and December 2009 at 15 medical centers in Korea; all patients received at least 1 chemotherapeutic regimen for MCL.
Results
The median age for the patients was 63 years (range, 26-78 years), and 77.9% were men. A total of 105 patients (80.1%) had stage III or IV MCL at diagnosis. Fifty-two patients (39.7%) were categorized with high- or high-intermediate risk MCL according to the International Prognostic Index (IPI). Eighteen patients (13.7%) were in the high-risk group according to the simplified MCL-IPI (MIPI). The overall incidence of extranodal involvement was 69.5%. The overall incidence of bone marrow and gastrointestinal involvements at diagnosis was 41.2% and 35.1%, respectively. Cyclophosphamide, doxorubicin, vincristine, prednisolone, and rituximab were used frequently as the first-line treatment (41.2%). With a median follow-up duration of 20.0 months (range, 0.2-77.0 months), the overall survival (OS) at 2 years was 64.7%, while the event-free survival (EFS) was 39.7%. Multivariate analysis showed that the simplified MIPI was significantly associated with OS. However, the use of a rituximab-containing regimen was not associated with OS and EFS.
Conclusion
Similar to results from Western countries, the current study found that simplified MIPI was an important prognostic factor in Korean patients with MCL.
Keywords Mantle cell lymphoma, Epidemiology, Trend, Survival, Chemotherapy, Rituximab
INTRODUCTION
Mantle cell lymphoma (MCL) is a distinct subtype of B-cell lymphoma and comprises approximately 5-10% of all lymphomas [1]. Moreover, the incidence of MCL has been increasing over the last decade, especially among elderly patients [2]. While extensive research has been exploring new and better ways to treat MCL, the histological diagnosis is invariably difficult and normally requires immunophenotyping; this is required even though MCL has been established as a new disease entity characterized by the t(11;14)(q13;q32) [3]. In particular, MCL is considered a heterogeneous disease on the basis of its development, growth, and prognosis [4]. The effect of chemotherapy also seems to vary depending on the tumor biology [5]. Clinically, the majority of patients present in an advanced stage, and up to 80% include the involvement of extranodal sites [6, 7]. These factors eventually lead to an aggressive clinical course, associated with rapid progression and a high recurrence rate. In Korea, MCL accounts for 2% of B-cell lymphomas, and it is typically characterized by an aggressive clinical course [8]. However, little is known about the clinical features and treatment outcomes in MCL patients in Korea.
Determining the optimal prognostic model for MCL is quite difficult owing to its rarity and diverse clinical course. Several studies have demonstrated that various prognostic factors are associated with survival in patients with MCL. For example, older age, elevated lactate dehydrogenase (LDH), advanced stage, presence of B symptoms, poor performance status, and high mitotic index (Ki-67) are often associated with poor prognosis [9, 10]. Recently, a simplified MCL Prognostic Index (MIPI) scoring system incorporating age, performance status, LDH level, and WBC count, has been established as a new prognostic model to predict the survival outcome for patients with MCL [11]. However, this index still requires validation when taking tumor and racial differences into consideration.
Although various chemotherapeutic regimens show significant activity in patients with MCL, no regimen has been found to be superior, and no standard treatment has been identified. Rituximab is a chimeric monoclonal antibody against the protein CD20, which is primarily found on the surface of malignant B-cells. The addition of rituximab to cyclophosphamide, doxorubicin, vincristine, and prednisolone (R-CHOP) has led to an impressive improvement in response rates and survival outcomes for patients with diffuse large B-cell lymphoma [12]. Several recent studies have also demonstrated that including rituximab in combination chemotherapy produces a significantly improved therapeutic effect for MCL [9, 13]. Other studies have also shown that rituximab can alleviate the negative impact of extranodal involvement [14]. Nevertheless, it is uncertain whether rituximab-based chemotherapy alters the clinical outcomes of patients with MCL.
As there is a lack of available data in this area, this study sought to provide basic clinical data for prospective clinical trials by evaluating the clinical features and treatment outcomes for patients with MCL in Korea.
MATERIALS AND METHODS
A retrospective review of the medical records of 131 patients who were newly diagnosed with MCL between January 2004 and December 2009 at 15 medical centers in Korea was conducted. Each medical center received unified case report forms. The collected data included the age, gender, performance status, presence of B symptoms (fever, night sweats, and weight loss), presence of extranodal disease, International Prognostic Index (IPI) score [15], simplified MIPI score [11], serum LDH, hemoglobin (Hb), WBC, platelets (Plt), initial date of diagnosis, and treatment modality utilized. All patients were evaluated by using standard laboratory tests, computed tomography (CT), bone marrow (BM) aspirate and biopsy, and endoscopy at diagnosis. Standard institutional protocols were used for central nervous system (CNS) prophylaxis. All patients were staged according to the Ann Arbor Staging classification by using CT scans [16]. Strict histologic and recently updated criteria were applied, and only patients with a confirmed MCL diagnosis were included in the study [17]. Cyclin D1 overexpression was present in 99/101 cases (98.0%), and CD5 overexpression was present in 68/86 cases (79.1%). The Ki-67 index was assessed in 57 cases (43.5%). Additional data obtained included the time to relapse, salvage treatment modality, and survival rates with salvage treatment. This study was approved by the institutional review board of each center.
The descriptive statistics are reported as the proportion and median. The response was evaluated by using revised response criteria for malignant lymphomas [18]. Overall survival (OS) was defined as death from any cause from the time of diagnosis. Event-free survival (EFS) was defined as the time from diagnosis to failure or death from any cause. The OS and EFS were analyzed by using the Kaplan-Meier test, and each group was compared by using a log-rank test. The Cox regression model was used to determine the clinical predictors for EFS and OS. An effect was considered statistically significant when
The total cohort included 131 patients (Table 1). The median age was 63 years (range, 26-78 years), and 77.9% were men. A total of 105 patients (80.1%) had stage III or IV MCL at diagnosis. On the basis of the IPI, 52 patients (39.7%) were categorized with high- or high-intermediate risk MCL. According to the simplified IPI, 18 patients (13.7%) were at high risk. B symptoms were noted in 34 patients (26.0%). The overall incidence of extranodal involvement was 69.5%. The most common extranodal sites were the BM (52.8%) and the gastrointestinal (GI) tract (34.7%); other extranodal sites included the CNS (8.4%), lungs (6.1%), liver (3.8%), and spleen (3.8%).
No patients were pretreated. As expected, the treatments were heterogeneous (Table 2). R-CHOP was frequently used as the first-line treatment (41.2%). Ten patients (7.6%) received rituximab plus hyperfractionated cyclophosphamide, vincristine, doxorubicin, and dexamethasone alternating with methotrexate-cytarabine (RHyperCVAD/RMTX-Ara-C). Seventy-one patients (54.2%) were treated with a rituximab-containing regimen, while 60 patients (45.8%) received a non-rituximab-containing regimen.
The treatment outcomes are shown in Table 3. A total of 121 patients were evaluated. The complete response (CR) and partial response (PR) rates were 45.0% and 27.5%, respectively. Overall, 73 patients experienced relapse, and 65 patients died. Among the relapsed patients, 66 received salvage treatment. The salvage regimens were heterogeneous, with 17 patients receiving fludarabine-based chemotherapy and 30 patients receiving cytarabine-containing chemotherapy.
With a median follow-up duration of 20.0 months (range, 0.2-77.0 months), the OS at 2 years was 64.7%, while the EFS was 39.7% (Fig. 1). As seen in Figs. 2 and 3, the IPI and MIPI had a statistically significant effect on OS (
MCL is characterized by an aggressive clinical course, and there is a pattern of frequent relapse after conventional chemotherapy. However, recent novel treatment options, such as rituximab and transplantation, have improved the response and survival outcomes [9]. As a result, the prognosis and survival of patients with MCL have considerably improved recently [5]. In addition, the significant improvement in treatment outcomes observed with the introduction of rituximab has altered the risk assessment for MCL. Therefore, an in-depth analysis of patients with MCL is important to help identify more adequate initial treatment modalities.
The present study found similar clinical characteristics to those reported previously. The patients in the current study had a median age of approximately 63 years and were predominantly men with mostly advanced stage MCL and frequent extranodal involvement, including the BM in the majority of cases [4, 7, 19, 20, 21, 22]. GI involvement was observed in 35.1% of the patients, which is similar to the rate described in other studies [19, 23]. In addition, several studies have demonstrated that consideration of MCL with GI involvement is important in the treatment planning, response assessment, and surveillance of patients with lymphoma [24, 25]. However, in contrast to other studies, the incidence of CNS involvement in the current study was relatively low. This discrepancy may be due to a lack of actual CNS examinations and a possible underestimation of CNS involvement. Indeed, the use of routine CNS examinations and prophylaxes remains controversial [16]. Similar to previous studies, other extranodal sites included the lungs, liver, and spleen, although these locations are considered rare [14, 26].
While a median survival of approximately 3 years has been common in previous reports, this has recently increased to 5 years [3]. Herrmann et al. [5] suggested that such superior outcomes may be a result of different patient selection, improved diagnosis, and improved treatment. In the current study, the 5-year OS rate was 23.1%, with a continuous decline of the survival curve. Although the addition of rituximab has improved the response rate and time-to-failure in the first-line setting, this has not translated into significant improvement in the OS. The results of the present study indicate that patients with MCL have a poor prognosis, even after rituximab-based chemotherapy [27]. Most patients in the current study also had poor clinical factors, such as advanced age, poor performance status, multiple extranodal involvements, and B symptoms at diagnosis. In addition, 45.8% of patients did not receive rituximab-based chemotherapy as a first-line treatment. The CR rate was 45.0%, which is similar to the results from other studies, where CR rate ranged from 30% to 80% [28]. The current study also showed that achieving CR prolonged OS. After relapse, the median life expectancy for a patient with MCL drops to 1-2 years [9]. Once relapse occurs, patients are offered aggressive chemotherapy; however, standard salvage chemotherapy has not yet been defined.
This study sought to provide an in-depth report on MCL subgroups with significantly worse clinical outcomes. Several previous studies have identified prognostic factors for MCL. While the IPI is a powerful tool for predicting clinical outcomes in patients with aggressive non-Hodgkin lymphoma [15], only a few studies have used IPI for predicting and examining MCL prognosis. However, a specific MCL prognostic score was recently proposed, and this score identifies 4 independent prognostic factors [11]. In terms of prognostic factors, the MIPI was found to correlate with OS in the current study including Korean patients. Older age and poor performance status are commonly mentioned as negative predictive factors for survival in cases of MCL [6, 11, 21]. Interestingly, patients with MCL and B symptoms displayed a worse survival trend. This agrees with previous reports showing that B symptoms have a negative impact on survival [29].
In conclusion, the present data reveal the clinical features and treatment outcomes for patients with MCL in Korea who received at least 1 chemotherapeutic regimen. Similar to the results from Western countries, patients with MCL in Korea were characterized by the aggressive clinical features and particularly poor clinical outcomes. The simplified MIPI was an important prognostic factor in patients with MCL in Korea. Although MIPI was a prognostic factor in the current study, an analysis of prognostic subgroups should be evaluated and validated for patients with MCL. In addition, rituximab did not significantly improve the therapeutic effect in patients with MCL in Korea; therefore, a more suitable treatment needs to be identified for patients with MCL in Korea.
Fig. 2. Kaplan-Meier analysis of (
Fig. 3. Kaplan-Meier analysis of (
Fig. 4. Kaplan-Meier analysis of (
Table 1 Baseline characteristics of patients.
Values are presented as numbers (%).
Abbreviations: ECOG, Eastern Cooperation Oncology Group; IPI, International Prognostic Index; MIPI, MCL International Prognostic Index; BM, bone marrow; CNS, central nervous system; GI, gastrointestinal tract.
Table 2 Types of first-line treatment.
Values are presented as numbers (%).
Abbreviations: R-CHOP, rituximab, cyclophosphamide, doxorubicin, and prednisone; RHyperCVAD/RMTX-Ara-C, rituximab, doxorubicin, vincristine, dexamethasone, methotrexate, and cytarabine; RCVP, rituximab, cyclophosphamide, vincristine, and prednisone; RICE, rituximab, ifosfamide, carboplatin, and etoposide; RESHAP, rituximab, etoposide, methylprednisone, cytarabine, and cisplatin; CHOP, cyclophosphamide, doxorubicin, and prednisone; HyperCVAD/MTX-Ara-C, doxorubicin, vincristine, dexamethasone, methotrexate, and cytarabine; CVP, cyclophosphamide, vincristine, and prednisone; ICE, ifosfamide, carboplatin, and etoposide; ESHAP, etoposide, methylprednisone, cytarabine, and cisplatin; GIDOX, gemcitabine, ifosfamide, dexamethasone, and oxaliplatin.
Table 3 Treatment outcomes of patients.
Values are presented as numbers (%).
Abbreviations: CR, complete response; PR, partial response; SD, stable disease; PD, progressive disease; CHOP, cyclophosphamide, doxorubicin, and prednisone; CVP, cyclophosphamide, vincristine, and prednisone; ICE, ifosfamide, carboplatin, and etoposide.
Table 4 Univariate and multivariate analyses for factors affecting EFS and OS.
a)Log-rank test for univariate analysis.
Abbreviations: HR, hazard ratio; MIPI, MCL International Prognostic Index; EFS, event-free survival; OS, overall survival; CI, confidence interval.
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- Herrmann, A, Hoster, E, Zwingers, T, et al. Improvement of overall survival in advanced stage mantle cell lymphoma. J Clin Oncol, 2009;27;511-518.
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Original Article
Blood Res 2014; 49(1): 15-21
Published online March 31, 2014 https://doi.org/10.5045/br.2014.49.1.15
Copyright © The Korean Society of Hematology.
Clinical features and treatment outcomes in patients with mantle cell lymphoma in Korea: Study by the Consortium for Improving Survival of Lymphoma
Byung Woog Kang1, Sang Kyun Sohn1,#*, Joon Ho Moon1, Yee Soo Chae1, Jong Gwang Kim1, Soo Jung Lee1, Won Seog Kim2, Je-Jung Lee3, Se Ryeon Lee4, Keon Uk Park5, Ho Sup Lee6, Won Sik Lee7, Jong-Ho Won8, Moo-Rim Park9, Jae-Yong Kwak10, Min Kyoung Kim11, Hyo Jung Kim12, Sung Yong Oh13, Hye Jin Kang14, and Cheolwon Suh15,#*
1Department of Hematology/Oncology, Internal Medicine, Kyungpook National University Hospital, Daegu, Korea.
2Department of Hematology/Oncology, Internal Medicine, Samsung Medical Center, Seoul, Korea.
3Department of Hematology/Oncology, Internal Medicine, Chonnam National University Hwasun Hospital, Hwasun, Korea.
4Department of Hematology/Oncology, Internal Medicine, Korea University Ansan Hospital, Ansan, Korea.
5Department of Hematology/Oncology, Internal Medicine, Keimyung University Dongsan Medical Center, Daegu, Korea.
6Department of Hematology/Oncology, Internal Medicine, Kosin University Gospel Hospital, Busan, Korea.
7Department of Hematology/Oncology, Internal Medicine, Inje University Busan Paik Hospital, Busan, Korea.
8Department of Hematology/Oncology, Internal Medicine, Soonchunhyang University Hospital, Seoul, Korea.
9Department of Hematology/Oncology, Internal Medicine, Wonkwang University Hospital, Iksan, Korea.
10Department of Hematology/Oncology, Internal Medicine, Chonbuk National University Hospital, Jeonju, Korea.
11Department of Hematology/Oncology, Internal Medicine, Yeungnam University Medical Center, Daegu, Korea.
12Department of Hematology/Oncology, Internal Medicine, Hallym University Scared Heart Hospital, Anyang, Korea.
13Department of Hematology/Oncology, Internal Medicine, Dong-A University Hospital, Busan, Korea.
14Department of Hematology/Oncology, Internal Medicine, Korea Cancer Center Hospital, Seoul, Korea.
15Department of Hematology/Oncology, Internal Medicine, Asan Medical Center, Seoul, Korea.
Correspondence to:Correspondence to Cheolwon Suh, M.D., Ph.D., Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, 88, Olympic-ro 43-gil, Songpa-gu, Seoul 138-736, Korea. Tel: +82-2-3010-3209, Fax: +82-2-3010-6961, csuh@amc.seoul.kr
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract
Background
We investigated the clinical features and treatment outcomes of patients with mantle cell lymphoma (MCL) in Korea.
Methods
We retrospectively analyzed the clinical characteristics and prognosis of 131 patients diagnosed with MCL between January 2004 and December 2009 at 15 medical centers in Korea; all patients received at least 1 chemotherapeutic regimen for MCL.
Results
The median age for the patients was 63 years (range, 26-78 years), and 77.9% were men. A total of 105 patients (80.1%) had stage III or IV MCL at diagnosis. Fifty-two patients (39.7%) were categorized with high- or high-intermediate risk MCL according to the International Prognostic Index (IPI). Eighteen patients (13.7%) were in the high-risk group according to the simplified MCL-IPI (MIPI). The overall incidence of extranodal involvement was 69.5%. The overall incidence of bone marrow and gastrointestinal involvements at diagnosis was 41.2% and 35.1%, respectively. Cyclophosphamide, doxorubicin, vincristine, prednisolone, and rituximab were used frequently as the first-line treatment (41.2%). With a median follow-up duration of 20.0 months (range, 0.2-77.0 months), the overall survival (OS) at 2 years was 64.7%, while the event-free survival (EFS) was 39.7%. Multivariate analysis showed that the simplified MIPI was significantly associated with OS. However, the use of a rituximab-containing regimen was not associated with OS and EFS.
Conclusion
Similar to results from Western countries, the current study found that simplified MIPI was an important prognostic factor in Korean patients with MCL.
Keywords: Mantle cell lymphoma, Epidemiology, Trend, Survival, Chemotherapy, Rituximab
INTRODUCTION
Mantle cell lymphoma (MCL) is a distinct subtype of B-cell lymphoma and comprises approximately 5-10% of all lymphomas [1]. Moreover, the incidence of MCL has been increasing over the last decade, especially among elderly patients [2]. While extensive research has been exploring new and better ways to treat MCL, the histological diagnosis is invariably difficult and normally requires immunophenotyping; this is required even though MCL has been established as a new disease entity characterized by the t(11;14)(q13;q32) [3]. In particular, MCL is considered a heterogeneous disease on the basis of its development, growth, and prognosis [4]. The effect of chemotherapy also seems to vary depending on the tumor biology [5]. Clinically, the majority of patients present in an advanced stage, and up to 80% include the involvement of extranodal sites [6, 7]. These factors eventually lead to an aggressive clinical course, associated with rapid progression and a high recurrence rate. In Korea, MCL accounts for 2% of B-cell lymphomas, and it is typically characterized by an aggressive clinical course [8]. However, little is known about the clinical features and treatment outcomes in MCL patients in Korea.
Determining the optimal prognostic model for MCL is quite difficult owing to its rarity and diverse clinical course. Several studies have demonstrated that various prognostic factors are associated with survival in patients with MCL. For example, older age, elevated lactate dehydrogenase (LDH), advanced stage, presence of B symptoms, poor performance status, and high mitotic index (Ki-67) are often associated with poor prognosis [9, 10]. Recently, a simplified MCL Prognostic Index (MIPI) scoring system incorporating age, performance status, LDH level, and WBC count, has been established as a new prognostic model to predict the survival outcome for patients with MCL [11]. However, this index still requires validation when taking tumor and racial differences into consideration.
Although various chemotherapeutic regimens show significant activity in patients with MCL, no regimen has been found to be superior, and no standard treatment has been identified. Rituximab is a chimeric monoclonal antibody against the protein CD20, which is primarily found on the surface of malignant B-cells. The addition of rituximab to cyclophosphamide, doxorubicin, vincristine, and prednisolone (R-CHOP) has led to an impressive improvement in response rates and survival outcomes for patients with diffuse large B-cell lymphoma [12]. Several recent studies have also demonstrated that including rituximab in combination chemotherapy produces a significantly improved therapeutic effect for MCL [9, 13]. Other studies have also shown that rituximab can alleviate the negative impact of extranodal involvement [14]. Nevertheless, it is uncertain whether rituximab-based chemotherapy alters the clinical outcomes of patients with MCL.
As there is a lack of available data in this area, this study sought to provide basic clinical data for prospective clinical trials by evaluating the clinical features and treatment outcomes for patients with MCL in Korea.
MATERIALS AND METHODS
A retrospective review of the medical records of 131 patients who were newly diagnosed with MCL between January 2004 and December 2009 at 15 medical centers in Korea was conducted. Each medical center received unified case report forms. The collected data included the age, gender, performance status, presence of B symptoms (fever, night sweats, and weight loss), presence of extranodal disease, International Prognostic Index (IPI) score [15], simplified MIPI score [11], serum LDH, hemoglobin (Hb), WBC, platelets (Plt), initial date of diagnosis, and treatment modality utilized. All patients were evaluated by using standard laboratory tests, computed tomography (CT), bone marrow (BM) aspirate and biopsy, and endoscopy at diagnosis. Standard institutional protocols were used for central nervous system (CNS) prophylaxis. All patients were staged according to the Ann Arbor Staging classification by using CT scans [16]. Strict histologic and recently updated criteria were applied, and only patients with a confirmed MCL diagnosis were included in the study [17]. Cyclin D1 overexpression was present in 99/101 cases (98.0%), and CD5 overexpression was present in 68/86 cases (79.1%). The Ki-67 index was assessed in 57 cases (43.5%). Additional data obtained included the time to relapse, salvage treatment modality, and survival rates with salvage treatment. This study was approved by the institutional review board of each center.
The descriptive statistics are reported as the proportion and median. The response was evaluated by using revised response criteria for malignant lymphomas [18]. Overall survival (OS) was defined as death from any cause from the time of diagnosis. Event-free survival (EFS) was defined as the time from diagnosis to failure or death from any cause. The OS and EFS were analyzed by using the Kaplan-Meier test, and each group was compared by using a log-rank test. The Cox regression model was used to determine the clinical predictors for EFS and OS. An effect was considered statistically significant when
RESULTS
The total cohort included 131 patients (Table 1). The median age was 63 years (range, 26-78 years), and 77.9% were men. A total of 105 patients (80.1%) had stage III or IV MCL at diagnosis. On the basis of the IPI, 52 patients (39.7%) were categorized with high- or high-intermediate risk MCL. According to the simplified IPI, 18 patients (13.7%) were at high risk. B symptoms were noted in 34 patients (26.0%). The overall incidence of extranodal involvement was 69.5%. The most common extranodal sites were the BM (52.8%) and the gastrointestinal (GI) tract (34.7%); other extranodal sites included the CNS (8.4%), lungs (6.1%), liver (3.8%), and spleen (3.8%).
No patients were pretreated. As expected, the treatments were heterogeneous (Table 2). R-CHOP was frequently used as the first-line treatment (41.2%). Ten patients (7.6%) received rituximab plus hyperfractionated cyclophosphamide, vincristine, doxorubicin, and dexamethasone alternating with methotrexate-cytarabine (RHyperCVAD/RMTX-Ara-C). Seventy-one patients (54.2%) were treated with a rituximab-containing regimen, while 60 patients (45.8%) received a non-rituximab-containing regimen.
The treatment outcomes are shown in Table 3. A total of 121 patients were evaluated. The complete response (CR) and partial response (PR) rates were 45.0% and 27.5%, respectively. Overall, 73 patients experienced relapse, and 65 patients died. Among the relapsed patients, 66 received salvage treatment. The salvage regimens were heterogeneous, with 17 patients receiving fludarabine-based chemotherapy and 30 patients receiving cytarabine-containing chemotherapy.
With a median follow-up duration of 20.0 months (range, 0.2-77.0 months), the OS at 2 years was 64.7%, while the EFS was 39.7% (Fig. 1). As seen in Figs. 2 and 3, the IPI and MIPI had a statistically significant effect on OS (
DISCUSSION
MCL is characterized by an aggressive clinical course, and there is a pattern of frequent relapse after conventional chemotherapy. However, recent novel treatment options, such as rituximab and transplantation, have improved the response and survival outcomes [9]. As a result, the prognosis and survival of patients with MCL have considerably improved recently [5]. In addition, the significant improvement in treatment outcomes observed with the introduction of rituximab has altered the risk assessment for MCL. Therefore, an in-depth analysis of patients with MCL is important to help identify more adequate initial treatment modalities.
The present study found similar clinical characteristics to those reported previously. The patients in the current study had a median age of approximately 63 years and were predominantly men with mostly advanced stage MCL and frequent extranodal involvement, including the BM in the majority of cases [4, 7, 19, 20, 21, 22]. GI involvement was observed in 35.1% of the patients, which is similar to the rate described in other studies [19, 23]. In addition, several studies have demonstrated that consideration of MCL with GI involvement is important in the treatment planning, response assessment, and surveillance of patients with lymphoma [24, 25]. However, in contrast to other studies, the incidence of CNS involvement in the current study was relatively low. This discrepancy may be due to a lack of actual CNS examinations and a possible underestimation of CNS involvement. Indeed, the use of routine CNS examinations and prophylaxes remains controversial [16]. Similar to previous studies, other extranodal sites included the lungs, liver, and spleen, although these locations are considered rare [14, 26].
While a median survival of approximately 3 years has been common in previous reports, this has recently increased to 5 years [3]. Herrmann et al. [5] suggested that such superior outcomes may be a result of different patient selection, improved diagnosis, and improved treatment. In the current study, the 5-year OS rate was 23.1%, with a continuous decline of the survival curve. Although the addition of rituximab has improved the response rate and time-to-failure in the first-line setting, this has not translated into significant improvement in the OS. The results of the present study indicate that patients with MCL have a poor prognosis, even after rituximab-based chemotherapy [27]. Most patients in the current study also had poor clinical factors, such as advanced age, poor performance status, multiple extranodal involvements, and B symptoms at diagnosis. In addition, 45.8% of patients did not receive rituximab-based chemotherapy as a first-line treatment. The CR rate was 45.0%, which is similar to the results from other studies, where CR rate ranged from 30% to 80% [28]. The current study also showed that achieving CR prolonged OS. After relapse, the median life expectancy for a patient with MCL drops to 1-2 years [9]. Once relapse occurs, patients are offered aggressive chemotherapy; however, standard salvage chemotherapy has not yet been defined.
This study sought to provide an in-depth report on MCL subgroups with significantly worse clinical outcomes. Several previous studies have identified prognostic factors for MCL. While the IPI is a powerful tool for predicting clinical outcomes in patients with aggressive non-Hodgkin lymphoma [15], only a few studies have used IPI for predicting and examining MCL prognosis. However, a specific MCL prognostic score was recently proposed, and this score identifies 4 independent prognostic factors [11]. In terms of prognostic factors, the MIPI was found to correlate with OS in the current study including Korean patients. Older age and poor performance status are commonly mentioned as negative predictive factors for survival in cases of MCL [6, 11, 21]. Interestingly, patients with MCL and B symptoms displayed a worse survival trend. This agrees with previous reports showing that B symptoms have a negative impact on survival [29].
In conclusion, the present data reveal the clinical features and treatment outcomes for patients with MCL in Korea who received at least 1 chemotherapeutic regimen. Similar to the results from Western countries, patients with MCL in Korea were characterized by the aggressive clinical features and particularly poor clinical outcomes. The simplified MIPI was an important prognostic factor in patients with MCL in Korea. Although MIPI was a prognostic factor in the current study, an analysis of prognostic subgroups should be evaluated and validated for patients with MCL. In addition, rituximab did not significantly improve the therapeutic effect in patients with MCL in Korea; therefore, a more suitable treatment needs to be identified for patients with MCL in Korea.
Fig 1.
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Kaplan-Meier analysis of overall survival and event-free survival.
Fig 2.
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Kaplan-Meier analysis of (
Fig 3.
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Kaplan-Meier analysis of (
Fig 4.
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Kaplan-Meier analysis of (
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Table 1 . Baseline characteristics of patients..
Values are presented as numbers (%)..
Abbreviations: ECOG, Eastern Cooperation Oncology Group; IPI, International Prognostic Index; MIPI, MCL International Prognostic Index; BM, bone marrow; CNS, central nervous system; GI, gastrointestinal tract..
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Table 2 . Types of first-line treatment..
Values are presented as numbers (%)..
Abbreviations: R-CHOP, rituximab, cyclophosphamide, doxorubicin, and prednisone; RHyperCVAD/RMTX-Ara-C, rituximab, doxorubicin, vincristine, dexamethasone, methotrexate, and cytarabine; RCVP, rituximab, cyclophosphamide, vincristine, and prednisone; RICE, rituximab, ifosfamide, carboplatin, and etoposide; RESHAP, rituximab, etoposide, methylprednisone, cytarabine, and cisplatin; CHOP, cyclophosphamide, doxorubicin, and prednisone; HyperCVAD/MTX-Ara-C, doxorubicin, vincristine, dexamethasone, methotrexate, and cytarabine; CVP, cyclophosphamide, vincristine, and prednisone; ICE, ifosfamide, carboplatin, and etoposide; ESHAP, etoposide, methylprednisone, cytarabine, and cisplatin; GIDOX, gemcitabine, ifosfamide, dexamethasone, and oxaliplatin..
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Table 3 . Treatment outcomes of patients..
Values are presented as numbers (%)..
Abbreviations: CR, complete response; PR, partial response; SD, stable disease; PD, progressive disease; CHOP, cyclophosphamide, doxorubicin, and prednisone; CVP, cyclophosphamide, vincristine, and prednisone; ICE, ifosfamide, carboplatin, and etoposide..
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Table 4 . Univariate and multivariate analyses for factors affecting EFS and OS..
a)Log-rank test for univariate analysis..
Abbreviations: HR, hazard ratio; MIPI, MCL International Prognostic Index; EFS, event-free survival; OS, overall survival; CI, confidence interval..
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