ACR Appropriateness Criteria®
Clinical Condition: Staging Evaluation for Patients with Hodgkin's Disease
Variant 1: Child with biopsy-proven CS IIA NSHD presenting with neck nodes and mediastinal disease on chest radiograph.
Radiologic Exam Procedure |
Appropriateness Rating |
Comments |
Computed Tomography |
Chest |
9 |
|
Abdomen |
9 |
|
Pelvis |
9 |
|
Nuclear Medicine |
PET scan |
8 |
|
Gallium scan |
4 |
Only if PET not available |
Bone scan |
2 |
|
Magnetic Resonance Imaging |
Chest |
2 |
|
Abdomen |
2 |
|
Laboratory Tests |
CBC with differential |
9 |
|
Liver function study |
9 |
|
Erythrocyte sedimentation rate |
8 |
|
Serum albumin |
8 |
|
Beta 2 microglobulin |
2 |
|
Soluble CD30 |
2 |
|
Bone marrow biopsy |
4 |
Indicated if platelet, WBC, or RBC counts are below normal. |
Appropriateness Criteria Scale
1 2 3 4 5 6 7 8 9
1 = Least appropriate 9 = Most appropriate
|
Note: Abbreviations used in the tables are listed at the end of the "Major Recommendations" field.
Variant 2: Young adult, male, with biopsy-proven CS IIIB NSHD with bulky mediastinal disease on chest radiograph and three para-aortic nodes on abdominal pelvic CT scan, located between L2-L4, measuring 1-1.5 cm.
Radiologic Exam Procedure |
Appropriateness Rating |
Comments |
Chest CT |
9 |
|
Bone marrow biopsy |
9 |
|
Nuclear Medicine |
PET scan |
8 |
|
Gallium scan |
4 |
Only if PET not available |
Bone scan |
2 |
|
Magnetic Resonance Imaging |
Chest |
2 |
|
Abdomen |
2 |
|
Laboratory Tests |
CBC with differential |
9 |
|
Liver function study |
9 |
|
Erythrocyte sedimentation rate |
8 |
|
Serum albumin |
8 |
|
Soluble CD30 |
4 |
|
Beta 2 microglobulin |
2 |
|
Appropriateness Criteria Scale
1 2 3 4 5 6 7 8 9
1 = Least appropriate 9 = Most appropriate
|
Note: Abbreviations used in the tables are listed at the end of the "Major Recommendations" field.
Variant 3: Young adult, male, with bulky mediastinal disease on chest radiograph, biopsy-proven CS 1A NSHD.
Radiologic Exam Procedure |
Appropriateness Rating |
Comments |
Computed Tomography |
Chest |
9 |
|
Abdomen |
9 |
|
Pelvis |
9 |
|
Nuclear Medicine |
PET scan |
8 |
|
Gallium scan |
4 |
Only if PET not available |
Bone scan |
2 |
|
Magnetic Resonance Imaging |
Chest |
2 |
|
Abdomen |
2 |
|
Laboratory Tests |
CBC with differential |
9 |
|
Liver function study |
8 |
|
Erythrocyte sedimentation rate |
8 |
|
Serum albumin |
8 |
|
Beta 2 microglobulin |
2 |
|
Soluble CD30 |
2 |
|
Bone marrow biopsy |
2 |
Indicated if platelet, WBC, or RBC counts are below normal. |
Appropriateness Criteria Scale
1 2 3 4 5 6 7 8 9
1 = Least appropriate 9 = Most appropriate
|
Note: Abbreviations used in the tables are listed at the end of the "Major Recommendations" field.
Variant 4: Young adult, male, with biopsy-proven CS 1A LPHD, high neck presentation.
Radiologic Exam Procedure |
Appropriateness Rating |
Comments |
Chest radiograph |
9 |
Chest CT can be performed in lieu of chest radiograph. |
Computed Tomography |
Neck |
9 |
|
Chest |
9 |
|
Abdomen |
9 |
|
Pelvis |
9 |
|
Nuclear Medicine |
PET scan |
8 |
|
Gallium scan |
4 |
Only if PET not available |
Bone scan |
2 |
|
Magnetic Resonance Imaging |
Chest |
2 |
|
Abdomen |
2 |
|
Laboratory Tests |
CBC with differential |
9 |
|
Liver function study |
8 |
|
Erythrocyte sedimentation rate |
8 |
|
Serum albumin |
8 |
|
Beta 2 microglobulin |
2 |
|
Soluble CD30 |
2 |
|
Bone marrow biopsy |
2 |
Indicated if platelet, WBC, or RBC counts are below normal. |
Appropriateness Criteria Scale
1 2 3 4 5 6 7 8 9
1 = Least appropriate 9 = Most appropriate
|
Note: Abbreviations used in the tables are listed at the end of the "Major Recommendations" field.
Variant 5: Young adult, male, with biopsy-proven CS 1A NSHD, axillary presentation.
Radiologic Exam Procedure |
Appropriateness Rating |
Comments |
Chest radiograph |
9 |
Chest CT can be performed in lieu of chest radiograph. |
Computed Tomography |
Chest |
9 |
|
Abdomen |
9 |
|
Pelvis |
9 |
|
Nuclear Medicine |
PET scan |
8 |
|
Gallium scan |
4 |
Only if PET not available |
Bone scan |
2 |
|
Magnetic Resonance Imaging |
Chest |
2 |
|
Abdomen |
2 |
|
Laboratory Tests |
CBC with differential |
9 |
|
Liver function study |
8 |
|
Erythrocyte sedimentation rate |
8 |
|
Serum albumin |
8 |
|
Beta 2 microglobulin |
2 |
|
Soluble CD30 |
2 |
|
Bone marrow biopsy |
2 |
Indicated if platelet, WBC, or RBC counts are below normal. |
Appropriateness Criteria Scale
1 2 3 4 5 6 7 8 9
1 = Least appropriate 9 = Most appropriate
|
Note: Abbreviations used in the tables are listed at the end of the "Major Recommendations" field.
Variant 6: Elderly patient, any gender, with biopsy-proven CS IIIA MCHD, with a left supraclavicular node and single 2-cm retroperitoneal node at L2.
Radiologic Exam Procedure |
Appropriateness Rating |
Comments |
Chest radiograph |
9 |
Chest CT can be performed in lieu of chest radiograph. |
Bone marrow biopsy |
8 |
|
Computed Tomography |
Chest |
9 |
|
Abdomen |
9 |
|
Pelvis |
9 |
|
Nuclear Medicine |
PET scan |
8 |
|
Gallium scan |
4 |
Only if PET not available |
Bone scan |
2 |
|
Magnetic Resonance Imaging |
Chest |
2 |
|
Abdomen |
2 |
|
Laboratory Tests |
CBC with differential |
9 |
|
Liver function study |
9 |
|
Erythrocyte sedimentation rate |
8 |
|
Serum albumin |
8 |
|
Beta 2 microglobulin |
2 |
|
Soluble CD30 |
2 |
|
Appropriateness Criteria Scale
1 2 3 4 5 6 7 8 9
1 = Least appropriate 9 = Most appropriate
|
Note: Abbreviations used in the tables are listed at the end of the "Major Recommendations" field.
Variant 7: Young adult, male, with biopsy-proven CS IIA NSHD, presenting with infradiaphragmatic left inguinal and femoral nodes and a 2-cm left external iliac node on pelvic CT scan.
Radiologic Exam Procedure |
Appropriateness Rating |
Comments |
Chest radiograph |
9 |
Chest CT can be performed in lieu of chest radiograph |
Computed Tomography |
Chest |
9 |
|
Abdomen |
9 |
|
Nuclear Medicine |
PET scan |
8 |
|
Gallium scan |
4 |
Only if PET not available |
Bone scan |
2 |
|
Magnetic Resonance Imaging |
Chest |
2 |
|
Abdomen |
2 |
|
Laboratory Tests |
CBC with differential |
9 |
|
Liver function study |
8 |
|
Erythrocyte sedimentation rate |
8 |
|
Serum albumin |
8 |
|
Beta 2 microglobulin |
2 |
|
Soluble CD30 |
2 |
|
Bone marrow biopsy |
2 |
Indicated if platelet, WBC, or RBC counts are below normal. |
Appropriateness Criteria Scale
1 2 3 4 5 6 7 8 9
1 = Least appropriate 9 = Most appropriate
|
Note: Abbreviations used in the tables are listed at the end of the "Major Recommendations" field.
Variant 8: Child, female, with biopsy-proven CS IIA MCHD presenting with left supraclavicular adenopathy and a non-bulky mediastinal mass on chest radiograph.
Radiologic Exam Procedure |
Appropriateness Rating |
Comments |
Computed Tomography |
Chest |
9 |
|
Abdomen |
9 |
|
Pelvis |
9 |
|
Nuclear Medicine |
PET scan |
8 |
|
Gallium scan |
4 |
Only if PET not available |
Bone scan |
2 |
|
Magnetic Resonance Imaging |
Chest |
2 |
|
Abdomen |
2 |
|
Laboratory Tests |
CBC with differential |
9 |
|
Liver function study |
9 |
|
Erythrocyte sedimentation rate |
8 |
|
Serum albumin |
8 |
|
Beta 2 microglobulin |
2 |
|
Soluble CD30 |
2 |
|
Bone marrow biopsy |
2 |
Indicated if platelet, WBC, or RBC counts are below normal. |
Appropriateness Criteria Scale
1 2 3 4 5 6 7 8 9
1 = Least appropriate 9 = Most appropriate
|
Note: Abbreviations used in the tables are listed at the end of the "Major Recommendations" field.
Variant 9: Young adult, male, with initial supradiaphragmatic PS IIA NSHD has an apparent pelvic nodal relapse following subtotal lymphoid irradiation.
Radiologic Exam Procedure |
Appropriateness Rating |
Comments |
Repeat biopsy |
9 |
|
Chest radiograph |
9 |
Chest CT can be performed in lieu of chest radiograph |
Bone marrow biopsy |
8 |
|
Computed Tomography |
Chest |
9 |
|
Abdomen |
9 |
|
Pelvis |
9 |
|
Nuclear Medicine |
PET scan |
8 |
|
Gallium scan |
4 |
Only if PET not available |
Bone scan |
2 |
|
Magnetic Resonance Imaging |
Chest |
2 |
|
Abdomen |
2 |
|
Laboratory Tests |
CBC with differential |
9 |
|
Liver function study |
9 |
|
Erythrocyte sedimentation rate |
8 |
|
Serum albumin |
2 |
No data for relapsed patients. |
Beta 2 microglobulin |
2 |
|
Soluble CD30 |
2 |
|
Appropriateness Criteria Scale
1 2 3 4 5 6 7 8 9
1 = Least appropriate 9 = Most appropriate
|
Note: Abbreviations used in the tables are listed at the end of the "Major Recommendations" field.
Variant 10: Young adult, male, with initial PS IIIA NSHD treated with ABVD chemotherapy alone, now with an apparent neck recurrence.
Radiologic Exam Procedure |
Appropriateness Rating |
Comments |
Repeat biopsy |
9 |
|
Chest radiograph |
9 |
Chest CT can be performed in lieu of chest radiograph |
Bone marrow biopsy |
8 |
|
Computed Tomography |
Chest |
9 |
|
Abdomen |
9 |
|
Pelvis |
9 |
|
Nuclear Medicine |
PET scan |
8 |
|
Gallium scan |
4 |
Only if PET not available |
Bone scan |
2 |
|
Magnetic Resonance Imaging |
Chest |
2 |
|
Abdomen |
2 |
|
Laboratory Tests |
CBC with differential |
9 |
|
Liver function study |
9 |
|
Erythrocyte sedimentation rate |
8 |
|
Serum albumin |
2 |
No data for relapsed patients. |
Beta 2 microglobulin |
2 |
|
Soluble CD30 |
2 |
|
Appropriateness Criteria Scale
1 2 3 4 5 6 7 8 9
1 = Least appropriate 9 = Most appropriate
|
Note: Abbreviations used in the tables are listed at the end of the "Major Recommendations" field.
In Hodgkin's disease, the purpose of staging is to define the anatomic extent of detectable disease. This provides prognostic information and can serve as the basis of rational treatment decisions.
The Ann Arbor staging system and subsequent proposed modifications include a designation based on clinical stage and pathological stage. Clinical stage is based on the results of the initial diagnostic biopsy, physical exam, laboratory data, and imaging studies. Pathological stage is based on the results of any additional biopsies, including bone marrow biopsy, percutaneous or laparoscopic biopsy of nodes, liver, and splenectomy.
Clinical Staging
History and Physical Examination
Clinical evaluation should include an initial history and physical examination to assess for signs and symptoms of Hodgkin's disease. Particular attention should be given to the presence of documented "B" symptoms since this represents an important prognostic factor with therapeutic implications. A clinical history of bone pain or cardiovascular/pulmonary complaints may direct further evaluation.
Laboratory Studies
Baseline laboratory evaluation should include a complete blood count with a differential, liver function studies, and an erythrocyte sedimentation rate (ESR).
One study has demonstrated that patients who present with abnormal blood counts, elevated alkaline phosphatase or lactate dehydrogenase levels, or an elevated ESR are at higher risk for involvement of bone marrow. Another study has also demonstrated that an elevated ESR may be associated with a higher risk for abdominal involvement.
The International Prognostic Factors Project on Advanced Hodgkin's Disease identified a seven-factor prognostic scoring system that could predict five-year rates of freedom from progression of disease. The prognostic score, which also was predictive of overall survival, included a serum albumin level of less than 4 grams per deciliter, a hemoglobin level less than 10.5 grams per deciliter, male gender, age 45 years or older, stage IV disease, leukocytosis (white cell count of at least 15,000 per cubic millimeter), and a lymphocyte count of less than 600 per cubic millimeter or a count less than 8% of the white cell count, or both.
Other markers such as elevated serum copper, zinc, and soluble CD30 levels have been noted to correlate with disease activity but are currently not part of the standard evaluation of the patient with Hodgkin's disease.
Imaging Studies
Plain Chest Radiograph
Posterior-anterior (PA) and lateral chest radiographs are required in all patients because intrathoracic presentation of disease is common.
Mediastinal adenopathy can be quantified by several methods. One such method involves measuring the maximum width of the mediastinal mass divided by the maximal transverse thoracic diameter at the level of the diaphragm (i.e., mediastinal mass ratio) on a standing PA chest radiograph. A second method involves taking the ratio of the greater transverse tumor diameter to the internal thoracic diameter at the level of the T5-T6 interspace. Patients with large mediastinal adenopathy, which has been defined as either a mediastinal mass ratio greater than one-third, a mass greater than 35% of the thoracic diameter at T5-T6, or a mass measuring more than 5-10 cm in width, are at increased risk for relapse when treated with radiation therapy alone.
Computed Tomography
Contrast-enhanced CT should be performed of the chest, abdomen, and pelvis in all patients.
Thoracic CT scans can result in upstaging of the patient by demonstrating abnormalities not appreciated on routine chest radiographs. Demonstration of intrathoracic abnormalities may also result in alteration of treatment fields or clinical management. Adenopathy in the mediastinal, hilar, subcarinal, and internal mammary areas may be detected with a thoracic CT scan, which can influence radiation treatment planning. Detection of extensive pericardial involvement or pulmonary parenchymal involvement can occasionally be demonstrated on chest CT scans and may alter the treatment plan.
CT scans of the abdomen have the ability to assess the upper abdominal nodes, the liver, and the spleen.
A CT of the neck may be helpful, especially in the situation where limited radiation therapy (involved field) is planned and the precise localization of enlarged lymph nodes in the neck will affect design of the radiation fields.
Magnetic Resonance Imaging
Magnetic resonance imaging (MRI) may be an alternative to chest or abdominal CT scanning for initial evaluation of the patient.
MRI has been evaluated as an initial staging tool compared with CT scan in a prospective study. Employing laparotomy to define pathologic extent of abdominal disease, investigators demonstrated that MRI was more sensitive but less specific than CT with similar accuracy rates.
Another study investigated the role of MRI in the initial staging of Hodgkin's disease and found this procedure to be a useful adjunct for staging thoracic disease and assessing the spleen. MRI has been used in evaluating the bone marrow to identify areas of abnormality for biopsy. Due to its low sensitivity (55.6%) and its low positive predictive value (38.5%), it is not a substitute for bone marrow biopsy in appropriate patients.
Some investigators have found MRI to be of benefit in restaging patients following definitive treatment to help differentiate fibrosis from tumor.
Nuclear Medicine Studies
Several imaging agents have been investigated in staging Hodgkin's disease, including gallium-67, fluorodeoxyglucose (FDG), technetium 99m, somatostatin, and thallium. They are utilized in the initial staging of Hodgkin's disease and in patients at risk for relapse who have residual radiographic abnormalities during or after completion of therapy.
Investigators looking at the role of gallium in the initial staging of Hodgkin's disease have observed a sensitivity of 64-80% and a specificity of 96%-98%. One study compared gallium scans to CT evaluation, physical exam, and lymphangiography. The authors concluded that initial staging with gallium scans was of no benefit in the majority of patients with Hodgkin's disease. Another study demonstrated a negative predictive value of 28% in a series of patients who were staged with laparotomy. Other investigators noted a low sensitivity of gallium scans in evaluating initial disease sites but found them to be of value in distinguishing fibrosis from Hodgkin's disease following treatment in the setting of residual radiographic abnormalities.
PET imaging has been used in the initial staging of Hodgkin's disease. One study reported on the pretreatment evaluation of 44 newly diagnosed patients with Hodgkin's disease using FDG-PET scans. As a consequence of PET imaging, five patients were upstaged and one patient was downstaged. PET scans were reported false positive in two patients and failed to visualize Hodgkin's disease in four patients. Another study retrospectively analyzed 44 patients staged with PET imaging and CT scans. One hundred and fifty nine sites of disease were demonstrated on PET imaging compared to 84 sites on CT. Eighteen patients (40.9%) were upstaged, nine with extranodal or splenic sites not identified on CT imaging.
Several studies have suggested that PET imaging is superior to gallium imaging in staging of Hodgkin's disease. One of these studies reported FDG-PET had a superior ability to clinically detect splenic disease compared with gallium imaging. PET scans demonstrated suspected disease below the diaphragm in three of five patients having FDG uptake in isolated splenic nodules that were not detected by gallium imaging. Another study compared PET imaging with conventional imaging methods in staging patients with Hodgkin's disease. The investigators reported an accuracy rate of 96% for PET versus 56% for conventional imaging.
Post treatment nuclear scintigraphy may help predict clinical outcome. Several authors have noted a significant difference in survival or an increased risk or relapse in patients who have a positive post treatment restaging gallium study. However, conversion of an initially positive study to a negative study following treatment does not rule out a subsequent relapse, particularly in the setting of stage III or IV disease.
Several investigators have demonstrated a potential role for PET imaging in conjunction with CT evaluation in the assessment of patients with residual masses following treatment. One study evaluated post treatment residual masses with PET imaging in patients with Hodgkin's disease and non-Hodgkin's lymphoma. Of 43 patients with Hodgkin's disease, no recurrences were noted in 39 patients with a negative PET scan; however, one of four patients with a positive scan relapsed. Another study compared PET to conventional CT imaging in the post treatment setting in patients with lymphoma (19 patients with Hodgkin's disease). They reported an increased relapse rate in patients with a positive post-treatment PET scan. Other investigators have recently reported similar results.
Pathological Staging
Bone Marrow Biopsy
In retrospective studies, the incidence of bone marrow involvement is low, approaching 5%. Bone marrow biopsy should be performed on patients with an abnormal complete blood count, "B" symptoms, advanced clinical stage, elevated alkaline phosphatase, or symptoms of bone pain.
Results from the German Hodgkin's Lymphoma Study Group demonstrate that the probability of bone marrow involvement increases with evidence of subdiaphragmatic disease (massive splenic involvement), more than one site of lymphatic involvement, the presence of "B" symptoms, and advanced clinical stage before bone marrow biopsy. Independent parameters when predicted for bone marrow involvement based on a logistic regression analysis included "B" symptoms (p<.00005); thrombocytopenia (p<.00005); large mediastinal tumor (p<.00005); stage before bone marrow biopsy (p=.00014); lactate dehydrogenase (LDH) level (p=.0004); and hemoglobin level (p=.0088).
Restaging
Following treatment for bulky mediastinal presentation of Hodgkin's disease, approximately 60% of patients will demonstrate residual adenopathy on a chest radiograph.
To avoid invasive restaging procedures, gallium scans and MRI have been used to ascertain whether a residual abnormality on chest radiograph represents fibrosis or viable tumor, with mixed results. Most investigators have found some predictive value; however, a significant number of false-negative and false-positive results have rendered these tests far from ideal. PET imaging may be more sensitive than gallium imaging in the restaging of patients with Hodgkin's disease. A negative result of these studies should not change further follow-up because subsequent relapse can occur. However, a positive result may suggest the need for additional tests, including biopsy if the implication of treatment failure is institution of additional therapy. Immunoscintigraphy and biological markers have also been used in an experimental setting to assess the question of persistent disease.
Conclusion
Staging procedures will continue to evolve as we develop new technological advances and our understanding of this disease process increases. New therapeutic approaches to this disease may also impact on our diagnostic evaluation of the patient.
Abbreviations
- ABVD, chemotherapy consisting of doxorubicin, bleomycin, vinblastine, and dacarbazine
- CBC, complete blood count
- CS, clinical stage
- CT, computed tomography
- LPHD, lymphocyte predominant Hodgkin's disease
- MCHD, mixed cellularity Hodgkin's disease
- NSHD, nodular sclerosis Hodgkin's disease
- PET, positron emission tomography
- PS, pathologic stage
- RBC, red blood cell
- WBC, white blood cell