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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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1094525 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
% Q' f, f- O; A: BNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
8 y0 b& Q: [0 m5 P" r3 I# q( X+ Author Affiliations
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; x* s  z7 U# k8 J: s/ d4 ~1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan 6 L& Z) N! h" q
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
1 x/ o! G7 ^$ O: t- r) \8 t7 w3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ; m8 o0 \$ E, i+ G9 C( u
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
. @. L' G7 T' a/ i$ F. u% W6 _5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan 0 x, N: Z" T6 Y% }: j
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 5 u# Z5 Q5 N( v. P7 G
7Kinki University School of Medicine, Osaka 589-8511, Japan
6 O$ H  p5 l# X: E4 v( ?& H8Izumi Municipal Hospital, Osaka 594-0071, Japan
* b6 a1 Y4 S( f9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
  ~' R9 H* U# }0 bCorrespondence 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 # w% x7 d4 U) c+ N
AbstractBackground: 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.
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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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9 [9 L6 o! b+ w: I4 W; ]  n" hAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato : Z; u( G& D" |! |9 {0 F: l0 ?: {

, p- F/ B! j, [4 {% JAffiliations: 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 # d$ a: L" r* g

" G* y9 p. r* S% B* k* KDoi: 10.3892/ol.2011.507   B6 A/ P7 ?. f# E( x6 Z- ~# s

3 L8 G4 `- t! ~' \( t( X4 vPages: 405-410 ( q9 p) l5 a+ D
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Abstract:
3 r) A) D' W: VS-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" G& S8 l' |$ m# J$ N
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 9 V8 c. X% q' `: }3 Y; C8 ^
+ Author Affiliations
0 w. X/ J9 S8 R9 @1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu : |7 m2 M1 v1 ~; ]. Q. b9 a) ]
2Department of Thoracic Surgery, Kyoto University, Kyoto
& ^7 z/ ~. d- |5 M3 R" C3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
. `4 l! V6 d* j% C( K+ ~&#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 # q: g7 x& M1 A$ W$ P! o
Received September 3, 2010.
/ H0 E! H4 M2 C$ @- a9 O  X4 xRevision received November 11, 2010.
/ d: _; d1 T" f9 e# G6 T/ N/ l% C! G" dAccepted November 17, 2010.
% ?0 T4 L& U: S. G' y* n0 jAbstract
* n1 I6 l" M( o  P1 WBackground: 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. % [0 A* B3 ?+ I! F
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. . ^1 }( ~& }% q6 n. J/ g+ b4 A+ o
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. 2 u8 P" A4 `" ~' b
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. # T" ?7 |( I' }* C9 F. \
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。
0 [6 q% @9 P: u7 f* R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?
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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
& T! O: f- i; hhttp://clinicaltrials.gov/ct2/show/NCT01523587
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: V' u# S  c  [, Z# SBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
+ A& p$ B" ?. ^4 \' Yhttp://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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( h. i3 n$ }; `' c' j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。; s! E( \( `6 Q
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 : @; {" \# A' O( ~+ U/ I. m0 c
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。  U4 G  E. V1 p  P/ B
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。( Y- v, ?+ D) A
不错。

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