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1 tt's lymphoma, nasopharyngeal carcinoma, and Hodgkin's disease.
2 effective in locally extensive and advanced Hodgkin's disease.
3 tutively activated in the malignant cells of Hodgkin's disease.
4 bulky mediastinal stage I/II or stage III/IV Hodgkin's disease.
5 nge, 2.65 to 29.88 years) after diagnosis of Hodgkin's disease.
6 The risk of breast cancer is increased after Hodgkin's disease.
7 men for children with relapsed or refractory Hodgkin's disease.
8 or effect on risk of second malignancy after Hodgkin's disease.
9 with heavily pretreated relapsed/refractory Hodgkin's disease.
10 tment with doxorubicin, and the diagnosis of Hodgkin's disease.
11 ervical-thoracic CT imaging of patients with Hodgkin's disease.
12 nd pairs in B-cell lymphoid malignancies and Hodgkin's disease.
13 eloid leukemia 17 months after treatment for Hodgkin's disease.
14 malignant neoplasms (SMNs) in children with Hodgkin's disease.
15 t biopsy samples from patients with relapsed Hodgkin's disease.
16 sion in EBV-induced lymphoproliferations and Hodgkin's disease.
17 apy for patients with relapsed or refractory Hodgkin's disease.
18 curring in untreated Reed-Sternberg cells of Hodgkin's disease.
19 ses of T- and null-cell NHL, and 18 cases of Hodgkin's disease.
20 athologically verified stage III or stage IV Hodgkin's disease.
21 31.6 years (mean, 13.1) after treatment for Hodgkin's disease.
22 have value in the treatment of EBV-positive Hodgkin's disease.
23 g cells and their variants from six cases of Hodgkin's disease.
24 year-old white girl diagnosed with stage IIa Hodgkin's disease.
25 ll lymphoma of T-cell lineage, and five with Hodgkin's disease.
26 eveloped AML 16 months from the diagnosis of Hodgkin's disease.
27 patients with nodular lymphocyte-predominant Hodgkin's disease.
28 OS in pediatric patients with advanced-stage Hodgkin's disease.
29 taneous T-cell lymphomas, and 5/38 classical Hodgkin's disease.
30 and autografting in the sustained control of Hodgkin's disease.
31 ells occur in nodular lymphocyte-predominant Hodgkin's disease.
32 5 years, and 12.2 years, respectively, after Hodgkin's disease.
33 developed multiple myeloma 16.5 years after Hodgkin's disease.
34 ted a 41% complete response in patients with Hodgkin's disease.
35 ased CD30+ lymphoproliferative disorders and Hodgkin's disease.
36 me patients with Epstein-Barr virus-positive Hodgkin's disease.
37 aining for CD95 was seen in 9 of 10 cases of Hodgkin's disease.
38 7 B- and 5 T-cell lymphomas, and 10 cases of Hodgkin's disease.
39 tment, age at treatment, sex, and time after Hodgkin's disease.
40 ho were treated with radiation for childhood Hodgkin's disease.
41 factor superfamily and a surface marker for Hodgkin's disease.
42 possible localization of primary extra nodal Hodgkin's disease.
43 ts who had prior mediastinal irradiation for Hodgkin's disease.
44 lymphomas and approximately 40% of cases of Hodgkin's disease.
45 c patients with unfavorable presentations of Hodgkin's disease.
46 been identified as effective treatments for Hodgkin's disease.
47 eive newer, combined modality treatments for Hodgkin's disease.
48 e standard regimen for treatment of advanced Hodgkin's disease.
49 xistence of chronic lymphocytic leukemia and Hodgkin's disease.
50 MOPP/ABV hybrid are effective therapies for Hodgkin's disease.
51 relapse after combined-modality therapy for Hodgkin's disease.
52 d with at least 35 Gy to the mediastinum for Hodgkin's disease.
53 d these regimens as initial chemotherapy for Hodgkin's disease.
54 ked in the first 5 years, predominantly from Hodgkin's disease.
55 monoclonal antibody (mAb)-based therapies of Hodgkin's disease.
56 an association between cigarette smoking and Hodgkin's disease.
57 er were treated for clinical stage IA to IIB Hodgkin's disease.
58 APEC-B in patients with previously untreated Hodgkin's disease.
59 or II) disease or advanced (stage III or IV) Hodgkin's disease.
60 is an important preventable risk factor for Hodgkin's disease.
61 -term follow-up care in patients treated for Hodgkin's disease.
63 ter steroid treatment (T5) in 40 patients (7 Hodgkin's Disease, 13 Acute Myeloblastic Leukemia, 5 Acu
64 s reacted with the BSAP antisera, whereas in Hodgkin's disease, 2 of 4 (50%) nodular lymphocytic pred
65 ll neoplasms, nodular lymphocyte-predominant Hodgkin's disease (7 cases), CD4+ cutaneous T-cell lymph
66 n KS and NHL, only angiosarcoma (36.7-fold), Hodgkin's disease (7.6-fold), multiple myeloma (4.5-fold
67 ific deaths at 25 years were 9.8%+/-1.6% for Hodgkin's disease, 8.1%+/-2.6% for second malignancy, 4.
68 n of a child who had completed treatment for Hodgkin's disease, a PET study strongly suggested recurr
72 lated CD30+ forms of lymphoma, such as CD30+ Hodgkin's disease and CD30+ cutaneous T-cell lymphoma.
74 asis to understand the genes responsible for Hodgkin's disease and develop novel diagnostic markers a
76 in splenectomized patients in remission from Hodgkin's disease and in healthy Afro-Caribbean subjects
80 roved useful in the staging and follow-up of Hodgkin's disease and non-Hodgkin's lymphoma (especially
81 ), and may be helpful to distinguish between Hodgkin's disease and non-Hodgkin's lymphoma in difficul
83 ular adverse effect of radiation exposure in Hodgkin's disease and other types of cancer manifesting
84 on library with TrAb sera from patients with Hodgkin's disease and paraneoplastic cerebellar degenera
85 ly untreated stages III2A, IIIB, IVA, or IVB Hodgkin's disease and patients in first relapse after ra
86 d of therapy is rarely seen in patients with Hodgkin's disease and should be considered a manifestati
87 erature on breast cancer after treatment for Hodgkin's disease and show that high risk is particularl
89 s expressed by vascular endothelial cells in Hodgkin's disease and various solid tumors in mice and h
90 otomy could be safely avoided in early-stage Hodgkin's disease and whether chemotherapy should be a p
92 isorders, including posttransplant lymphoma, Hodgkin's disease, and Burkitt's lymphoma, as well as na
93 e expression in nasopharyngeal carcinoma and Hodgkin's disease, and differs from the full spectrum of
95 of HIV-associated non-Hodgkin's lymphoma and Hodgkin's disease, and include further work on virologic
98 the management of early stage breast cancer, Hodgkin's disease, and to a lesser extent other thoracic
99 erse non-Hodgkin's lymphomas overexpress the Hodgkin's disease antigen CD30 (CD30(hi)), a tumor necro
101 Unusual types of NHL and manifestations of Hodgkin's disease are seen in HIV-infected individuals a
106 age, diagnosis of non-Hodgkin's lymphoma or Hodgkin's disease, bone marrow involvement, prior radiat
107 e marrow transplant (BMT) can cure recurrent Hodgkin's disease, but more than half of patients will p
109 tric patients with stages I and II favorable Hodgkin's disease can be cured with limited therapy that
113 caspase-3 is commonly expressed in classical Hodgkin's disease (CHD); however, the biological signifi
114 ighty-two patients with previously untreated Hodgkin's disease, clinical stages I/II (plus mediastina
115 ogeneity and paucity of "malignant" cells in Hodgkin's disease continue to limit our ability to artic
117 IV and developing non-Hodgkin's lymphoma and Hodgkin's disease continues to improve as insights into
119 ker for Reed-Sternberg cells and variants of Hodgkin's disease (except L&H types), and may be helpful
120 demonstrated that patients with early-stage Hodgkin's disease experience a short-term decrease in QO
122 nal diagnosis of bone tumor, brain tumor, or Hodgkin's disease; female sex; and an income less than $
126 fective treatment strategy for patients with Hodgkin's disease for whom induction chemotherapy fails.
127 , whereas patients with multiple myeloma and Hodgkin's disease had worse outcomes as a result of high
129 ticular, extended follow-up of patients with Hodgkin's disease has revealed an increased risk of brea
130 sfully treated children and adolescents with Hodgkin's disease have a substantial risk for the occurr
132 -AIDS-defining cancers, germ cell tumors and Hodgkin's disease, have been reported in the setting of
133 rative disorders (PTLD); however, reports of Hodgkin's disease (HD) after transplantation are rare.
134 n expression was also studied in 51 cases of Hodgkin's disease (HD) and 17 large B-cell lymphomas (LB
136 large-cell lymphomas (DLCL) and 128 cases of Hodgkin's disease (HD) and discusses the clinical featur
137 homa (BL), post-transplant B cell lymphomas, Hodgkin's disease (HD) and nasopharyngeal carcinoma (NPC
138 y (HDT) with autologous stem cell rescue for Hodgkin's disease (HD) and non-Hodgkin's lymphoma (NHL)
140 patients with a history of presumably cured Hodgkin's disease (HD) and non-Hodgkin's lymphoma (NHL).
141 as documented survival benefits for relapsed Hodgkin's disease (HD) and non-Hodgkin's lymphoma (NHL).
142 carboxy (C)-terminal mutations occurring in Hodgkin's disease (HD) and reactive tissues from two dif
143 men who are exposed to chest irradiation for Hodgkin's disease (HD) are at increased risk of breast c
145 ts Study Group cohort of 1,380 children with Hodgkin's disease (HD) diagnosed between 1955 and 1986 i
147 m 190 patients with histologically confirmed Hodgkin's disease (HD) for the presence of Epstein-Barr
148 the Hodgkin's Reed-Sternberg (H-RS) cells in Hodgkin's disease (HD) had the greatest abundance of hsp
150 non-Hodgkin's lymphoma (NHL) in 48 patients, Hodgkin's disease (HD) in 14 patients, other neoplastic
156 lymphoma with the characteristic features of Hodgkin's disease (HD) occasionally develops in patients
159 ineteen patients with relapsed or refractory Hodgkin's disease (HD) received high-dose therapy follow
162 Cardiovascular status was assessed in 48 Hodgkin's disease (HD) survivors at a median of 14.3 yea
164 in patients with lymphocyte-predominant (LP) Hodgkin's disease (HD) to determine whether these patien
165 CL), other non-Hodgkin's lymphomas (NHL), or Hodgkin's disease (HD) were eligible if their cancer was
166 ield radiotherapy in patients with favorable Hodgkin's disease (HD) who have been laparotomy-staged.
167 heral T cell, 13 with low-grade NHL, 31 with Hodgkin's disease (HD), and 6 with lymphomatoid papulosi
168 nasopharyngeal carcinoma (NPC), a subset of Hodgkin's disease (HD), and in EBV-associated lymphoprol
169 six had lymphoplasmacytic lymphoma, six had Hodgkin's disease (HD), and one each had diffuse large B
171 and Reed-Sternberg (HRS) cells of classical Hodgkin's disease (HD), but its clinical significance re
172 mortality after the successful treatment of Hodgkin's disease (HD), little is known about the molecu
173 dian, 40) with non-Hodgkin's lymphoma (NHL), Hodgkin's disease (HD), multiple myeloma (MM), or acute
174 n 1982 and 1995 were included in this study: Hodgkin's disease (HD), n = 12; intermediate/high-grade
175 -424 of EBNA-4 in 25 cases of EBV-associated Hodgkin's disease (HD), nine cases of AIDS-related non-H
187 with diffuse large B-cell lymphoma (n = 12), Hodgkin's disease (HD; n = 12), multiple myeloma (n = 2)
188 y disease is effective in bulky and advanced Hodgkin's disease in a multi-institutional setting.
189 s of this study show that, in advanced-stage Hodgkin's disease in children, equivalent results can be
191 o cure acute childhood leukemia and advanced Hodgkin's disease in the 1960s and early 1970s overcame
193 rd therapy for children and adolescents with Hodgkin's disease includes combination chemotherapy and
195 ednisone (NOVP) combination chemotherapy for Hodgkin's disease increases the frequencies of the speci
197 tra nodal and extra lymphatic propagation of Hodgkin's disease is a characteristic of the fourth stag
199 alone in selected patients with early-stage Hodgkin's disease is associated with disease control rat
200 urate disease status in patients treated for Hodgkin's disease is discussed, along with recommendatio
201 tion for patients with early-stage/favorable Hodgkin's disease is highly effective and without demons
203 major consequence of successful treatment of Hodgkin's disease is the development of second malignant
206 ransplant-related mortality rates decline in Hodgkin's disease, it is predicted that cure rates and l
209 elated cancers, elevated SIRs were found for Hodgkin's disease (male, 8.0; female, 6.4; heterosexuall
210 lso present in the cytoplasmic domain of the Hodgkin's disease marker, CD30, and binds TRAF3 in vitro
211 C promoter or Cp) in Burkitt's lymphoma and Hodgkin's disease may play an important role in the path
213 ts, alternative malignancies were diagnosed (Hodgkin's disease; metastatic neuroendocrine carcinoma;
215 S leads to a significantly increased risk of Hodgkin's disease, multiple myeloma, brain cancer, and s
216 of follow-up, 71 fatal events resulted from Hodgkin's disease (n=36), second malignancies (n=14), in
217 nfection including posttransplant lymphomas, Hodgkin's disease, nasopharyngeal carcinoma, and AIDS-re
218 methylated and silent in Burkitt's lymphoma, Hodgkin's disease, nasopharyngeal carcinoma, and nasal l
219 and B strains contrasts with EBV-associated Hodgkin's disease, nasopharyngeal carcinoma, and post-tr
220 apy and low-dose radiotherapy in early stage Hodgkin's disease need our attention in rigorously desig
221 d be generated ex vivo from 13 patients with Hodgkin's disease: nine with active relapsed disease and
222 clonality of nodular lymphocyte-predominant Hodgkin's disease (NLPHD) and the relationship to compos
224 caspase-3 in nodular lymphocyte predominance Hodgkin's disease (NLPHD) was evaluated by immunohistoch
225 reticulum cell, for the neoplastic cells of Hodgkin's disease, notably in nodular sclerosis type.
228 mokers had a significantly increased risk of Hodgkin's disease (odds ratio (OR) = 1.8, 95% confidence
230 chronic lymphocytic leukemia (one patient), Hodgkin's disease (one patient), and adult T-cell leukem
233 contrast, Burkitt's lymphoma (P=0.0047) and Hodgkin's disease (P=0.016) were only observed in late P
234 healthy men and to repeated samples of eight Hodgkin's disease patients before treatment, 35-50 days
235 tumors in pathologically staged and treated Hodgkin's disease patients followed for long intervals t
236 52 patients, compared with three (4%) of 68 Hodgkin's disease patients in a comparison cohort who di
237 nd Marrow Transplant Registry (ABMTR) on 122 Hodgkin's disease patients who failed to achieve complet
239 whole saliva flow rates were measured in 11 Hodgkin's disease patients who received therapeutic dose
241 59 children and adolescents with unfavorable Hodgkin's disease received three alternating cycles (tot
246 mortality from all causes, causes other than Hodgkin's disease, second tumors, and cardiac disease re
247 er (PTLD; SIR = 54.3; 95% CI, 39.5 to 41.1), Hodgkin's disease (SIR = 14.8; 95% CI, 3.9 to 32.9), or
250 es in non-AIDS-defining malignancies such as Hodgkin's disease, skin, lung, anal, and kidney cancers
251 n a randomized clinical trial in early-stage Hodgkin's disease (Southwest Oncology Group [SWOG] 9133)
253 elangiectasia (AT) gene, ATM, in a cohort of Hodgkin's disease survivors with secondary malignancies.
254 neoplasms were observed in this cohort of 52 Hodgkin's disease survivors, with 18 patients (35%) deve
256 is an effective treatment for all stages of Hodgkin's disease that present with a large mediastinal
261 creening of patients who have recovered from Hodgkin's disease to aid early diagnosis and ensure the
262 roup followed a cohort of 1380 children with Hodgkin's disease to determine the incidence of second n
263 neck and chest are obtained at diagnosis of Hodgkin's disease to establish disease extent, plan radi
267 A cohort of 5,519 British patients with Hodgkin's disease treated during 1963 through 1993 was a
268 ns in children and adolescents with low-risk Hodgkin's disease treated with vinblastine, doxorubicin,
270 ith lymphomatoid papulosis (fourteen cases), Hodgkin's disease (twelve cases), and CD30+ large-cell l
271 ren), Kaposi's sarcoma (KS; three children), Hodgkin's disease (two children), vaginal carcinoma in s
272 and in the FRC and endothelium of classical Hodgkin's disease, two tumor types that also showed an a
274 fects for smoking in relation to the risk of Hodgkin's disease using data from the Selected Cancers S
275 lative risk for invasive breast cancer after Hodgkin's disease was 4.7 (95% confidence interval, 3.4
276 ond neoplasm 15 years after the diagnosis of Hodgkin's disease was 7.0 percent (95 percent confidence
277 it was observed that successful treatment of Hodgkin's disease was associated with risk of a second m
278 ldren and adolescents with stages III and IV Hodgkin's disease was conducted by the Children's Cancer
279 The risk for developing breast cancer after Hodgkin's disease was greatest in women who were under t
281 odular sclerosing and lymphocyte predominant Hodgkin's disease were derived from an unusual B-cell li
282 age (PS) IA to IIA or clinical stage (CS) IA Hodgkin's disease were entered onto a single-arm prospec
283 escents with stages IIB, IIIA2, IIIB, and IV Hodgkin's disease were randomized to receive eight cycle
284 clinical stage IA to IIA supradiaphragmatic Hodgkin's disease were randomized without staging laparo
286 0 and April 1993, 56 pediatric patients with Hodgkin's disease were treated on a single-arm trial at
287 diatric patients with clinical stage I to IV Hodgkin's disease were treated with chemotherapy and low
288 inical stages I and II, favorable (nonbulky) Hodgkin's disease were treated with four cycles of VAMP
290 patients with laparotomy staged (PS) IA-IIIB Hodgkin's disease were treated with radiation therapy (R
291 like B-cell chronic lymphocytic leukemia and Hodgkin's disease, where IL-13 modulates apoptosis or tu
294 lants should be considered for patients with Hodgkin's disease who do not achieve complete remission
295 We analyzed retrospectively 81 patients with Hodgkin's disease who had serial [(18)F]FDG-PET scans pe
296 acial zygomycosis in a 24-year-old male with Hodgkin's disease who underwent chemotherapy and autolog
297 control populations, survivors of pediatric Hodgkin's disease who were treated before 1990 face an i
298 secutive, previously untreated patients with Hodgkin's disease who were younger than 20 years of age
299 ms focus on obtaining a relapse-free cure of Hodgkin's disease with judicious use of radiation and al
300 = cisplatinum), in a group of patients with Hodgkin's disease with such poor risk characteristics.
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