Intravascular lymphomas

The gene, chromosome, and gene expression abnormalities in IVBCL have not been fully evaluated. Studies to date indicate that the malignant cells in this disease have mutations in their MYD88 (44% of cases) and CD79B (26% of cases) genes.[5] The exact mutation seen in the MYD88 (i.e. L265P)[10] and some or the mutations in CD79B[11] occur in diverse types of lymphoma. Other abnormalities seen in the small numbers of cases that have been studied so far include translocations between chromosome 14 and 18; tandem triplications of both the BCL2 gene located on the long arm of chromosome 18 at position q21 and the KMT2A gene located on the long arm of chromosome 11 between positions 22 and 25.[5] The product protein of BCL2 viz., Bcl-2, regulates cell survival and apoptosis (i.e. programmed cell death) and the product protein of KMT2a viz., MLL regulates cell maturation. Abnormalities in BCL2[12] and KMT2A[13] are associated with other types of B-cell lymphomas. It seems likely that these or other gene, chromosome, and/or gene expression abnormalities contribute to the development and/or progression of IVBCL.

The malignant B-cells in IVBCL fail to express the CD29 protein while the endothelial cells in close proximity to the intravascular accumulations of the malignant B-cells fail to express key CXC chemokine receptor proteins particularly CxcL12 but also Cxcr5, Ccr6, and/or Ccr7. The failure of the endothelial cells to express these receptor proteins may be due to the action of nearby malignant B-cells. In any event, all of the cited proteins are involved in the movement of B-cells from the intravascular space across the vascular endothelium and into tissues. The lack of these proteins may explain the accumulation of the malignant B-cells of IVLBC within blood vessels.[5]

In about 80% of cases, the malignant B-cells in IVBCL are "non-germinal center B-cells" as defined by the Hans algorithm[14] rather than the "germinal center B-cells" that are commonly found in less aggressive B-cell lymphomas. This factor may contribute to the aggressiveness of IVBCL.[5]

Individuals presenting with the classical variant of IVLBL are typically middle-aged or elderly (39–90 years) that have one or more of the following: systemic symptoms, particularly fever (45% of cases);[5] cutaneous lesions (40%); central nervous system disorders (35%);[2] and clinical and laboratory abnormalities involving the bone marrow (~18%), lung (~6%), and, rarely, endocrine glands (e.g. pituitary, thyroid, adrenal gland[2]), liver, prostate, uterus, eye, intestine, and in individual cases almost any other organ or tissue.[15] These findings are based primarily on studies of 740 patients conducted in Europe; a study conducted in Quebec, Canada on 29 patients gave similar results.[15] Individuals may present with one, two, or more of these abnormalities. Systemic symptoms include not only the most commonly seen one viz., fever, but also malaise, weight loss, and other B symptoms; the cutaneous lesions include singular or multiple plaques, nodules, tumors, and ulcerations, some of which may be painful and most of which are located on the breast, lower abdomen, and/or extremities. Central nervous system defects include sensory and/or motor neuropathy, spinal nerve root pain, paresthesia, hypoesthesia, aphasia, dysarthria, hemiparesis, seizures, myoclonus, transient visual loss, vertigo, altered conscious states, and, particularly in relapsed disease, neurolymphomatosis (i.e. direct invasion of one or more nerves in the peripheral nervous system by the malignant B-cells).[5] Laboratory studies generally show non-specific abnormalities: elevated levels of serum lactate dehydrogenase and soluble IL2RA;[16] anemia, decreases in blood platelet levels, and decreases in white blood cell levels in 25%->50% of cases.[7] Circulating malignant B-cells are not found in 90-95% of cases[5] and laboratory evidence of organ injury is found in those cases involving these organs.[7]

The diagnosis of IVBCL is heavily dependent upon obtaining biopsy specimens from involved tissues, particularly the skin but in cases without skin lesions, other apparently involved tissues. Microscopic examination of these tissues typically shows medium-sized to large-sized lymphocytes located within small- to medium-sized blood vessels of the skin, lung, and other tissues or the sinusoids of the liver, bone marrow, and spleen. On occasion, these malignant cells have the appearance of Reed-Sternberg cells. The lesions should show no or very little extension outside of blood vessels. As determined by immunohistochemistry analyses, the intravascular malignant lymphocytes express typical B-cell proteins, particularly CD20, which is found in almost all cases, CD79a and Pax5, which are found in most cases,[5] and MUM1 and Bcl-2, which are found in 95% and 91% of cases, respectively.[2] These B-cells are usually (80% of cases) non-germinal center B-cells (see Pathophysiology section) and may express one or more of the gene, chromosome, and gene expression abnormalities described in the above Pathophysiology section. Since the classical variant can present with a wide range of clinical signs, symptoms, and organ involvements, its presence may not be apparent, particularly in cases that do not exhibit clinically apparent skin lesions. Accordingly, random skin biopsies have been used to obtain evidence of IVL in cases that have signs and/or symptoms of the disease that are restricted to non-cutaneous sites,[2] even in cases that present with no other finding except unexplained fever.[17] The diagnosis of IVBCL, classical variant is solidified by finding these pathological features in more than one site.[2]

At diagnosis, IVBCL must be regarded as an aggressive and disseminated malignancy requiring systemic chemotherapy. In the absence of long- or short-term, controlled clinical trials on treating this lymphoma, individuals with IVBCL have been treated with the standard regimen used to treat diffuse large B-cell lymphomas viz., the CHOP chemotherapy regimen which consists of cyclophosphamide, hydroxydaunorubicin (also termed doxorubicin or adriamycin), oncovin (also termed vincristine), and a corticosteroid (i.e. either prednisone or prednisolone) plus the monoclonal antibody immunotherapy agent, Rituximab. This immunochemotherapeutic regimen has achieved an overall survival rate at 3 years of 81%; this overall survival rate using CHOP before Retuximab was added to the regimen was only 33%. However, highly toxic reactions to Rituximab such as pulmonary failure may occur and require delay or interrupting the use of this drug. High dose chemotherapy regimens followed by autologous stem-cell transplantation has offered clinical improvement similar to that found with the CHOP plus Rituximabn. However, only a small percentage of patients with IVBCL are young and healthy enough to receive this regimen.[5] Intravenous methotrexate may be a useful addition to the rituximab-CHOP regiment in individuals with central nervous system involvement.[18][19]

The cutaneous variant, which comprises a small percentage of all IVBCL cases, occurs almost exclusively in females and younger individuals (median age 59 years) than the classical variant (median age 72 years).[5] Individuals present with lesions that are exclusively or greatly confined to the skin.[2] The clinical features of these lesions are similar to those described in the section on Presentation of the classical variant. Individuals with the cutaneous variant may have systemic symptoms but this occurs less frequently (30% of cases) than those in the classical variant (45% of cases). In general, cutaneous variant patients are in much better physical shape than those with other forms of IVBCL and have a better long-term prognosis.[5]

The diagnosis of IVL, cutaneous variant depends on finding the pathological picture in the skin as described for the classical variant except that the lesions occur exclusively or predominantly in the skin. Ideally, these pathological findings should be found in more than one skin site.[5] However, cutaneous involvement is frequently detected in a single site such as the hypervascular lesions of cherry hemangiomas and angiolipomas.[20]

Historically, individuals with the cutaneous variant survive significantly longer than that those with the classical variant (3 year overall survival 56% versus 22%). Early intervention in the cutaneous variant would appear to be highly desirable.[5] Virtually all reports on the treatment of the cutaneous variant were made before Rituximab was used to treat IVL. Historically, patients with localized disease obtained prolonged remission with conventional CHOP therapy. However, individuals with single cutaneous lesions were long‐term survivors: when treated with just radiation therapy or surgical removal, these single-lesion patients had prolonged remissions both at initial diagnosis and after relapse. In contrast, patients with multiple lesions had a far worse outcome after treatment with CHOP: they had an objective response in 86% of cases but nonetheless the majority relapsed within a year of treatment with and only a few being successfully managed with salvage chemotherapy.[21] Rituximab may improve the latter situation.

The hemophagocytic syndrome-associated variant of IVBCL is a very rare variant of IVBCL. Its previous name, intravascular large B-cell lymphoma, Asian variant, was recently changed to its current name by the world Health Organization, 2016. Unlike the classical and cutaneous variants, the hemophagocytic syndrome-associated variant presents with the hemophagocytic syndrome. This syndrome is characterized by bone marrow involvement, reduced numbers of circulating blood platelets[5] as well as the reduced levels of other circulating blood cells,[22] and enlarged liver and spleen. Less often, it is also associated with overt hemophagocytosis (i.e. the engulfment by non-malignant histiocytes of red blood cells, white blood cells, platelets, and their precursor cells that is most commonly found in the bone marrow and other tissues.[5] The syndrome often reflects excessive secretion of inflammatory cytokines and severe systemic inflammation similar to that seen in the cytokine storm syndrome.[2] In general, individuals present with a rapidly progressive disease (median time from onset to diagnosis~4 weeks, range 2–12 weeks).[12] Patients are often extremely ill[12] and experience multiple organ failures.[2]

The diagnosis of the intravascular large B-cell lymphoma, hemophagocytic syndrome-associated variant depends on the individual presenting with clinical and laboratory findings compatible with the hemphagocytic syndrome (see previous section) and on the histology of biopsied tissues of the bone marrow, spleen, liver, brain, or other organ that clinical and/or laboratory findings suggest are involved in the disease. Its histology is described in the Diagnosis section of the classical variant but also includes the presence of hemophagocytosis, i.e. the engulfment of red blood cells and/or other mature and immature blood cells.[5] Hemophagocytosis can also be found in sites removed from the intravascular lesions such as the cerebrospinal fluid in patients with central nervous system involvement.[22]

Prior to the use of rituximab, individuals with this variant generally followed a rapidly (i.e. weeks to months) fatal course even when treated with the CHOP regimen. However, addition of rituximab to the CHOP regimen appears to have improved the treatment of this disease. Intravenous methotrexate may be a useful addition to the rituximab-CHOP regiment in individuals with central nervous system involvement.[18][19]

Three studies have examine gene mutations and gene expression abnormalities in IVNK/TL. A retrospective study of 25 patients identified numerous gene abnormalities including tumor-specific splicing alterations in oncogenes and tumor suppressor genes such as HRAS, MDM2, and VEGFA as well as premature termination mutations or copy number losses in a total of 15 splicing-regulator genes such as SF3B5 and TNPO3.[23] A study of two patients with IVNKL identified mutations in genes that produce histone proteins (HIST1H2BE, HIST1H2BN and H3F3A), the histone deacetylase gene, HDAC5, two genes that produce helicase proteins (WRN and DDX3X), two genes that make DNA methylation-related enzymes (TET2 and DNMT1) and a gene in the SWI/SNF family of chromatin remodeling genes, ARID1A.[24] In a third study of a single patient, copy number analysis identified driver gene alterations in ARID1B, HACE1, and SMAD4 genes and gain of the SOX2 gene.[8] While further studies are needed before conclusions can be made, one or more of these gene abnormalities may contribute to the development and/or progression of IVNK/TL.

The malignant NK and T cells that accumulate within the vascular of individuals with IVNK/TL are usually infected with the Epstein–Barr virus (EBV). This suggests that most IVNK/TL cases are examples of the Epstein-Barr virus-associated lymphoproliferative diseases and, like these diseases, are EBV-driven.[8] About 95% of the world's population is infected with EBV. During the initial infection, the virus may cause infectious mononucleosis, only minor non-specific symptoms, or no symptoms. Regardless of this, the virus enters a latency phase and the infected individual becomes a lifetime asymptomatic carrier of EBV. Weeks, months, years, or decades thereafter, a small percentage of these carriers develop an EBV-associated lymphoproliferative disease,[25][26] including in extremely rare cases IVNK/TL.[8] EBV is well known to infect NK- and T-cells, to express some of its genes that promote the survival and proliferation of the cells it infects, and thereby to cause various and far more common NK- and T-cell lymphomas.[27] It seems likely that the virus acts similarly to cause IVNK/TL.[8] IVNK/TL may differ from the other types of NK- and T-cell lymphomas which EBV produces because its NK- and T-cells and nearby endothelial cells have defects in the expression of proteins required for the NK/T-cells to pass through the endothelium and into the surrounding tissues (see above section on the Pathopysiology IVBCL).[28]

Individuals (age range 23–81 years[8]) with IVNK/TL typically have a rapidly progressive disease. They commonly present with skin lesions, less commonly symptoms due to central nervous system involvement, and in a minority of cases symptoms due to the involvement of the bone marrow, liver, kidneys, ovaries, and/or cervix.[1] They often show signs of an disseminated disease such as fever, weight loss, night sweats, arthralgias, jaundice, decreased numbers of circulating red blood cells, white blood cells, and/or platelets, bone marrow involvement as determined by biopsy, and signs/symptoms of multiple organ involvement.[8]

The diagnosis of IVNK/TL depends upon obtaining histology findings in the skin and/or other involved tissue that resembles that seen in IVBCL except that the malignant lymphocytes are not B-cells but rather: 1) NK-cells as evidenced by their expression of NK-cell selective marker proteins (e.g. CD3e, CD2, CD30, CD43, CD56, and/or CD79), expression of granule-bound enzymes (e.g. granzyme B),[8] and expression of EBV proteins (e.g. Epstein–Barr virus latent membrane protein 1[8] and EBV-produced small RNAs[1]); but not the expression of B-cell (e.g. CD20, CD79a, and Pax5) or cytotoxic T cell marker proteins;[8] and 2) cytotoxic T-cell lymphoma as evidenced by the neoplastic cells' expression of T-cell co-receptor proteins (e.g. CD3, CD4, and/or CD8) as well as EBV marker proteins and/or small RNAs but usually not B-cell or NK-cell marker proteins.[9]

Patients with IVNK/TL have been treated with various chemotherapy regimens, particularly CHOP or, less commonly, hyperCVAD. Rare patients have been treated with chemotherapy followed by hematopoietic stem cell transplantation or chemotherapy plus a proteasome inhibitor, bortezomib. In general, patients have responded poorly to treatment, have short (i.e. up to 12 months) survival times regardless of the chemotherapy regimen used.[8][9][29][30] Rituximab does not target NK- or T-cells and therefore is not used to treat IVNK/TL.