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Analysis of the response time to involved-field radiotherapy in primary gastrointestinal low-grade B-cell lymphoma

Abstract

Background

Early-stage primary gastrointestinal (GI) low-grade B-cell lymphoma shows good therapeutic response to primary radiotherapy. However, there is no clear guideline for the evaluation of response to radiation therapy currently. The aim of this study was to analyze the relationship between the best response time and the clinical course after radiotherapy.

Methods

Patients who underwent radiotherapy for treatment of primary GI low-grade B-cell lymphoma from September 2007 to December 2018 at Seoul St. Mary’s Hospital were included. Early responders were defined by best response within 6 months after radiotherapy, and delayed responders after 6 months. Clinical and pathological factors associated with delayed response and survival analyses were performed to investigate the recurrence and survival during follow-up.

Results

A total of 43 patients were evaluated and the number of gastric mucosa-associated lymphoid tissue and duodenal follicular lymphoma was 36 and 7, respectively. All of 43 patients showed complete remission to radiotherapy and the best response time after radiotherapy was a median of 3 months. There were 8 delayed responders with a median duration of 8.9 months. Early and delayed responders were characterized by a significant difference in depth of invasion beyond the mucosal layer.

Conclusions

Delayed responders did not show differences in oncological outcomes compared with early responders. They were allowed to watch and wait for an additional 6 to 12 months without further treatment.

Background

Gastrointestinal (GI) lymphoma is the most common extranodal lymphomas and primary GI lymphoma is usually diagnosed in the stomach, duodenum, esophagus and rectum [1, 2]. More than 90% of all GI lymphomas are of B-cell lineage and treatment modalities differ according to the pathological subtype [3]. Systemic involvement of B-cell lymphomas in early stage with low-grade pathology such as mucosa-associated lymphoid tissue (MALT) or follicular lymphoma is rare and it can be cured by local radiotherapy or observed without treatment.

Factors known to cause primary GI lymphoma include bacterial infections such as H.pylori and C.jejuni, preexisting intestinal diseases, and immunosuppression [4]. In the case of gastric lymphoma infected with H.pylori, H.pylori eradication (HPE) consisted of proton pump inhibitors, amoxicillin, and clarithromycin is the primary treatment resulting in an efficacy of over 80% [5, 6]. Involved-field radiotherapy (IFRT) is indicated for patients with H.pylori-positive lymphoma refractory to HPE as the second-line treatment or H.pylori-negative lymphoma as first-line [7, 8]. Gastric lymphoma tends to be a multifocal disease, so the entire stomach should be irradiated according to the International Lymphoma Radiation Oncology Group (ILROG) guidelines [9].

Primary GI low-grade follicular lymphoma is predominantly found in the second portion of the duodenum, with polypoid lesions appearing sporadically in the affected organs. Early-stage GI follicular lymphoma has been monitored without any treatments in the past; however, radiotherapy has been administered to patients with GI follicular lymphoma because of the relatively better overall survival rate [10]. The dose of ≤30 Gy showed an effective local control rate of ≥90%. And ILROG also recommend ≥24 Gy as radiation dose of early stage GI low-grade follicular lymphoma, and the entire duodenum should be included as radiotherapy field [9, 11]. Recently, options for radiation doses of less than 4 Gy (2 × 2 Gy) in recurrent follicular lymphoma have also been proposed and have shown an acceptable response rate of 92% [12]. However, as a rare disease, there is no standardized guideline for the duration and frequency of follow-up in patients receiving radiotherapy.

Clinical and endoscopic factors associated with delayed response after radiotherapy or the timing of follow-up in primary GI low-grade B-cell lymphoma (PG-LGBCL) have not been studied and the protocol of follow-up varies from institution to institution. This study was conducted to analyze the duration of the response and delayed responders to radiotherapy in PG-LGBCL at a single institution. The purpose of this study was to determine the interval of follow-up needed and avoid unnecessary additional treatment.

Materials and methods

Patients with PG-LGBCL treated with curative radiotherapy at Seoul St. Mary’s Hospital from September 2007 to December 2018 were analyzed retrospectively. Patients underwent blood tests, endoscopy, endoscopic biopsy, abdominal CT, and fluorine-18 fluorodeoxyglucose (18F-FDG) positron emission tomography (PET) at initial diagnosis. Endoscopic ultrasound (EUS) to confirm the depth of the lesion was performed in stomach lymphoma patients. This study was approved by the ethical review board (Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, reference number: KC19RESI0121).

Patients completed treatment courses of IFRT, and patients involved ≥2 organs were excluded. The clinical target volume (CTV) included the entire involved organ and the regional lymph nodes if involved. The internal target volume (ITV) was set using the motion information obtained from the 4-dimensional CT for assessment of breathings and abdominal motions. Planning target volume (PTV) was defined by expanding 5 mm from ITV considering the patient’s set-up error. Radiotherapy was prescribed as 30.6 Gy over 17 fractions on stomach or 24 Gy over 12 fractions on duodenum. Images presenting an example of CTV, ITV and PTV are illustrated in Fig. 1. The dose constraints to organ at risk used for radiotherapy planning were as follows: the maximum dose (Dmax) to spinal cord < 40 Gy, Dmax of the duodenum < 50 Gy, V50 of the small intestine < 5%, V20 of both kidneys < 20%, and V30 of the liver < 30% (Vx, the percentage of organ receiving x Gy).

Fig. 1
figure1

Images presenting examples of CTV (red-colored line), ITV (green-colored) and PTV (blue-colored) in this study (a, stomach; b, duodenum). CTV, clinical target volume; ITV, internal target volume; PTV, planning target volume

After treatment completion, patients underwent CT, endoscopy and biopsy every 3 months for the first year, every 6 months for the next 5 years, and then annually. The complete remission (CR) was pathologic and radiologic remission in endoscopic biopsy and imaging. The first CR of the follow-up was defined as the best response. The duration of best response was the time period between the completion of radiotherapy and the best response. The best response within 6 months after radiotherapy was defined as early response and that after > 6 months was defined as delayed response. The National Comprehensive Cancer Network (NCCN) guideline recommends evaluation of the lesion at 3 to 6 months in patients diagnosed with PG-LGBCL. The hypothesis of this study was that clinical outcomes of delayed responders after > 6 months may differ from those of early responders.

During the follow-up period, we analyzed the recurrence and survival rates of patients using Kaplan-Meier survival analysis and evaluated the clinical and pathological factors of delayed responders using multivariate logistic regression analysis. P-values less than 0.05 were considered statistically significant. Statistical analysis was performed using SPSS software version 24 (SPSS Inc., Chicago, IL, U.S.A.). Furthermore, the medical records were reviewed in accordance with the National Cancer Institute’s Common Terminology Criteria for Adverse Events (NCI CTCAE) version 5.0 to investigate the acute and chronic side effects of radiotherapy.

Results

A total of 43 patients were included in this study and the median follow-up period was 27.9 months (range, 8.8–117 months). The clinical characteristics of 43 patients are summarized in Table 1. They comprised 36 gastric MALT lymphomas and 7 duodenal follicular lymphomas, and clinical stage of all patients was Lugano I or II1. Fourteen of gastric lymphoma patients were refractory to the eradication therapy in H.pylori infection and received radiotherapy as the second-line treatment. The other 22 gastric lymphomas patients with negative for H.pylori infection were treated with radiotherapy as primary treatment. Five patients were tested for BIRC3/MALT1 translocation before treatment, one of which yielded positive results. Seven patients in duodenal lesions were follicular lymphomas and all received radiotherapy as the primary treatment. The treatment technique included 3-dimensional conformal radiotherapy and intensity-modulated radiotherapy in 38 and 5 patients, respectively.

Table 1 The clinical and tumor characteristics of 43 patients

All of 43 patients achieved pathologic CR after radiotherapy with a median duration of 3 months (range, 2.1–14.6 months). Radiologic or metabolic CR in CT or PET-CT was also demonstrated in regional node metastasis of 5 patients. Thirty-five patients showed the best responses in the endoscopy and biopsy at the first follow-up within 6 months. Eight patients were delayed responders, and their median duration of best response was 8.9 months (range, 6.1–14.6 months). Of 8 delayed responders, five patients had CR at the second follow-up (6.1–9 months) after completion of treatment and 3 patients at the third follow-up (9.7–14.6 months). Thirty-five patients who had CR within 6 months and 8 patients after > 6 months were classified into early and delayed responder groups, respectively.

One patient received salvage chemotherapy during follow-up period because of other organ involvement out of radiation field 7.7 months after completion of radiotherapy. She was a patient with early response of pathologic CR to radiotherapy at the first-line treatment. Another patient died at 7 years because of lymphoma-unrelated cause. The 2-year overall survival (OS) and recurrence-free survival (RFS) rates were 100 and 97.1%, respectively. The 5-year OS and RFS rates were 100 and 97.1%, respectively. Figure 2 shows Kaplan-Meier curves for OS and RFS of the 43 patients. The OS and RFS between two responder groups were not significantly different (P = 0.633). Grade 1 and 2 GI toxicity according to NCI CTCAE version 5.0 was observed in 12 patients (27.9%) and 6 patients (14.0%), respectively. Their main complaints were nausea or epigastric discomfort and improved after conservative treatment. No adverse events of grade 3 or higher were noted, and there were no stomach or duodenal ulcers or perforations.

Fig. 2
figure2

Kaplan-Meier curves for OS (a) and RFS (b) of the 43 patients. OS, overall survival; RFS, recurrence-free survival

Multivariate logistic regression analysis to evaluate the factors associated with significant differences between 35 early responders and 8 delayed responders was conducted (Table 2). There was no significant difference in the pathologic type or tumor location between the early and delayed responders. The lactate dehydrogenase (LDH), Lugano stage, IPI score, and SUV uptake in PET-CT before treatment did not differ significantly between the two groups. The endoscopic and EUS factors related to response to radiotherapy were analyzed (Table 3). There was no significant difference in location, size, multiplicity, or endoscopic pattern of the tumor. EUS was performed in 30 out of 36 gastric lymphoma patients, and there was statistically significant difference of deep invasion beyond the mucosal layer in EUS between two responder groups (P = 0.027). The odds ratio was 0.400 and 95% confidence interval was 0.155–1.031.

Table 2 Multivariate logistic regression analysis to assess clinical factors affecting the duration of best response
Table 3 Multivariate logistic regression analysis to assess endoscopic factors affecting the duration of best response

Discussion

PG-LGBCL in early stage can be cured with local radiotherapy, and this study resulted that pathologic CR after IFRT was achieved in all patients, suggesting radiation dose of 25–30 Gy showed adequate tumor control. Previous studies also reported a high response rate of 90% to radiotherapy in cases diagnosed with PL-LGBCL, with RFS rate of 90–100% and an OS rate of 75–100% [13,14,15,16,17]. A recent retrospective study analyzed the efficacy of the radiotherapy field reduction in low-grade follicular and MALT lymphoma, and reported that there was no difference in local control and survival between the existing IFRT and involved-site radiotherapy [18]. Further research is underway to reduce radiation fields and doses in low-grade B-cell lymphoma [19, 20]. However, the clinical factors that affect the response time and oncologic outcome of delayed response to radiation therapy have not yet been evaluated in previous studies.

The current study demonstrated that local tumor control was good even with delayed response to radiotherapy. Only one patient in early responder group developed out-field recurrence and there was no recurrence in delay responder group. This results suggested that the lesion can be cured without further treatment even if the response to radiation therapy was delayed. In addition, initial evaluation of radiotherapy after 6 months or interval increases could reduce unnecessary invasive tests.

For treatment of H.pylori-positive gastric lymphoma, eradication therapy using antibiotics is the first-line treatment and highly invasive lymphomas are known to respond later more than 6 months [21, 22]. Previous studies have shown that patients with lymphoma extending beyond the submucosal layer can respond after 1 year of HPE, so endoscopy and biopsy are recommended every 6 months for the first 2 years [23,24,25]. The heterogeneity of H.pylori strain may result in different responses or different tumor location might affect different responses to HPE [21, 26, 27]. Therefore, secondary treatment after eradication therapy is recommended if the gross lesion persists for 6 months and microscopic lymphomatous infiltration occurs up to 2 years [28]. A delayed response to eradication therapy indicates poor prognosis warranting secondary treatment such as radiotherapy.

On the other hand, few studies investigating delayed response to radiotherapy have been conducted. Cheson et al. [29] and the NCCN guidelines recommended an evaluation of endoscopy and biopsy at 3 to 6 months after radiotherapy. However, 8 of the 43 patients manifested the delayed response after > 6 months, which may require further follow-up to evaluate the final response to radiotherapy.

Interestingly, clinical and endoscopic factors that affect delayed response after radiation therapy were analyzed in this study. In multivariate logistic regression analysis, the depth of invasion beyond mucosal layer showed a significant difference between two responder groups. Other characteristics such as age, stage, LDH, and IPI score did not show statistical difference between two groups. Previous studies reported differences in eradication therapy depending on sex or tumor location; however, no significant difference in response time of radiotherapy was demonstrated [26, 27]. Although there were delayed response in deeply invasive lymphoma, the patients were observed without salvage treatment and all achieved CRs finally.

The endoscopic findings such as ulcerative pattern indicated the high grade lymphoma in previous study [30]. In the endoscopic findings of current study, there was no significant difference in endoscopic patterns between two responder groups. However, the first endoscopic finding of the 7 patients in 8 delayed responders was characterized by diffuse or deep nodularity and ulceration rather than erosion or erythema at the initial examination. The number of patients was small so there was no difference between endoscopic findings and delayed response.

The aim of the current study was not only to evaluate the response rate but also to analyze the factors associated with the delayed response. The limitation of this study are its retrospective nature with small number of patients, as well as short follow up with median of 27.9 months, and therefore it is difficult to compare the oncological outcome in this short period. A prospective large-scale study is needed to analyze the factors that may cause delayed response and to establish a protocol for evaluation of response to radiotherapy of PG-LGBCL. To evaluate the oncologic outcome and late toxicity results in radiotherapy for PG-LGBCL, longer follow-up will be necessary.

Second, the different prescription doses of duodenal follicular lymphoma and gastric MALT lymphoma show limitations in the dose inhomogeneity of retrospective studies. In the UK, a 3-phase multicenter prospective study was conducted comparing the local control rates of 40 Gy and 24 Gy in indolent lymphoma, and the local control rates were 93% and 92%, respectively, which did not differ between the two groups [19]. In addition, Lee et al. reported 95% complete remission of the duodenal follicular lymphoma after 24 Gy irradiation [20]. Therefore, 24 Gy for duodenal follicular lymphoma and 30.6 Gy for gastric MALT lymphoma were prescribed in our instution, and there was no difference in local control between 24 Gy and 30.6 Gy in this study.

In conclusion, PG-LGBCL showed an adequate response rate, RFS, and OS with limited toxicity with radiotherapy. And there were no significant difference of recurrence and local control between response time to radiotherapy. Furthermore, deep invasion beyond mucosal layer affected delayed response to radiotherapy. This study suggested more studies of factors and prognosis affecting the delayed response. Additional clinical studies are needed, but PG-LGBCL with response to radiation therapy may be followed up without further treatment.

Availability of data and materials

The dataset used and analyzed during the current study are available from the corresponding author on reasonable request.

Abbreviations

GI:

Gastrointestinal

MALT:

Mucosa-associated lymphoid tissue

HPE:

H.pylori eradication

IFRT:

Involved-field radiotherapy

ILROG:

International Lymphoma Radiation Oncology Group

PG-LGBCL:

Primary GI low-grade B-cell lymphoma

18F-FDG:

Fluorine-18 fluorodeoxyglucose

PET:

Positron emission tomography

EUS:

Endoscopic ultrasound

CTV:

Clinical target volume

ITV:

Internal target volume

PTV:

Planning target volume

Dmax:

Maximum dose

Vx:

the percentage of organ receiving x Gy

CR:

Complete remission

NCCN:

National Comprehensive Cancer Network

NCI CTCAE:

National Cancer Institute’s Common Terminology Criteria for Adverse Events

OS:

Overall survival

RFS:

Recurrence-free survival

LDH:

Lactate dehydrogenase

References

  1. 1.

    Nakamura S, Matsumoto T. Gastrointestinal lymphoma: recent advances in diagnosis and treatment. Digestion. 2013;87:182–8.

    Article  Google Scholar 

  2. 2.

    Nakamura S, Matsumoto T, Iida M, Yao T, Tsuneyoshi M. Primary gastrointestinal lymphoma in Japan: a clinicopathologic analysis of 455 patients with special reference to its time trends. Cancer. 2003;97:2462–73.

    Article  Google Scholar 

  3. 3.

    Ghimire P, Wu GY, Zhu L. Primary gastrointestinal lymphoma. World J Gastroenterol. 2011;17:697–707.

    Article  Google Scholar 

  4. 4.

    Juarez-Salcedo LM, Sokol L, Chavez JC, Dalia S. Primary gastric lymphoma, epidemiology, clinical diagnosis, and treatment. Cancer Control. 2018;25:1073274818778256.

    Article  Google Scholar 

  5. 5.

    Gong EJ, Ahn JY, Jung HY, Park H, Ko YB, Na HK, Jung KW, Kim Do H, Lee JH, Choi KD, Song HJ, Lee GH, Kim JH. Helicobacter pylori eradication therapy is effective as the initial treatment for patients with H. pylori-negative and disseminated gastric mucosa-associated lymphoid tissue lymphoma. Gut Liver. 2016;10:706–13.

    Article  Google Scholar 

  6. 6.

    Stathis A, Chini C, Bertoni F, Proserpio I, Capella C, Mazzucchelli L, Pedrinis E, Cavalli F, Pinotti G, Zucca E. Long-term outcome following helicobacter pylori eradication in a retrospective study of 105 patients with localized gastric marginal zone B-cell lymphoma of MALT type. J Ann Oncol. 2009;20:1086–93.

    CAS  Article  Google Scholar 

  7. 7.

    Pinotti G, Zucca E, Roggero E, Pascarella A, Bertoni F, Savio A, Savio E, Capella C, Pedrinis E, Saletti P, Morandi E, Santandrea G, Cavalli F. Clinical features, treatment and outcome in a series of 93 patients with low-grade gastric MALT lymphoma. Leuk Lymphoma. 1997;26:527–37.

    CAS  Article  Google Scholar 

  8. 8.

    Aleman BM, Haas RL, van der Maazen RW. Role of radiotherapy in the treatment of lymphomas of the gastrointestinal tract. J Best Pract Res Clin Gastroenterol. 2010;24:27–34.

    Article  Google Scholar 

  9. 9.

    Yahalom J, Illidge T, Specht L, Hoppe RT, Li YX, Tsang R, Wirth A. Modern radiation therapy for extranodal lymphomas: field and dose guidelines from the international lymphoma radiation oncology group. Int J Radiat Oncol Biol Phys. 2015;92:11–31.

    Article  Google Scholar 

  10. 10.

    Mac Manus MP, Hoppe RT. Is radiotherapy curative for stage I and II low-grade follicular lymphoma? Results of a long-term follow-up study of patients treated at Stanford University. J Clin Oncol. 1996;14:1282–90.

    CAS  Article  Google Scholar 

  11. 11.

    Brady JL, Binkley MS, Hajj C, Chelius M, Chau K, Balogh A, Levis M, Filippi AR, Jones M, Mac Manus M, Wirth A, Oguchi M, Vistisen AK, Andraos TY, Ng AK, Aleman BMP, Choi SH, Kirova Y, Hardy S, Reinartz G, Eich HT, Bratman SV, Constine LS, Suh CO, Dabaja B, El-Galaly TC, Hodgson DC, Ricardi U, Yahalom J, Hoppe RT, et al. Definitive radiotherapy for localized follicular lymphoma staged by (18)F-FDG PET-CT: a collaborative study by ILROG. Blood. 2019;133:237–45.

    CAS  Article  Google Scholar 

  12. 12.

    Haas RL, Poortmans P, de Jong D, Aleman BM, Dewit LG, Verheij M, Hart AA, van Oers MH, van der Hulst M, Baars JW, Bartelink H. High response rates and lasting remissions after low-dose involved field radiotherapy in indolent lymphomas. J Clin Oncol. 2003;21:2474–80.

    CAS  Article  Google Scholar 

  13. 13.

    Koch P, del Valle F, Berdel WE, Willich NA, Reers B, Hiddemann W, Grothaus-Pinke B, Reinartz G, Brockmann J. Temmesfeld A: Primary gastrointestinal non-Hodgkin’s lymphoma: II. Combined surgical and conservative or conservative management only in localized gastric lymphoma—results of the prospective German multicenter study GIT NHL 01/92. J Clin Oncol. 2001;19:3874–83.

    CAS  Article  Google Scholar 

  14. 14.

    Tsang RW, Gospodarowicz MK. Radiation therapy for localized low-grade non-Hodgkin's lymphomas. J Hematol oncol. 2005;23:10–7.

    Article  Google Scholar 

  15. 15.

    Vrieling C, de Jong D, Boot H, de Boer JP, Wegman F, Aleman BM. Long-term results of stomach-conserving therapy in gastric MALT lymphoma. J Radiotherapy. 2008;87:405–11.

    Article  Google Scholar 

  16. 16.

    Goda JS, Gospodarowicz M, Pintilie M, Wells W, Hodgson DC, Sun A, Crump M, Tsang RW. Long-term outcome in localized extranodal mucosa-associated lymphoid tissue lymphomas treated with radiotherapy. J Cancer. 2010;116:3815–24.

    Article  Google Scholar 

  17. 17.

    Kim S-W, YCA DHL, Kim WS, Kim SJ, Ko YH, Kim K-M. Clinical outcomes of radiation therapy for early-stage gastric mucosa-associated lymphoid tissue lymphoma. J World J Gastroenterol. 2013;19:6062.

    Article  Google Scholar 

  18. 18.

    Elsayad K, Reinartz G, Oertel M, Rehn S, Eismann J, Scobioala S, Berssenbrügge H, Eter N, Weishaupt C, Schmidt HH, Friedrichs B, Grünewald I, Hartmann W, Lenz G, Wardelmann E, Willich N, Eich HT. Radiotherapy of extranodal low-grade follicular and marginal zone lymphomas: long-term follow-up of 159 patients. Strahlenther Onkol. 2020;196:117–25.

    Article  Google Scholar 

  19. 19.

    Lowry L, Smith P, Qian W, Falk S, Benstead K, Illidge T, Linch D, Robinson M, Jack A, Hoskin P. Reduced dose radiotherapy for local control in non-Hodgkin lymphoma: a randomised phase III trial. Radiother Oncol. 2011;100:86–92.

    Article  Google Scholar 

  20. 20.

    Lee H, Oh D, Yang K, Ko YH, Ahn YC, Kim WS, Kim SJ. Radiation therapy outcome and clinical features of duodenal-type follicular lymphoma. Cancer Res Treat. 2019;51:547–55.

    Article  Google Scholar 

  21. 21.

    Ruskone-Fourmestraux A, Lavergne A, Aegerter P, Megraud F, Palazzo L, De Mascarel A, Molina T, Rambaud JL. Predictive factors for regression of gastric MALT lymphoma after anti-helicobacter pyloritreatment. Gut. 2001;48:297–303.

    CAS  Article  Google Scholar 

  22. 22.

    Hussell T, Isaacson PG, Crabtree JE, Spencer J. The response of cells from low-grade B-cell gastric lymphomas of mucosa-associated lymphoid tissue to helicobacter pylori. Lancet. 1993;342:571–4.

    CAS  Article  Google Scholar 

  23. 23.

    Savio A, Zamboni G, Capelli P, Negrini R, Santandrea G, Scarpa A, Fuini A, Pasini F, Ambrosetti A, Paterlini A, Buffoli F, Angelini GP, Cesari P, Rolfi F, Graffeo M, Pascarella A, Valli M, Mombello A, Ederle A, Franzin G. Relapse of low-grade gastric MALT lymphoma after Helicobacter pylori eradication: true relapse or persistence? Long-term post-treatment follow-up of a multicenter trial in the north-east of Italy and evaluation of the diagnostic protocol's adequacy. Recent Results Cancer Res. 2000;156:116–24.

    CAS  Article  Google Scholar 

  24. 24.

    Vetro C, Romano A, Chiarenza A, Conticello C, Donnarumma D, Gorgone A, Coppolino F, Palumbo GA, Bonanno G, Di Raimondo F. Endoscopic ultrasonography in gastric lymphomas: appraisal on reliability in long-term follow-up. Hematol Oncol. 2012;30:180–5.

    Article  Google Scholar 

  25. 25.

    El-Zahabi LM, Jamali FR, El H II, Naja M, Salem Z, Shamseddine A, El-Saghir NS, Zaatari G, Geara F, Soweid AM. The value of EUS in predicting the response of gastric mucosa-associated lymphoid tissue lymphoma to helicobacter pylori eradication. Gastrointest Endosc. 2007;65:89–96.

    Article  Google Scholar 

  26. 26.

    Steinbach G, Ford R, Glober G, Sample D, Hagemeister FB, Lynch PM, McLaughlin PW, Rodriguez MA, Romaguera JE, Sarris AH, Younes A, Luthra R, Manning JT, Johnson CM, Lahoti S, Shen Y, Lee JE, Winn RJ, Genta RM, Graham DY, Cabanillas FF. Antibiotic treatment of gastric lymphoma of mucosa-associated lymphoid tissue. An uncontrolled trial. Ann Intern Med. 1999;131:88–95.

    CAS  Article  Google Scholar 

  27. 27.

    Nakamura S, Matsumoto T, Suekane H, Takeshita M, Hizawa K, Kawasaki M, Yao T, Tsuneyoshi M, Iida M, Fujishima M. Predictive value of endoscopic ultrasonography for regression of gastric low grade and high grade MALT lymphomas after eradication of helicobacter pylori. Gut. 2001;48:454–60.

    CAS  Article  Google Scholar 

  28. 28.

    Ruskoné-Fourmestraux A, Fischbach W, Aleman BMP, Boot H, Du MQ, Megraud F, Montalban C, Raderer M, Savio A, Wotherspoon A. EGILS consensus report. Gastric extranodal marginal zone B-cell lymphoma of MALT. Gut. 2011;60:747–58.

    Article  Google Scholar 

  29. 29.

    Cheson BD, Fisher RI, Barrington SF, Cavalli F, Schwartz LH, Zucca E, Lister TA, Alliance AL, Lymphoma G, Eastern Cooperative Oncology G, European Mantle Cell Lymphoma C, Italian Lymphoma F, European Organisation for R, Treatment of Cancer/Dutch Hemato-Oncology G, Grupo Español de Médula Ó, German High-Grade Lymphoma Study G, German Hodgkin's Study G, Japanese Lymphorra Study G, Lymphoma Study A, Group NCT, Nordic Lymphoma Study G, Southwest Oncology G, United Kingdom National Cancer Research I: Recommendations for initial evaluation, staging, and response assessment of Hodgkin and non-Hodgkin lymphoma: the Lugano classification. J Clin Oncol 2014, 32:3059–3068.

  30. 30.

    Zullo A, Hassan C, Andriani A, Cristofari F, Cardinale V, Spinelli GP, Tomao S, Morini S. Primary low-grade and high-grade gastric MALT-lymphoma presentation. J Clin Gastroenterol. 2010;44:340–4.

    Article  Google Scholar 

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Acknowledgements

We would like to thank the participants who made this study possible.

Funding

The study did not receive specific grants from public or commercial funding agencies.

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Authors

Contributions

All of the authors participated in designing this study. KHC and BOC performed the data collection. KHC, HHL, BOC, and SGC undertook the statistical analyses. KHC, HHL, SEJ, KSP, JHO, and YWJ analyzed and interpreted the data. KHC wrote the first draft of the manuscript, which was reviewed by all of the other authors, who also provided further contributions and suggestions. The author(s) read and approved the final manuscript.

Corresponding authors

Correspondence to Byung-Ock Choi or Seok-Goo Cho.

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Ethics approval and consent to participate

This study was approved by the Institutional Review Board of the Korea Association of Health Promotion (approval No. KC19RESI0121). Informed consent was waived due to the retrospective study design.

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All authors declare that they have no conflict of interest.

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Choi, K.H., Lee, H.H., Jung, S. et al. Analysis of the response time to involved-field radiotherapy in primary gastrointestinal low-grade B-cell lymphoma. Radiat Oncol 15, 210 (2020). https://doi.org/10.1186/s13014-020-01649-6

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