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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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1466521 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
* j& o: _# H( ^+ u$ v( y% BNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
' m/ z- t' O/ q) p) ]* C+ Author Affiliations# C; c5 a8 K( D
4 [$ l2 o; z* I2 ]
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan   r" V5 b6 a* z4 }/ t0 x" K3 A
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
% o* C! T  p9 Y) P6 l3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ( h# d; R( z( P3 z1 y  V' `
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
3 N: b) c8 D+ z7 j1 u5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan 1 X" i" N9 j# W& P+ B: k, [2 `" e
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
& W3 V8 ~3 r  v* G7 |# n7Kinki University School of Medicine, Osaka 589-8511, Japan
# J& l5 k2 @) |' F8Izumi Municipal Hospital, Osaka 594-0071, Japan 6 R7 s4 @/ Z3 s
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
* H$ }- G* S  z/ TCorrespondence 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 * U2 e5 s  P' o5 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
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3 z8 \* o: H% Z! s6 qAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato 6 c+ W& ?% R& v( J3 e
, |4 ?2 W( N* H' E: T2 l
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  : w" A/ x9 j8 A0 {. e- h

& O; ~2 N% h0 C0 _8 M0 }  RPublished online on: Thursday, December 1, 2011 - T. F0 }9 q2 Z, R2 L, v8 U  k4 s

% k1 a3 t' Y7 y: w/ ^Doi: 10.3892/ol.2011.507 - G0 S4 j5 M! b' ]0 @

7 l. ]1 X  ]$ m! U7 RPages: 405-410 1 \% F% {( r4 ^- A) o

; x$ ?# t; G+ eAbstract:4 p% ^- `7 @7 x+ A
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.& C) b7 c2 {9 L

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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! o: t9 C) |8 X! o$ ^
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 4 i% x3 V) w! G( r! ^6 U
+ Author Affiliations
) H$ a5 n& L1 _+ Z+ Y+ v9 H3 {. f1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
4 y# m9 A. C0 J) ]2Department of Thoracic Surgery, Kyoto University, Kyoto 1 D' ^, y  X- X' u5 T- x
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
) [1 u0 E7 x0 {8 P. R7 G' l&#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
  C3 |$ o4 B3 M. ?. pReceived September 3, 2010.
+ ~, k6 ~' {: T+ L1 A1 V  pRevision received November 11, 2010. 8 [( y$ B* J, K: x( r9 O
Accepted November 17, 2010.
* J6 q7 P+ Y6 R$ b* a8 SAbstract# o" n- P' l# O
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 W% a; E2 f, p) |- K6 fPatients 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. ' U( T$ I1 N5 w% }2 B
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 l' h" X  ?7 ~/ U
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 3 y  Q8 }: G: v/ {
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。
; w2 ^3 \9 p1 T) o9 x% p; X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
! f+ `9 ~% O6 S+ Q2 ^8 ]9 vhttp://clinicaltrials.gov/ct2/show/NCT01523587
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC7 q  E" G- V2 c
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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/ X* q+ e& K9 Q8 i0 z# [" c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。
# ~* L3 ]' G3 ~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

2 T$ d4 H0 r& I5 C$ D' S5 _没有副作用是第一追求,效果显著是第二追求。: a3 j8 z4 i0 z/ k3 a# f) ^) p
不错。

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