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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1176190 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type
3 B; }$ a# R+ M# KNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
1 B$ U1 m. B* z+ Author Affiliations# X, W; M/ g+ p# w7 H4 r& P% c

% u5 l) D- r9 s$ @' l# C6 g/ ^; Y0 R' W1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan / R  O# s: r/ D" j. x) \# s2 q
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
4 B$ L# w3 r- ]' U4 M6 _3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan / O% P2 S( J! [  G3 P; [5 l
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan ; n2 t1 H3 _7 Z+ e- @! ?
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan # n* _( P6 r% A  g, }
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan + u2 }; G: z) O* `. `
7Kinki University School of Medicine, Osaka 589-8511, Japan / i( {- F4 A  m6 U6 V
8Izumi Municipal Hospital, Osaka 594-0071, Japan & A  Y, m9 p/ u, [& ~( _5 l. j2 f
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan # a9 }2 M( a% b* M5 f& c
Correspondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp
/ s7 k6 T$ M  KAbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type. 3 T# Y  S; [/ O: y
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type
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; [3 S0 q( U0 EAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
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1 c8 s7 v3 o. \0 C9 a& nAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
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Published online on: Thursday, December 1, 2011   ^! H% P9 w3 ^. y: @

" @9 M5 n- q1 k4 i7 c# h; v. i. }Doi: 10.3892/ol.2011.507 9 i0 B% J+ t5 k$ H6 N& z, N* _7 @' U

: L6 y8 S0 z" s' p" R  Y: |Pages: 405-410 ! l$ l' M) d! }$ R% t4 c3 j

' Q' U; \4 z1 S, S! VAbstract:
" X2 l" [5 A; q1 z4 fS-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population" _# x! ?0 S; j, v
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 4 E' ^2 c$ o0 L. C- q7 j0 @# w. j$ V
+ Author Affiliations
- N2 \4 c3 f( H1 B  X+ B; [7 x1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
* S/ @7 p) z1 k2 v2Department of Thoracic Surgery, Kyoto University, Kyoto & C8 M# y1 W0 K, M# D. l+ e: e/ i
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
$ h, F; {+ t. E8 V&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp
4 i1 [8 J, \# S% X* gReceived September 3, 2010. / ~# O# O. L$ F; i; D
Revision received November 11, 2010. 8 B5 K( d# p: r; Y" [
Accepted November 17, 2010. * Y2 v& E( R; n; g2 g  |& N
Abstract
; R; Y( }  f7 h+ G5 NBackground: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed.
+ A$ t) I2 P  A, x* k7 EPatients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes.   I" u+ B0 j0 Q  _. s3 A  }; _$ _
Results: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression. 8 G# r" B) O% j
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
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个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。* Z- M: b: [! q+ Z  a* f6 p" K
今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?/ D1 B! u. C* M- g% S3 l
老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy" F$ V8 ]" |8 n5 G1 s$ \  z7 r
http://clinicaltrials.gov/ct2/show/NCT01523587
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' j5 J8 |& P- s: }3 e; UBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
, T: y# d# |6 z7 khttp://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑
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从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
6 n- T, y) e6 u5 `至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
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没有副作用是第一追求,效果显著是第二追求。
+ B, k/ b1 d4 B1 j不错。

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