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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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1279020 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 Type1 Y6 [9 A) }. e( W, W# y' w! U
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
) A1 ]- ~9 w) B9 ^4 ?5 @+ Author Affiliations
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan ' x' V2 r% M# m
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ) o/ T% P4 v' m: E. C  y
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
3 f+ _! K% f, ^4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
) [% g3 _% B7 C9 ^5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan & x: I" b  Z( I" @! T' q
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 7 y* [  B* T% ~" ^: E2 ]
7Kinki University School of Medicine, Osaka 589-8511, Japan
- U7 h, C$ {/ R1 \' l' r8Izumi Municipal Hospital, Osaka 594-0071, Japan 4 A5 l5 Q3 l/ u" C- s# g
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan % v# [2 I. A/ L  N
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
* i1 |( W8 V: X9 t( `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. ' A0 X8 m- W6 r. Z
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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 9 V4 Q5 r/ J% L7 }  O& w- {2 J

4 b4 s- q: [1 t/ j" mAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato / ^( H* r: U& ^$ D

/ R$ X9 j" y* bAffiliations: 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
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Doi: 10.3892/ol.2011.507 0 ~$ ?& r0 u7 G$ m" N. |! P' A

& |5 V4 C. u4 I3 }- KPages: 405-410 # v% V7 X4 Y, X1 H" A  G

' ], W$ j! M4 |8 ]/ QAbstract:. f% e* [9 K! e- |
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( U# S7 u, |3 {, ?3 F' _% I. z% ]
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 & b0 _6 p. [$ Y
+ Author Affiliations
" V4 ^1 h7 @* M1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu 1 C( ~5 C6 M0 y, v  \
2Department of Thoracic Surgery, Kyoto University, Kyoto , @$ G" [* [) U" L) [; Y
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
7 Y/ p1 q, p$ f: j&#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 8 Z% ^- `- T& j0 H; \( V: I
Received September 3, 2010. 4 t3 t# |' Y' R  z% ]7 t
Revision received November 11, 2010.
, g: j# i( s7 `/ C$ W7 Q4 ]8 j# rAccepted November 17, 2010.
$ Z0 a' ]- F) \, X, OAbstract4 j- s; K+ A$ I% ^
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.
0 B, `" U/ E% V" o! j* v* y* t- _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. " O6 S+ s- [; H* A5 P
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.
( [3 L' ^' `& pConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. " [* W& j8 O! t: o- I; d3 v( 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。
  m: [$ ]9 I8 G  y5 F" O3 v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?" c5 _: w$ `9 E
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
' C/ z& {4 M/ t, n. b6 K7 Mhttp://clinicaltrials.gov/ct2/show/NCT01523587
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC- C3 n; w3 u$ u! R) _
http://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 $ {3 K( A6 P+ E4 Y" v
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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 v  y4 W7 v& u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
. l1 g9 O8 K, a' L/ m4 L1 Y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。5 \) |9 W" p  |. I/ U1 W
至今为止,未出 ...

7 p6 p! M) A4 i  v/ J& i没有副作用是第一追求,效果显著是第二追求。
; O/ g- Z" b% ~0 P5 m8 I. D8 ^不错。

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