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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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1093534 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
, x4 A3 n7 I  A9 F* T7 @: YNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 ( F& Y1 A8 p  {  J9 j4 x, P
+ Author Affiliations- ~9 w/ s6 Z: G% P9 w) O
: F& w) N  |7 U; F
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
, Y. Y( ]2 i% C' M* K! I$ p+ L2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan + K% S+ h9 r9 j" ^3 ^
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
4 X6 H# B/ }8 |, c8 S+ ]; P4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan ) }, y+ p+ |  {
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
3 i  i- Q4 B+ ~6 z9 A6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 4 e/ A0 \4 K7 c5 D. _4 n2 R; `  o
7Kinki University School of Medicine, Osaka 589-8511, Japan ' _7 K+ N0 z+ C1 U! o6 d
8Izumi Municipal Hospital, Osaka 594-0071, Japan $ u; `! w9 F3 l
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
1 k  g; M, F& w$ {/ KCorrespondence 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 * Q4 v! `* U, y( c8 _
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. . L: e. o9 q& V" i. L2 @/ r
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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
" ]  T6 J' E* P+ O* A+ l' u& t9 \& @; |, l% [1 _
Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
) |& n. c1 {$ J6 E( F. O6 ~7 n( L7 r5 s( |& }' g+ }. Z5 R- z, H; p
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  : q+ `: I; D$ b. |

6 w( R) e4 f1 WPublished online on: Thursday, December 1, 2011 3 H0 m2 l6 r, }6 e+ p2 ^. ]

" C! z2 B7 P1 r/ e1 _7 UDoi: 10.3892/ol.2011.507 ' Y8 i  o+ E7 \% v

$ B. }$ O* ]$ [2 U2 ^Pages: 405-410 ! H" E0 u- a6 q9 _. S
* X4 }' ^0 s. ]
Abstract:) T4 Z( e! R7 X8 u, k4 L
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.; C7 V. ^- J' O! G0 e* B$ ~: O

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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, F* _+ U( Q# x( J/ i- l$ D
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 % m# ?6 {, \' U. Y. L: c9 i
+ Author Affiliations6 m/ q  |9 A6 ~0 k
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
. `4 o# i3 w- e* F2Department of Thoracic Surgery, Kyoto University, Kyoto
1 L! O; Q; S0 S7 N$ v- ]3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
" @7 L0 W, X' D! K  u+ \/ H&#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
1 h& E; v! [8 b1 p- F' `) B( SReceived September 3, 2010.   x' p$ Z# v1 Q& ]$ R
Revision received November 11, 2010. ( t: l3 T! D7 i/ \9 ]
Accepted November 17, 2010.
+ R4 a: u! Q* d, @# J$ yAbstract
& g. b5 h: i5 g  m( d5 ]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. , n  K2 v; w9 r7 Z0 e
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. . B' d) ]* z3 a  w& S$ w0 r6 h) {
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.
9 H) U1 f  x! z3 iConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 9 E1 p6 [/ z* Z! z
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。2 Z/ y2 H$ ]) ?, f
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?( u% `  _$ h3 N4 J- A9 c) z) n/ Q
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# _+ W# e, `* J
http://clinicaltrials.gov/ct2/show/NCT01523587  ?* e1 n1 [! L

/ h9 ~( m$ Y" p) I& q7 L0 mBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
# V: s  y( L7 d* z8 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
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# |2 b0 [  {3 [  r* g' S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。* b' w4 |' }  ]6 A
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 ; ]* d* ?$ N( ^" M2 t3 s! w9 A
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。
$ u) v4 C7 g  L, \( I至今为止,未出 ...

1 W$ t+ s9 B& w; y没有副作用是第一追求,效果显著是第二追求。1 N* P9 W1 @4 j' E
不错。

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