Axillary Recurrence in Breast Cancer Patients with Isolated Tumor Cells in the Sentinel Lymph Node [AJCC N0(i+)]

Background  

Completion axillary lymph node dissection (CALND) is controversial in patients with sentinel lymph node (SLN) metastases ≤ 0.2 mm [N0 (i+)]. Our goal was to characterize patients with SLN isolated tumor cells regarding surgical management and axillary recurrence.     

Acute toxicity and first clinical results of intensive postinduction therapy using a modified busulfan and cyclophosphamide regimen with autologous bone marrow rescue in first remission of acute myeloid leukemia [see comments]

The combination of high-dose busulfan (16 mg/kg) and 200 mg/kg cyclophosphamide is gaining increasing significance as a preparative regimen prior to autologous, syngeneic, or allogeneic marrow transplantation. A new regimen of high-dose busulfan in conjunction with a reduced dose of 120 mg/kg cyclophosphamide has recently been described as a preparative regimen prior to allogeneic transplantation. To determine the drug-related nonhematologic toxic effects of this new regimen without confounding factors associated with allogeneic transplantation, we conducted a pilot study using this new regimen in 20 patients with acute myeloid leukemia (AML) in first remission prior to autologous unpurged marrow transplantation. All patients experienced transient non-life-threatening acute drug-related toxicity with skin reactions in 20 (100%), nausea and vomiting in 20 (100%), oral mucositis in 18 (90%), hepatic functional impairment in 17 (85%), hemorrhagic cystitis in three (15%), and generalized seizures in two (10%) of these patients, respectively. Two procedural, fatal complications resulted from infectious causes that were not directly related to the speed of hematopoietic reconstitution or the toxicity of the preparative regimen. The 3-year event-free survival estimate (55% +/- 11%) and probability of leukemic recurrence (38% +/- 11%) attained with this new regimen in recipients of autografts in first remission of AML are promising and challenge comparisons with preparative regimens employing combinations of cytotoxic agents or total body irradiation (TBI).     

Kr-81m ventilation imaging: clinical utility in suspected pulmonary embolism

The results of Kr-81m/Tc-99m ventilation-perfusion (VP) lung scintigraphy were correlated with the results of pulmonary angiography for 74 patients suspected of having pulmonary embolism (PE). Among patients having a diagnostic scan, the sensitivity and specificity of scintigraphy were 91% and 94%, respectively. Also, 157 consecutive cases of Kr-81m/Tc-99m VP lung scintigraphy were reviewed, and the frequency of an indeterminate scan was found to be 22%. A similar frequency was found for VP scintigraphy with xenon-133. Of eight patients who had indeterminate scans due to the presence of a single VP mismatch, four were demonstrated to have PE by angiography. Kr-81m is an excellent agent for VP scanning in cases of suspected PE, offering accuracy in diagnosis as well as favorable physical properties.     

Curcumin causes superoxide anion production and p53-independent apoptosis in human colon cancer cells

Curcumin from the rhizome of the Curcuma longa plant has chemopreventative activity and inhibits the growth of neoplastic cells. Since p53 has been suggested to be important for anticancer activity by curcumin, we investigated curcumin-induced cytotoxicity in cultures of p53^+/+ and p53^−/− HCT-116 colon cancer cells, as well as mutant p53 HT-29 colon cancer cells. Curcumin killed wild-type p53 HCT-116 cells and mutant p53 HT-29 cells in a dose- and time-dependent manner. In addition, curcumin-treated p53^+/+ HCT-116 cells and mutant p53 HT-29 cells showed upregulation of total and activated p53, as well as increased expression of p53-regulated p21, PUMA (p53 upregulated modulator of apoptosis), and Bax; however, an equivalent cytotoxic effect by curcumin was observed in p53^+/+ and p53^−/− HCT-116 cells, demonstrating that curcumin-induced cytotoxicity was independent of p53 status. Similar results were obtained when the cytotoxic effect of curcumin was assessed in wild-type p53 HCT-116 cells after siRNA-mediated p53 knockdown. Chromatin condensation, poly (ADP-ribose) polymerase-1 cleavage and reduced pro-caspase-3 levels in curcumin-treated p53^+/+ and p53^−/− HCT-116 cells suggested that curcumin caused apoptosis. In addition, exposure to curcumin resulted in superoxide anion production and phosphorylation of oxidative stress proteins in p53^+/+ and p53^−/− HCT-116 cells. Collectively, our results indicate that, despite p53 upregulation and activation, curcumin-induced apoptosis in colon cancer cells was independent of p53 status and involved oxidative stress. Curcumin may therefore have therapeutic potential in the management of colon cancer, especially in tumors that are resistant to conventional chemotherapy due to defects in p53 expression or function.     

Noninvasive measurement of aortic aneurysm sac tension with vibrometry

OBJECTIVE: Currently, the risk of aneurysm sac rupture after endovascular abdominal aortic aneurysm repair (EVAR) is estimated by using a group of anatomic variables. Available techniques for pressure monitoring include either direct measurement using catheter-based techniques or indirect measurement requiring implantation of a pressure sensor during aneurysm repair. None of these methods is without limitations. Radiation pressure, such as that generated by a modulated ultrasound (US) beam, can induce surface vibration at a distance. The velocity of the resulting surface waves depends on the tensile stress of the vibrated surface. By measuring the change in wave velocity, it is possible to detect the change in tensile stress and calculate the pressure through the vibrated surface. We tested this concept in an in vitro aneurysm model. METHODS: Rubber tubes and explanted porcine abdominal aortas were used to model an aneurysm sac. The surface of the model was vibrated with an amplitude-modulated US beam. The resulting motion was detected either by reflected laser light or by Doppler US. The phase of the propagating wave was measured to assess changes in velocity with different pressures. RESULTS: Increasing hydrostatic pressure in the rubber model correlated well with the cumulative phase shift (R(2) = 0.96-0.99; P < .0001). By using a pump to generate dynamic pressure (between 110 and 200 mm Hg), the cumulative phase shift correlated well with the square of the mean pressure (R(2) = 0.92; P < .0001); however, the correlation with pulse pressure was poor (24-36 mm Hg; r = 0.38; P < .02). In the porcine in vitro aortic sac model, the cumulative phase shift detected with both laser (r = 0.94-0.99; P < .0001) and Doppler (r = 0.96-0.99; P < .0001) correlated well with the aneurysm pressure. CONCLUSIONS: Application of vibrometry for noninvasive measurement of aortic aneurysm sac tension is feasible in an in vitro setting. The concept of vibrometry may be used to detect endotension noninvasively after EVAR. Vibrometry may also be used to estimate wall stress in native aneurysms, and it may predict the risk of aneurysm rupture. CLINICAL RELEVANCE: Vibrometry may offer a technique for completely noninvasive monitoring of aneurysm sac pressure after EVAR. Vibrometry is based on the following principles: radiation pressure, such as that generated by modulated US, can induce surface vibration at a distance; by measuring the change in wave velocity of vibration, it is possible to detect changes in tensile stress and calculate the pressure through the vibrated surface. We tested this concept in an in vitro model and found that application of vibrometry for noninvasive measurement of aortic aneurysm sac tension is feasible. Vibrometry may also be used to estimate wall stress in native aneurysms.     

商陆多糖Ⅱ体外对小鼠脾细胞增殖及产生集落刺激因子的影响

用[³H]TdR参入法检测小鼠脾细胞增殖能力及产生集落刺激因子(colony stimulating factor. CSF)含量.证明商陆多糖Ⅱ(PAP-Ⅱ)在31～500 μg·m^-1范围内显著促进小鼠稗细胞增殖。PAP-Ⅱ,31～125 μg·ml^-1可剂量依赖性地促进Con A(1,2.8μg·ml^-1),LPS(3,10,30 μg·ml^-1)诱导的淋巴细胞细咆增殖,随着PAP-Ⅱ剂量加大,对丝裂原诱导的淋巴细胞增殖反呈抑制作用。PAP-Ⅱ。10～500μg·ml^-1呈剂量及时间依赖性地促进脾细胞产生CSF,其最适剂量为100 μg·ml^-1。最佳时间为5 d,提示PAP-Ⅱ能增强免疫及促进造血功能。