A multi-institutional and case-matched control study on treatment outcomes of consolidative radiotherapy after a full course of R-CHOP compared with R-CHOP alone in Stage I-II diffuse large B-cell lymphoma (KROG 17-02)
Creators
- 1. Department of Radiation Oncology, Kyung Hee University Hospital at Gangdong, College of Medicine, Kyung Hee University, Seoul (Korea, Republic of)
- 2. Department of Radiation Oncology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul (Korea, Republic of)
- 3. Department of Radiation Oncology, Seoul National University Bundang Hospital, Seongnam (Korea, Republic of)
- 4. Department of Radiation Oncology, Dongsan Medical Center, Keimyung University School of Medicine, Daegu (Korea, Republic of)
- 5. Department of Radiation Oncology, Inha University Hospital, Inha University of Medicine, Inchon (Korea, Republic of)
- 6. Department of Radiation Oncology, St Vincent's Hospital, College of Medicine, The Catholic University of Korea, 442-723, 93-6, Ji-dong, Paldal-gu, Suwon, Kyeonggi-do, Republic of (Korea, Republic of)
Description
We compared treatment outcomes between rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) chemotherapy alone with R-CHOP followed by consolidative radiation therapy (RT) in diffuse large B-cell lymphoma (DLBCL). We analyzed 404 patients with Stage I-II DLBCL who received six to eight cycles of R-CHOP and achieved a good response after a full course of chemotherapy. Propensity-score matching was used to assess the role of consolidative RT. The R-CHOP alone group (n = 184) was matched in a 1:2 ratio with the R-CHOP plus RT group (n = 92). Twenty-four (13.0%) of 184 patients receiving R-CHOP alone and 8 (8.7%) of 92 patients receiving R-CHOP plus RT had bulky diseases (>7.5 cm). A Deauville score of 1-2 was achieved for 159 (86.4%) of 184 patients receiving R-CHOP alone and 84 (91.3%) of 92 patients receiving R-CHOP plus RT. After a median follow-up time of 42 months, the recurrence-free survival (RFS) rate (86.7% vs 93.0%, P = 0.464) and overall survival rate (88.3% vs 95.1%, P = 0.295) at 5 years did not differ significantly between the R-CHOP alone and R-CHOP plus RT arms. In the additional multivariate analyses, large tumor size (>7.5 cm) was significantly associated with decreased RFS (hazard ratio, 2.368 and confidence interval, 1.837-6.697; P = 0.048). Consolidative radiation was not a significant factor for RFS (P = 0.563). Tumor size was a significant factor for RFS in the rituximab era. The outcome of omitting consolidative RT for good responders after six to eight cycles of R-CHOP chemotherapy was acceptable in early-stage DLBCL without a bulky disease.
Availability note (English)
Available from http://dx.doi.org/10.1093/jrr/rrz043; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6806014Additional details
Identifiers
Publishing Information
- Journal Title
- Journal of Radiation Research
- Journal Volume
- 60
- Journal Issue
- 5
- Journal Page Range
- p. 677-684
- ISSN
- 0449-3060
INIS
- Country of Publication
- Japan
- Country of Input or Organization
- Japan
- INIS RN
- 54118596
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- CHEMOTHERAPY; COMBINED THERAPY; COMPARATIVE EVALUATIONS; DOXORUBICIN; ENDOXAN; FRACTIONATED IRRADIATION; GY RANGE 10-100; IMMUNITY; LYMPHOCYTES; LYMPHOMAS; MULTIVARIATE ANALYSIS; PATIENTS; PREDNISONE; RADIOTHERAPY; SIZE; SURVIVAL CURVES
- Descriptors DEC
- ABSORBED DOSE RANGE; ADRENAL HORMONES; ALKYLATING AGENTS; ANIMAL CELLS; ANTIBIOTICS; ANTI-INFECTIVE AGENTS; ANTINEOPLASTIC DRUGS; BIOLOGICAL MATERIALS; BLOOD; BLOOD CELLS; BODY FLUIDS; CONNECTIVE TISSUE CELLS; CORTICOSTEROIDS; DISEASES; DRUGS; EVALUATION; GLUCOCORTICOIDS; GY RANGE; HORMONES; HYDROXY COMPOUNDS; IMMUNE SYSTEM DISEASES; IMMUNOSUPPRESSIVE DRUGS; IRRADIATION; KETONES; LEUKOCYTES; MATERIALS; MATHEMATICS; MEDICINE; NEOPLASMS; NUCLEAR MEDICINE; ORGANIC COMPOUNDS; PREGNANES; RADIATION DOSE RANGES; RADIOLOGY; SOMATIC CELLS; STATISTICS; STEROID HORMONES; STEROIDS; THERAPY
Optional Information
- Copyright
- Copyright (c) The Author(s) 2019. Published by Oxford University Press on behalf of The Japan Radiation Research Society and Japanese Society for Radiation Oncology.
- Notes
- PMCID: PMC6806014; PMID: 31251343; PMID: 31251343; PUBLISHER-ID: rrz043; OAI: oai:pubmedcentral.nih.gov:6806014