Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021 Sep 2;138(9):785-789.
doi: 10.1182/blood.2020010497.

The bidirectional increased risk of B-cell lymphoma and T-cell lymphoma

Affiliations

The bidirectional increased risk of B-cell lymphoma and T-cell lymphoma

Dai Chihara et al. Blood. .

Abstract

Lymphoma survivors have a significantly higher risk of developing second primary lymphoma than the general population; however, bidirectional risks of developing B- and T-cell lymphomas (BCLs and TCLs) specifically are less well understood. We used population-based cancer registry data to estimate the subtype-specific risks of second primary lymphoma among patients with first BCL (n = 288 478) or TCL (n = 23 747). We observed nearly fivefold increased bidirectional risk between BCL and TCL overall (TCL following BCL: standardized incidence ratio [SIR] = 4.7, 95% confidence interval [CI] = 4.2-5.2; BCL following TCL: SIR = 4.7, 95% CI = 4.1-5.2), but the risk varied substantially by lymphoma subtype. The highest SIRs were observed between Hodgkin lymphoma (HL) and peripheral T-cell lymphoma not otherwise specified (PTCL-NOS) (PTCL-NOS following HL: SIR = 27.5; HL following PTCL-NOS: SIR = 31.6). Strikingly elevated risks also were notable for angioimmunoblastic T-cell lymphoma (AITL) and diffuse large B-cell lymphoma (DLBCL) (AITL following DLBCL: SIR = 9.7; DLBCL following AITL: SIR = 15.3). These increased risks were strongest within the first year following diagnosis but remained persistently elevated even at ≥5 years. In contrast, SIRs were <5 for all associations of TCL with chronic lymphocytic leukemia/small lymphocytic lymphoma and follicular lymphoma. These patterns support etiologic heterogeneity among lymphoma subtypes and provide further insights into lymphomagenesis.

PubMed Disclaimer

Figures

None
Graphical abstract
Figure 1.
Figure 1.
SIRs with 95% CIs for the reciprocal associations between BCL and TCL. (A) HL. (B) DLBCL. (C) FL. (D) CLL/SLL. (E) MZL. Numbers shown represent the observed cases of second primary lymphoma. Red diamonds correspond to TCL following BCL, and white diamonds correspond to BCL following TCL. leuk/lymph, leukemia/lymphoma.

References

    1. Morton LM, Curtis RE, Linet MS, et al. . Second malignancy risks after non-Hodgkin’s lymphoma and chronic lymphocytic leukemia: differences by lymphoma subtype. J Clin Oncol. 2010;28(33):4935-4944. - PMC - PubMed
    1. Brennan P, Scélo G, Hemminki K, et al. . Second primary cancers among 109 000 cases of non-Hodgkin’s lymphoma. Br J Cancer. 2005;93(1):159-166. - PMC - PubMed
    1. Dores GM, Metayer C, Curtis RE, et al. . Second malignant neoplasms among long-term survivors of Hodgkin’s disease: a population-based evaluation over 25 years. J Clin Oncol. 2002;20(16):3484-3494. - PubMed
    1. Goyal A, O’Leary D, Goyal K, et al. . Increased risk of second primary hematologic and solid malignancies in patients with mycosis fungoides: a surveillance, epidemiology, and end results analysis. J Am Acad Dermatol. 2020;83(2):404-411. - PMC - PubMed
    1. Huang KP, Weinstock MA, Clarke CA, McMillan A, Hoppe RT, Kim YH. Second lymphomas and other malignant neoplasms in patients with mycosis fungoides and Sezary syndrome: evidence from population-based and clinical cohorts. Arch Dermatol. 2007;143(1):45-50. - PubMed

Publication types