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Schenkein et al. 189<br />

Toxicity<br />

Toxic effects occurred in 10 patients receiving IFRT after HDS chemotherapy<br />

<strong>and</strong> PBSCT. Grade 3 toxicity occurred in three cases, all of which were<br />

hematologic. These patients experienced a significant break in the course of their<br />

radiation treatments (14-15 days) due to myelosuppression <strong>and</strong> required<br />

transfusions <strong>and</strong> hematologic growth factors. There were no grade 4 or 5 toxicities.<br />

Esophagitis was the most common form of toxicity recorded; however, all cases<br />

were minor, grade 1 symptoms.<br />

DISCUSSION<br />

The International Non-Hodgkin's Lymphoma Prognostic Factors Project 18<br />

identified four risk groups based on prognostic factors. The age-adjusted index<br />

used advanced tumor stage, LDH level, <strong>and</strong> performance status to model the four<br />

risk groups. The present study identified <strong>and</strong> treated newly diagnosed NHL patients<br />

with two or three risk factors.<br />

Several studies that incorporate high-dose therapy as part of initial therapy or in<br />

first CR/PR have been reported with both positive <strong>and</strong> negative results. No trial has<br />

directly compared early vs. late autotransplant, although the Parma trial clearly<br />

demonstrates the utility of this modality in first chemosensitive relapse.<br />

We have confirmed the extremely positive results reported by Gianni with a<br />

high OS <strong>and</strong> RFS at extended follow-up for a cohort of high-risk untreated NHL<br />

patients. We have also examined the role of involved-field x-ray therapy in this<br />

patient population. Our preliminary results indicate that the addition of IFRT is<br />

well tolerated in this group of patients with high-risk, newly diagnosed NHL.<br />

While the small patient numbers limit the statistical power of this analysis, there<br />

was nonetheless a strong trend toward improved RFS with the use of involved-field<br />

radiation therapy. Additional studies, including the ongoing ECOG trial of CHOP<br />

vs. HDS <strong>and</strong> initial PBPC <strong>transplantation</strong>, are needed to address the controversy of<br />

early vs. late <strong>transplantation</strong>.<br />

REFERENCES<br />

l.Shipp MA, Klatt MM, Yeap B, et al.: Patterns of relapse in large cell lymphoma patients<br />

with bulk disease: Implications for the use of adjuvant radiation therapy. J Clin Oncol<br />

7:613-618,1989.<br />

2.Schenkein D, Roitman D, Miller K, et al.: A phase II multicenter trial of high-dose sequen­<br />

tial chemotherapy <strong>and</strong> peripheral <strong>blood</strong> stem cell <strong>transplantation</strong> as initial therapy for<br />

patients with high-risk non-Hodgkin's lymphoma. Biol Blood Marrow Transplant<br />

3:210-216,1997.

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