A case of Hodgkin’s lymphoma with severely impaired liver function treated successfully with gemcitabine followed by ABVD

Abstract

Hodgkin’s lymphoma (HL) originates from clonal B cells and is the most common malignancy in the second decade of life. Liver involvement is uncommon at presentation in patients with HL and there is a paucity of data for treatment of patients with severely impaired liver function. We present an unusual case of HL with severe hepatic impairment, splenomegaly and multiple chromosomal abnormalities that was treated initially with gemcitabine and steroids. Once liver function tests improved, six cycles of Adriamycin, bleomycin, vinblastine, and dacarbazine were administered. The patient remains in remission at 3.5 years of follow-up.

Keywords:

• hepatomegaly
• cytogenetics
• remission

Case report

A 27-year-old Hispanic man was admitted to the Queens Hospital Center because of cough, weakness, night sweats, and weight loss.

The patient was well until 1 month before admission when he started having weakness, coughing, and sweats. He had traveled to Puerto Rico 1 month prior to admission. On return to the United States he saw a physician for the above symptoms and was prescribed azithromycin for 5 days. However, the symptoms progressively worsened over weeks and at presentation also included drenching night sweats and dizziness. His coworkers noted him to be paler. On interview, he was noted to have lost 25 pounds over 4 to 6 weeks. He denied any fever, chills, and rigors. He had fatigue, and felt early satiety due to pressure in the left upper quadrant of abdomen. He denied any travel to the countryside, significant outdoor activities, hiking or spelunking. He also denied any bright red blood per rectum, melena, myalgia, arthralgia, hematuria or dark colored urine.

The patient had no prior medical or surgical history. He denied taking any medications. He was a non-smoker, drank socially, and did not take any illicit or recreational drugs. His father was recently diagnosed with multiple myeloma and his mother had diabetes mellitus.

On physical examination, the patient was alert and oriented. The blood pressure was 119/76 mmHg, the temperature 100.0°F, the pulse 119/min with regular rhythm, the respiratory rate 16/min with oxygen saturation 100% on ambient air. The patient had pale conjunctiva, icteric sclera, non-tender left supraclavicular and cervical lymphadenopathy, hepatomegaly with palpable liver edge 2–3 cm below right costal margin and splenomegaly.

On hospital day (HD) 1, his complete blood count showed white blood cell count 3,100/mcL, hemoglobin 6.6 g/dL, hematocrit 20% and platelets 76,000/mcL. Liver function tests (LFTs) were abnormal with alkaline phosphatase of 611 u/L, aspartate aminotransferase (AST) of 42 u/L, gamma glutamyl transpeptidase (GGT) of 68 u/L, lactate dehydrogenase (LDH) of 581 u/L, total bilirubin of 2.67 mg/dL and conjugated bilirubin of 1.25 mg/dL. Anemia workup revealed a reticulocyte count of 1,231/μL with reticulocytes 5.53% (0.5%–1.5%), iron 60 μg/dL (60–160 μg/dL), total iron binding capacity (TIBC) of 213 μg/dL (250–460 μg/dL), ferritin of 3,128 ng/mL (15–200 ng/mL), vitamin B12 level of 1,387 pg/mL (200–900 pg/mL) and serum folate 11.25 ng/mL (2.5–20 ng/mL).

Initial review of a peripheral blood smear showed thrombocytopenia with occasional large platelets, poikilocytosis, polychromasia, decreased white blood cells without toxic granulation and no schistocytes. Tests for hemolysis, including direct anti-globulin test and haptoglobin level, were negative on HD 2.

A computed tomography (CT) scan of chest, abdomen, and pelvis done on HD 1 revealed enlarged lymph nodes in the mediastinum, retroperitoneum and splenomegaly and hepatomegaly.

A workup for infectious etiologies was performed as summarized in Table 1. Testing for human immunodeficiency virus was negative. A bone marrow biopsy was performed on HD 4. A lymph node biopsy was requested, given pancytopenia and concurrent lymphadenopathy and performed on HD 6.

Table 1 Laboratory data (infectious and autoimmune workup)

Variable	Reference range	Value	Interpretation	Day
Hepatitis B surface Ab		Reactive	Positive	1
Hepatitis B surface Ag		Non-reactive	Negative	1
Hepatitis B core Ab		Non-reactive	Negative	1
Hepatitis C Ab		Non-reactive	Negative	1
CMV Ab (IgM)	<0.91	0.39	Negative	2
EBV capsid Ab IgG	<0.91	1.41	Positive	2
EBV capsid Ab IgM	<0.91	0.00	Negative	2
EBNA Ab IgG	<0.91	4.10	Positive	2
CMV Ab (IgG)	<0.9	1.12	Positive	2
Parvovirus B19 Ab (IgG)	<0.9	4.1	Positive	2
Parvovirus B19 Ab (IgM)	<0.9	0.3	Negative	2
Mono heterophile Ab		Negative	Negative	2
Haptoglobin	16–200 mg/dL	203	Elevated	2
Urine histoplasma Ag			Negative	6
Serum histoplasma Ab			Negative	6
JAK 2 mutation			Negative	8
HIV-1 RNA, quantitative	<48 copies/mL	<48 copies/mL	Negative	11
Dengue IgG Ab	<0.9	0.23	Negative	12
Dengue IgM Ab	<0.9	0.24	Negative	12
Syphilis IgG		Negative	Negative	12
ANA		Negative	Negative	21
Anti-SM Ab	<1:20	1:80	Positive	21
Anti-mitochondrial Ab		Negative	Negative	21
CMV DNA quantitative	<200 copies/mL	<200 copies/mL	Negative	25

Abbreviations: ANA, anti-nuclear antibody; Anti-SM, anti-smith antibody; CMV, cytomegalovirus; EBNA, Epstein–Barr nuclear antigen; EBV, Epstein–Barr virus.

Initial diagnostic results

The bone marrow biopsy showed a markedly hypercellular marrow (90%–100%) with erythroid hyperplasia, left shifted granulocytic series, and increased megakaryocytes with atypical and dysplastic forms, suggesting a myelodysplastic or myeloproliferative disorder. The bone marrow aspirate smears showed occasional abnormal mononuclear cells, likely vacuolated lymphoid precursors and mature myeloid and erythroid lines with no evidence of blasts. The findings were later interpreted as an unusual reaction to Hodgkin’s lymphoma (HL).

Cytogenetic analysis of a bone marrow specimen revealed tetraploidy, aneuploidy, and multiple abnormalities including XXY, add(2)(p25), add(5)(p15)×2, add(6)(q27), add(10)(q23), add(13)(p11), add(14), del(10)(q22,q23), +5, +8 and +9.

Patient outcome and initial hospital course

The patient was initially treated with supportive transfusions while a diagnosis was being established. The liver enzymes including total and direct bilirubin worsened while awaiting results from the biopsies. Total bilirubin reached 9.22 mg/dL by HD 14 (Table 2).

Table 2 Laboratory data

Variable	Reference range	Hospital Day (D)
		D 1	D 10	D 12	D 20	D 30	D 33	2 months	6 months	2 years
Hemoglobin (g/dL)	13.5–17.5	6.6	9.3	8.6	8.7	9.4	8.9	13	14.4	15.7
Hematocrit (%)	41–53	20	26.9	25.1	25.3	27.3	25.8	38.2	43.1	46.5
White cell count (k/mm^3)	4.5–11	3.1	1.7	1.6	1.9	3.5	3.4	4.1	2.9	8.2
Neutrophils (%)	40–70	58.3	60.1	63	72.2	70.1	59.6	48.9	21.4	69.7
Lymphocytes (%)	22.2–43.6	19.9	19.7	19.5	17.8	25.7	36.8	47.7	63.7	22.7
Monocytes (%)	2–11	21.2	19.9	17.5	9.8	3.7	3.2	1.5	13.3	5.6
Eosinophils (%)	0–7.5	0.4	0.5	0.0	0.1	0.2	0.3	0.2	1.6	0.3
Basophils (%)	0–2	0.2	0.1	0.0	0.1	0.3	0.1	1.7	0	1.7
Platelets (k/mm^3)	130–400	76	57	38	41	10	52	223	247	175
Alkaline phosphatase (u/L)	30–115	611	546	666	821	597	597	107	77	74
Aspartate aminotransferase (u/L)	5–40	42	75	107	106	34	34	27	30	22
Alanine aminotransferase (u/L)	5–50	28	37	60	190	125	125	42	41	25
Gamma glutamyl transpeptidase (u/L)	3–40	68	126	128	253	178	178	122	122	27
Lactate dehydrogenase (u/L)	90–225	581	510	553	412	125	125	149	126	141
Albumin (g/dL)	3.5–5	2.2	1.7	1.5	1.5	2.7	2.7	4.2	4.4	4.4
Total bilirubin (mg/dL)	0–1.5	2.67	2.62	5.39	9.22	2.39	2.39	1.02	0.66	0.63
Conjugated bilirubin (mg/dL)	0–0.3	1.25	1.51	3.64	5.76	1.05	1.05	0.20	0.05	0.15
Serum creatinine (mg/dL)	0.4–1.6	0.9	0.8	0.8	0.8	0.5	0.5	0.5	0.8	0.9

A workup for causes of increased LFTs had been initiated on HD 1. A magnetic resonance cholangiopancreatography did not show any intra or extra hepatic biliary obstruction or any clear involvement of the liver by lymphoma, but it identified multiple hypodensities in the spleen. A hepatobiliary iminodiacetic acid scan showed marked hepatomegaly with smooth contour, but no evidence of focal defects.

Drug-induced hepatitis was considered as the patient had been on fluconazole and acetaminophen during the course of his hospital stay. LFTs showed a predominantly obstructive pattern initially and the serum acetaminophen level at presentation was less than 10 μg/mL. Workup was done to rule out autoimmune disorders (Table 1).

Prednisone was started on HD 14 in an attempt to stop further decline in LFTs. Despite steroids, his total bilirubin on HD 20 had increased up to 9.22 mg/dL with conjugated bilirubin of 5.76 mg/dL.

Lymph node biopsy

A left cervical lymph node biopsy revealed mixed cellularity classical HL with multiple Reed Sternberg and Hodgkin cells with immunohistochemical expression of PAX5, CD30 and CD15, background CD3 positive T cells and CD 20-positive residual follicles. The patient clinically appeared to have stage IVB mixed cellularity classical HL.

Definitive treatment and follow-up

Due to elevated LFTs, major dose reductions or omission of most chemotherapeutic agents would be needed. Gemcitabine was considered because of its ability to be used even with hepatic impairment and its effectiveness as a salvage regimen. Gemcitabine was administered at a dose of 600 mg/m². Intravenous methylprednisone was started along with gemcitabine. After first dose of gemcitabine with methylprednisone, total bilirubin, conjugated bilirubin and alkaline phosphatase levels decreased. Ten days after gemcitabine, conjugated bilirubin was 2.73mg/dL. Patient developed thrombocytopenia with a nadir of 10,000/mL and was supported with platelet transfusions.

Thirteen days after the administration of gemcitabine, LFTs were still abnormal but improved sufficiently that dose reduced Adriamycin, bleomycin, vinblastine, and dac-arbazine (ABVD) could be administered. He subsequently completed six cycles of ABVD.

A follow-up bone marrow biopsy was done after completing six cycles of ABVD, which showed 70% cellularity with trilineage hematopoiesis, all three cell lines proceeding to maturity and no cytogenetic evidence of an abnormal clone. A repeat CT scan of the chest, abdomen, and pelvis showed decrease in the size of mediastinal, left supraclavicular, abdominal, and pelvic lymph nodes. A follow-up whole body positron emission tomography/CT scan showed no evidence of fluorodeoxy (FDG) avid tumor and decreased splenomegaly.

Discussion

HL originates from clonotypic B cells.¹ The standard regimens used in the USA at the time the patient presented were ABVD, Stanford V Regimen and, less commonly, dose escalated BEACOPP (bleomycin, etoposide, Adriamycin, cyclophosphamide, vincristine, procarbazine, prednisone). Older regimens such as MOPP (mechlorethamine, vincristine, procarbazine, prednisone) are less effective than ABVD.^2,3 There is a paucity of data and published case reports for treatment of patients with HL and severely impaired liver function as this patient presented. Case reports have been published using chemotherapy agents for patients with HL presenting with high bilirubin levels.^4–6

Many of the active agents used in treatment for HL require extensive dose reduction for severe liver impairment (Table 3). Liver involvement is uncommon at presentation in patients with HL, and is exceptionally rare in the absence of splenic involvement.^7,8 The hepatic involvement could range from hepatic infiltration by lymphoma to biliary obstruction by lymph node masses or infiltration of the common bile duct.^9–11 The LFTs in our case revealed a cholestatic picture with high alkaline phosphatase and conjugated hyperbilirubinemia.

Table 3 Manufacturer recommended dose reduction of chemotherapeutic agents used in Hodgkin’s lymphoma

Drug	Moderate hepatic impairment	Severe hepatic impairment	Renal impairment
Doxorubicin	50% dose reduction for bilirubin 1.2–3.0 mg/dL^Citation1	75% dose reduction for bilirubin 3.1–5.0 mg/dL^Citation1	No dose adjustment needed
Bleomycin	No dose adjustment needed	No dose adjustment needed	CrCl 40 to 50 mL/min (70% dose); CrCl 30 to 40 mL/min (60% dose); CrCl 20 to 30 mL/min (55% dose); CrCl 10 to 20 (45% dose); CrCl 5 to 10 mL/min (40% dose)^Citation2
Vinblastine	No dose adjustment needed	50% dose reduction for direct bilirubin greater than 3 mg/dL^Citation3	No dose adjustment needed
Dacarbazine	Precaution recommended	Precaution recommended	Precaution recommended
Mechlorethamine	No dose adjustment needed	No dose adjustment needed	No dose adjustment needed
Vincristine	No dose adjustment needed	50% dose reduction if direct serum bilirubin greater than 3 mg/dL^Citation4	No dose adjustment needed
Procarbazine	No dose adjustment needed	No dose adjustment needed	No dose adjustment needed
Etoposide	Dose reduction by 50% for bilirubin 1.5–3.0 mg/dL^Citation5	Not recommended for bilirubin greater than 3.0 mg/dL^Citation5	25% dose reduction recommended for CrCl 15–50 mL/min
Methylprednisolone	No dose adjustment needed	No dose adjustment needed	No dose adjustment needed
Cytarabine	Dose may need to be reduced, exact data not available	Dose may need to be reduced, exact data not available	Dose may need to be reduced, increased neurotoxicity associated with CrCl less than 60 mL/min
Cisplatin	Data not available	Data not available	Repeat courses not recommended until serum creatinine less than 1.5 mg/dL and/or BUN is less than 25 mg/dL^Citation6
Cyclophosphamide	No dose adjustment needed	No dose adjustment needed	No dose adjustment needed

Abbreviations: BUN, blood urea nitrogen; CrCl, creatinine clearance rate.

Vanishing bile duct syndrome as a cause of jaundice has also been reported to be associated with HL.^4,12,13 In one case report, bilirubin level normalized after two cycles of MOPP, one cycle of reduced dose P(V)AG (prednisone, vinblastine was excluded due to potential neurotoxicity, doxorubicin and gemcitabine) followed by six cycles of full dose P(V) AG from 5.4 to 0.15 mg/dL.⁴ However, the treatment course in that case was complicated with prolonged fever, pancytopenia, severe peripheral polyneuropathy and toxic interstitial pneumonitis, requiring intensive care after receiving two cycles of MOPP. A case report of successful use of DHAP (full-dose dexamethasone, high-dose cytarabine, and cisplatin) in a patient with stage IV nodular sclerosis classical HL with severe hepatic dysfunction resulted in significant improvement in the hepatic function after the administration of DHAP regimen as evidenced by the normalization of serum bilirubin from 6.5 mg/dL to 1.2 mg/dL.⁵

Gemcitabine has been shown to be effective as a salvage regimen in patients with refractory HL with a response rate of 39% with mild drug related toxicities.¹⁴ Currently, three gemcitabine based regimens, GVD (gemcitabine, vinorelbine and pegylated liposomal doxorubicin),¹⁵ GDP (gemcitabine, dexamethasone and cisplatin),¹⁶ and GCD(R) (gemcitabine, carboplatin, dexamethasone, rituximab)¹⁷ have been evaluated for use in relapsed and/or refractory HL. A retrospective study has shown that gemcitabine combined with vinorelbine or cisplatinum and steroid is an effective treatment option with a manageable toxicity profile in patients with post-transplant progression of HL and in patients eligible for allogeneic or second autologous stem cell transplantation as a pre-transplant option.¹⁸ Manufacturer drug package insert and Phase I pharmacokinetic trials of gemcitabine in patients with hepatic or renal dysfunction have demonstrated that dose adjustments are not necessary for elevated transaminases nor elevated bilirubin and creatinine levels.^19,20

Finally, chromosomal abnormalities in HL have not been well studied to characterize a coherent cytogenetic picture.²¹ Recent studies have designated some common chromosomal aberrations including gains of short arm of chromosome 2 involving REL oncogene locus^1,22 and chromosomal breakpoints involving immunoglobulin loci.²³ Frequent occurrence of abnormalities involving 1p, 1q and 6q chromosomal arms was shown in a case series.²¹ The cytogenetic studies in our case were not typical for HL except 6q involvement and the clinical significance of these chromosomal findings and its disappearance in complete remission still remains to be elucidated.

In summary, we present an unusual case of HL with severe hepatic impairment, splenomegaly and multiple chromosomal abnormalities, which was treated successfully with gemcitabine and steroids to initially improve LFTs, such that six cycles of ABVD could be given. The patient remains in remission at 3.5 years after his initial diagnosis.

Disclosure

The authors report no conflicts of interest in this work.