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1.
AJNR Am J Neuroradiol ; 28(10): 1878-9, 2007.
Article in English | MEDLINE | ID: mdl-17905891

ABSTRACT

BACKGROUND AND PURPOSE: The purpose of this study was to review the imaging findings of nasal septal abscess in 2 patients with immunosuppression. MATERIALS AND METHODS: Two patients with immunosuppression were identified as having a nasal septal abscess, and correlative CT imaging in both patients was evaluated. RESULTS: The characteristic radiographic appearance of a nasal septal abscess included a fluid collection with thin rim enhancement, located within the cartilaginous nasal septum. After CT examination, incision and drainage was performed in both patients, and appropriate antibiotic coverage was initiated. Clinical and imaging follow-up demonstrated no signs of residual infection. CONCLUSION: Nasal septal abscess has a characteristic appearance on CT examination. Prompt diagnosis and treatment, including incision and drainage and appropriate antibiotic coverage, are necessary to avoid serious complications.


Subject(s)
Abscess/diagnostic imaging , Immunocompromised Host , Nasal Septum/diagnostic imaging , Adolescent , Aged , Humans , Male , Nose Diseases/diagnostic imaging , Tomography, X-Ray Computed
2.
Blood ; 98(9): 2784-90, 2001 Nov 01.
Article in English | MEDLINE | ID: mdl-11675352

ABSTRACT

The malignant Hodgkin and Reed-Sternberg (H/RS) cells of Hodgkin disease (HD) express several members of the tumor necrosis factor (TNF) receptor family, including CD30 and CD40, and secrete several cytokines and chemokines. However, little is known about what regulates cytokine and chemokine secretion in H/RS cells. Although H/RS cells are predominantly of B-cell origin, they frequently share phenotypic and functional features with dendritic cells (DCs). Previous studies reported that receptor activator of nuclear factor kappaB (NF-kappaB) (RANK), a member of the TNF receptor family, is expressed on DCs, and that RANK ligand (RANKL) enhances DC survival and induces them to secrete cytokines. This study reports that, similar to DCs, cultured H/RS cells expressed RANK. However, unlike DCs, H/RS cells also expressed RANKL. Soluble RANKL activated NF-kappaB and induced messenger RNA expression of interferon-gamma, interleukin-8 (IL-8), IL-13, IL-9, IL-15, and RANTES, in addition to the receptors for IL-9, IL-13, IL-15, and CCR4. RANKL increased IL-8 and IL-13 levels in the supernatants of H/RS cell lines, an effect that was blocked by soluble RANK. Furthermore, soluble RANK decreased the basal level of IL-8 in one cell line, suggesting that IL-8 was induced by an autocrine RANKL/RANK loop. RANKL had no effect on H/RS cell survival in culture, and it did not modulate the expression of bcl-2, bcl-xL, bax, or inhibitors of apoptosis proteins. These data provide evidence of further functional similarities between DCs and H/RS cells. The coexpression of RANK and RANKL in H/RS cells suggests that they may regulate cytokine and chemokine secretion in H/RS cells by an autocrine mechanism.


Subject(s)
Hodgkin Disease/pathology , Receptors, Tumor Necrosis Factor/metabolism , Antigens, Surface/drug effects , Antigens, Surface/metabolism , Autocrine Communication , Carrier Proteins/metabolism , Carrier Proteins/pharmacology , Cell Survival/drug effects , Cytokines/drug effects , Cytokines/metabolism , Glycoproteins/metabolism , Hodgkin Disease/metabolism , Humans , Membrane Glycoproteins/metabolism , Membrane Glycoproteins/pharmacology , Osteoprotegerin , RANK Ligand , Receptor Activator of Nuclear Factor-kappa B , Receptors, Cytoplasmic and Nuclear/metabolism , Receptors, Tumor Necrosis Factor/drug effects , Receptors, Tumor Necrosis Factor/physiology , Reed-Sternberg Cells/metabolism , Tumor Cells, Cultured , Up-Regulation/drug effects
3.
Int J Radiat Oncol Biol Phys ; 51(1): 4-9, 2001 Sep 01.
Article in English | MEDLINE | ID: mdl-11516844

ABSTRACT

PURPOSE: Fluoro-2-deoxy-d-glucose-positron emission tomography (FDG-PET) is a functional imaging modality that measures the relative uptake of 18FDG with PET. The purpose of this review is to assess the potential contribution of FDG-PET scans to the treatment of head-and-neck cancer patients. METHODS AND MATERIALS: Data were assessed from the literature with attention to what additional information may be gained from the use of FDG-PET in four clinical settings: (1) detection of occult metastatic disease in the neck, (2) detection of occult primaries in patients with neck metastases, (3) detection of synchronous primaries or metastatic disease in the chest, and (4) detection of residual/recurrent locoregional disease. RESULTS: Although the data are somewhat conflicting, FDG-PET appears to add little additional value to the physical examination and conventional imaging studies (supplemented by biopsy when appropriate) for the detection of subclinical nodal metastases, unknown primaries, or disease in the chest. However, FDG-PET scans are quite useful in differentiating residual/recurrent disease from treatment-induced normal tissue changes. A positive FDG-PET scan at 1 month after radiotherapy is highly indicative of the presence of residual disease, and a negative scan at 4 months after treatment is highly predictive of tumor eradication. CONCLUSIONS: Large-scale studies using newer generation equipment and more defined methods are needed to more rigorously assess the potential of FDG-PET in the detection of subclinical primary or simultaneous secondary tumors and of nodal or systemic spread. Currently, however, FDG-PET can contribute to the detection of residual/early recurrent tumors, leading to the timely institution of salvage therapy or the prevention of unnecessary biopsies of irradiated tissues, which may aggravate injury.


Subject(s)
Fluorodeoxyglucose F18 , Head and Neck Neoplasms/diagnostic imaging , Radiopharmaceuticals , Tomography, Emission-Computed , Head and Neck Neoplasms/radiotherapy , Humans , Lymphatic Metastasis/diagnostic imaging , Neoplasm, Residual , Neoplasms, Unknown Primary/diagnostic imaging
4.
Arch Otolaryngol Head Neck Surg ; 127(2): 149-54, 2001 Feb.
Article in English | MEDLINE | ID: mdl-11177031

ABSTRACT

BACKGROUND: Merkel cell carcinoma is a rare malignant neoplasm of the skin that most often arises in the head and neck region. Despite the innocuous appearance of the primary lesion, Merkel cell carcinoma often has an aggressive clinical course with frequent locoregional recurrences and distant metastases. We evaluated the association of the width of surgical margins and the use of postoperative radiation therapy with locoregional control and survival rates. METHODS: The medical records of 66 patients with head and neck Merkel cell carcinoma seen between 1945 and 1995 were retrospectively reviewed. The Fisher exact test was used to compare outcomes. Kaplan-Meier survival curves were constructed. RESULTS: Eighteen patients for whom there was adequate information were divided into the following groups according to the width of their surgical margins: smaller than 1 cm, 1 to 2 cm, and larger than 2 cm. No statistical difference in locoregional control or survival was found among these groups owing to the small patient population. In contrast, a comparison of the patients who did (n = 26) and did not (n = 34) receive postoperative radiation therapy revealed a significant difference in local (3 [12%] vs 15 [44%], respectively; P<.01) and regional (7 [27%] vs 29 [85%], respectively; P<.01) recurrence rates. There was, however, no significant difference in the disease-specific survival between these groups (P = .30). Distant disease developed in 36% of all patients regardless of therapy. CONCLUSIONS: Any effect of the width of surgical margins on outcome was not detectable in the small number of patients analyzed. The use of postoperative radiation therapy was associated with a significant improvement in locoregional control. There was no detectable influence of the type of initial therapy on the rates of distant metastases or on survival. Future therapeutic innovations should be directed toward controlling the development of distant metastases in patients with Merkel cell carcinoma.


Subject(s)
Carcinoma, Merkel Cell/therapy , Head and Neck Neoplasms/therapy , Adult , Aged , Aged, 80 and over , Carcinoma, Merkel Cell/mortality , Combined Modality Therapy , Disease-Free Survival , Female , Head and Neck Neoplasms/mortality , Humans , Male , Middle Aged , Neoplasm Metastasis , Neoplasm Recurrence, Local , Radiotherapy, Adjuvant , Retrospective Studies , Surgical Procedures, Operative/methods , Survival Rate
5.
AJNR Am J Neuroradiol ; 21(7): 1315-9, 2000 Aug.
Article in English | MEDLINE | ID: mdl-10954286

ABSTRACT

BACKGROUND AND PURPOSE: The pterygopalatine fossa (PPF) is an important anatomic location of the deep portion of the face. It is essential to review this area on both pre- and posttreatment studies of head and neck malignancies to assess local extent of disease or recurrence and perineural tumor spread. The purpose of this study was to review the postoperative appearance of the PPF on MR images. METHODS: Imaging and clinical data of 10 patients who underwent surgical resection of tumor in which the PPF was violated at surgery were reviewed. Patients were included in the study if there was no imaging or clinical evidence of tumor in the PPF pre- or postoperatively. Postoperative MR studies were examined to assess the appearance of the PPF. RESULTS: The PPF is consistently and persistently abnormal after surgical violation. There is loss of the normal T1 signal hyperintensity and abnormal, increased contrast enhancement, as seen on fat-suppressed T1-weighted images. These postoperative changes are strikingly similar to those of tumor involvement. CONCLUSION: After surgical violation, the PPF will always appear abnormal on MR images, and the expected imaging findings must be recognized to avoid the misdiagnosis of tumor recurrence.


Subject(s)
Magnetic Resonance Imaging , Maxillary Sinus Neoplasms/surgery , Neoplasm Recurrence, Local/diagnosis , Palate/surgery , Postoperative Complications/diagnosis , Pterygoid Muscles/surgery , Aged , Diagnosis, Differential , Female , Humans , Male , Maxillary Sinus/pathology , Maxillary Sinus/surgery , Maxillary Sinus Neoplasms/diagnosis , Middle Aged , Palate/pathology , Pterygoid Muscles/pathology
6.
Clin Cancer Res ; 6(8): 3172-6, 2000 Aug.
Article in English | MEDLINE | ID: mdl-10955800

ABSTRACT

The p57KIP2 is a maternally expressed and paternally imprinted cyclin-dependent kinase inhibitor located on chromosome 11p15.5. Because of its location, biochemical functions, and imprinting status, p57KIP2 has been considered a candidate tumor suppressor gene. To determine, for the first time, the involvement of this gene in the development of head and neck squamous carcinoma (HNSC), we analyzed the imprinting and expression status and loss of heterozygosity (LOH) within the p57KIP2 gene flanking loci on the 11p15.5 region in 64 primary untreated tumors. Of the 30 (47%) informative cases for this gene, loss of imprinting and LOH were noted in 4 (13%) and 10 tumors (33%), respectively. Analysis of the microsatellite markers flanking the p57KIP2 gene on chromosome 11p showed infrequent alterations at these loci. p57KIP2 was expressed in all tumors with LOH within and around the gene. Quantitative reverse transcription-PCR analysis showed elevated p57 mRNA expression in tumor with loss of imprinting. Sequencing analysis of exons 1 and 2 of the p57KIP gene failed to detect any mutations. Our data indicate: (a) infrequent genomic abnormalities at the p57KIP2 gene in HNSC; (b) leaky or incomplete imprinting of the paternal allele is associated with increased expression of this gene in a subset of tumors; and (c) minimal evidence for suppressor function for this gene in HNSC.


Subject(s)
Carcinoma, Squamous Cell/genetics , Genomic Imprinting , Loss of Heterozygosity , Mouth Neoplasms/genetics , Nuclear Proteins/genetics , Carcinoma, Squamous Cell/metabolism , Chromosomes, Human, Pair 11 , Cyclin-Dependent Kinase Inhibitor p57 , Exons , Gene Expression , Humans , Microsatellite Repeats , Mouth Neoplasms/metabolism , Nuclear Proteins/biosynthesis , Polymorphism, Genetic , Polymorphism, Single-Stranded Conformational , RNA, Messenger/biosynthesis , RNA, Messenger/genetics , Reverse Transcriptase Polymerase Chain Reaction
7.
Nat Med ; 6(8): 879-85, 2000 Aug.
Article in English | MEDLINE | ID: mdl-10932224

ABSTRACT

ONYX-015 is an adenovirus with the E1B 55-kDa gene deleted, engineered to selectively replicate in and lyse p53-deficient cancer cells while sparing normal cells. Although ONYX-015 and chemotherapy have demonstrated anti-tumoral activity in patients with recurrent head and neck cancer, disease recurs rapidly with either therapy alone. We undertook a phase II trial of a combination of intratumoral ONYX-015 injection with cisplatin and 5-fluorouracil in patients with recurrent squamous cell cancer of the head and neck. There were substantial objective responses, including a high proportion of complete responses. By 6 months, none of the responding tumors had progressed, whereas all non-injected tumors treated with chemotherapy alone had progressed. The toxic effects that occurred were acceptable. Tumor biopsies obtained after treatment showed tumor-selective viral replication and necrosis induction.


Subject(s)
Adenoviruses, Human/genetics , Cisplatin/therapeutic use , Fluorouracil/therapeutic use , Genetic Therapy/methods , Head and Neck Neoplasms/drug therapy , Head and Neck Neoplasms/therapy , Neoplasm Recurrence, Local/drug therapy , Neoplasm Recurrence, Local/therapy , Adenoviruses, Human/physiology , Adult , Aged , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Carcinoma, Squamous Cell/drug therapy , Carcinoma, Squamous Cell/pathology , Carcinoma, Squamous Cell/therapy , Combined Modality Therapy , Female , Genetic Therapy/adverse effects , Head and Neck Neoplasms/pathology , Humans , Male , Middle Aged , Neoplasm Recurrence, Local/pathology , Virus Replication
8.
Photochem Photobiol ; 72(1): 103-13, 2000 Jul.
Article in English | MEDLINE | ID: mdl-10911734

ABSTRACT

There is no satisfactory mechanism to detect premalignant lesions in the upper aero-digestive tract. Fluorescence spectroscopy has potential to bridge the gap between clinical examination and invasive biopsy; however, optimal excitation wavelengths have not yet been determined. The goals of this study were to determine optimal excitation-emission wavelength combinations to discriminate normal and precancerous/cancerous tissue, and estimate the performance of algorithms based on fluorescence. Fluorescence excitation-emission matrices (EEM) were measured in vivo from 62 sites in nine normal volunteers and 11 patients with a known or suspected premalignant or malignant oral cavity lesion. Using these data as a training set, algorithms were developed based on combinations of emission spectra at various excitation wavelengths to determine which excitation wavelengths contained the most diagnostic information. A second validation set of fluorescence EEM was measured in vivo from 281 sites in 56 normal volunteers and three patients with a known or suspected premalignant or malignant oral cavity lesion. Algorithms developed in the training set were applied without change to data from the validation set to obtain an unbiased estimate of algorithm performance. Optimal excitation wavelengths for detection of oral neoplasia were 350, 380 and 400 nm. Using only a single emission wavelength of 472 nm, and 350 and 400 nm excitation, algorithm performance in the training set was 90% sensitivity and 88% specificity and in the validation set was 100% sensitivity, 98% specificity. These results suggest that fluorescence spectroscopy can provide a simple, objective tool to improve in vivo identification of oral cavity neoplasia.


Subject(s)
Mouth Neoplasms/diagnosis , Spectrometry, Fluorescence/methods , Algorithms , Case-Control Studies , Humans , Photobiology , Precancerous Conditions/diagnosis
9.
Head Neck ; 22(2): 142-8, 2000 Mar.
Article in English | MEDLINE | ID: mdl-10679901

ABSTRACT

BACKGROUND: Tracheostoma breathing valves permit hands-free tracheoesophageal (TE) speech production; however, few laryngectomees routinely use them because of problems with attachment. METHODS: We retrospectively reviewed the charts of 45 TE speakers to determine the success rate and factors associated with successful breathing valve use based on attachment. All patients attempted to use a tracheostoma breathing valve with either a standard or customized peristomal housing, or a standard or customized Barton button. Device selection was based on inspection of the patient's neck and peristomal contour. Six to eight consecutive hours of attachment defined success. RESULTS: Overall, 9% of subjects succeeded with any peristomal attachment as compared to 68% with either a standard (57%) or customized (85%) Barton button. Smooth stomal contour, a contiguous stomal lip, and correct button length were important for successful Barton button use. CONCLUSIONS: Standard or customized Barton buttons offer excellent alternatives to peristomal housing attachments for hands-free TE speech in select patients.


Subject(s)
Laryngeal Neoplasms/surgery , Laryngectomy , Speech, Esophageal/instrumentation , Surgical Stomas , Tracheostomy/instrumentation , Voice Disorders/rehabilitation , Equipment Design , Female , Humans , Male , Patient Satisfaction , Respiration , Retrospective Studies , Voice Disorders/etiology , Voice Quality
10.
Arch Otolaryngol Head Neck Surg ; 125(10): 1083-9, 1999 Oct.
Article in English | MEDLINE | ID: mdl-10522499

ABSTRACT

OBJECTIVES: To evaluate the efficacy and secondarily the toxic effects of biochemopreventive therapy (high-dose isotretinoin [13-cis-retinoic acid], alpha-tocopherol, and interferon alfa) in the reversal of advanced premalignant lesions of the upper aerodigestive tract and to correlate the therapeutic events with modulation of biomarkers. DESIGN: Prospective, nonrandomized chemoprevention trial. SETTING: Tertiary cancer care referral center and ambulatory care. PARTICIPANTS: Thirty-six patients with advanced premalignant lesions of the upper aerodigestive tract, without cancer during the 2 years before the intervention, with evaluable lesions, and without retinoid therapy for 3 months before the trial. INTERVENTION: Administration of oral isotretinoin (100 mg/m2 per day), oral alpha-tocopherol (1200 IU/d), and subcutaneous interferon alfa (3 megaunits per square meter twice weekly) for 12 months, with serial biopsies and clinical examination at 0, 6, 12, and 18 months from study start. MAIN OUTCOME MEASURES: Clinical and histologic responses to the intervention. RESULTS: Of the 36 patients, evaluation was possible in 30 for response at 6 months and in 21 at 12 months. At 6 months, there were 10 pathologic complete responses and 7 partial responses; at 12 months, 7 complete and 3 partial responses. A striking difference in response was observed in favor of laryngeal lesions (9/19 [47%] complete response rate at 6 months and 7/14 [50%] at 12 months vs 1/11 [9%] and 0/7 [0%], respectively, for oral lesions). Toxic effects were acceptable and did not exceed grade 3. CONCLUSION: Biochemoprevention is a promising biologic approach for laryngeal dysplasia and needs to be investigated further.


Subject(s)
Antineoplastic Agents/therapeutic use , Interferon-alpha/therapeutic use , Isotretinoin/therapeutic use , Laryngeal Neoplasms/prevention & control , Mouth Neoplasms/prevention & control , Precancerous Conditions/drug therapy , Vitamin E/therapeutic use , Adult , Aged , Antineoplastic Agents/administration & dosage , Chemoprevention , Female , Humans , Interferon-alpha/administration & dosage , Isotretinoin/administration & dosage , Male , Middle Aged , Prospective Studies , Treatment Outcome , Vitamin E/administration & dosage
11.
Semin Surg Oncol ; 16(1): 19-29, 1999.
Article in English | MEDLINE | ID: mdl-9890736

ABSTRACT

Well-differentiated thyroid cancer usually progresses slowly and rarely invades other tissues. However, the rare cases with invasion of local structures, such as the larynx, trachea, or esophagus, present particular management difficulties. In situations with limited involvement of the larynx or trachea, there is controversy over whether a "shave excision" that may leave microscopic disease at the site, or a complete resection that includes removal of a portion of these structures is the better approach. In the case of more extensive involvement of upper aerodigestive tract structures by thyroid carcinomas, the most appropriate method of resection and reconstruction is also at issue. We discuss the literature pertaining to the surgical management of laryngotracheal and esophageal invasion by thyroid carcinoma, review the incidence and presentation of this disease, and make recommendations based on our own experience.


Subject(s)
Esophageal Neoplasms/surgery , Laryngeal Neoplasms/surgery , Thyroid Neoplasms/pathology , Tracheal Neoplasms/surgery , Esophageal Neoplasms/mortality , Esophageal Neoplasms/pathology , Humans , Laryngeal Neoplasms/mortality , Laryngeal Neoplasms/pathology , Neoplasm Invasiveness , Survival Rate , Tracheal Neoplasms/mortality , Tracheal Neoplasms/pathology
12.
Laryngoscope ; 108(5): 760-3, 1998 May.
Article in English | MEDLINE | ID: mdl-9591559

ABSTRACT

Sarcomatoid carcinoma of head and neck mucosal sites is a rare high-grade malignancy that may cause diagnostic and therapeutic controversies. A characteristic of this entity consistently reported but not entirely validated is its relative radioresistance and the general belief is that surgery is the treatment of choice. The objective of this retrospective study was to determine if patients treated with radiation for early glottic sarcomatoid carcinoma had worse outcomes than those achieved with irradiation for the more typical squamous cell carcinoma. Twenty-eight cases of early stage (T1-T2) sarcomatoid carcinoma of the larynx treated with definitive doses of megavoltage irradiation between 1969 and 1995 at The University of Texas M. D. Anderson Cancer Center form the cohort for this analysis. All pathologic material was reviewed to confirm the diagnosis. All tumors manifested spindle cell features with marked cytomorphologic abnormalities characteristic of this entity. Sixteen tumors (57%) had the more typical polypoid gross morphology of sarcomatoid carcinoma. Twenty-one patients (75%) were staged T1 and seven patients (25%) had stage T2 disease. All patients were treated with small laryngeal fields, median size 20 cm2, and to a median dose of 65 Gy. Follow-up ranged from 1.5 to 24 years (median, 10 years). Four patients (14%) had local disease recurrence, and all had salvage total laryngectomies and remained free of local disease. The 5-year actuarial local control rates for patients with T1 and T2 lesions were 94% and 54%, respectively. Only one patient developed regional and distant disease. The 10-year actuarial disease-specific and overall survival rates were 92% and 63%, respectively. Patients with early stage sarcomatoid carcinoma of the glottis treated with radiation had similar control rates to irradiated patients with similar volume disease with the more typical squamous cell carcinoma. The authors contend that the histologic diagnosis of sarcomatoid carcinoma by itself should not influence the decision to treat a patient with early stage glottic disease with irradiation.


Subject(s)
Carcinosarcoma/radiotherapy , Laryngeal Neoplasms/radiotherapy , Vocal Cords , Adult , Aged , Aged, 80 and over , Carcinosarcoma/pathology , Disease-Free Survival , Female , Humans , Laryngeal Neoplasms/pathology , Male , Middle Aged , Radiotherapy Dosage , Retrospective Studies , Treatment Outcome
13.
J Clin Oncol ; 16(4): 1325-30, 1998 Apr.
Article in English | MEDLINE | ID: mdl-9552033

ABSTRACT

PURPOSE: To assess the activity and toxicity profile of combined taxol (paclitaxel), ifosfamide, and platinum (cisplatin) (TIP) in patients with recurrent or metastatic squamous cell carcinoma (SCC) of the head and neck. PATIENTS AND METHODS: Recurrent or metastatic head and neck SCC patients received paclitaxel 175 mg/m2 in a 3-hour infusion on day 1; ifosfamide 1,000 mg/m2 in a 2-hour infusion on days 1 through 3; mesna 600 mg/m2 on days 1 through 3; and cisplatin 60 mg/m2 on day 1, repeated every 3 to 4 weeks. All were premedicated with dexamethasone, diphenhydramine, and cimetidine. Prophylactic hematopoietic growth factors were not permitted. RESULTS: Fifty-two patients were assessable for response and toxicity; 53 for survival (local-regional recurrence alone in 57% and distant metastasis with or without local-regional recurrence in 43%). Overall response rate was 58% (30 of 52) of patients; complete response rate was 17% (nine of 52) of patients, with six complete responses that continued for a median 15.7+ months. Median follow-up of all patients was 17.7 months. Median survival was 8.8 months (95% confidence interval [CI] 8.1 to 17.5 months). Toxicity was relatively well tolerated and caused no deaths. The most frequent moderate-to-severe toxicity (90% of patients) was transient grades 3 to 4 neutropenia; neutropenic fever occurred in 27%. Grade 3 peripheral neuropathy occurred in three patients, none had grade 4. Grade 3 mucositis occurred in only one patient, none had grade 4. CONCLUSION: TIP had major activity in this setting, with a 58% objective response rate, 17% complete response rate, durable complete responses (six of nine persisting), and relatively well-tolerated toxicity, with no toxic deaths. The activity of TIP, a novel taxol-cisplatin-based regimen, in recurrent or metastatic head and neck SCC should be confirmed in a phase III trial.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Carcinoma, Squamous Cell/drug therapy , Head and Neck Neoplasms/drug therapy , Neoplasm Recurrence, Local/drug therapy , Adult , Aged , Antineoplastic Agents, Phytogenic/administration & dosage , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Carcinoma, Squamous Cell/pathology , Cisplatin/administration & dosage , Cisplatin/adverse effects , Cisplatin/therapeutic use , Dose-Response Relationship, Drug , Female , Head and Neck Neoplasms/pathology , Humans , Ifosfamide/administration & dosage , Ifosfamide/adverse effects , Ifosfamide/therapeutic use , Male , Middle Aged , Neoplasm Metastasis , Paclitaxel/administration & dosage , Paclitaxel/adverse effects , Paclitaxel/therapeutic use , Survival Rate , Taxoids
14.
Cancer Treat Res ; 90: 149-69, 1997.
Article in English | MEDLINE | ID: mdl-9367082

ABSTRACT

During the past years advances have been made in the understanding of the molecular mechanisms involved in the initiation and progression of thyroid carcinoma. Mutations in tumor suppressor genes such as p53 and oncogenes such as N-ras may be important for progression of well-differentiated thyroid carcinomas. Activation of the ret protooncogene located on chromosomal region 10q11.2 has been identified as a key factor in the initiation of papillary and medullary carcinoma. Integration of these discoveries into a prognostic classification scheme may allow us to better predict the biologic behavior of tumors in individual patients. Despite the recent advances in our understanding of the molecular events occurring during thyroid carcinogenesis, major questions persist regarding aspects of patient management. New diagnostic modalities may enable us to noninvasively discriminate between benign and malignant thyroid nodules, and to detect recurrent disease earlier. Although the optimal surgical procedure for well-encapsulated tumors is still debated, recent clinical studies have shown that for those patients with tumors > 1.5 cm, the routine use of RAI and hormone suppression can improve local control and survival rates. Findings in two recent reviews suggest that patients with widely invasive thyroid masses benefit from the surgical removal of all gross tumor. Further investigation is required to define the role of adjuvant radiotherapy and the most appropriate management of unresectable disease. Incorporation of prognostic markers into clinical staging systems should allow surgeons to better tailor their treatment plans for each patient. Translation of recent basic science advances into the clinical arena may also aid in the development of novel treatment strategies for patients with aggressive tumors.


Subject(s)
Thyroid Neoplasms/therapy , Carcinoma, Medullary/therapy , Chromosome Aberrations , Genes, Tumor Suppressor , Humans , Prognosis , Thyroid Neoplasms/diagnosis , Thyroid Neoplasms/genetics
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