Elsevier

Seminars in Oncology

Volume 36, Issue 5, October 2009, Pages 381-418
Seminars in Oncology

Impact of malignant disease on young adults II
Lymphoma in Adolescents and Young Adults

https://doi.org/10.1053/j.seminoncol.2009.07.009Get rights and content

Non-Hodgkin (NHL) and Hodgkin (HL) lymphomas are represented prominently in the adolescent and young adult (AYA) population. These diseases represent 11% of total cancer diagnoses in children, 4% in those 40 years of age and older, and 13% in AYA (aged 15–39 years). Although age-adjusted incidence rates of NHL increase with age, the more aggressive lymphomas are seen more commonly in the younger population with a transition to low-grade, indolent subtypes as the population ages. Burkitt lymphoma, diffuse large B-cell lymphoma, lymphoblastic lymphoma, and anaplastic large cell lymphoma make up the most common subtypes in the AYA population, although within the subgroup age 30–39 years, follicular lymphoma becomes more prominent. As a result, much of the armamentarium in the treatment of aggressive NHL and HL in adults is based on data from pediatric clinical trials. There are obvious limitations to this approach. It is vital that we gain a more thorough understanding of the biology and therapeutic responsiveness of NHL and HL in the AYA population. Thus, we must leverage the large prospective and retrospective trials that have been completed to date and redirect our approaches to cancer care in this unique population. We review the epidemiological data on NHL and HL from the Surveillance, Epidemiology and End Results registries as a cornerstone for a comparative analysis of therapeutic outcomes available in this population.

Section snippets

Epidemiology

As demonstrated in Figure 1, the risk of developing NHL increases with age. Clarke et al reported that, from 1973–1998, the incidence of NHL demonstrated an increase that was dependent on age at diagnosis, sex, and race.5 In our own independent review of the Surveillance, Epidemiology and End Results (SEER) registry, using nine US geographic areas from 1973–2004 (SEER 9), age-adjusted rates of NHL were calculated using the 2000 US standard population and analyzed with SEER*Stat software. From

Epidemiology

HL was first described in 1832, when Thomas Hodgkin presented postmortem findings on a series of patients, all of whom had massive enlargements of lymph nodes and spleen. It is one of the most common tumors in AYA, and represents approximately one third of lymphomas in children.169, 170 Among 15- to 29-year-olds, it accounts for 12% of cancers and is the most common hematologic malignancy. As is evident in Figure 13A, HL has a bimodal distribution, with incidence peaks in the 20- to 24-year age

Conclusion

Many improvements in our understanding of NHL and HL have occurred over the last several decades. Outcome improvements have mirrored our better understanding of the molecular, epidemiological, and genetic aspects of lymphomas. Unfortunately, our awareness of the unique aspects of lymphoma in the AYA age range lags behind our insights in children and older adults. In order to continue our course of improved mortality and morbidity across all age ranges, a comprehensive and coordinated approach

References (239)

  • A. Reiter et al.

    Improved treatment results in childhood B-cell neoplasms with tailored intensification of therapy: a report of the Berlin-Frankfurt-Munster group trial NHL-BFM 90

    Blood

    (1999)
  • C. Patte et al.

    The Societe Francaise d'Oncologie Pediatrique LMB89 protocol: highly effective multiagent chemotherapy tailored to the tumor burden and initial response in 561 unselected children with B-cell lymphomas and L3 leukemia

    Blood

    (2001)
  • C. Patte et al.

    Results of the randomized international FAB/LMB96 trial for intermediate risk B-cell non-Hodgkin lymphoma in children and adolescents: it is possible to reduce treatment for the early responding patients

    Blood

    (2007)
  • K.J. Savage et al.

    The molecular signature of mediastinal large B-cell lymphoma differs from that of other diffuse large B-cell lymphomas and shares features with classical Hodgkin lymphoma

    Blood

    (2003)
  • M.A. Epstein et al.

    Virus particles in cultured lymphoblasts from Burkitt's lymphoma

    Lancet

    (1964)
  • K.A. Blum et al.

    Adult Burkitt leukemia and lymphoma

    Blood

    (2004)
  • N. Wollner

    Non-Hodgkin's lymphoma in children

    Pediatr Clin North Am

    (1976)
  • I.T. Magrath et al.

    An effective therapy for both undifferentiated (including Burkitt's) lymphomas and lymphoblastic lymphomas in children and young adults

    Blood

    (1984)
  • M.S. Cairo et al.

    Results of a randomized international study of high-risk central nervous system B non-Hodgkin lymphoma and B acute lymphoblastic leukemia in children and adolescents

    Blood

    (2007)
  • G.M. Mead et al.

    An international evaluation of CODOX-M and CODOX-M alternating with IVAC in adult Burkitt's lymphoma: results of United Kingdom Lymphoma Group LY06 study

    Ann Oncol

    (2002)
  • R.B. Lorsbach et al.

    Clinicopathologic analysis of follicular lymphoma occurring in children

    Blood

    (2002)
  • G. Ott et al.

    Cytomorphologic, immunohistochemical, and cytogenetic profiles of follicular lymphoma: 2 types of follicular lymphoma grade 3

    Blood

    (2002)
  • C.D. Jennings et al.

    Recent advances in flow cytometry: application to the diagnosis of hematologic malignancy

    Blood

    (1997)
  • J.C. Aster et al.

    Detection of BCL2 rearrangements in follicular lymphoma

    Am J Pathol

    (2002)
  • E. Yang et al.

    Molecular thanatopsis: a discourse on the BCL2 family and cell death

    Blood

    (1996)
  • A. Lopez-Guillermo et al.

    Correlation of bcl-2 rearrangement with clinical characteristics and outcome in indolent follicular lymphoma

    Blood

    (1999)
  • A. Lopez-Guillermo et al.

    The clinical significance of molecular response in indolent follicular lymphomas

    Blood

    (1998)
  • A.L. Shaffer et al.

    BCL-6 represses genes that function in lymphocyte differentiation, inflammation, and cell cycle control

    Immunity

    (2000)
  • P. Solal-Celigny et al.

    Follicular lymphoma international prognostic index

    Blood

    (2004)
  • K.M. Ardeshna et al.

    Long-term effect of a watch and wait policy versus immediate systemic treatment for asymptomatic advanced-stage non-Hodgkin lymphoma: a randomised controlled trial

    Lancet

    (2003)
  • W. Hiddemann et al.

    Frontline therapy with rituximab added to the combination of cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) significantly improves the outcome for patients with advanced-stage follicular lymphoma compared with therapy with CHOP alone: results of a prospective randomized study of the German Low-Grade Lymphoma Study Group

    Blood

    (2005)
  • A. Jemal et al.

    Cancer Statistics, 2009

    CA Cancer J Clin

    (2009)
  • C. Percy et al.
  • C. Percy et al.

    Non-Hodgkin's lymphomasApplication of the International Classification of Diseases for Oncology (ICD-O) to the Working Formulation

    Cancer

    (1984)
  • C.A. Clarke et al.

    Changing incidence of non-Hodgkin lymphomas in the United States

    Cancer

    (2002)
  • The Non-Hodgkin's Lymphoma Classification Project

    Blood

    (1997)
  • R.J. Lukes et al.

    Immunologic characterization of human malignant lymphomas

    Cancer

    (1974)
  • N.L. Harris et al.

    World Health Organization classification of neoplastic diseases of the hematopoietic and lymphoid tissues: report of the Clinical Advisory Committee meeting-Airlie House, Virginia, November 1997

    J Clin Oncol

    (1999)
  • N.L. Harris et al.

    Who Classification of Tumours of Haematopoietic and Lymphoid Tissues. Vol 4

    (2008)
  • P. Zeppa et al.

    Fine-needle cytology and flow cytometry immunophenotyping and subclassification of non-Hodgkin lymphoma: a critical review of 307 cases with technical suggestions

    Cancer

    (2004)
  • S.T. Hehn et al.

    Utility of fine-needle aspiration as a diagnostic technique in lymphoma

    J Clin Oncol

    (2004)
  • E. Ravinsky et al.

    Diagnosis of lymphoma by image-guided needle biopsies: fine needle aspiration biopsy, core biopsy or both?

    Acta Cytol

    (2005)
  • G.B. Slap et al.

    When to perform biopsies of enlarged peripheral lymph nodes in young patients

    JAMA

    (1984)
  • S.B. Murphy et al.

    End results of treating children with localized non-Hodgkin's lymphomas with a combined modality approach of lessened intensity

    J Clin Oncol

    (1983)
  • P.P. Carbone et al.

    Report of the Committee on Hodgkin's Disease Staging Classification

    Cancer Res

    (1971)
  • A predictive model for aggressive non-Hodgkin's lymphomaThe International Non-Hodgkin's Lymphoma Prognostic Factors Project

    N Engl J Med

    (1993)
  • S.B. Murphy

    Classification, staging and end results of treatment of childhood non-Hodgkin's lymphomas: dissimilarities from lymphomas in adults

    Semin Oncol

    (1980)
  • M. O’Leary et al.

    Lymphomas and reticuloendothelial neoplasms

  • J.T. Sandlund et al.

    Non-Hodgkin's lymphoma in childhood

    N Engl J Med

    (1996)
  • H. Stein et al.

    Diffuse large B-cell lymphoma. Vol 4

    (2008)
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