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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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1360371 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
; u  a& J6 \1 g" K2 z% E7 |7 YNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
! |* G' X! H" j+ c7 f) p+ Author Affiliations
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, L) ~$ `6 J2 S4 m1 J2 |. q4 _6 y1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan 1 l& Y6 y5 R2 ~  g4 j
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan + z! l6 V1 G5 a/ s
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
& V/ j$ t2 v2 v3 W4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan $ y1 Y  |: J, h& H* s9 ^' [' z
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
% d/ Q! P, Z! }& S4 O4 y& y: m6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 8 L; ~3 a$ P  G0 m
7Kinki University School of Medicine, Osaka 589-8511, Japan # Y+ \6 ^1 T2 K
8Izumi Municipal Hospital, Osaka 594-0071, Japan 5 W4 H) c& o0 [/ q3 U) E
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan 2 }7 x) K/ N/ K6 I7 y+ Y2 z: W+ h
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
- m+ q) r3 i, B2 wAbstractBackground: 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 1 ~6 K9 o% `' C8 X) `+ j
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Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
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  V: ^' R! u! _5 Y- l0 |5 iAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
+ {: h2 ~' ~# j, |/ H$ S! E, _: b: A$ r! U+ c. g% B  _
Published online on: Thursday, December 1, 2011 + _& P7 F; t( I0 R0 {& l

8 J/ u+ @: O% q$ u' E( y7 r% p2 u0 DDoi: 10.3892/ol.2011.507 - C6 Q" n! A4 O% O0 Q

4 N# x3 ?: \7 h# E# |9 ZPages: 405-410
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7 d3 z" E& N2 XAbstract:4 i0 Z& K( F$ U1 G
S-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
8 \% T7 U8 z( r2 o6 i1 A1 D  \1 GF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
6 G. u# i! ^- b+ Author Affiliations& B8 p2 k1 h% D' I' W/ L* M
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
/ s; c4 B$ P5 Y3 X0 f9 z0 ^5 P$ u9 I' R' C2Department of Thoracic Surgery, Kyoto University, Kyoto 0 R, C6 V1 }3 s0 Z
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
  b$ n8 K" r  H  @7 E  p&#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 * o# D# a1 t, n
Received September 3, 2010. + `! S- q& \1 q3 m
Revision received November 11, 2010. 5 d( p( h8 |1 F5 P% x8 \# b- O- M
Accepted November 17, 2010.
$ M1 M7 ^, n! q9 CAbstract
3 _: [" d$ Q& K& V; w1 ^: _Background: 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.
6 D  O1 d# O( h! L( @  KPatients 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.
! C2 |- M2 B- G3 q1 I1 jResults: 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.
% q' O6 j+ z9 D8 _( F8 J# z+ A+ hConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. - P  P$ _9 D' e6 Y9 L5 N
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。
+ f  T7 s* a2 y" Z; v# R- i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?9 |( [* k/ n9 L! ]( A. |
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" ^1 Q$ I8 t  o+ ]5 W
http://clinicaltrials.gov/ct2/show/NCT015235879 d8 \1 r4 t5 u8 i$ q7 M' K: |( R5 b

# D, j& y0 }: z  iBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
5 f' @4 y! `) T6 x! M! Thttp://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 ! ^, ]: c+ d; b- V$ c6 Z
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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。' \5 Q  U) k: ~" E- W" Q# K
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 7 W* M; E, }7 C( w
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。: i; a! s# ]/ X# r* ~' q6 j
至今为止,未出 ...

. W2 `9 J1 F! d  {; i  N5 @没有副作用是第一追求,效果显著是第二追求。
/ c$ m9 Y! B6 @' C不错。

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