Literature DB >> 25341750

Clinical features and outcome of primary pancreatic lymphoma.

Eran Sadot1, Joachim Yahalom, Richard Kinh Gian Do, Julie Teruya-Feldstein, Peter J Allen, Mithat Gönen, Michael I D'Angelica, T Peter Kingham, William R Jarnagin, Ronald P DeMatteo.   

Abstract

INTRODUCTION: Primary pancreatic lymphoma (PPL) is a rare tumor that is often misdiagnosed. Clinicopathologic features, optimal therapy, and outcomes are not well defined. We reviewed our institutional experience with PPL.
METHODS: Search of our institutional database identified that between 1987-2012, 21,760 patients with lymphoma and 11,286 patients with a primary pancreatic tumor were evaluated. There were 44 patients with pathologically confirmed PPL. Clinical data were obtained by chart review and survival distributions were estimated using the Kaplan-Meier method and compared using the log-rank test.
RESULTS: At baseline, LDH was elevated in 55 % of the patients, CA 19-9 in 25 %, and CEA in 20 %. Imaging characteristics included large, unresectable tumors (67 %), and lymphadenopathy inferior to the renal vein (50 %). Twenty-three patients underwent surgery for resection (5), diagnosis (13), or palliation (5). Chemotherapy alone achieved a 75 % complete response rate. Eight patients experienced relapse, 88 % of which occurred at distant sites. Median overall survival was 6.1 years and 10-year disease-specific survival (DSS) was 69 %. Patients with a low risk International Prognostic Index (IPI) and those with a follicular histologic subtype demonstrated 5-year DSS of 100 %.
CONCLUSIONS: Chemotherapy for PPL results in a high complete response rate and long DSS, which is similar to nodal non-Hodgkin's lymphoma (NHL). A favorable outcome is expected for IPI low risk patients and follicular histologic subtype. Systemic therapy should generally be the initial therapy when the diagnosis is known. Prolonged follow up is recommended to detect relapses. Surgery alone should be reserved for non-curative intent (i.e. diagnostic or palliative).

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Year:  2014        PMID: 25341750      PMCID: PMC4574284          DOI: 10.1245/s10434-014-4176-6

Source DB:  PubMed          Journal:  Ann Surg Oncol        ISSN: 1068-9265            Impact factor:   5.344


  30 in total

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3.  Pancreatic adenocarcinoma: putting a hump in survival.

Authors:  Peter J Allen
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4.  Primary pancreatic lymphoma.

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Journal:  Surgery       Date:  1998-04       Impact factor: 3.982

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Authors:  Muhammad Wasif Saif
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7.  Late relapse in patients with diffuse large-cell lymphoma treated with MACOP-B.

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Review 8.  Primary pancreatic lymphoma: diagnostic and therapeutic dilemma.

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Journal:  Pancreas       Date:  2006-08       Impact factor: 3.327

9.  Pancreatic lymphoma: is it a surgical disease?

Authors:  K E Behrns; M G Sarr; J G Strickler
Journal:  Pancreas       Date:  1994-09       Impact factor: 3.327

10.  Primary diffuse large B-cell lymphoma of the breast: prognostic factors and outcomes of a study by the International Extranodal Lymphoma Study Group.

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  8 in total

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Journal:  J Blood Med       Date:  2021-05-05

Review 3.  Pancreatic T/histiocyte-rich large B-cell lymphoma: A case report and review of literature.

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4.  [Epigastralgia revealing primary pancreatic large B-cell lymphoma in a young patient: about a case].

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Review 5.  Primary hepatopancreatobiliary lymphoma: Pathogenesis, diagnosis, and management.

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6.  CT imaging of primary pancreatic lymphoma: experience from three referral centres for pancreatic diseases.

Authors:  Enrico Boninsegna; Giulia A Zamboni; Davide Facchinelli; Charikleia Triantopoulou; Sofia Gourtsoyianni; Maria Chiara Ambrosetti; Dino Veneri; Achille Ambrosetti; Roberto Pozzi Mucelli
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  8 in total

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