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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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1227322 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 Type8 @0 K8 R4 r' H+ a1 @8 c
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
8 C: Z% l! ~* _% k! `+ S; \1 e+ Author Affiliations
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan 5 j  g, N0 o) c
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
! ~* u2 K: s  G+ {9 ?$ P3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ) q4 n: x" U2 j: A  V, G6 y/ T
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 6 b/ H' C8 Z/ ^) S$ A
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
3 w' M/ T% }" p, a& j6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan , K  C+ b, S9 o7 y
7Kinki University School of Medicine, Osaka 589-8511, Japan ) `# \: Z7 ~/ I& h
8Izumi Municipal Hospital, Osaka 594-0071, Japan ( p" R7 i% T. ~! A) h' A9 U
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
# v& v4 Y/ `# f6 ICorrespondence 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
- I! Y, S. K( S; o) tAbstractBackground: 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. 8 s, m4 }+ I6 i' H7 a9 q" |" j- {+ g

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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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/ I4 u0 _! f; }2 k  G: vAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato ! _9 D  f/ V$ F# Z7 z- D
' t/ d9 V# S! R: A  f% h& i
Affiliations: 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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4 D/ h0 N. F, E3 m; N$ `$ G% G: PPublished online on: Thursday, December 1, 2011 $ G3 r$ r' X9 [) U3 }
6 s) s$ N+ W& |  L6 d
Doi: 10.3892/ol.2011.507 7 I# b- R3 D: T/ o0 b" _
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Pages: 405-410
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Abstract:
) P4 H9 P! |: i4 p+ T1 NS-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.9 W( `* L* M* |. [

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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
& r: o( x; A' n0 I' S1 s+ V; H1 |* ~F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 * B* f. p1 [; Y: \" n
+ Author Affiliations
3 R' `+ q- G  |  s) d3 u1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
2 d9 I; M1 L! c+ g: a) B) g( C" `- T2Department of Thoracic Surgery, Kyoto University, Kyoto
, Y/ V5 o8 T/ z8 i6 W1 F3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan ; k3 s5 {% _: `
&#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
* y5 V8 g$ |9 ^3 @! e4 eReceived September 3, 2010.
0 A$ l/ ]: P  R& f7 k  O6 I! IRevision received November 11, 2010.
$ ]( L& w  q" |9 s& e0 x: O0 z% AAccepted November 17, 2010.
" D5 U! o* R0 ^8 J1 W8 Y! b: tAbstract
, e9 k" u/ n$ i2 `; Z( LBackground: 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. % M+ h* P( c0 C3 J  Z
Patients 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.
5 s2 o- L$ {% C& Z6 D' ^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.
+ U7 C9 `6 e9 ?5 X/ {8 ^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。
6 u( @, q- m0 S8 @4 T, I/ e8 t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?  a, x2 V; L, F# i
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
( R7 y/ L: B* E! R" ]# q9 F( D8 mhttp://clinicaltrials.gov/ct2/show/NCT01523587) D6 e& {+ i5 Y: y9 ?7 F
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
$ @" Y( X5 `5 G/ \9 ~7 Ihttp://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 8 ]) a# Z1 u) C

3 Q/ ]' H" I3 e! K8 j; V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。3 G  {4 L- T- ?
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
老马 发表于 2012-4-29 20:53 ! {) {2 \) w& O- G4 r
从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
2 T! X$ y/ b( x$ W, \9 p& y1 p至今为止,未出 ...
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没有副作用是第一追求,效果显著是第二追求。& `7 Y0 t5 [; c: h
不错。

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