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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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1243190 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& p7 [7 t8 }; a$ _
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 : @' T, S, o$ r# I' G) I
+ Author Affiliations% {7 g; B' R0 k3 L+ W1 z; d

! ?# U0 W" ?. B" `0 d1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan   \( Z% L8 x9 t: u: W( A: h
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
2 s% J) h. D) t1 F2 T3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan & K& b; U0 ~! X" d0 l
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan $ g9 H7 g  b) Z# i, T/ V8 L$ P. X
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan 1 b  Q4 ~  K( I) Q
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
3 w. K# T) ~& [$ d0 _0 ^: i0 F7Kinki University School of Medicine, Osaka 589-8511, Japan & D; G) R  Y8 q" p0 n& r1 N6 k
8Izumi Municipal Hospital, Osaka 594-0071, Japan
) H. N/ D/ ~) p( a1 g9 I1 y: S9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan 2 |" d- Z( L/ Z1 O# P& Y/ o$ {
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 ' J! n3 K9 h' k# r( c
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 ; _8 S: J  p9 g

* P  ^, t% Z- k) R/ r6 J7 J3 f- vAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
0 b$ c) W3 m% P5 p- [
8 f: ]/ H% ^" d$ g! WAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  - r9 N( L& I$ ?! s$ R, I2 [

' h) h- ^+ T) v. H$ Y7 VPublished online on: Thursday, December 1, 2011
3 D! a) d% w, m: H% Z# ]+ C# ]& D, X  A5 H, U7 l7 a
Doi: 10.3892/ol.2011.507 0 u8 o& L2 D0 m9 R* X: {
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Pages: 405-410
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Abstract:
1 }4 Q% b: n) g, C  Y' SS-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
& {; h0 D& u1 [F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 ( n! m4 w0 U9 j: J, u. A+ K, _
+ Author Affiliations6 e8 t/ \* h. l; b" V. r# t; \
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
4 b2 z/ o9 I& @; j3 z& e2Department of Thoracic Surgery, Kyoto University, Kyoto
  L5 x! }+ e! B3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan ) J! }. a) o6 {/ _: T, Y
&#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
0 |0 `* T4 f/ kReceived September 3, 2010. ) C$ P+ P' L, e/ L5 b/ q$ C
Revision received November 11, 2010.
* a" ^& j1 y) D3 b! m! a8 t4 b; SAccepted November 17, 2010.
$ `) u. v5 h# n* q: ]0 b% f9 Z. JAbstract
3 `: B# l3 i2 E3 O; s7 S" [0 p  yBackground: 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 o: H5 k9 G& u& a; j8 w) wPatients 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. / `# n' n* S7 _3 d) |7 `1 V* w
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.
1 }' _8 Y; s; N. B* F4 v5 KConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 5 a" C& D# C1 \
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。
* o! }' q) Y% ~4 y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?8 {: F4 J2 m2 k. u; G7 X
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
; l' H6 Z4 ~6 h6 h4 c4 _' ?3 a8 [3 ohttp://clinicaltrials.gov/ct2/show/NCT015235877 D& z' Z  o, m, O# ^4 B; @- r

) i4 v& o& m( E- l# `# s7 u) }BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC, v! A  Z- K& {3 ]& B) X
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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2 C2 w- b0 ]: ~3 a+ Z4 \) T! `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。
8 Z3 W& G4 {8 e; F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 / h# U- W  ~- x: [( w+ z; F0 I+ M! ]
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。
$ G8 E! v, ]* q2 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。3 n: J& R6 r% D+ B: J, z  o/ U
不错。

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