Single-Institution Experience in the Treatment of Primary Mediastinal B Cell Lymphoma Treated With Immunochemotherapy in the Setting of Response Assessment by 18Fluorodeoxyglucose Positron Emission Tomography
Creators
- Pinnix, Chelsea C.1
- Dabaja, Bouthaina1
- Ahmed, Mohamed Amin2
- Chuang, Hubert H.3
- Costelloe, Colleen4
- Wogan, Christine F.1
- Reed, Valerie1
- Romaguera, Jorge E.2
- Neelapu, Sattva2
- Oki, Yasuhiro2
- Rodriguez, M. Alma5, 2
- Fayad, Luis2
- Hagemeister, Frederick B.2
- Nastoupil, Loretta2
- Turturro, Francesco2
- Fowler, Nathan2
- Fanale, Michelle A.2
- Nieto, Yago6
- Khouri, Issa F.6
- Ahmed, Sairah6
- and others
- 1. Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas (United States)
- 2. Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, Texas (United States)
- 3. Department of Nuclear Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas (United States)
- 4. Department of Diagnostic Radiology, The University of Texas MD Anderson Cancer Center, Houston, Texas (United States)
- 5. Office of Medical Affairs, The University of Texas MD Anderson Cancer Center, Houston, Texas (United States)
- 6. Department of Stem Cell Transplantation, The University of Texas MD Anderson Cancer Center, Houston, Texas (United States)
Description
Purpose: Excellent outcomes obtained after infusional dose-adjusted etoposide, doxorubicin, cyclophosphamide, vincristine, prednisone, and rituximab (R-EPOCH) alone have led some to question the role of consolidative radiation therapy (RT) in the treatment of primary mediastinal B cell lymphoma (PMBL). We reviewed the outcomes in patients treated with 1 of 3 rituximab-containing regimens (cyclophosphamide, doxorubicin, vincristine, prednisone [R-CHOP]; hyperfractionated cyclophosphamide, vincristine, doxorubicin and dexamethasone [R-HCVAD], or R-EPOCH) with or without RT. We also evaluated the ability of positron emission tomography–computed tomography (PET-CT) to identify patients at risk of relapse. Methods and Materials: We retrospectively identified 97 patients with diagnoses of stage I/II PMBCL treated at our institution between 2001 and 2013. The clinical characteristics, treatment outcomes, and toxicity were assessed. We analyzed whether postchemotherapy PET-CT could identify patients at risk for progressive disease according to a 5 point scale (5PS) Deauville score assigned. Results: Among 97 patients (median follow-up time, 57 months), the 5-year overall survival rate was 99%. Of patients treated with R-CHOP, 99% received RT; R-HCVAD, 82%; and R-EPOCH, 36%. Of 68 patients with evaluable end-of-chemotherapy PET-CT scans, 62% had a positive scan (avidity above that of the mediastinal blood pool [Deauville 5PS = 3]), but only 9 patients experienced relapse (n=1) or progressive disease (n=8), all with a 5PS of 4 to 5. Of the 25 patients who received R-EPOCH, 4 experienced progression, all with 5PS of 4 to 5; salvage therapy (RT and autologous stem cell transplantation) was successful in all cases. Conclusion: Combined modality immunochemotherapy and RT is well tolerated and effective for treatment of PMBCL. A postchemotherapy 5PS of 4 to 5, rather than 3 to 5, can identify patients at high risk of progression who should be considered for therapy beyond chemotherapy alone after R-EPOCH
Availability note (English)
Available from http://dx.doi.org/10.1016/j.ijrobp.2015.02.006Additional details
Identifiers
- DOI
- 10.1016/j.ijrobp.2015.02.006;
- PII
- S0360-3016(15)00168-6;
Publishing Information
- Journal Title
- International Journal of Radiation Oncology, Biology and Physics
- Journal Volume
- 92
- Journal Issue
- 1
- Journal Page Range
- p. 113-121
- ISSN
- 0360-3016
- CODEN
- IOBPD3
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 47028277
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- BLOOD; CHEMOTHERAPY; DEXAMETHASONE; DIAGNOSIS; DOXORUBICIN; ENDOXAN; HAZARDS; LYMPHOMAS; PATIENTS; POSITRON COMPUTED TOMOGRAPHY; PREDNISONE; RADIATION DOSES; RADIOTHERAPY; REVIEWS; STEM CELLS; TOXICITY
- Descriptors DEC
- ADRENAL HORMONES; ALKYLATING AGENTS; ANIMAL CELLS; ANTIBIOTICS; ANTI-INFECTIVE AGENTS; ANTINEOPLASTIC DRUGS; BIOLOGICAL MATERIALS; BODY FLUIDS; COMPUTERIZED TOMOGRAPHY; CORTICOSTEROIDS; DIAGNOSTIC TECHNIQUES; DISEASES; DOCUMENT TYPES; DOSES; DRUGS; EMISSION COMPUTED TOMOGRAPHY; GLUCOCORTICOIDS; HORMONES; HYDROXY COMPOUNDS; IMMUNE SYSTEM DISEASES; IMMUNOSUPPRESSIVE DRUGS; KETONES; MATERIALS; MEDICINE; NEOPLASMS; NUCLEAR MEDICINE; ORGANIC COMPOUNDS; PREGNANES; RADIOLOGY; SOMATIC CELLS; STEROID HORMONES; STEROIDS; THERAPY; TOMOGRAPHY
Optional Information
- Copyright
- Copyright (c) 2015 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.