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Surgical treatment of primitive gastro-intestinal lymphomas: a systematic review

Abstract

Primitive Gastrointestinal Lymphomas (PGIL) are uncommon tumours, although time-trend analyses have demonstrated an increase. The role of surgery in the management of lymphoproliferative diseases has changed over the past 40 years. Nowadays their management is centred on systemic treatments as chemo-/radio- therapy. Surgery is restricted to very selected indications, always discussed in a multidisciplinary setting. The aim of this systematic review is to evaluate the actual role of surgery in the treatment of PGIL.

A systematic review of literature was conducted according to the recommendations of The Cochrane Collaboration. Main outcomes analysed were overall survival (OS) and disease free survival (DFS).

There are currently 1 RCT and 4 non-randomised prospective controlled studies comparing surgical versus medical treatment for PGIL. Seven hundred and one patients were analysed, divided into two groups: 318 who underwent to surgery alone or associated with chemotherapy and/or radiotherapy (surgical group) versus 383 who were treated with chemotherapy and/or radiotherapy (medical group).

Despite the OS at 10 years between surgical and medical groups did not show relevant differences, the DFS was significantly better in the medical group (P = 0.00001). Accordingly a trend was noticed in the recurrence rate, which was lower in the medical group (6.06 vs. 8.57%); and an higher mortality was revealed in the surgical group (4.51% vs. 1.50%).

The chemotherapy confirms its primary role in the management of PGIL as part of systemic treatment in the medical group. Surgery remains the treatment of choice in case of PGIL acutely complicated, although there is no evidence in literature regarding the utility of preventive surgery.

Introduction

Primitive Gastrointestinal Lymphomas (PGIL) are uncommon tumours, although time-trend analyses have demonstrated an increase of 2.7% per annum in incidence for gastric (6.3%) and small bowel diseases (5.9%) [1].

PGIL could be localised in any site of the gastrointestinal tract [1–7]. The most frequent site is the stomach (44-75%). Other locations might be the jejunum or the ileo-cecal region, while duodenum, colon and rectum are rare. Multiple gastrointestinal lesions are very infrequent.

The treatment of patient with PGIL is quite undefined. In fact, although the efficacy of chemotherapy (CT) is well recognised and all treatment strategies for PGIL include CT, with or without radiotherapy (RT); whether or not CT should be performed as unique medical treatment or as part of a combined treatment, which includes the surgical resection of the primary lymphoma, is still discussed. Moreover, surgery is sometime necessary to manage acute complications, such as haemorrhage, abscess, gastrointestinal occlusion or perforation during systemic therapies or suggested for prevention of such emergencies.

The aim of this systematic review is to evaluate the actual role of surgery in the treatment of PGIL, analysing overall and disease free survival as main outcomes.

Methods of meta-analysis

We conducted the review according to the recommendations of The Cochrane Collaboration and performed the statistical analysis using Review Manager 5 (RevMan) software.

Research methods for identification of studies

We searched for all published and unpublished randomised controlled trials (RCT) and controlled clinical trials (CCT) using the following electronic databases: Cochrane Central Register of Controlled Trials, MEDLINE, Science Citation Index, ISI Proceedings, Current Controlled Trials metaRegister, Zetoc, CINAHL and EMBASE. The following medical search headings (MeSH) and free text words were used: ''surgery''; "chemotherapy"; "radiotherapy"; "gastric lymphoma"; ''gastrointestinal lymphoma", "colonic lymphoma". We checked the reference lists of all relevant studies obtained from our search and from previously published systematic reviews in order to identify other possible articles. The latest date for this search was February 25th 2010.

Data Extraction

Three authors (RC and ST) assessed titles or abstracts of all the studies identified by the initial search and excluded clearly non-relevant studies. They obtained the full text of all potentially relevant studies and also those with unclear methodology. These studies were assessed by the authors as to whether they met the inclusion criteria for this review. Disagreements on inclusion were resolved by discussing and, if necessary, by involving an independent third author (EF).

Inclusion Criteria

To be included in the analysis, the studies had to compare surgery alone or associated with chemotherapy and/or radiotherapy (surgical group) versus chemotherapy and/or radiotherapy (medical group) in the treatment of gastrointestinal lymphoma tumours.

Exclusion Criteria

Studies were excluded from the meta-analysis if the outcomes of interest were not reported for both groups, or solid tumours were considered, or there was a considerable overlap between authors, centres or patient cohorts evaluated.

Outcomes of Interest

Primary outcomes analysed were: overall survival (OS) and disease free survival (DFS). Secondary outcomes measured were: recurrence rate and mortality.

Measures of treatment effect

Statistical analysis for categorical variables was performed by using the odds ratio (OR). This ratio represents the odds of an adverse event occurring in the surgical treatment group compared with the medical treatment group. The Mantel-Haenszel method was used to combine the ORs for the outcomes of interest. Intention-to-treat analyses were performed extracting the number of patients originally allocated to each treatment group irrespective of compliance. Results were presented on a forest plot graphs.

Assessment of heterogeneity

Heterogeneity was first tested using Chi-squared test. A Chi-squared test with a P value < 0.100 representing statistical significance. However, since tests of heterogeneity had a relative low power when there were few study we further explored heterogeneity derived from another statistical method named "inconsistency" or I2 metric, which is independent of the number of combined studies. If I2 is equal 0%, there is no heterogeneity. If I2 > 50% heterogeneity is indicated.

Results for the meta-analysis

Eligible Studies

Using the search strategy listed above, 114 publications were identified. Fifty-two studies were excluded following title and abstract review. The remaining 62 studies were investigated in detail and 57 studies were excluded as they did not meet the inclusion criteria for this review (Figure 1).

Figure 1
figure 1

Study selection flow chart.

There were 1 RCT and 4 non-randomised prospective controlled studies comparing surgical versus medical treatment for PGIL, which fulfilled the inclusion criteria and were analysed in the systematic review (Table 1) [6, 8–11]. Seven hundred and one patients were analysed, divided into two groups: 318 who underwent to surgery alone or associated with chemotherapy and/or radiotherapy (surgical group) versus 383 who were treated with chemotherapy and/or radiotherapy (medical group). Only in the randomised trial [8] the patients were divided in three different group: surgery (80 patients), radiotherapy (78 patients) and chemotherapy (83 patients).

Table 1 Characteristics of the included studies

Results of Meta-analysis

Despite the OS at 10 years between surgical and medical groups did not show relevant differences (P = 0.25) (Figure 2), the DFS was significantly better in the medical group (P = 0.00001) (Figure 3). Despite not statistically significant, a trend was noticed in the recurrence rate, which was lower in the medical group (6.06 vs. 8.57%) (P = 0.63) (Figure 4). Furthermore the recurrences after surgical treatment were associated with higher mortality (50% vs. 0%) (P = 0.10) (Figure 5). Similarly an higher mortality was revealed in the surgical group (4.51% vs. 1.50%) (P = 0.29) (Figure 6).

Figure 2
figure 2

The overall survival at 10 years in patients with PGIL treated with chemo and/or radiotherapy versus the surgical approach associated with adjuvant treatments. Surgical Group (SG): surgery alone or associated with chemotherapy and/or radiotherapy. Medical Group (MG): chemotherapy and/or radiotherapy.

Figure 3
figure 3

The disease free survival at 10 years in patients with PGIL treated with chemo and/or radiotherapy versus the surgical approach associated with adjuvant treatments. Surgical Group (SG): surgery alone or associated with chemotherapy and/or radiotherapy. Medical Group (MG): chemotherapy and/or radiotherapy.

Figure 4
figure 4

The incidence of recurrences in patients with PGIL treated with chemo and/or radiotherapy versus the surgical approach associated with adjuvant treatments. Surgical Group (SG): surgery alone or associated with chemotherapy and/or radiotherapy. Medical Group (MG): chemotherapy and/or radiotherapy.

Figure 5
figure 5

The mortality in patients with recurrence from PGIL treated with chemo and/or radiotherapy versus the surgical approach associated with adjuvant treatments. Surgical Group (SG): surgery alone or associated with chemotherapy and/or radiotherapy. Medical Group (MG): chemotherapy and/or radiotherapy.

Figure 6
figure 6

The mortality in patients with PGIL treated with chemo and/or radiotherapy versus the surgical approach associated with adjuvant treatments. Surgical Group (SG): surgery alone or associated with chemotherapy and/or radiotherapy. Medical Group (MG): chemotherapy and/or radiotherapy.

Discussion

Based on the assumption that PGIL is a localised disease, the surgical treatment was traditionally considered the cornerstone of the therapeutical strategy showing impressive results in terms of long DFS and OS [3, 12–16].

Nowadays this approach has been extensively revised and the management of PGIL is centred on systemic treatments such as chemo- and radiotherapy.

The current National Comprehensive Cancer Network (NCCN) guidelines [17, 18] suggests for the gastric MALT lymphoma chemotherapy mainly and Helicobacter pylori eradication therapy in the early stage. Surgery is restricted to the treatment of complications, such as occlusion, bleeding or perforation. Preventive surgery is sometime advocated in bulky tumours, when rapid tumour necrosis secondary to chemo-/radiotherapy may be associated with a high risk of life threatening complications. Surgery is also required for removal of residual disease after medical debulking [19]. Total gastrectomy is the most frequent procedure performed for gastric MALT lymphomas, given the evidence that they are multicentric; a D2 lymphadenectomy is recommended [20].

The majority of small bowel lymphomas are represented by B-large cell lymphomas. The NCCN guidelines proposes surgery or radiotherapy as equally effective in the early stage of MALT lymphomas, while chemotherapy for B-large cell lymphomas and advanced stage of MALT lymphomas. In locally advanced lymphomas of the small bowel, surgical resection is indicated during laparotomy/laparoscopy for tumours of undefined histology or complicated by intestinal occlusion, bleeding, and perforation. Surgery may be advocated before chemotherapy in bulky lesions in order to prevent bowel perforation. A segmental intestinal resection with the own mesentery containing at least 12 lymph nodes is recommended.

In the colon-rectum localization, the MALT lymphomas are more common. The NCCN proposed for the colon the same protocols as for the small intestine. In this cases the surgical approach is represented by the segmental resection of the colon, or a local excision for rectal tumours.

The MALT lymphomas represent the majority of PGIL [21], therefore the disease stage is commonly IE [6] with a favourable prognosis [21].

Given the actual dominant role of chemotherapy in the treatment of PGIL, in our literature research most of outcomes resulted from combined therapy. We could identify only one trial [8] analysing surgery, radiotherapy and chemotherapy separately. In this trial, Aviles et al included only patients with diagnosis of low-grade gastric MALT lymphoma, who were randomised to be treated with primary surgical resection (total gastrectomy and D2 limphadenectomy), radiotherapy or chemotherapy. At 4 weeks complete response was achieved in all patients, but relapse in another abdominal site were more frequent in patients treated with surgery or radiotherapy. At 10 years DFS and OS were statistical significantly higher in the chemotherapy group (p = 0.01 and p = 0.04).

Surgery lost its leading role, becoming the treatment of choice only in acute complicated cases or in the prevention of chemotherapy and/or radiotherapy related complications secondary to rapid tumour necrosis [22]. The aim of preventive surgery is to reduce the high incidence of severe morbidity and mortality due to an emergency laparotomy in highly compromised patients [23]. In the past this risk was overestimated and a surgical management was more frequently advocated; actually it stands at 5% [24]: surgery has more than 5% of procedure related morbidity [25] and similarly, from our meta-analysis resulted a higher mortality (P = 0, 29). Therefore surgery must be reserved to very selected patients.

One of the main limitations of our study is the retrospective nature of the majority of studies included in the systematic review. These studies are heterogeneous, combining different types of malignant lymphoma, using different histology classifications and staging systems. Moreover, the aim of this review was the comparison of surgery versus medical therapies but only one study confronted these two approaches. In the others studies, surgery was part of a multimodal treatment, associated to chemo with or without radiotherapy. Besides, case history considers different type of lymphomas, in different stages, with different prognosis, without stratification. Therefore, the application of selective methods and statistical analysis, even if apparently they are in line with what is the generally accepted, they cannot bring to evidence based conclusions.

It would be interesting to analyze only studies including surgery during not surgical treatments in order to evaluate if, when and why surgery was used. From this type of analysis prognostic factors for development of acute complications could be evident and could help selecting high risk patients that are preemptively candidate for surgery.

Conclusions

Although from our meta-analysis there was not any significant difference in terms of OS between surgical and medical groups, DFS was significantly better in the medical group. Accordingly a lower recurrence rate was reported in the medical group. Moreover, our meta-analysis showed an higher mortality in the surgical group. This confirms the widely recognized primary role of the chemotherapy, as part of systemic treatment in the medical group. Surgery remains the treatment of choice in case of PGIL acutely complicated, although there is no evidence in literature regarding the utility of preventive surgery.

Despite the absence in literature of high quality studies (RCT) demonstrating the effectiveness of chemotherapy without local surgical resection in patient with PGIL, the evidence present in literature and analyzed in our review well support a systemic approach for PGIL patients.

References

  1. Gurney KA, Cartwright RA, Gilman EA: Descriptive epidemiology of gastrointestinal non-Hodgkin's lymphoma in a population-based registry. Br J Cancer. 1999, 79 (11-12): 1929-34.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  2. Freeman C, Berg JW, Cutler SJ: Occurrence and prognosis of extranodal lymphomas. Cancer. 1972, 29 (1): 252-60. 10.1002/1097-0142(197201)29:1<252::AID-CNCR2820290138>3.0.CO;2-#.

    Article  CAS  PubMed  Google Scholar 

  3. Radaszkiewicz T, Dragosics B, Bauer P: Gastrointestinal malignant lymphomas of the mucosa-associated lymphoid tissue: factors relevant to prognosis. Gastroenterology. 1992, 102 (5): 1628-38.

    CAS  PubMed  Google Scholar 

  4. d'Amore F, Brincker H, Gronbaek K, Thorling K, Pedersen M, Jensen MK, Mortensen LS: Non-Hodgkin's lymphoma of the gastrointestinal tract: a population-based analysis of incidence, geographic distribution, clinicopathologic presentation features, and prognosis. Danish Lymphoma Study Group. J Clin Oncol. 1994, 12 (8): 1673-84.

    PubMed  Google Scholar 

  5. Liang R, Todd D, Chan TK, Chiu E, Lie A, Kwong YL, Choy D, Ho FC: Prognostic factors for primary gastrointestinal lymphoma. Hematol Oncol. 1995, 13 (3): 153-63. 10.1002/hon.2900130305.

    Article  CAS  PubMed  Google Scholar 

  6. Koch P, del Valle F, Berdel WE, Willich NA, Reers B, Hiddemann W, Grothaus-Pinke B, Reinartz G, Brockmann J, Temmesfeld A, Schmitz R, RĂĽbe C, Probst A, Jaenke G, Bodenstein H, Junker A, Pott C, Schultze J, Heinecke A, Parwaresch R, Tiemann M: 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 (18): 3874-83.

    CAS  PubMed  Google Scholar 

  7. 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 (10): 2462-73. 10.1002/cncr.11415.

    Article  PubMed  Google Scholar 

  8. Aviles A, Nambo MJ, Neri N, Talavera A, Cleto S: Mucosa-associated lymphoid tissue (MALT) lymphoma of the stomach: results of a controlled clinical trial. Med Oncol. 2005, 22 (1): 57-62. 10.1385/MO:22:1:057.

    Article  PubMed  Google Scholar 

  9. Popescu RA, Wotherspoon AC, Cunningham D, Norman A, Prendiville J, Hill ME: Surgery plus chemotherapy or chemotherapy alone for primary intermediate- and high-grade gastric non-Hodgkin's lymphoma: the Royal Marsden Hospital experience. Eur J Cancer. 1999, 35 (6): 928-34. 10.1016/S0959-8049(99)00069-6.

    Article  CAS  PubMed  Google Scholar 

  10. Gobbi PG, Ghirardelli ML, Cavalli C, Baldini L, Broglia C, Clo V, Bertè R, Ilariucci F, Carotenuto M, Piccinini L, Stelitano C, Attardo-Parrinello G, Ascari E: The role of surgery in the treatment of gastrointestinal lymphomas other than low-grade MALT lymphomas. Haematologica. 2000, 85 (4): 372-80.

    CAS  PubMed  Google Scholar 

  11. Binn M, Ruskone-Fourmestraux A, Lepage E, Haioun C, Delmer A, Aegerter P, Lavergne A, Guettier C, Delchier JC: Surgical resection plus chemotherapy versus chemotherapy alone: comparison of two strategies to treat diffuse large B-cell gastric lymphoma. Ann Oncol. 2003, 14 (12): 1751-7. 10.1093/annonc/mdg495.

    Article  CAS  PubMed  Google Scholar 

  12. Cogliatti SB, Schmid U, Schumacher U, Eckert F, Hansmann ML, Hedderich J, Takahashi H, Lennert K: Primary B-cell gastric lymphoma: a clinicopathological study of 145 patients. Gastroenterology. 1991, 101 (5): 1159-70.

    CAS  PubMed  Google Scholar 

  13. Seifert E, Schulte F, Stolte M: Long-term results of treatment of malignant non-Hodgkin's lymphoma of the stomach. Z Gastroenterol. 1992, 30 (8): 505-8.

    CAS  PubMed  Google Scholar 

  14. Montalban C, Castrillo JM, Abraira V, Serrano M, Bellas C, Piris MA: Gastric B-cell mucosa-associated lymphoid tissue (MALT) lymphoma. Clinicopathological study and evaluation of the prognostic factors in 143 patients. Ann Oncol. 1995, 6 (4): 355-62.

    CAS  PubMed  Google Scholar 

  15. Pasini F, Ambrosetti A, Sabbioni R, Todeschini G, Santo A, Meneghini V, Perona G, Cetto GL: Postoperative chemotherapy increases the disease-free survival rate in primary gastric lymphomas stage IE and IIE. Eur J Cancer. 1994, 30A (1): 33-6.

    Article  CAS  PubMed  Google Scholar 

  16. Bartlett DL, Karpeh MS, Filippa DA, Brennan MF: Long-term follow-up after curative surgery for early gastric lymphoma. Ann Surg. 1996, 223 (1): 53-62. 10.1097/00000658-199601000-00008.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  17. National Comprehensive Cancer Network. http://www.nccn.org/professionals/physician_gls/PDF/nhl.pdf

  18. Zucca E, Cavalli F: Gut lymphomas. Baillieres Clin Haematol. 1996, 9 (4): 727-41. 10.1016/S0950-3536(96)80051-5.

    Article  CAS  PubMed  Google Scholar 

  19. Yoon SS, Coit DG, Portlock CS, Karpeh MS: The diminishing role of surgery in the treatment of gastric lymphoma. Ann Surg. 2004, 240 (1): 28-37. 10.1097/01.sla.0000129356.81281.0c.

    Article  PubMed Central  PubMed  Google Scholar 

  20. Kodera Y, Yamamura Y, Nakamura S, Shimizu Y, Torii A, Hirai T, Yasui K, Morimoto T, Kato T, Kito T: The role of radical gastrectomy with systematic lymphadenectomy for the diagnosis and treatment of primary gastric lymphoma. Ann Surg. 1998, 227 (1): 45-50. 10.1097/00000658-199801000-00007.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  21. Day D, Jass J, Price A, Shepherd N, JM S: Non-epithelial tumours of the stomach. 2003, Malden (USA): Blackwell Publishing Inc.

    Chapter  Google Scholar 

  22. Aviles A, Nambo MJ, Neri N, Huerta-Guzman J, Cuadra I, Alvarado I, Castañeda C, Fernández R, González M: The role of surgery in primary gastric lymphoma: results of a controlled clinical trial. Ann Surg. 2004, 240 (1): 44-50. 10.1097/01.sla.0000129354.31318.f1.

    Article  PubMed Central  PubMed  Google Scholar 

  23. Al-Refaie W, Abdalla E, Ahmad S, Mansfield P: Gastric cancer. 2006, Houston (USA) Lippincott Williams & Wilkins

    Google Scholar 

  24. Mercer DW, Robinson EK, editors: Gastric neoplasia. 2007, Philadelphia

    Google Scholar 

  25. Friedberg J, Mauch P, Rimsza L, Fisher R, editors: 2008, Non-Hodgkin's Lymphomas: Lippincott Williams & Wilkins

    Google Scholar 

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Correspondence to Roberto Cirocchi.

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* All authors contributed equally to this work and approved the final manuscript.

Roberto Cirocchi, Eriberto Farinella, Stefano Trastulli, Davide Cavaliere, Piero Covarelli, Chiara Listorti, Jacopo Desiderio, Francesco Barberini, Nicola Avenia, Antonio Rulli, Giorgio Maria Verdecchia, Giuseppe Noya and Carlo Boselli contributed equally to this work.

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Cirocchi, R., Farinella, E., Trastulli, S. et al. Surgical treatment of primitive gastro-intestinal lymphomas: a systematic review. World J Surg Onc 9, 145 (2011). https://doi.org/10.1186/1477-7819-9-145

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