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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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1206560 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
# b  w6 \/ `# B2 A4 ^; ~0 }NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
/ y, n2 A3 r# Z+ {+ Author Affiliations
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1 M" ?* ^6 K1 P$ e* s1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan ) u! Z( l6 {! w; R
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan + o" Y; K& d) ?; ]- z) C* |, ]
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
3 M' P0 r& X1 F5 b, F4 J2 e7 @+ t4 L! H4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 5 M( P5 v0 x; _2 w6 @
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
6 c5 U7 n9 P  j. \4 m& _3 K5 [6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan # \# U2 V5 l4 Z. A  ?% c5 Y
7Kinki University School of Medicine, Osaka 589-8511, Japan   Z9 c% `" V8 X" L( n3 t9 K
8Izumi Municipal Hospital, Osaka 594-0071, Japan # b8 q  Q, a9 J7 u& j
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
0 x+ p( f8 K8 i  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 % W7 G3 b4 z; Q4 B9 J
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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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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) \" l4 f) o2 b  X& CAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  0 [+ |4 y) \% j( g: R% t4 A2 g$ i

0 K9 `5 I; t% v  ^+ M. G  yPublished online on: Thursday, December 1, 2011 . h+ x$ Q2 [1 A; V" q

$ g' E* I. O- `  `2 jDoi: 10.3892/ol.2011.507 4 [8 {  t+ y2 K. Z5 R

0 N" |: s4 U; W) YPages: 405-410 0 W' Z% v" b- J4 I$ l1 k

( z; f, R  b5 K6 r  I' N' CAbstract:
# y" s5 ~% n& P% A4 u; s4 }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.6 \* _+ m# t3 G& q
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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 population8 K" N" [9 O* R$ Z
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
3 ~" \; E9 A. t- p7 N4 G. T4 e9 A% `+ Author Affiliations
7 Z. g% r4 R/ r' {1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu 2 N- {1 A& j- Q- e% p8 a  G& ?
2Department of Thoracic Surgery, Kyoto University, Kyoto . e( N( J! V/ g% r
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan 7 }% R1 U3 o1 B  @9 I  R& v( s/ N
&#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
& [6 p) t3 N  ]6 }2 X0 ?Received September 3, 2010.
: e! [. k4 s1 t. t- G) ]Revision received November 11, 2010. 6 c5 \/ ]4 }8 N) r
Accepted November 17, 2010.
" @& A6 z- f# n. b' g3 w1 NAbstract. i. |( {% v4 O: V1 v4 c
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.
1 _" ~, N* ^; V% q* X1 LPatients 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. ' Z6 _8 I- ]9 a4 l) \# x9 L, E
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. 6 ]  r8 Z8 G3 |; w8 \& \+ n
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。( P: x; q. d; f# y+ c% H
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?: x  }# W+ r6 i- t
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
' k- E4 Y/ F3 u3 P. S6 O! yhttp://clinicaltrials.gov/ct2/show/NCT015235874 z  M' X  r& v! O  N
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC0 b) D# {2 U$ i( Z# m
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
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7 W" g4 x8 r& K- f7 L6 _9 Z( Q9 ~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。, _% d- B. S& r5 u# B
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 $ o6 M1 I& ^$ n6 C6 f
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。
8 Q* W. {7 w3 A  H3 L# ?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。+ @" [9 Z" c" v' f/ F8 A
不错。

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