Chemotherapy Based on Positron Emission Tomography Scan in Treating Patients With Stage I or Stage II Hodgkin Lymphoma



Status:Completed
Conditions:Lymphoma
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - 60
Updated:1/26/2018
Start Date:May 2010
End Date:January 2018

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Phase II Trial of Response-Adapted Chemotherapy Based on Positron Emission Tomography for Non-Bulky Stage I and II Hodgkin Lymphoma

This phase II trial studies how well chemotherapy based on positron emission tomography (PET)
scan works in treating patients with stage I or stage II Hodgkin lymphoma. Drugs used in
chemotherapy work in different ways to stop the growth of cancer cells, either by killing the
cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy)
may kill more cancer cells. Radiation therapy uses high energy x-rays to kill cancer cells.
Giving combination chemotherapy together with radiation therapy may kill more cancer cells
and allow doctors to save the part of the body where the cancer started. Comparing results of
diagnostic procedures, such as PET scan, done before, during, and after chemotherapy may help
doctors predict a patient's response to treatment and help plan the best treatment.

PRIMARY OBJECTIVES:

I. To determine the progression-free survival (PFS) from enrollment for patients with
non-bulky stage I and II Hodgkin lymphoma.

II. To compare the PFS of patients who are PET positive versus PET negative following 2
cycles of doxorubicin hydrochloride, bleomycin, vinblastine, and dacarbazine (ABVD).

SECONDARY OBJECTIVES:

I. To evaluate the complete response (CR) rate of patients diagnosed with non-bulky stage I
and II Hodgkin lymphoma following PET response-adapted chemotherapy with or without radiation
therapy.

II. To determine the predictive value of fludeoxyglucose (FDG) uptake using various
semi-quantitative approaches, at baseline, after 2 cycles of AVBD and at completion of
therapy.

III. To determine the predictive value of volumetric changes on computed tomography (CT) vs
2-dimensional (2-D) analyses after 2 cycles and 4 cycles and compare with PET parameters with
and without combination analyses (PET + dedicated CT data).

IV. To compare the predictive value of metabolic parameters/changes that are measured both
visually and semi-quantitatively, International Harmonization Project (IHP) criteria, 2-D and
volumetric CT changes, molecular parameters, and conventional parameters, including
International Prognostic Score (IPS).

V. To assess whether elevated baseline circulating markers of inflammation (including soluble
cluster of differentiation CD30 [sCD]30, soluble CD 163 [CD163], interleukin-10 (IL10),
chemokine (C-C motif) ligand 17 (CCL17), and chemokine (C-C motif) ligand 22 [CCL22])
correlate with clinical response and PFS and PET scan results.

VI. To assess whether persistent or recurrent elevated serial circulating markers of
inflammation (including soluble CD30 [sCD30], soluble CD163 [sCD163], IL10, CCL17, or CCL22)
correlate with relapse/progression or PET scan results.

VII. To confirm independently useful tissue biomarkers for risk stratification in patients
with non-bulky stage I and II Hodgkin lymphoma treated with this regimen.

VIII. To compare mediastinal bulk on standing posterior-anterior (PA) and lateral chest x-ray
(> 0.33 maximum chest diameter) with chest CT (mass > 10 cm).

OUTLINE:

ABVD CHEMOTHERAPY: Patients receive doxorubicin hydrochloride intravenously (IV) over 3-5
minutes, bleomycin sulfate IV over 3-5 minutes, vinblastine IV over 3-5 minutes, and
dacarbazine IV over 30 minutes on days 1 and 15. Treatment repeats every 28 days for 2
courses. Patients then undergo PET scan. Patients achieving complete response (CR), partial
response (PR), or stable disease (SD) with a negative PET scan receive 2 additional courses
of ABVD chemotherapy in the absence of disease progression or unacceptable toxicity. Patients
achieving CR, PR, or SD with a positive PET scan proceed to escalated BEACOPP chemotherapy.

ESCALATED BEACOPP* CHEMOTHERAPY: Patients receive doxorubicin hydrochloride IV over 3-5
minutes and cyclophosphamide IV over 60 minutes on day 1, etoposide IV over 45-60 minutes on
days 1-3, procarbazine orally (PO) on days 1-7, prednisone PO on days 1-14, and bleomycin
sulfate IV and vincristine IV on day 8. Treatment repeats every 21 days for 2 courses in the
absence of disease progression or unacceptable toxicity. Within 4-6 weeks after completion of
BEACOPP chemotherapy, patients undergo involved-field radiotherapy (IFRT) 5 days a week for
3½ weeks.

NOTE: * HIV-positive patients receive standard BEACOPP instead of escalated BEACOPP.

Patients undergo fludeoxyglucose F^18 PET/CT scan at baseline, and within 8-10 days after
completion of chemotherapy. Patients also undergo additional PET/CT scans within 3-4 weeks
after completion of ABVD or within 12 weeks after completion of BEACOPP and IFRT. Patients
with a negative PET scan proceed to follow up. Patients with a positive PET scan undergo
biopsy**. Patients with a negative biopsy proceed to follow up, and patients with a positive
biopsy are treated at the discretion of the investigator.

NOTE: ** Patients for whom biopsy is neither clinically appropriate nor medically feasible
proceed to follow-up. Patients for whom biopsy is neither clinically indicated nor medically
appropriate undergo a repeat PET/CT scan after 3 months. If PET/CT scan remains positive,
patients undergo biopsy as above.

After completion of study therapy, patients are followed up every 3 months for 1 year, every
6 months for 2-3 years, and then annually for a maximum of 5 years.

DISEASE CHARACTERISTICS:

- Histologically confirmed* Hodgkin lymphoma

- Clinical stage IA, IB, IIA, or IIB disease according to the modified Ann Arbor
Staging Classification system

- Subclassified according to the WHO modification of the Rye Classification

- "E" extension allowed provided all other criteria have been met NOTE: *Pathology
materials must be submitted within 60 days of study registration. Core-needle
biopsies are acceptable provided they contain adequate tissue for primary
diagnosis and immunophenotyping. Fine-needle aspirates not allowed. If multiple
specimens are available, submit the most recent.

- No nodular lymphocyte-predominant Hodgkin lymphoma

- No mediastinal mass > 0.33 maximum intrathoracic diameter by standing postero-anterior
chest x-ray or peripheral or retroperitoneal adenopathy > 10 cm in its largest
diameter

- Measurable disease by physical examination or imaging studies

- Any tumor mass measurable in two dimensions and > 1 cm (or 1.5 cm if 0.5 cm
slices are used, as in spiral CT scans) allowed

- Lesions that are considered intrinsically non-measurable include:

- Bone lesions

- Leptomeningeal disease

- Ascites

- Pleural/pericardial effusion

- Lymphangitis cutis/pulmonis

- Abdominal masses that are not confirmed and followed by imaging techniques

- Cystic lesions

- Lesions that are situated in a previously irradiated area

PATIENT CHARACTERISTICS:

- Performance status 0-2

- ANC ≥ 1,000/μL

- Platelet count ≥ 100,000/μL

- Serum creatinine ≤ 2 mg/dL

- Bilirubin ≤ 2 mg/dL

- AST ≤ 2 times upper limit of normal

- LVEF normal by ECHO or MUGA

- DLCO ≥ 60% with no symptomatic pulmonary disease

- Not pregnant or nursing

- Negative pregnancy test

- Fertile patients must use effective contraception

- Patients with known HIV allowed provided they have CD4 counts ≥ 350/mcL

- Patients must not have multi-drug resistant HIV infections (i.e., concurrent
AIDS-defining conditions)

- An HIV test is required for patients with a history of IV drug abuse or any
behavior associated with an increased risk of HIVinfection

- No "currently active" second malignancy other than nonmelanoma skin cancers

- Patients are not considered to have a "currently active" malignancy provided they
have completed therapy and are considered by their physician to be at < 30% risk
of relapse

PRIOR CONCURRENT THERAPY:

- See Disease Characteristics

- No prior chemotherapy or radiotherapy for Hodgkin lymphoma

- 1 course of ABVD (doxorubicin, bleomycin, vinblastine, and dacarbazine) allowed
and will be considered the first course
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